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NAD+ in Brain Aging and Neurodegenerative Disorders
Open accessAbstract
NAD+ is a pivotal metabolite involved in cellular bioenergetics, genomic stability, mitochondrial homeostasis, adaptive stress responses, and cell survival. Multiple NAD+-dependent enzymes are involved in synaptic plasticity and neuronal stress resistance. Here, we review emerging findings that reveal key roles for NAD+ and related metabolites in the adaptation of neurons to a wide range of physiological stressors and in counteracting processes in neurodegenerative diseases, such as those occurring in Alzheimer's, Parkinson's, and Huntington diseases, and amyotrophic lateral sclerosis. Advances in understanding the molecular and cellular mechanisms of NAD+-based neuronal resilience will lead to novel approaches for facilitating healthy brain aging and for the treatment of a range of neurological disorders.
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TL;DR
This review argues that NAD+ availability declines with brain aging and in Alzheimer’s, Parkinson’s, Huntington’s, and ALS, while NAD+-boosting strategies improve pathology and function in many preclinical models. It also surveys human trial evidence and cautions that causal human data, optimal precursors, and long-term safety remain unresolved.
Key findings
- NAD+ depletion is reported across species and tissues: human brain NAD+ and NAD+/NADH decline with age by non-invasive 31P MR assay; mouse hippocampus shows nearly 40% lower NAD+ at 10–12 months versus 1 month; aged worms also show lower organismal NAD+.
- The review links NAD+ loss to the 10 hallmarks of brain aging, including mitochondrial dysfunction, oxidative damage, impaired autophagy/proteasome function, disturbed calcium handling, weakened adaptive stress responses, reduced network plasticity, defective DNA repair, inflammation, impaired neurogenesis, and senescence/telomere changes.
- In neurodegenerative disease models, NAD+ augmentation with precursors such as NR, NMN, NAM, or NA, or by PARP inhibition/SIRT activation, reduces pathology and improves behavior. Examples include a 30% NAD+ reduction in LRRK2 G2019S dopaminergic neurons, 69% lower NAD+ in PINK1 mutant flies, 78% lower NAD+ in parkin mutant flies, and about 50% lower total NAD+ in Fbxo7-deficient cells or patient fibroblasts.
- Human trials show bioavailability and some safety signals: oral NR at 1,000 mg/day for 7 days raised blood NAD+ up to 2.7-fold and NAAD 45-fold; NRPT raised whole-blood NAD+ by 90%; however, a phase II NAM trial in 15 mild-to-moderate AD patients showed no significant benefit, and NAD+ precursors may carry cancer-related concerns in some contexts.
Methods
- Narrative review synthesizing mechanistic, preclinical, and clinical literature on NAD+ synthesis, metabolism, subcellular balance, brain aging, and neurodegenerative disorders.
- Evidence discussed includes animal models (mice, C. elegans, Drosophila, rhesus monkeys), human postmortem tissue, patient-derived cells/iPSCs, and clinical trials; no new primary data are generated.
- Main analysis is conceptual synthesis, including a proposed model connecting NAD+ depletion to the hallmarks of brain aging and disease-specific pathologies, with tables summarizing preclinical and clinical findings.
Limitations
- The paper states that human data on NAD+ changes during normal aging are sparse and require large, well-controlled population studies; a direct causal role for impaired NAD+-dependent processes in human neurodegenerative disease remains to be established.
- The paper notes unresolved questions about mechanisms upstream/downstream of NAD+ depletion, whether NAD+ precursors increase cancer risk in the general population, and the lack of direct human comparisons among NR, NMN, NA, and NAM.
- Evident from the text: as a review, it does not perform a systematic search or meta-analysis, and many cited clinical trials are small or short (for example, 15 AD patients in the NAM phase II trial and 20 ALS patients in the EH301 pilot), with mixed outcomes.
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In the paper
“While the aspartate pathway is the de novo NAD+ pathway in most photosynthetic eukaryotes, the kynurenine pathway is the only de novo NAD+ synthetic pathway in mammals.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
- Not checked yetcites Vécsei et al., 2013 source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIn the paper
“Three mammalian NMNATs exist, NMNAT1–3, showing neuroprotective effects in both mice and D. melanogaster models (Ali et al., 2013).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
- Not checked yetcites Ali et al., 2013 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIn the paper
“The kynurenine pathway exhibits “double-edged sword” effects on neurons with both neuroprotective metabolites (tryptophan, kynurenic acid, and picolinic acid) and neurotoxic intermediates, including 3-hydroxykynure-nine (3-HK) that generates free radicals, 3-hydroxyanthranilic acid (3-HAA), and quinolinic acid (that induces glutamate receptor excitotoxicity) (Figure 1).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
- Not checked yetcites Vécsei et al., 2013 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIn the paper
“In addition to ATP loss, hyperactivation of PARP1-induced NAD+ depletion can induce neuronal loss and accelerated aging (Fang et al., 2016a).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not checked yetcites Fang et al., 2016a
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesNone of the sources cited for this claim could be matched to a paper in Crossref, so there is nothing to check it against.
In the paper
“However, excessive PARP1 activation can trigger cell death, termed parthanatos, through a mechanism in which PAR formation triggers the release of mitochondrial apoptosis-inducing factor (AIF) from the cytosolic side of the mitochondrial outer membrane. AIF is then translocated to the nucleus to activate macrophage migration inhibitory factor (MIF, a nuclease), which finally results in MIF-depend”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not matchedcites Wang et al., 2011, 2016
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not matchedcites Yu et al., 2002
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Not matched
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“In addition to cellular bioenergetics, NAD+ is also a substrate for different NAD+-consuming proteins, which catabolize NAD+ to NAM. They are class III histone deacetylases sirtuins (SIRTs), poly (ADP-ribose) polymerases (PARPs), ADP ribosyl-cyclases (CD38/CD157), and NADase sterile alpha and TIR motif-containing 1 (SARM1) (Figure 1).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesNone of the sources cited for this claim have been checked yet.
In the paper
“For example, SIRT1 consumes NAD+ to regulate glycolysis, gluconeogenesis, and mitochondrial homeostasis via the balance between mitochondrial biogenesis and mitophagy and adaptive responses of neurons to exercise and metabolic/excitatory challenges (Bonkowski and Sinclair, 2016; Cheng et al., 2016; Fang, 2019).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not checked yetcites Bonkowski and Sinclair, 2016
- Not checked yetcites Cheng et al., 2016 source
- Not checked yetcites Fang, 2019
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesNone of the sources cited for this claim have been checked yet.
In the paper
“In neurons, NMNAT2 localizes to Golgi and Rab7-containing late endosomes as well as to both synaptic terminals and axons (Gilley and Coleman, 2010; Mayer et al., 2010).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
What the sources say
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIn the paper
“In line with the role of NAD+ in maintaining healthy brain function, genetic approaches to reduce brain NAD+ production via CA1-region-specific knockdown of Nampt recapitulate hippocampal cognitive phenotypes of old mice (Johnson et al., 2018).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ in Normal Brain Aging
What the sources say
- Not checked yetcites Johnson et al., 2018 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIn the paper
“In mice, there was a nearly 40% decrease of NAD+ levels in the hippocampus in 10- to 12-month-old mice compared with 1-month-old mice (Stein and Imai, 2014).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ in Normal Brain Aging
What the sources say
- Not checked yetcites Stein and Imai, 2014
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes
- It may state two separate claims as one. 123
- Probably not a substantial claim. 25
- The quote only partly states this claim. 1
In the paper
“The ambient levels of these metabolites are determined by different enzymes, which in the brain are preferentially localized in microglia and astrocytes, suggesting necessary glial cell-neuron communication (Schwarcz and Pellicciari, 2002).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
- Not checked yetcites Schwarcz and Pellicciari, 2002
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“The NAD+ salvage pathway starts from the recycling of nicotinamide (NAM) to nicotinamide mononucleotide (NMN) by intracellular nicotinamide phosphoribosyltransferase (iNAMPT), followed by the conversion of NMN into NAD+ via the NMNATs (Bogan and Brenner, 2008; Verdin, 2015).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Experimental evidence suggests that blood NA and NAM are able to cross the plasma membrane, while blood NAD+ cannot be taken up by cells directly but needs to be converted to smaller uncharged molecules to enter the cells (Hara et al., 2007; Ratajczak et al., 2016).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“While kynurenic acid is an NMDA receptor antagonist, quinolinic acid is an NMDA receptor agonist (Vécsei et al., 2013).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
- Not checked yetcites Vécsei et al., 2013 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“While NMNAT1 and NMNAT3 are ubiquitously expressed, NMNAT2 is enriched in the brain, and adequate levels of NMNAT2 seem to be essential for axon development and survival (Gilley et al., 2019).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
- Not checked yetcites Gilley et al., 2019 source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“The kynurenine pathway modulates neuronal functions as it is involved in the synthesis of two fundamental neuro-transmitters (glutamate and acetylcholine) as well as regulates N-methyl-D-aspartate (NMDA) receptor activity and free radical production (Vécsei et al., 2013).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
- Not checked yetcites Vécsei et al., 2013 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Additionally, nicotinamide riboside (NR) integrates in this pathway via the conversion of NR into NMN by nicotinamide riboside kinase 1 (NRK1) or NRK2 (Bieganowski and Brenner, 2004; Ratajczak et al., 2016).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“NAD+ is a vital redox cofactor for metabolism and ATP production, and a key substrate for at least four families of enzymes involved in healthspan and longevity (Fang et al., 2017; Gomes et al., 2013; Verdin, 2015).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“The ratio of NAD+/NADH is important in various bioenergetic reactions in different subcellular compartments, and increased activity of one of these reactions can influence the metabolic homeostasis via changes in the NAD+/NADH ratio (Ying, 2008).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not checked yetcites Ying, 2008 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“NAD+ plays an essential role in glycolysis and the citric acid (TCA) cycle, by its ability to accept hydride equivalents, forming NADH during ATP production (Krebs, 1970; Wallace, 2012).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“Extracellularly, NAD+ can be digested to NAM by the membrane-bound CD38 and CD157, with NAM further metabolized into NMN by extracellular NAMPT (eNAMPT); however, NAD+ can also be converted directly into NMN by CD73 (Bogan and Brenner, 2008; Verdin, 2015).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“A newly reported NMN transporter, the Slc12a8, is highly expressed and regulated by NAD+, in the murine small intestine, and Slc12a8 deficiency abrogates the uptake of NMN in vitro and in vivo (Grozio et al., 2019).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
- Not checked yetcites Grozio et al., 2019 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Additionally, the conversion of NAD+ to NADP+/NADPH is important in the involvement of different cellular functions, including antioxidation and generation of oxidative stress, calcium homeostasis, and cell survival or death (Ying, 2008).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not checked yetcites Ying, 2008 source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“NADH is one of the central electron donors in oxidative phosphorylation (OXPHOS) in the mitochondria, providing electrons to the electron transport chain (ETC) to generate ATP (Krebs, 1970; Wallace, 2012).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Studies in mice and humans indicate that NR supplementation dramatically upregulates intracellular NAAD, suggesting unknown NAD+ metabolic pathways, including possibilities of NAD+ conversion to NAAD and/or NMN to nicotinic acid mononucleotide (NAMN) (Trammell et al., 2016a).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Synthesis in Cells
What the sources say
- Not checked yetcites Trammell et al., 2016a
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Furthermore, SIRT1 has been shown to promote neurite outgrowth and axon development, in addition to regulating dendritic arborization, long-term potentiation and learning, and memory (Gao et al., 2010).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not checked yetcites Gao et al., 2010 source
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Experimental evidence supports that PARP1 transfers the first ADP-ribose moiety from NAD+ to lysine, arginine, glutamate, aspartate, and serine residues on an acceptor protein, followed by addition of multiple ADP-ribose units to the preceding ones, thereby forming poly(ADP-ribose) (PAR) chains (Bonfiglio et al., 2017; Daniels et al., 2014).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“In mammals, there are seven SIRTs, which regulate a large number of cellular pathways, including neuronal survival, stem cell rejuvenation, cancer, and healthy longevity (Chalkiadaki and Guarente, 2015).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not checked yetcites Chalkiadaki and Guarente, 2015
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“The majority of PARylation is executed by PARP1, which participates in a number of necessary cellular processes, such as DNA repair, DNA/RNA metabolism, and cellular stress response.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“PARP1 is critical in the stabilization of DNA repair forks, with its catalytic activity necessary for multiple DNA repair pathways, such as the repair of single-strand breaks, bulky lesions, and double-strand breaks (DSBs) (Ray Chaudhuri and Nussenzweig, 2017).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not checked yetcites Ray Chaudhuri and Nussenzweig, 2017 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Notably, excessive PARP1 activation induces ATP depletion through PAR-dependent inhibition of hexokinase activity, resulting in dysfunctional glycolysis, a mechanism likely independent of NAD+ depletion (Andrabi et al., 2014; Fouquerel et al., 2014).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Among the 17 PARPs, only four of them are capable of adding multiple ADP-ribose units (poly[ADP-ribosyl]ation) or PARylation; they are PARP1, PARP2, PARP5a (tankyrase 1), and PARP5b (tankyrase 2) (Leung, 2017; Rouleau et al., 2010).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“While a small fraction of NAMPT has been shown to co-purify with mitochondria in liver extracts (Yang et al., 2007), results from mitochondrial purification and immunofluorescence in cell lines suggested an exclusion of NAMPT from the mitochondrial matrix, suggesting the lack of NAM recycling to NAD+ in the mitochondria (Pittelli et al., 2010).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
What the sources say
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“SARM1 is a newly recognized class of NADase that cleaves NAD+ into NAM, ADPR, and cADPR via its TIR domain. It is expressed in both brain and non-brain tissues, including the liver (Essuman et al., 2017; Pan and An, 2018).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Despite CD38 being a lymphocyte differentiation antigen, it is also expressed in the brain (Mizuguchi et al., 1995), and CD38 knockout mice show significant protection against ischemic brain damage (Long et al., 2017).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“CD38 catalyzes the synthesis of the Ca2+-responsive messenger cyclic ADP-ribose (cADPR) by use of NAD+ and plays a key role in multiple physiological processes such as immunity, metabolism, inflammation, and even social behaviors (Jin et al., 2007).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not checked yetcites Jin et al., 2007 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“SIRTS, PARPs, CD38/CD157, and SARM1 compete with each other to consume cellular NAD+; thus, the hyperactivation of one enzyme can impair the activities of other NAD+-dependent enzymes.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Two major mechanisms are involved in the regulation of subcellular balance of NAD+, including the expression of subcellular-specific NAD+-synthetic enzymes and subcellular transporters for NAD+ and related metabolites.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“NAD+ is in constant equilibrium between synthesis, consumption, and recycling in various subcellular compartments, including the cytoplasm, nucleus, mitochondria, and Golgi apparatus.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“The three mammalian NMNATs include the nuclear NMNAT1, the cytoplasmic NMNAT2, and the mitochondrial NMNAT3, which is also present in the cytosol (Berger et al., 2005).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
What the sources say
- Not checked yetcites Berger et al., 2005 source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Similarly, NAMPT (Figure 1) is primarily localized in the nucleus and cytoplasm, where it regulates subcellular NAD+ levels.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“While CD38 molecules are expressed in both a type II form(i.e., large extracellular C-terminal) and a type III form (with its catalytic domain facing the cytosol) (Liu et al., 2017, 2008), there is an age-dependent increase of CD38, which may contribute to cellular NAD+ depletion and impaired mitochondrial function (Camacho-Pereira et al., 2016).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not checked yetcites Camacho-Pereira et al., 2016 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“The NADase activity of SARM1 may contribute to its role in axonal degeneration (Essuman et al., 2017) and is therefore a potential target for therapeutic intervention in neurodegenerative diseases.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not checked yetcites Essuman et al., 2017 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“SARM1 exhibits both cyclase and glycohydrolase activities, and the estimated Michaelis constant (Km) is 24 μM, which is similar to that of the other known NAD+-consumers (PARP1, 50–97 μM; SIRT1, 94–96 μM; CD38, 15–25 μM) (Cantó et al., 2015).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Has Numerous Functions in Cells
What the sources say
- Not checked yetcites Cantó et al., 2015 source
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“While the existence of mitochondrial NAD+ transporters is well documented in yeast and plants, a mammalian counterpart has yet to be identified.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
Strength:boosted· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Furthermore, some NAD+ transporters (SLC25A17) localize in peroxisomes, where NAD+ participates in b-oxidation like in mitochondria (Agrimi et al., 2012).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
What the sources say
- Not checked yetcites Agrimi et al., 2012 source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Peroxisomes have recently been shown to have a shared mitochondrial and endoplasmic reticulum (ER) origin, further linking the function of mitochondria and peroxisomes (Sugiura et al., 2017).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
What the sources say
- Not checked yetcites Sugiura et al., 2017 source
Strength:boosted· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“Recent studies have demonstrated that both NMN and NAD+/NADH can be transported into the mitochondria by unknown systems, and that NMN is converted to NAD+ by NMNAT3 within the mitochondrial matrix, whereas NR is likely converted to NMN or NAD+ in the cytoplasm before transport into mitochondria (Davila et al., 2018; Nikiforov et al., 2011).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
What the sources say
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“In addition to a role in mitophagy, USP30 was recently demonstrated to be involved in the peroxisome-specific degradation process, pexophagy. Peroxisomes have a half-life of 1.5–2.5 days, though pexophagy can be regulated by the metabolic state of the cells. This suggests a role for NAD+ in pexophagy regulation (Marcassa et al., 2018).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
What the sources say
- Not checked yetcites Marcassa et al., 2018 source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Furthermore, in the pentose phosphate pathway (PPP), glucose-6-phosphate (G6P) dehydrogenase (G6PD) converts G6P to 6-p-gluconate, when the NAD+-dependent SIRT2 deacetylates and activates G6PD. The PPP pathway converts NADP+ to NADPH and regenerates the antioxidant glutathione (GSH), thus promoting cell survival during oxidative stress (Wu and Sinclair, 2014).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Synthesis and Metabolism > NAD+ Subcellular Equilibrium
What the sources say
- Not checked yetcites Wu and Sinclair, 2014
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Possible explanations for reduced cellular NAD+ during aging include increased NAD+ consumption by PARPs and CD38 (Camacho-Pereira et al., 2016; Fang et al., 2014) and reduced NAD+ production, such as that evidenced by reduced eNAMPT in the aged mice and humans (Yoshida et al., 2019).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ in Normal Brain Aging
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“The mechanism underlying the benefits of NAD+ augmentation likely involves reduced levels of DNA damage, leading to decreased PARP1 activity.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ Depletion in Premature Aging Diseases with Neurodegeneration
What the sources say
- Not checked yetcites Fang et al., 2016b
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Additionally, increased SIRT1 and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) activities were observed after NAD+ augmentation, which, when combined with enhanced DNA repair, suggest improved nuclear-to-mitochondrial communication (Fang et al., 2016b).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ Depletion in Premature Aging Diseases with Neurodegeneration
What the sources say
- Not checked yetcites Fang et al., 2016b
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Furthermore, adding extracellular vesicles containing eNAMPT improved cognitive/neuronal function and extended lifespan in WT mice (Yoshida et al., 2019).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ in Normal Brain Aging
What the sources say
- Not checked yetcites Yoshida et al., 2019 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Moreover, NAD+ augmentation restores mitochondrial function and bioenergetics, leading to enhanced neuronal survival and improved cognitive function in premature aging animal models.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ Depletion in Premature Aging Diseases with Neurodegeneration
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“During aging, the cellular milieu of the brain exhibits mitochondrial dysfunction, intracellular accumulation of oxidatively damaged macromolecules (DNA, lipids, and proteins), dysregulated energy metabolism, impaired cellular “waste disposal” mechanisms, impaired adaptive stress response signaling, compromised DNA repair, aberrant neuronal network activity, dysregulated neuronal Ca2+ handling,”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Mattson and Arumugam, 2018
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“NMN treatment improved cognition in this Nampt-knockdown (CA1) mouse model, partially through upregulation of calcium/calmodulin-dependent serine protein kinase (Cask), a potential downstream effector, in a SIRT1-dependent manner (Johnson et al., 2018).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ in Normal Brain Aging
What the sources say
- Not checked yetcites Johnson et al., 2018 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Two hallmarks of aging in proliferative tissues, including cellular senescence and telomere damage, may also apply in some types of glial cells and neural progenitor cells in the brain, but this remains elusive (Mattson and Arumugam, 2018).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Mattson and Arumugam, 2018
Strength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Mitochondria generate ATP to support neuronal activities including neurotransmission and Ca2+ homeostasis and are a source of signals that regulate nuclear-mitochondrial communication and even the arbitration of neuronal survival and death (Mattson et al., 2008).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Mattson et al., 2008 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“NAD+ is central to mitochondrial homeostasis, including in mitochondrial biogenesis, mitophagy, the mitochondrial unfolded protein response (UPRmt), and nuclear-mitochondrial communication (Fang et al., 2014; Gomes et al., 2013; Mouchiroud et al., 2013).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Mitochondria isolated from animal and post-mortem human brain tissues show an age-dependent rise in mitochondrial functional heterogeneity, increased oxidative damage, reduced function of the ETC, disrupted membrane potential, impaired Ca2+ handling, and/or an accumulation of dysfunctional mitochondria (Lin and Beal, 2006; Mattson et al., 2008; Sorrentino et al., 2017).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“During aging, neurons accumulate dysfunctional proteins and subcellular organelles as a result of the actions of reactive oxygen species (ROS). This has been exemplified by the observed increase in oxidative damage to DNA, proteins, and lipids in the aging brain (Mattson and Arumugam, 2018).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Mattson and Arumugam, 2018
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Superoxide produced during mitochondrial electron transport and via the activity of NADPH oxidase are the two major routes of cellular ROS production, and both NAD+/NADH and NADP+/NADPH play key roles in cellular antioxidant systems (Ying, 2008).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Ying, 2008 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“In quiescent NSCs from old mice, an age-dependent reduction of lysosome activity with accumulated protein aggregates was observed.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Leeman et al., 2018 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“In the adult brain, the autophagy-lysosome pathway keeps healthy brain function via the maintenance of the survival and function of mature neurons and keeping a “youthful state” of NSC pool.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Accordingly, long-lived animals, including the naked mole-rat, rodents maintained on calorie restricted (CR) and intermittent fasting (IF) diets, and long-lived daf-2 mutant worms exhibit decreased levels of oxidative damage and are more resistant to oxidative stress (Fontana and Partridge, 2015; Guarente and Kenyon, 2000; Pérez et al., 2009).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Reduced NAD+ levels play a pivotal role in brain aging and neurodegenerative disorders because NAD+ replenishment improves mitochondrial function and mitochondrial biogenesis and reduces accumulation of damaged mitochondria in both premature aging models and Alzheimer’s disease (AD) models (Fang et al., 2014, 2016a; Scheibye-Knudsen et al., 2014).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not matchedcites Fang et al., 2014, 2016a
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
- Not checked yetcites Scheibye-Knudsen et al., 2014 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Not matched
None of the sources cited for this claim have been checked yet.
In the paper
“As we age, levels of autophagy and proteasomal degradation gradually decline, leading to proteinopathies, a result of aberrant protein misfolding and aggregation (Menzies et al., 2015; Nixon, 2013).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Genetic (expression of the transcription factor EB/TFEB, a master regulator of autophagy and lysosome biogenesis) or pharmacological (feeding with the mTOR inhibitor rapamycin) enhancement of the lysosome activity in old quiescent NSCs cleared protein aggregates and inhibited the NSCs’ activation to maintain the “youthful state” (Leeman et al., 2018).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Leeman et al., 2018 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Similar to age-dependent reduction of autophagy, evidence of impaired UPS in the aging brain arises from studies showing age-dependent accumulation of polyubiquitinated proteins in neurons and a brain region-specific reduction of age-dependent proteasome activity in the hippocampus and cerebral cortex (Keller et al., 2002; Mattson and Arumugam, 2018).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Keller et al., 2002 source
- Not checked yetcites Mattson and Arumugam, 2018
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Impaired UPS can be caused by the global aging process and by intracellular proteinopathies, such as Ab and tau aggregates (Saez and Vilchez, 2014).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Saez and Vilchez, 2014
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“NAD+ levels are reduced in many neurodegenerative diseases, and NAD+ augmentation forestalls pathologies in animal and cell culture models of AD, PD, and HD, at least partially through induction of autophagy/mitophagy (detailed in the next section).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Impaired autophagy with accumulated proteinopathies are common pathological features in many age-predisposed neurodegenerative diseases, including AD, Parkinson’s disease (PD), Huntington disease (HD), and tauopathies. Importantly, impaired lysosome function and autophagy/mitophagy are common features among them (Kerr et al., 2017; Lou et al., 2019; Menzies et al., 2015; Nixon, 2013).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Recently, it was shown that knockdown of any of three mitophagy-related genes (pink1, pdr-1, and dct-1) in a C. elegans AD model eliminated benefits of NAD+ augmentation on behavioral deficits, and a similar pivotal role for mitophagy was demonstrated in AD mice and AD patient-derived induced pluripotent stem cells (iPSCs) (Fang et al., 2019).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Fang et al., 2019
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Accordingly, enhancement of UPS can improve healthy aging as well as longevity in disease and aged animals, although the specific benefits to neurons and brain function are still elusive (Saez and Vilchez, 2014; Walther et al., 2015).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Saez and Vilchez, 2014
- Not checked yetcites Walther et al., 2015 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“With advancing age, these stress responses might become impaired, which will render the neurons more vulnerable to various forms of stress of either endogenous or exogenous origin (Mattson et al., 2018). This will in turn compromise synaptic function due to reduced expression and activity of neurotrophic factors and decreased mitochondrial function.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Mattson et al., 2018
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Interestingly, the reduced form of NAD+, NADH, binds and stabilizes 26S proteasomes, and may also regulate the function of 20S proteasomes, the two main proteolytic complexes (Asher et al., 2005; Tsvetkov et al., 2014).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“During aging, the neurons suffer impaired proteostasis and energy production as well as increased oxidative damage, resulting in compromised subcellular Ca2+ handling, which may lead to caspase-regulated apoptosis and PARP1-mediated neuronal death (Bezprozvanny and Mattson, 2008; Mairet-Coello et al., 2013).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Collectively, there is a strong link between impaired autophagy-lysosome and UPS pathways in the aging brain, while detailed linkages between NAD+ levels and such pathways in the aging brain remain to be further studied.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
Strength:boosted· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“As previously mentioned, the strong links between NAD+ and mitochondrial function (ATP production), ROS, and Ca2+ signaling suggest that bolstering cellular NAD+ levels can improve adaptive cellular stress responses in neurons.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“NAD(P) is a precursor of nicotinic acid adenine dinucleotide phosphate (NAADP), cADPR, and ADPR, which are key regulators of Ca2+ signaling and are synthesized by CD38 and CD157 by the use of NAD+ (Figure 1) (Guse, 2015).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Guse, 2015 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“NAADP and cADPR stimulate the release of Ca2+ from ER stores, whereas cADPR regulates the entry of Ca2+ from the extracellular space.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“In neurons, SIRT3 mediates the adaptive responses of neurons to exercise, intermittent fasting, and excitatory challenges and helps prevent noise-induced hearing loss and spiral ganglia neurite degeneration (Brown et al., 2014; Cheng et al., 2016; Liu et al., 2019).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Moreover, NAD+ depletion is evident as a phenotypic driver in many of these DNA damage-induced diseases, including at least CS, XPA, and A-T, since restoration of tissue NAD+ through PARPs inhibition ameliorates disease pathologies (Fang et al., 2014).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Fang et al., 2014 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“For example, mitochondrial NAD+ levels remain unchanged following genotoxic stress and can maintain cell viability in the conditions of depleted nuclear and cytoplasmic NAD+.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Yang et al., 2007 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“In AD mouse models, supplementation with the NAD+ precursor NR inhibited the disease-associated neuroinflammation, decreased the numbers of activated microglia and astrocytes, and reduced pro-inflammatory cytokines (Fang et al., 2019; Hou et al., 2018).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Fang et al., 2019
- Not checked yetcites Hou et al., 2018 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“In different neurodegenerative mouse models including AD, HD, and the premature aging disease A-T, NAD+ augmentation increases the expression and activity of BDNF, leading to enhanced synaptic plasticity and function (Fang et al., 2016a; Hathorn et al., 2011; Liu et al., 2013).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“The neurotrophin brain-derived neurotrophic factor (BDNF) is important in the development, maintenance, and plasticity of the central and peripheral nervous system; it also protects the aging brain against injury and disease through stimulation of glucose transport and mitochondrial biogenesis (Marosi and Mattson, 2014).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
- Not checked yetcites Marosi and Mattson, 2014 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Collectively, impaired DNA repair byproducts and intermediates accumulate in cells of the aging brain and may contribute to numerous human neurological diseases, at least partially through NAD+ depletion driven by hyperactivation of PARP.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“In primary cell culture, supplementation with NR delays cellular senescence (Wiley et al., 2016), and NR treatment also reduces the senescent state in both NSCs and other stem cell types (Zhang et al., 2016).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Collectively, the knowledge so far suggests an important role of reduced NAD+ levels in senescence, though further research is needed to understand the mechanisms upstream and downstream of NAD+ depletion in cell senescence in the aging brain.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ in Brain Aging > NAD+ and the Hallmarks of Brain Aging
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Neurons affected by Aβ and p-Tau neurofibrillary pathology in AD exhibit oxidative damage, impaired Ca2+ handling, defective lysosome function and mitophagy, and reduced DNA repair (Canter et al., 2016; Fang et al., 2019; Mattson et al., 2018; Polanco et al., 2018).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
- Not checked yetcites Canter et al., 2016 source
- Not checked yetcites Fang et al., 2019
- Not checked yetcites Mattson et al., 2018
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“While Aβ, p-Tau, and inflammation are major contributors to AD pathogenesis, NAD+ augmentation can ameliorate cognitive deficits in AD mouse models by suppressing these pathologies.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Knockdown of CD38 in APPswePS1ΔE9 (APP.PS) mice reduced Aβ plaques and soluble Aβ levels, and increased spatial learning, possibly through upregulation of brain NAD+ levels (Blacher et al., 2015).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
- Not checked yetcites Blacher et al., 2015 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Accordingly, NAD+ augmentation inhibited AD-related pathology and cognitive decline in different AD animal models, including 3xTgAD mice treated with NAM (Liu et al., 2013), 3xTgAD/Polβ+/− mice treated with NR (Hou et al., 2018), and in neuronal Aβ1–42 and the neuronal Tau (pro-aggregant F3ΔK280 tau fragment) transgenic C. elegans models (Fang et al., 2019) (summarized in Table 1).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“NAD+ augmentation inhibited Tau phosphorylation at different sites (Thr181, Ser202, Thr205, and Thr231) possibly through suppression of cyclin-dependent kinase 5 (Cdk5)-p25 complex activity (Fang et al., 2019; Green et al., 2008).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
- Not checked yetcites Fang et al., 2019
- Not checked yetcites Green et al., 2008 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Consistent with NHEJ being bolstered by NAD+, NR treatment of ATM-deficient neurons improved neuronal NHEJ activity through deacetylation and activation of the key NHEJ protein Ku70 in addition to facilitating the chromatin binding of Ku70 and DNA-PKcs, an additional NHEJ repair protein (Fang et al., 2016a).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
- Not checked yetcites Fang et al., 2016a
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Four months of NAM treatment increased the level of p25 2-fold, reduced p-TauThr231 levels, and improved cognitive function in 3xTgAD mice (Green et al., 2008).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
- Not checked yetcites Green et al., 2008 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“While LTP is impaired in the 3xTgAD mice, NR restores LTP, correlating with improvements in learning and memory (Hou et al., 2017).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
- Not checked yetcites Hou et al., 2017 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“In mice, the expression and activity of CD38 increase during aging, and CD38 contributes significantly to age-related NAD+ depletion and mitochondrial dysfunction at least in part via inhibition of NAD+/SIRT3 activity (Camacho-Pereira et al., 2016).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
- Not checked yetcites Camacho-Pereira et al., 2016 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In summary, NAD+ augmentation enhances synaptic plasticity and improves memory in different AD mouse models possibly through the reduction of Aβ and p-Tau pathologies and suppression of inflammation (see below).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“Senolytic elimination of Aβ-associated senescent OPCs or Tau pathology-associated senescent glial cells ameliorates cognitive impairment in different AD mouse models (Bussian et al., 2018; Zhang et al., 2019).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“NR supplementation delayed senescence of adult NSCs in 2-year-old mice (Zhang et al., 2016), suggesting a role for a deficit in NAD+ or one or more of the enzymes it supports in neural-cell senescence.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
- Not checked yetcites Zhang et al., 2016 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“ALS has been linked to NAD+ metabolism via impairment of the kynurenine pathway and the potential involvement of altered SIRT1 and SIRT3 activities.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and ALS
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“As evidenced, neurons expressing the LRRK2 G2019S mutation exhibit mitochondrial dysfunction and a 30% reduction of NAD+ levels.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and PD
What the sources say
- Not checked yetcites Schwab et al., 2017 source
- Not checked yetcites Sison and Ebert, 2018
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“NAD+-induced mitophagy likely plays a major role in the observed benefits, as mutation of key mitophagy genes (pink1, parkin/pdr-1, and nix/dct-1) abolishes NAD+- dependent memory improvement in Aβ and p-Tau C. elegans models (Fang et al., 2019).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
- Not checked yetcites Fang et al., 2019
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“NAD+ augmentation via NR supplementation induced UPS in both the hippocampus and cortex of Tg2576 AD mice (Gong et al., 2013) and restored UPRmt in APPswe/PSEN1dE9 AD mice.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and AD
What the sources say
- Not checked yetcites Gong et al., 2013 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Knockdown of PINK1 expression in primary neurons and neuroblastoma cells causes increased oxidative stress and 50% reduction of NADH levels (Gandhi et al., 2009).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and PD
What the sources say
- Not checked yetcites Gandhi et al., 2009 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“PD is a progressive fatal neurological disorder of aging that profoundly impairs one’s ability to control body movements as the result of loss of dopaminergic neurons in the substantia nigra, which exhibit abnormal accumulation of α-synuclein fibrils in their cell body and neurites (Kam et al., 2018; Spillantini et al., 1997).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and PD
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Dopaminergic neurons derived from iPSCs expressing mutant GBA exhibit a reduced cytosolic NAD+/NADH ratio, although no significant change of total cellular NAD+ was seen (Schöndorf et al., 2018).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and PD
What the sources say
- Not checked yetcites Schöndorf et al., 2018 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“In ALS patients, there were higher levels of CSF and serum tryptophan, kynurenine, and quinolinic acid, and decreased serum picolinic acid”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and ALS
What the sources say
- Not checked yetcites Chen et al., 2010 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“SIRT3 expression has been linked to ALS in a PGC-1α-dependent pathway, though the mechanism remains unknown”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and ALS
What the sources say
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Though NAD+ levels were not reported, all the data suggest an inflammation-related excitotoxic-chelation defective mechanism in ALS patients.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and ALS
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The discrepancies between the findings on SIRT1 levels in ALS might be due to different cell lines used or altered expression of SIRT1 during disease progression.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and ALS
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“there was higher microglial inflammation and increased neuronal and microglial expression of indoleamine 2,3-dioxygenase and quinolinic acid in the motor cortex and spinal cord tissues from ALS patients”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and ALS
What the sources say
- Not checked yetcites Chen et al., 2010 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“SIRT1, SIRT3, and/or SIRT6 are likely activated as a result of improved NAD+ salvage, leading to decreased acetylation of IDH2 and activation of Nrf2, thereby improving the resistance of motor neurons to oxidative stress and the mitochondrial function”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and ALS
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“SIRT1 activity is altered in mouse models of ALS and in postmortem tissue samples from ALS patients; however, the direction of change has been debated”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and ALS
What the sources say
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“enhancement of the NAD+ salvage pathway protects astrocytes expressing an ALS-linked mutant SOD1 and thereby promotes motor neuron survival”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and ALS
What the sources say
- Not checked yetcites Harlan et al., 2016 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“NAD+ precursor treatment (NMN or NR) or NAMPT overexpression results in increased oxidative stress resistance in motor neurons and prevents the toxicity of co-cultured SOD1-mutant astrocytes.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and ALS
What the sources say
- Not checked yetcites Harlan et al., 2016 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“up to 2.7-fold increased NAD+ levels and 45-fold increase in the intermediate NAAD in human blood after oral NR supplementation (1,000 mg/day for 7 days)”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
- Not checked yetcites Trammell et al., 2016a
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“NR is orally bioavailable, and it is well tolerated and elevates NAD+ in healthy middle-aged and older adults as well as in old diabetic males.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The involvement of cellular NAD+ depletion and the potential therapeutic benefits of treatments that bolster NAD+ levels include, but are not limited to, AD, PD, HD, and ALS.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Depletion in Different Neurological Disorders with NAD+ Replenishment in Neural Resilience > NAD+ and ALS
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“the data confirmed that NR was bioavailable and safe, with potential cardiovascular benefits”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
- Not checked yetcites Martens et al., 2018 source
Tests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“at least four independent clinical trials indicate NR supplementation (1–2 g/day for up to 3 months) is orally bioavailable and relatively safe.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“the clinical data showing NAM is relatively safe (1,000–2,000 mg/day) and is readily absorbed from the gastrointestinal tract with peak serum concentrations in 1 h after oral ingestion”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“NRPT treatment increased whole blood NAD+ levels by 90% with no serious adverse events”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
- Not checked yetcites Dellinger et al., 2017 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“However, NAM did not show any significant effects”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
- Not checked yetcites Phelan et al., 2017
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesThe quote only partly states this claim.
In the paper
“All patients in the EH301 group choose to continue the treatment after 4 months, and thus the treatment was finalized after 1-year treatment, where no deterioration, except of FVC, was observed”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
- Not checked yetcites de la Rubia et al., 2019 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“increased NAD+, through either overexpressed NAD+ synthetic enzymes or supplementation with NAD+ precursors, promotes cancer cell proliferation, migration, and resistance to anticancer chemo-/radiotherapy”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > A Cautionary Note on Interventions that Bolster NAD+ Levels
What the sources say
- Not checked yetcites Demarest et al., 2019 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“strategies to deplete cellular NAD+ and the inhibition of NAD+ synthetic enzymes can trigger cancer cell death”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > A Cautionary Note on Interventions that Bolster NAD+ Levels
What the sources say
- Not checked yetcites Buonvicino et al., 2018 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“NRPT/EH301 treatment improved ALS functional rating scale revised (ALSFRS-R), increased the MRC grading scale index (grades muscle power), and forced vital capacity (FVC, functional respiratory capacity test), as well as increased electrical activity in muscles.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
- Not checked yetcites de la Rubia et al., 2019 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“500 mg NA twice a day improved rigidity and bradykinesia, while a higher dose at 1,000 mg twice a day produced severe nightmares and skin rash”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
- Not checked yetcites Alisky, 2005 source
Tests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“painful flushing is a common side effect of high NA doses”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
- Not checked yetcites DiPalma and Thayer, 1991
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“The study was a randomized double-blind design and included both males and females.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
- Not checked yetcites de la Rubia et al., 2019 source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Despite the low level of participants in this study, it sets the stage for the potential for NAD+ augmentation/SIRT1 activation as a treatment for ALS, and large-scale phase trials are warranted.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Clinical Trials
What the sources say
- Not checked yetcites de la Rubia et al., 2019 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim. It may state two separate claims as one.
In the paper
“the gut-to-brain axis may also show effects of NAD+ augmentation and, hereby, provide a new target of interest in neurodegenerative diseases”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Outstanding Questions and Future Perspectives
What the sources say
- Not checked yetcites Blacher et al., 2019 source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“cancer cells and post-mitotic cells exhibit a completely different metabolism, which may explain why the neuroprotective conditions of NAD+ augmentation and autophagy (Sousa et al., 2016) can also promote the growth of specific cancers (e.g., pancreatic cancer).”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > A Cautionary Note on Interventions that Bolster NAD+ Levels
What the sources say
- Not checked yetcites Sousa et al., 2016 source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Rests on an assumption: Cancer cells and post-mitotic cells have fundamentally different metabolism despite both having high energy demand.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Emerging findings are revealing a critical role for NAD+ in neural resilience and in the molecular mechanisms of the hallmarks of brain aging.”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Outstanding Questions and Future Perspectives
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“A phase-III randomized large clinical trial reported that oral NAM was safe and effective in reducing the rates of new nonmelanoma skin cancers and actinic keratosis in high-risk patients”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > A Cautionary Note on Interventions that Bolster NAD+ Levels
What the sources say
- Not checked yetcites Chen et al., 2015 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Emerging evidence suggests NAD+ depletion in brain cells is common during aging and is accentuated in many neurodegenerative disorders including AD, PD, HD, and ALS, and that NAD+ augmentation inhibits pathological features in animal models of these disorders”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Outstanding Questions and Future Perspectives
What the sources say
- Not checked yetcites Table 1
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“NAD+ depletion and mitochondrial abnormalities have been shown, and beneficial effects of NAM treatment of mouse models have been reported”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Outstanding Questions and Future Perspectives
What the sources say
- Not checked yetcites Williams et al., 2017 source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
None of the sources cited for this claim have been checked yet.
In the paper
“the ketone β-hydroxybutyrate, which elevates NAD+ levels in neurons and has been shown to suppress Aβ and p-Tau pathologies and ameliorate behavioral deficits in a mouse model of AD”
§ NAD+ in Brain Aging and Neurodegenerative Disorders > NAD+ Restoration as a Therapeutic Strategy > Outstanding Questions and Future Perspectives
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The paper relies on this without support.
Mechanisms of NAD+ depletion and benefits of NAD+ augmentation observed in animal models apply to human brain aging and neurodegenerative disorders.
“While mounting evidence in animals shows age-dependent NAD+ depletion, similar data on NAD+ changes through normal aging in humans are sparse, and data from large, well-controlled population studies will be required.”
The paper relies on this without support.
Understanding NAD+-based neuronal resilience mechanisms will lead to novel approaches for healthy brain aging and treatment of neurological disorders.
“Advances in understanding the molecular and cellular mechanisms of NAD+-based neuronal resilience will lead to novel approaches for facilitating healthy brain aging and for the treatment of a range of neurological disorders.”
The paper relies on this without support.
Cancer cells and post-mitotic cells have fundamentally different metabolism despite both having high energy demand.
“Despite both being nutrition demanding, cancer cells and post-mitotic cells exhibit a completely different metabolism”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“NAD+ augmentation ameliorates both Aβ and p-tau pathologies and neuroinflammation.125”
From Antiageing strategy for neurodegenerative diseases: from mechanisms to clinical advances (2025) · cites this paper as [125]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Opposite effects of lysosome activation on neural stem-cell activation
MinorThe review says enhancing lysosome activity inhibited activation of quiescent neural stem cells, but the cited reference's title says lysosome activation enhanced it.
“Genetic (expression of the transcription factor EB/TFEB, a master regulator of autophagy and lysosome biogenesis) or pharmacological (feeding with the mTOR inhibitor rapamycin) enhancement of the lysosome activity in old quiescent NSCs cleared protein aggregates and inhibited the NSCs’ activation to maintain the “youthful state” (Leeman et al., 2018).”
“Lysosome activation clears aggregates and enhances quiescent neural stem cell activation during aging.”
Citations
Cites
2 retracted
RETRACTED ARTICLE: Parkin and PINK1 mitigate STING-induced inflammation
Sliter, D. A., Martinez, J., Hao, L., Chen, X., Sun, N., Fischer, T. D., Burman, J. L., Li, Y., Zhang, Z., Narendra, D. P., et al. (2018) · Nature · doi:10.1038/s41586-018-0448-9 · Cited by 1,287
RetractedAge related changes in NAD+ metabolism oxidative stress and Sirt1 activity in wistar rats
Braidy, N., Guillemin, G. J., Mansour, H., Chan-Ling, T., Poljak, A., & Grant, R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019194 · Cited by 594
RetractedRepertoires of Autophagy in the Pathogenesis of Ocular Diseases
Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351
Spillantini, M. G., Schmidt, M. L., Lee, V. M.-Y., Trojanowski, J. Q., Jakes, R., & Goedert, M. (1997) · Nature · doi:10.1038/42166 · Cited by 8,382
Mitochondrial Dysfunction and Oxidative Stress in Neurodegenerative Diseases
Lin, M. T., & Beal, M. F. (2006) · Nature · doi:10.1038/nature05292 · Cited by 6,455
Dementia prevention, intervention, and care
Livingston, G., Sommerlad, A., Orgeta, V., Costafreda, S. G., Huntley, J., Ames, D., Ballard, C., Banerjee, S., Burns, A., Cohen-Mansfield, J., et al. (2017) · The Lancet · doi:10.1016/s0140-6736(17)31363-6 · Cited by 6,072
Poewe, W., Seppi, K., Tanner, C. M., Halliday, G. M., Brundin, P., Volkmann, J., Schrag, A.-E., & Lang, A. E. (2017) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2017.13 · Cited by 5,415
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
Kitada, T., Asakawa, S., Hattori, N., Matsumine, H., Yamamura, Y., Minoshima, S., Yokochi, M., Mizuno, Y., & Shimizu, N. (1998) · Nature · doi:10.1038/33416 · Cited by 5,227
Cui, C., Cui, J., Jin, F., Cui, Y., Li, R., Jiang, X., Tian, Y., Wang, R. C., Jiang, P., & Gao, J. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479571 · Cited by 5,214
Transcriptional silencing and longevity protein Sir2 is an NAD-dependent histone deacetylase
Imai, S.-I., Armstrong, C. M., Kaeberlein, M., & Guarente, L. (2000) · Nature · doi:10.1038/35001622 · Cited by 3,510
Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1
Valente, E. M., Abou-Sleiman, P. M., Caputo, V., Muqit, M. M. K., Harvey, K., Gispert, S., Ali, Z., Del Turco, D., Bentivoglio, A. R., Healy, D. G., et al. (2004) · Science · doi:10.1126/science.1096284 · Cited by 3,481
Complement and microglia mediate early synapse loss in Alzheimer mouse models
Hong, S., Beja-Glasser, V. F., Nfonoyim, B. M., Frouin, A., Li, S., Ramakrishnan, S., Merry, K. M., Shi, Q., Rosenthal, A., Barres, B. A., et al. (2016) · Science · doi:10.1126/science.aad8373 · Cited by 3,343
Wallace, D. C. (2012) · Nature Reviews Cancer · doi:10.1038/nrc3365 · Cited by 2,404
Ravikumar, B., Vacher, C., Berger, Z., Davies, J. E., Luo, S., Oroz, L. G., Scaravilli, F., Easton, D. F., Duden, R., O'Kane, C. J., et al. (2004) · Nature Genetics · doi:10.1038/ng1362 · Cited by 2,347
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
Sidransky, E., Nalls, M. A., Aasly, J. O., Aharon-Peretz, J., Annesi, G., Barbosa, E. R., Bar-Shira, A., Berg, D., Bras, J., Brice, A., et al. (2009) · New England Journal of Medicine · doi:10.1056/nejmoa0901281 · Cited by 2,135
The role of autophagy in neurodegenerative disease
Nixon, R. A. (2013) · Nature Medicine · doi:10.1038/nm.3232 · Cited by 2,059
Li, J.-Y., Englund, E., Holton, J. L., Soulet, D., Hagell, P., Lees, A. J., Lashley, T., Quinn, N. P., Rehncrona, S., Björklund, A., et al. (2008) · Nature Medicine · doi:10.1038/nm1746 · Cited by 1,845
Mediation of Poly(ADP-Ribose) Polymerase-1-Dependent Cell Death by Apoptosis-Inducing Factor
Yu, S.-W., Wang, H., Poitras, M. F., Coombs, C., Bowers, W. J., Federoff, H. J., Poirier, G. G., Dawson, T. M., & Dawson, V. L. (2002) · Science · doi:10.1126/science.1072221 · Cited by 1,826
The multifaceted roles of PARP1 in DNA repair and chromatin remodelling
Ray Chaudhuri, A., & Nussenzweig, A. (2017) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.53 · Cited by 1,786
Fang, E. F., Hou, Y., Palikaras, K., Adriaanse, B. A., Kerr, J. S., Yang, B., Lautrup, S., Hasan-Olive, M. M., Caponio, D., Dan, X., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-018-0332-9 · Cited by 1,740
Self-citationCantó, C., Menzies, K. J., & Auwerx, J. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.05.023 · Cited by 1,648
Moreno-Jiménez, E. P., Flor-García, M., Terreros-Roncal, J., Rábano, A., Cafini, F., Pallas-Bazarra, N., Ávila, J., & Llorens-Martín, M. (2019) · Nature Medicine · doi:10.1038/s41591-019-0375-9 · Cited by 1,577
Mechanisms of mitophagy in cellular homeostasis, physiology and pathology
Palikaras, K., Lionaki, E., & Tavernarakis, N. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0176-2 · Cited by 1,556
Ying, W. (2008) · Antioxidants & Redox Signaling · doi:10.1089/ars.2007.1672 · Cited by 1,494
Gomes, A. P., Price, N. L., Ling, A. J. Y., Moslehi, J. J., Montgomery, M. K., Rajman, L., White, J. P., Teodoro, J. S., Wrann, C. D., Hubbard, B. P., et al. (2013) · Cell · doi:10.1016/j.cell.2013.11.037 · Cited by 1,482
Self-citationTransfer of mitochondria from astrocytes to neurons after stroke
Hayakawa, K., Esposito, E., Wang, X., Terasaki, Y., Liu, Y., Xing, C., Ji, X., & Lo, E. H. (2016) · Nature · doi:10.1038/nature18928 · Cited by 1,423
Kim, S., Kwon, S.-H., Kam, T.-I., Panicker, N., Karuppagounder, S. S., Lee, S., Lee, J. H., Kim, W. R., Kook, M., Foss, C. A., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.035 · Cited by 1,397
Multiple types of neuronal calcium channels and their selective modulation
Tsien, R. W., Lipscombe, D., Madison, D. V., Bley, K. R., & Fox, A. P. (1988) · Trends in Neurosciences · doi:10.1016/0166-2236(88)90194-4 · Cited by 1,381
Yoshino, J., Mills, K. F., Yoon, M. J., & Imai, S.-I. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.08.014 · Cited by 1,340
Genetic pathways that regulate ageing in model organisms
Guarente, L., & Kenyon, C. J. (2000) · Nature · doi:10.1038/35041700 · Cited by 1,337
NAD + in aging, metabolism, and neurodegeneration
Verdin, E. (2015) · Science · doi:10.1126/science.aac4854 · Cited by 1,319
PARP inhibition: PARP1 and beyond
Rouleau, M., Patel, A., Hendzel, M. J., Kaufmann, S. H., & Poirier, G. G. (2010) · Nature Reviews Cancer · doi:10.1038/nrc2812 · Cited by 1,298
Clearance of senescent glial cells prevents tau-dependent pathology and cognitive decline
Bussian, T. J., Aziz, A., Meyer, C. F., Swenson, B. L., van Deursen, J. M., & Baker, D. J. (2018) · Nature · doi:10.1038/s41586-018-0543-y · Cited by 1,289
Mitochondrial Dysfunction Induces Senescence with a Distinct Secretory Phenotype
Wiley, C. D., Velarde, M. C., Lecot, P., Liu, S., Sarnoski, E. A., Freund, A., Shirakawa, K., Lim, H. W., Davis, S. S., Ramanathan, A., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2015.11.011 · Cited by 1,275
NAD + repletion improves mitochondrial and stem cell function and enhances life span in mice
Zhang, H., Ryu, D., Wu, Y., Gariani, K., Wang, X., Luan, P., D’Amico, D., Ropelle, E. R., Lutolf, M. P., Aebersold, R., et al. (2016) · Science · doi:10.1126/science.aaf2693 · Cited by 1,255 · cited 12×
“At a younger age, sufficient cellular NAD+ maintains mitochondrial quality to sustain normal neuronal function via the NAD+dependent regulations of autophagy/mitophagy, UPRmt, proteasome degradation, and mitochondrial biogenesis.”
InfluentialPromoting Health and Longevity through Diet: From Model Organisms to Humans
Fontana, L., & Partridge, L. (2015) · Cell · doi:10.1016/j.cell.2015.02.020 · Cited by 1,245
Hallmarks of Brain Aging: Adaptive and Pathological Modification by Metabolic States
Mattson, M. P., & Arumugam, T. V. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.05.011 · Cited by 1,242
Self-citationMouchiroud, L., Houtkooper, R. H., Moullan, N., Katsyuba, E., Ryu, D., Cantó, C., Mottis, A., Jo, Y.-S., Viswanathan, M., Schoonjans, K., et al. (2013) · Cell · doi:10.1016/j.cell.2013.06.016 · Cited by 1,210
Pancreatic stellate cells support tumour metabolism through autophagic alanine secretion
Sousa, C. M., Biancur, D. E., Wang, X., Halbrook, C. J., Sherman, M. H., Zhang, L., Kremer, D., Hwang, R. F., Witkiewicz, A. K., Ying, H., et al. (2016) · Nature · doi:10.1038/nature19084 · Cited by 1,122
Mitochondria in neuroplasticity and neurological disorders
Mattson, M. P., Gleichmann, M., & Cheng, A. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.010 · Cited by 1,081
Self-citationKim, D., Nguyen, M. D., Dobbin, M. M., Fischer, A., Sananbenesi, F., Rodgers, J. T., Delalle, I., Baur, J. A., Sui, G., Armour, S. M., et al. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601758 · Cited by 1,074
Self-citationNAD+ Intermediates: The Biology and Therapeutic Potential of NMN and NR
Yoshino, J., Baur, J. A., & Imai, S.-I. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2017.11.002 · Cited by 1,061
Zhang, P., Kishimoto, Y., Grammatikakis, I., Gottimukkala, K., Cutler, R. G., Zhang, S., Abdelmohsen, K., Bohr, V. A., Misra Sen, J., Gorospe, M., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0372-9 · Cited by 977
Self-citationA novel pathway regulates memory and plasticity via SIRT1 and miR-134
Gao, J., Wang, W.-Y., Mao, Y.-W., Gräff, J., Guan, J.-S., Pan, L., Mak, G., Kim, D., Su, S. C., & Tsai, L.-H. (2010) · Nature · doi:10.1038/nature09271 · Cited by 975
Nutrient-Sensitive Mitochondrial NAD+ Levels Dictate Cell Survival
Yang, H., Yang, T., Baur, J. A., Perez, E., Matsui, T., Carmona, J. J., Lamming, D. W., Souza-Pinto, N. C., Bohr, V. A., Rosenzweig, A., et al. (2007) · Cell · doi:10.1016/j.cell.2007.07.035 · Cited by 950
Self-citationNeuronal calcium mishandling and the pathogenesis of Alzheimer's disease
Bezprozvanny, I., & Mattson, M. P. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.06.005 · Cited by 938
Self-citationCamacho-Pereira, J., Tarragó, M. G., Chini, C. C. S., Nin, V., Escande, C., Warner, G. M., Puranik, A. S., Schoon, R. A., Reid, J. M., Galina, A., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.05.006 · Cited by 901
Autophagy maintains the metabolism and function of young and old stem cells
Ho, T. T., Warr, M. R., Adelman, E. R., Lansinger, O. M., Flach, J., Verovskaya, E. V., Figueroa, M. E., & Passegué, E. (2017) · Nature · doi:10.1038/nature21388 · Cited by 896
Mitophagy and Alzheimer’s Disease: Cellular and Molecular Mechanisms
Kerr, J. S., Adriaanse, B. A., Greig, N. H., Mattson, M. P., Cader, M. Z., Bohr, V. A., & Fang, E. F. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.01.002 · Cited by 870
Self-citationCompromised autophagy and neurodegenerative diseases
Menzies, F. M., Fleming, A., & Rubinsztein, D. C. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3961 · Cited by 851
Slowing ageing by design: the rise of NAD+ and sirtuin-activating compounds
Bonkowski, M. S., & Sinclair, D. A. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2016.93 · Cited by 834
Self-citationCoordination of mitophagy and mitochondrial biogenesis during ageing in C. elegans
Palikaras, K., Lionaki, E., & Tavernarakis, N. (2015) · Nature · doi:10.1038/nature14300 · Cited by 770
Autophagy as a promoter of longevity: insights from model organisms
Hansen, M., Rubinsztein, D. C., & Walker, D. W. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-018-0033-y · Cited by 754
Bieganowski, P., & Brenner, C. (2004) · Cell · doi:10.1016/s0092-8674(04)00416-7 · Cited by 750
Defective Mitophagy in XPA via PARP-1 Hyperactivation and NAD+/SIRT1 Reduction
Fang, E. F., Scheibye-Knudsen, M., Brace, L. E., Kassahun, H., SenGupta, T., Nilsen, H., Mitchell, J. R., Croteau, D. L., & Bohr, V. A. (2014) · Cell · doi:10.1016/j.cell.2014.03.026 · Cited by 711
Self-citationBogan, K. L., & Brenner, C. (2008) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.28.061807.155443 · Cited by 707
Potential roles of gut microbiome and metabolites in modulating ALS in mice
Blacher, E., Bashiardes, S., Shapiro, H., Rothschild, D., Mor, U., Dori-Bachash, M., Kleimeyer, C., Moresi, C., Harnik, Y., Zur, M., et al. (2019) · Nature · doi:10.1038/s41586-019-1443-5 · Cited by 700
Nicotinamide riboside is uniquely and orally bioavailable in mice and humans
Trammell, S. A. J., Schmidt, M. S., Weidemann, B. J., Redpath, P., Jaksch, F., Dellinger, R. W., Li, Z., Abel, E. D., Migaud, M. E., & Brenner, C. (2016) · Nature Communications · doi:10.1038/ncomms12948 · Cited by 697
Gandhi, S., Wood-Kaczmar, A., Yao, Z., Plun-Favreau, H., Deas, E., Klupsch, K., Downward, J., Latchman, D. S., Tabrizi, S. J., Wood, N. W., et al. (2009) · Molecular Cell · doi:10.1016/j.molcel.2009.02.013 · Cited by 682
CD38 is critical for social behaviour by regulating oxytocin secretion
Jin, D., Liu, H.-X., Hirai, H., Torashima, T., Nagai, T., Lopatina, O., Shnayder, N. A., Yamada, K., Noda, M., Seike, T., et al. (2007) · Nature · doi:10.1038/nature05526 · Cited by 665
A Phase 3 randomized trial of nicotinamide for skin-cancer chemoprevention
Chen, A. C., Martin, A. J., Choy, B., Fernández-Peñas, P., Dalziell, R. A., McKenzie, C. A., Scolyer, R. A., Dhillon, H. M., Vardy, J. L., Kricker, A., et al. (2015) · New England Journal of Medicine · doi:10.1056/nejmoa1506197 · Cited by 648 · cited 2×
“A phase-III randomized large clinical trial reported that oral NAM was safe and effective in reducing the rates of new nonmelanoma skin cancers and actinic keratosis in high-risk patients (Chen et al., 2015).”
Kynurenines in the CNS: recent advances and new questions
Vécsei, L., Szalárdy, L., Fülöp, F., & Toldi, J. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd3793 · Cited by 641
Enhancing mitochondrial proteostasis reduces amyloid-β proteotoxicity
Sorrentino, V., Romani, M., Mouchiroud, L., Beck, J. S., Zhang, H., D’Amico, D., Moullan, N., Potenza, F., Schmid, A. W., Rietsch, S., et al. (2017) · Nature · doi:10.1038/nature25143 · Cited by 630
Intermittent metabolic switching, neuroplasticity and brain health
Mattson, M. P., Moehl, K., Ghena, N., Schmaedick, M., & Cheng, A. (2018) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.156 · Cited by 624
Self-citationEssuman, K., Summers, D. W., Sasaki, Y., Mao, X., DiAntonio, A., & Milbrandt, J. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.022 · Cited by 619
Vitamin B 3 modulates mitochondrial vulnerability and prevents glaucoma in aged mice
Williams, P. A., Harder, J. M., Foxworth, N. E., Cochran, K. E., Philip, V. M., Porciatti, V., Smithies, O., & John, S. W. M. (2017) · Science · doi:10.1126/science.aal0092 · Cited by 617
SARM1 activation triggers axon degeneration locally via NAD + destruction
Gerdts, J., Brace, E. J., Sasaki, Y., DiAntonio, A., & Milbrandt, J. (2015) · Science · doi:10.1126/science.1258366 · Cited by 593
Basal Mitophagy Occurs Independently of PINK1 in Mouse Tissues of High Metabolic Demand
McWilliams, T. G., Prescott, A. R., Montava-Garriga, L., Ball, G., Singh, F., Barini, E., Muqit, M. M. K., Brooks, S. P., & Ganley, I. G. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2017.12.008 · Cited by 591
Martens, C. R., Denman, B. A., Mazzo, M. R., Armstrong, M. L., Reisdorph, N., McQueen, M. B., Chonchol, M., & Seals, D. R. (2018) · Nature Communications · doi:10.1038/s41467-018-03421-7 · Cited by 588
Fang, E. F., Kassahun, H., Croteau, D. L., Scheibye-Knudsen, M., Marosi, K., Lu, H., Shamanna, R. A., Kalyanasundaram, S., Bollineni, R. C., Wilson, M. A., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.09.004 · Cited by 575
Self-citationWidespread Proteome Remodeling and Aggregation in Aging C. elegans
Walther, D. M., Kasturi, P., Zheng, M., Pinkert, S., Vecchi, G., Ciryam, P., Morimoto, R. I., Dobson, C. M., Vendruscolo, M., Mann, M., et al. (2015) · Cell · doi:10.1016/j.cell.2015.03.032 · Cited by 569
BDNF mediates adaptive brain and body responses to energetic challenges
Marosi, K., & Mattson, M. P. (2014) · Trends in Endocrinology & Metabolism · doi:10.1016/j.tem.2013.10.006 · Cited by 568
Self-citationThe road to restoring neural circuits for the treatment of Alzheimer's disease
Canter, R. G., Penney, J., & Tsai, L.-H. (2016) · Nature · doi:10.1038/nature20412 · Cited by 565
Manipulation of Brain Kynurenines: Glial Targets, Neuronal Effects, and Clinical Opportunities
Schwarcz, R. M., & Pellicciari, R. (2002) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.102.034439 · Cited by 556
The role of leucine-rich repeat kinase 2 (LRRK2) in Parkinson's disease
Cookson, M. (2010) · Nature reviews. Neuroscience · doi:10.1038/nrn2935 · Cited by 552
Leeman, D. S., Hebestreit, K., Ruetz, T., Webb, A. E., McKay, A., Pollina, E. A., Dulken, B. W., Zhao, X., Yeo, R. W., Ho, T. T., et al. (2018) · Science · doi:10.1126/science.aag3048 · Cited by 528
Kynurenine 3-Monooxygenase Inhibition in Blood Ameliorates Neurodegeneration
Zwilling, D., Huang, S., Sathyasaikumar, K. V., Notarangelo, F. M., Guidetti, P., Wu, H., Lee, J. H., Truong, J. K., Andrews-Zwilling, Y. S., Hsieh, E., et al. (2011) · Cell · doi:10.1016/j.cell.2011.05.020 · Cited by 519
The multifaceted functions of sirtuins in cancer
Chalkiadaki, A., & Guarente, L. (2015) · Nature reviews. Cancer · doi:10.1038/nrc3985 · Cited by 513
Berger, F., Lau, C., Dahlmann, M., & Ziegler, M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m508660200 · Cited by 508
NAD(+) in aging: molecular mechanisms and translational implications
Fang, E. F., Lautrup, S., Hou, Y., Demarest, T. G., Croteau, D. L., Mattson, M. P., & Bohr, V. A. (2017) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2017.08.001 · Cited by 501
Self-citationMacrophage de novo NAD+ synthesis specifies immune function in aging and inflammation
Minhas, P. S., Liu, L., Moon, P. K., Joshi, A. U., Dove, C., Mhatre, S., Contrepois, K., Wang, Q., Lee, B. A., Coronado, M., et al. (2019) · Nature Immunology · doi:10.1038/s41590-018-0255-3 · Cited by 501
D-β-Hydroxybutyrate rescues mitochondrial respiration and mitigates features of Parkinson disease
Tieu, K., Perier, C., Caspersen, C., Teismann, P., Wu, D.-C., Yan, S.-D., Naini, A., Vila, M., Jackson-Lewis, V., Ramasamy, R., et al. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200318797 · Cited by 497
Impairment of an endothelial NAD(+)-H2S signaling network is a reversible cause of vascular aging
Das, A., Huang, G. X., Bonkowski, M. S., Longchamp, A., Li, C., Schultz, M. B., Kim, L.-J., Osborne, B., Joshi, S., Lu, Y., et al. (2018) · Cell · doi:10.1016/j.cell.2018.02.008 · Cited by 496 · cited 2×
“Mounting evidence supports a critical role for NAD+ in stem cell rejuvenation, including in HSCs, endothelial stem cells, muscle stem cells, and melanocyte stem cells (Das et al., 2018; Vannini et al., 2019; Zhang et al., 2016).”
Self-citationWang, Y., Kim, N. S., Haince, J.-F., Kang, H. C., David, K. K., Andrabi, S. A., Poirier, G. G., Dawson, V. L., & Dawson, T. M. (2011) · Science Signaling · doi:10.1126/scisignal.2000902 · Cited by 476
Poly(ADP-ribose) drives pathologic α-synuclein neurodegeneration in Parkinson’s disease
Kam, T.-I., Mao, X., Park, H., Chou, S.-C., Karuppagounder, S. S., Umanah, G. E., Yun, S. P., Brahmachari, S., Panicker, N., Chen, R., et al. (2018) · Science · doi:10.1126/science.aat8407 · Cited by 476
Endogenous Nmnat2 Is an Essential Survival Factor for Maintenance of Healthy Axons
Gilley, J., & Coleman, M. P. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000300 · Cited by 472
Hou, Y., Lautrup, S., Cordonnier, S., Wang, Y., Croteau, D. L., Zavala, E., Zhang, Y., Moritoh, K., O’Connell, J. F., Baptiste, B. A., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1718819115 · Cited by 472
Self-citationZhu, X.-H., Lu, M., Lee, B.-Y., Ugurbil, K., & Chen, W. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1417921112 · Cited by 468
Lou, G., Palikaras, K., Lautrup, S., Scheibye‐Knudsen, M., Tavernarakis, N., & Fang, E. F. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2019.07.002 · Cited by 455
Self-citationAcetylation Targets Mutant Huntingtin to Autophagosomes for Degradation
Jeong, H., Then, F., Melia, T. J., Mazzulli, J. R., Cui, L., Savas, J. N., Voisine, C., Paganetti, P., Tanese, N., Hart, A. C., et al. (2009) · Cell · doi:10.1016/j.cell.2009.03.018 · Cited by 438
A nuclease that mediates cell death induced by DNA damage and poly(ADP-ribose) polymerase-1
Wang, Y., An, R., Umanah, G. K., Park, H., Nambiar, K., Eacker, S. M., Kim, B., Bao, L., Harraz, M. M., Chang, C., et al. (2016) · Science · doi:10.1126/science.aad6872 · Cited by 421
Pérez, V. I., Buffenstein, R., Masamsetti, V., Leonard, S., Salmon, A. B., Mele, J., Andziak, B., Yang, T., Edrey, Y., Friguet, B., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0809620106 · Cited by 418
Biosensor reveals multiple sources for mitochondrial NAD +
Cambronne, X. A., Stewart, M. L., Kim, D., Jones-Brunette, A. M., Morgan, R. K., Farrens, D. L., Cohen, M. S., & Goodman, R. H. (2016) · Science · doi:10.1126/science.aad5168 · Cited by 407
Extracellular vesicle-contained eNAMPT delays aging and extends lifespan in mice
Yoshida, M., Satoh, A., Lin, J. B., Mills, K. F., Sasaki, Y., Rensing, N., Wong, M., Apte, R. S., & Imai, S.-I. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.05.015 · Cited by 407
Green, K. N., Steffan, J. S., Martinez-Coria, H., Sun, X., Schreiber, S. S., Thompson, L. M., & LaFerla, F. M. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.3203-08.2008 · Cited by 404 · cited 6×
“Based on the promising data from ADmice (Green et al., 2008), a phase II clinical trial of NAMon 15ADpatients withmild tomoderate dementia (1,500 mg twice daily) for 24 weeks was performed (NCT00580931) (Phelan et al., 2017).”
InfluentialNAD+ metabolism governs the proinflammatory senescence-associated secretome
Nacarelli, T., Lau, L., Fukumoto, T., Zundell, J., Fatkhutdinov, N., Wu, S., Aird, K. M., Iwasaki, O., Kossenkov, A. V., Schultz, D., et al. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0287-4 · Cited by 402
Nuclear DNA damage signalling to mitochondria in ageing
Fang, E. F., Scheibye-Knudsen, M., Chua, K. F., Mattson, M. P., Croteau, D. L., & Bohr, V. A. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2016.14 · Cited by 387
Self-citationNewly born peroxisomes are a hybrid of mitochondrial and ER-derived pre-peroxisomes
Sugiura, A., Mattie, S., Prudent, J., & McBride, H. M. (2017) · Nature · doi:10.1038/nature21375 · Cited by 386 · cited 1×
“Peroxisomes have recently been shown to have a shared mitochondrial and endoplasmic reticulum (ER) origin, further linking the function of mitochondria and peroxisomes (Sugiura et al., 2017).”
Aβ inhibits the proteasome and enhances amyloid and tau accumulation
Tseng, B. P., Green, K. N., Chan, J. L., Blurton-Jones, M., & LaFerla, F. M. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.04.014 · Cited by 384
Amyloid-β and tau complexity — towards improved biomarkers and targeted therapies
Polanco, J. C., Li, C., Bodea, L., Martínez‐Mármol, R., Meunier, F. A., & Götz, J. (2017) · Nature Reviews Neurology · doi:10.1038/nrneurol.2017.162 · Cited by 383
NRK1 controls nicotinamide mononucleotide and nicotinamide riboside metabolism in mammalian cells
Ratajczak, J., Joffraud, M., Trammell, S. A. J., Ras, R., Canela, N., Boutant, M., Kulkarni, S. S., Rodrigues, M., Redpath, P., Migaud, M. E., et al. (2016) · Nature Communications · doi:10.1038/ncomms13103 · Cited by 378
Cheng, A., Yang, Y., Zhou, Y., Maharana, C., Lu, D., Peng, W., Liu, Y., Wan, R., Marosi, K., Misiak, M., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2015.10.013 · Cited by 371
Self-citationComplement C3-Deficient Mice Fail to Display Age-Related Hippocampal Decline
Shi, Q., Colodner, K. J., Matousek, S. B., Merry, K., Hong, S., Kenison, J. E., Frost, J. L., Le, K. X., Li, S., Dodart, J.-C., et al. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.1698-15.2015 · Cited by 368
A mechanism of ubiquitin-independent proteasomal degradation of the tumor suppressors p53 and p73
Asher, G., Tsvetkov, P., Kahana, C., & Shaul, Y. (2005) · Genes & Development · doi:10.1101/gad.319905 · Cited by 367 · cited 2×
“There is also evidence showing that a-synuclein competes with NAD+ for binding to the partially oxidized glycolytic enzyme glyceraldehyde-3-phosphate dehydrogenase (GAPDH), which co-localizes with a-synuclein in Lewy bodies in PD (Barinova et al., 2018).”
Kashiwaya, Y., Bergman, C., Lee, J.-H., Wan, R., King, M. T., Mughal, M. R., Okun, E., Clarke, K., Mattson, M. P., & Veech, R. L. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.11.023 · Cited by 363
Self-citationBasal mitophagy is widespread in Drosophila but minimally affected by loss of Pink1 or parkin
Lee, J. J., Sánchez-Martínez, Á., Martinez, A., Benincá, C., Mayor, U., Clague, M. J., & Whitworth, A. J. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201801044 · Cited by 353
A high-fat diet and NAD(+) activate Sirt1 to rescue premature aging in Cockayne syndrome
Scheibye-Knudsen, M., Mitchell, S. J., Fang, E. F., Iyama, T., Ward, T., Wang, J., Dunn, C. A., Singh, N., Veith, S., Hasan-Olive, M. M., et al. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.10.005 · Cited by 352
Self-citationSerine ADP-ribosylation depends on HPF1
Bonfiglio, J. J., Fontana, P., Zhang, Q., Colby, T., Gibbs-Seymour, I., Atanassov, I., Bartlett, E., Zaja, R., Ahel, I., & Matic, I. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.01.003 · Cited by 352
Mairet-Coello, G., Courchet, J., Pieraut, S., Courchet, V., Maximov, A., & Polleux, F. (2013) · Neuron · doi:10.1016/j.neuron.2013.02.003 · Cited by 351
Gong, B., Pan, Y., Vempati, P., Zhao, W., Knable, L., Ho, L., Wang, J., Sastre, M., Ono, K., Sauve, A. A., et al. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.12.005 · Cited by 345
The Parkinson's disease–linked proteins Fbxo7 and Parkin interact to mediate mitophagy
Burchell, V., Nelson, D. E., Sánchez-Martínez, Á., Delgado-Camprubi, M., Ivatt, R. M., Pogson, J. H., Randle, S. J., Wray, S., Lewis, P. A., Houlden, H., et al. (2013) · Nature Neuroscience · doi:10.1038/nn.3489 · Cited by 342
Schöndorf, D. C., Ivanyuk, D., Baden, P., Sanchez-Martinez, A., De Cicco, S., Yu, C., Giunta, I., Schwarz, L. K., Di Napoli, G., Panagiotakopoulou, V., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.05.009 · Cited by 337
The Mechanistic Links Between Proteasome Activity, Aging and Agerelated Diseases
Sáez, I., & Vı́lchez, D. (2014) · Current Genomics · doi:10.2174/138920291501140306113344 · Cited by 331
Pathways and Subcellular Compartmentation of NAD Biosynthesis in Human Cells
Nikiforov, A., Dölle, C., Niere, M., & Ziegler, M. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.213298 · Cited by 326
Beal, M. F., Matson, W. R., Swartz, K. J., Gamache, P. H., & Bird, E. D. (1990) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1990.tb03143.x · Cited by 312
The kynurenine pathway and neurodegenerative disease
Maddison, D. C., & Giorgini, F. (2015) · Seminars in Cell & Developmental Biology · doi:10.1016/j.semcdb.2015.03.002 · Cited by 309
PINK1 signalling rescues amyloid pathology and mitochondrial dysfunction in Alzheimer’s disease
Du, F., Yu, Q., Yan, S., Hu, G., Lue, L., Walker, D., Wu, L., Yan, S. F., Tieu, K., & Yan, S. S. (2017) · Brain · doi:10.1093/brain/awx258 · Cited by 308
Poly(ADP-ribose) polymerase-dependent energy depletion occurs through inhibition of glycolysis
Andrabi, S. A., Umanah, G. K. E., Chang, C., Stevens, D. A., Karuppagounder, S. S., Gagné, J.-P., Poirier, G. G., Dawson, V. L., & Dawson, T. M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1405158111 · Cited by 307
mTORC1 and SIRT1 Cooperate to Foster Expansion of Gut Adult Stem Cells during Calorie Restriction
Igarashi, M., & Guarente, L. (2016) · Cell · doi:10.1016/j.cell.2016.05.044 · Cited by 305
Han, X., Tai, H., Wang, X., Wang, Z., Zhou, J., Wei, X., Ding, Y., Gong, H., Mo, C., Zhang, J., et al. (2016) · Aging Cell · doi:10.1111/acel.12446 · Cited by 302
Nicotinamide Riboside Opposes Type 2 Diabetes and Neuropathy in Mice
Trammell, S. A. J., Weidemann, B. J., Chadda, A., Yorek, M. S., Holmes, A., Coppey, L. J., Obrosov, A., Kardon, R. H., Yorek, M. A., & Brenner, C. (2016) · Scientific Reports · doi:10.1038/srep26933 · Cited by 301
Slc12a8 is a nicotinamide mononucleotide transporter
Grozio, A., Mills, K. F., Yoshino, J., Bruzzone, S., Sociali, G., Tokizane, K., Lei, H. C., Cunningham, R., Sasaki, Y., Migaud, M. E., et al. (2019) · Nature Metabolism · doi:10.1038/s42255-018-0009-4 · Cited by 287
Lysosomal signaling molecules regulate longevity in Caenorhabditis elegans
Folick, A., Oakley, H. D., Yu, Y., Armstrong, E. H., Kumari, M., Sanor, L., Moore, D. D., Ortlund, E. A., Zechner, R., & Wang, M. C. (2015) · Science · doi:10.1126/science.1258857 · Cited by 283
Dollerup, O. L., Christensen, B., Svart, M., Schmidt, M. S., Sulek, K., Ringgaard, S., Stødkilde-Jørgensen, H., Møller, N., Brenner, C., Treebak, J. T., et al. (2018) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/nqy132 · Cited by 282
Brown, K. D., Maqsood, S., Huang, J.-Y., Pan, Y., Harkcom, W., Li, W., Sauve, A., Verdin, E., & Jaffrey, S. R. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.11.003 · Cited by 277
Fischer, A., Sananbenesi, F., Pang, P. T., Lu, B., & Tsai, L.-H. (2005) · Neuron · doi:10.1016/j.neuron.2005.10.033 · Cited by 277
The kynurenine pathway as a therapeutic target in cognitive and neurodegenerative disorders
Stone, T. W., & Darlington, L. G. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12230 · Cited by 276
Pallos, J., Bodai, L., Lukácsovich, T., Purcell, J. M., Steffan, J. S., Thompson, L. M., & Marsh, J. (2008) · Human Molecular Genetics · doi:10.1093/hmg/ddn273 · Cited by 272
Disease-associated tau impairs mitophagy by inhibiting Parkin translocation to mitochondria
Cummins, N., Tweedie, A., Zuryn, S., Bertran‐Gonzalez, J., & Götz, J. (2019) · The EMBO Journal · doi:10.15252/embj.201899360 · Cited by 267
Stein, L. R., & Imai, S. (2014) · The EMBO Journal · doi:10.1002/embj.201386917 · Cited by 265
The Kynurenine Pathway Modulates Neurodegeneration in a Drosophila Model of Huntington's Disease
Campesan, S., Green, E. W., Breda, C., Sathyasaikumar, K. V., Muchowski, P. J., Schwarcz, R. M., Kyriacou, C. P., & Giorgini, F. (2011) · Current Biology · doi:10.1016/j.cub.2011.04.028 · Cited by 261
Keller, J. (2002) · Ageing Research Reviews · doi:10.1016/s1568-1637(01)00006-x · Cited by 247
Marosi, K., Kim, S. W., Moehl, K., Scheibye‐Knudsen, M., Cheng, A., Cutler, R., Camandola, S., & Mattson, M. P. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13868 · Cited by 242
Self-citationLiu, D., Pitta, M., Jiang, H., Lee, J.-H., Zhang, G., Chen, X., Kawamoto, E. M., & Mattson, M. P. (2013) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2012.11.020 · Cited by 238
Self-citationMaintaining genome stability in the nervous system
McKinnon, P. J. (2013) · Nature Neuroscience · doi:10.1038/nn.3537 · Cited by 229
Vannini, N., Campos, V., Girotra, M., Trachsel, V., Rojas-Sutterlin, S., Tratwal, J., Ragusa, S., Stefanidis, E., Ryu, D., Rainer, P. Y., et al. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.02.012 · Cited by 218
ARTD1/PARP1 Negatively Regulates Glycolysis by Inhibiting Hexokinase 1 Independent of NAD+ Depletion
Fouquerel, E., Goellner, E. M., Yu, Z., Gagné, J.-P., Barbi de Moura, M., Feinstein, T., Wheeler, D., Redpath, P., Li, J., Romero, G., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.08.036 · Cited by 212 · cited 1×
“Despite NAMPT being relatively highly expressed in brown adipocyte, liver, and kidney tissues compared to brain tissue in mice, several studies have supported an essential role of iNAMPT in neuronal NAD+ metabolism (Stein and Imai, 2014; Stein et al., 2014; Zhang et al., 2010).”
Molecular aspects of age-related cognitive decline: the role of GABA signaling
McQuail, J. A., Frazier, C. J., & Bizon, J. L. (2015) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2015.05.002 · Cited by 207
Hara, N., Yamada, K., Shibata, T., Osago, H., Hashimoto, T., & Tsuchiya, M. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m610357200 · Cited by 205
Arumugam, T. V., Tang, S., Lathia, J. D., Cheng, A., Mughal, M. R., Chigurupati, S., Magnus, T., Chan, S. L., Jo, D., Ouyang, X., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700506104 · Cited by 204
Self-citationRate control of the tricarboxylic acid cycle
Krebs, H. A. (1970) · Advances in Enzyme Regulation · doi:10.1016/0065-2571(70)90028-2 · Cited by 196
Adult Hippocampal Neurogenesis: A Coming-of-Age Story
Kuhn, H. G., Toda, T., & Gage, F. H. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2144-18.2018 · Cited by 195
Complement in the pathogenesis of Alzheimer’s disease
Morgan, B. P. (2018) · Seminars in Immunopathology · doi:10.1007/s00281-017-0662-9 · Cited by 194
Inhibition of Nicotinamide Phosphoribosyltransferase
Pittelli, M., Formentini, L., Faraco, G., Lapucci, A., Rapizzi, E., Cialdai, F., Romano, G., Moneti, G., Moroni, F., & Chiarugi, A. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.136739 · Cited by 189
A conserved NAD + binding pocket that regulates protein-protein interactions during aging
Li, J., Bonkowski, M. S., Moniot, S., Zhang, D., Hubbard, B. P., Ling, A. J. Y., Rajman, L. A., Qin, B., Lou, Z., Gorbunova, V. A., et al. (2017) · Science · doi:10.1126/science.aad8242 · Cited by 188
Self-citationTelomere Dysfunction Induces Sirtuin Repression that Drives Telomere-Dependent Disease
Amano, H., Chaudhury, A., Rodriguez-Aguayo, C., Lu, L., Akhanov, V., Catic, A., Popov, Y. V., Verdin, E., Johnson, H., Stossi, F., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2019.03.001 · Cited by 182
Self-citationDellinger, R. W., Santos, S. R., Morris, M., Evans, M., Alminana, D., Guarente, L., & Marcotulli, E. (2017) · npj Aging and Mechanisms of Disease · doi:10.1038/s41514-017-0016-9 · Cited by 181
A lysosomal switch triggers proteostasis renewal in the immortal C. elegans germ lineage
Bohnert, K. A., & Kenyon, C. J. (2017) · Nature · doi:10.1038/nature24620 · Cited by 179
Liu, Y., Cheng, A., Li, Y.-J., Yang, Y., Kishimoto, Y., Zhang, S., Wang, Y., Wan, R., Raefsky, S. M., Lu, D., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09897-1 · Cited by 176
Self-citationA new function for CD38/ADP-ribosyl cyclase in nuclear Ca2+ homeostasis
Adebanjo, O. A., Anandatheerthavarada, H. K., Ap, K., Moonga, B. S., Biswas, G., Sun, L., Sodam, B. R., Bevis, P. J. R., Huang, C. L.-H., Epstein, S., et al. (1999) · Nature Cell Biology · doi:10.1038/15640 · Cited by 158
Grozio, A., Sociali, G., Sturla, L., Caffa, I., Soncini, D., Salis, A., Raffaelli, N., De Flora, A., Nencioni, A., & Bruzzone, S. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.470435 · Cited by 158 · cited 3×
“into NAM, which is able to cross the plasma membrane (Camacho-Pereira et al., 2016; Grozio et al., 2013; Sauve et al., 1998).”
Dual role of USP30 in controlling basal pexophagy and mitophagy
Marcassa, E., Kallinos, A., Jardine, J., Rusilowicz‐Jones, E. V., Martinez, A., Kuehl, S., Islinger, M., Clague, M. J., & Urbé, S. (2018) · The EMBO Reports · doi:10.15252/embr.201745595 · Cited by 158
The human gene SLC25A17 encodes a peroxisomal transporter of coenzyme A, FAD and NAD+
Agrimi, G., Russo, A., Scarcia, P., & Palmieri, F. (2012) · Biochemical Journal · doi:10.1042/bj20111420 · Cited by 154
Nicotinamide adenine dinucleotide is transported into mammalian mitochondria
Davila, A., Liu, L., Chellappa, K., Redpath, P., Nakamaru-Ogiso, E., Paolella, L. M., Zhang, Z., Migaud, M. E., Rabinowitz, J. D., & Baur, J. A. (2018) · eLife · doi:10.7554/elife.33246 · Cited by 142
The kynurenine pathway and inflammation in amyotrophic lateral sclerosis
Chen, Y., Stankovic, R., Cullen, K. M., Meininger, V., Garner, B., Coggan, S., Grant, R., Brew, B. J., & Guillemin, G. J. (2010) · Neurotoxicity Research · doi:10.1007/s12640-009-9129-7 · Cited by 141
Mitophagy and NAD + inhibit Alzheimer disease
Fang, E. F. (2019) · Autophagy · doi:10.1080/15548627.2019.1596497 · Cited by 140
Self-citationChini, C., Hogan, K. A., Warner, G. M., Tarragó, M. G., Peclat, T. R., Tchkonia, T., Kirkland, J. L., & Chini, E. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.03.199 · Cited by 138
Apollo-NADP+: a spectrally tunable family of genetically encoded sensors for NADP+
Cameron, D. W., Bui, C. V., Hutchinson, A., Loppnau, P., Gräslund, S., & Rocheleau, J. V. (2016) · Nature Methods · doi:10.1038/nmeth.3764 · Cited by 126
Fletcher, R. S., Ratajczak, J., Doig, C. L., Oakey, L. A., Callingham, R., Xavier, G. D. S., Garten, A., Elhassan, Y., Redpath, P., Migaud, M. E., et al. (2017) · Molecular Metabolism · doi:10.1016/j.molmet.2017.05.011 · Cited by 125
Hathorn, T., Snyder-Keller, A., & Messer, A. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2010.08.017 · Cited by 123
Sauve, A. A., Munshi, C. B., Lee, H. C., & Schramm, V. L. (1998) · Biochemistry · doi:10.1021/bi981248s · Cited by 120
Genome instability in Alzheimer disease
Hou, Y., Song, H., Croteau, D. L., Akbari, M., & Bohr, V. A. (2017) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.04.005 · Cited by 120
Phosphoproteomic approach to characterize protein mono- and poly(ADP-ribosyl)ation sites from cells
Daniels, C. M., Ong, S.-E., & Leung, A. K. L. (2014) · Journal of Proteome Research · doi:10.1021/pr401032q · Cited by 119
Alzheimer's disease pathology is attenuated in a CD 38‐deficient mouse model
Blacher, E., Dadali, T., Bespalko, A., Haupenthal, V. J., Grimm, M. O. W., Hartmann, T., Lund, F. E., Stein, R., & Levy, A. (2015) · Annals of Neurology · doi:10.1002/ana.24425 · Cited by 117
Kishimoto, Y., Zhu, W. S., Hosoda, W., Sen, J. M., & Mattson, M. P. (2019) · NeuroMolecular Medicine · doi:10.1007/s12017-019-08539-5 · Cited by 115
Self-citationJarome, T. J., Ferrara, N. C., Kwapis, J. L., & Helmstetter, F. J. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.01.001 · Cited by 112
Pawlosky, R. J., Kemper, M. F., Kashiwaya, Y., King, M. T., Mattson, M. P., & Veech, R. L. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.13958 · Cited by 108
Self-citationDiPalma, & THAYER, W. S. (1991) · Annual Review of Nutrition · doi:10.1146/annurev.nu.11.070191.001125 · Cited by 106
Liu, H.-W., Smith, C. B., Schmidt, M. S., Cambronne, X. A., Cohen, M. S., Migaud, M. E., Brenner, C., & Goodman, R. H. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1809392115 · Cited by 105
Microglial mitophagy mitigates neuroinflammation in Alzheimer's disease
Lautrup, S., Lou, G., Aman, Y., Nilsen, H., Tao, J., & Fang, E. F. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.104469 · Cited by 105
Self-citationJia, H., Li, X., Gao, H., Feng, Z., Li, X., Zhao, L., Jia, X., Zhang, H., & Liu, J. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21650 · Cited by 98
Neuronal localization of CD38 antigen in the human brain
Mizuguchi, M., Otsuka, N., Sato, M., Ishii, Y., Kon, S.-I., Yamada, M., Nishina, H., Katada, T., & Ikeda, K. (1995) · Brain Research · doi:10.1016/0006-8993(95)00885-t · Cited by 97
Latta, C. H., Sudduth, T. L., Weekman, E. M., Brothers, H. M., Abner, E. L., Popa, G. J., Mendenhall, M. D., Gonzalez-Oregon, F., Braun, K. J., & Wilcock, D. M. (2015) · Journal of Neuroinflammation · doi:10.1186/s12974-015-0243-6 · Cited by 96
Pathways to mitochondrial dysfunction in ALS pathogenesis
Carrì, M. T., D’Ambrosi, N., & Cozzolino, M. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.07.055 · Cited by 96
Enhancing NAD+ salvage metabolism is neuroprotective in a PINK1 model of Parkinson's disease
Lehmann, S., Loh, S. H. Y., & Martins, L. M. (2016) · Biology Open · doi:10.1242/bio.022186 · Cited by 96
Fitzgerald, J. C., Zimprich, A. A., Berrio, D. A. C., Schindler, K. M., Maurer, B., Schulte, C., Bus, C., Hauser, A., Kübler, M., Lewin, R., et al. (2017) · Brain · doi:10.1093/brain/awx202 · Cited by 96
Birkmayer, J. G. D., Vrecko, C., Volc, D., & Birkmayer, W. (1993) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.1993.tb00018.x · Cited by 94
Harlan, B. A., Pehar, M., Sharma, D. R., Beeson, G., Beeson, C. C., & Vargas, M. R. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.698779 · Cited by 94
Global Metabolic Shifts in Age and Alzheimer’s Disease Mouse Brains Pivot at NAD + /NADH Redox Sites
Dong, Y., & Brewer, G. J. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-190408 · Cited by 93
de la Rubia, J. E., Drehmer, E., Platero, J. L., Benlloch, M., Caplliure-Llopis, J., Villaron-Casales, C., de Bernardo, N., AlarcÓn, J., Fuente, C., Carrera, S., et al. (2019) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.1080/21678421.2018.1536152 · Cited by 92
NMNATs, evolutionarily conserved neuronal maintenance factors
Ali, Y. O., Li-Kroeger, D., Bellen, H. J., Zhai, R. G., & Lu, H.-C. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.07.002 · Cited by 91
CRISPR/Cas9-mediated PINK1 deletion leads to neurodegeneration in rhesus monkeys
Yang, W., Liu, Y., Tu, Z., Xiao, C., Yan, S., Ma, X., Guo, X., Chen, X., Yin, P., Yang, Z., et al. (2019) · Cell Research · doi:10.1038/s41422-019-0142-y · Cited by 90
Neuronal Protective Role of PBEF in a Mouse Model of Cerebral Ischemia
Zhang, W., Xie, Y., Wang, T., Bi, J., Li, H., Zhang, L. Q., Ye, S. Q., & Ding, S. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2010.71 · Cited by 86
Mayer, P. R., Huang, N., Dewey, C. M., Dries, D. R., Zhang, H., & Yu, G. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.178913 · Cited by 82
Calcium mobilizing second messengers derived from NAD
Guse, A. H. (2015) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2014.12.015 · Cited by 82
Decreased sirtuin deacetylase activity in LRRK2 G2019S iPSC-derived dopaminergic neurons
Schwab, A. J., Sison, S. L., Meade, M. R., Broniowska, K. A., Corbett, J. A., & Ebert, A. D. (2017) · Stem Cell Reports · doi:10.1016/j.stemcr.2017.10.010 · Cited by 80
Murata, H., Khine, C. C., Nishikawa, A., Yamamoto, K.-I., Kinoshita, R., & Sakaguchi, M. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.004578 · Cited by 80
Birkmayer, J. G. D. (1996) · PubMed · Cited by 77
Higashida, H., Yokoyama, S., Huang, J., Liu, L., Ma, W., Akther, S., Higashida, C., Kikuchi, M., Minabe, Y., & Munesue, T. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.01.030 · Cited by 74
Identification of the nicotinamide salvage pathway as a new toxification route for antimetabolites
Buonvicino, D., Mazzola, F., Zamporlini, F., Resta, F., Ranieri, G., Camaioni, E., Muzzi, M., Zecchi, R., Pieraccini, G., Dölle, C., et al. (2018) · Cell Chemical Biology · doi:10.1016/j.chembiol.2018.01.012 · Cited by 73
Delgado-Camprubi, M., Esteras, N., Soutar, M. P., Plun-Favreau, H., & Abramov, A. Y. (2017) · Cell Death & Differentiation · doi:10.1038/cdd.2016.104 · Cited by 71
Dölle, C., Niere, M., Lohndal, E., & Ziegler, M. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-0190-4 · Cited by 70
Antitumor effect of combined NAMPT and CD73 inhibition in an ovarian cancer model
Sociali, G., Raffaghello, L., Magnone, M., Zamporlini, F., Emionite, L., Sturla, L., Bianchi, G., Vigliarolo, T., Nahimana, A., Nencioni, A., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.6502 · Cited by 70
Lehmann, S., Costa, A. C., Celardo, I., Loh, S. H. Y., & Martins, L. M. (2016) · Cell Death & Disease · doi:10.1038/cddis.2016.72 · Cited by 69
Körner, S., Böselt, S., Thau, N., Rath, K. J., Dengler, R., & Petri, S. (2013) · Neurodegenerative Diseases · doi:10.1159/000338048 · Cited by 64
Lee, H. J., Hong, Y., Jun, W., & Yang, S. J. (2015) · Journal of Medicinal Food · doi:10.1089/jmf.2015.3439 · Cited by 63
Cytosolic interaction of type III human CD38 with CIB1 modulates cellular cyclic ADP-ribose levels
Liu, J., Zhao, Y. J., Li, W. H., Hou, Y. N., Li, T., Zhao, Z. Y., Fang, C., Li, S. L., & Lee, H. C. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1703718114 · Cited by 63
Low levels of NMNAT2 compromise axon development and survival
Gilley, J., Mayer, P. R., Yu, G., & Coleman, M. P. (2019) · Human Molecular Genetics · doi:10.1093/hmg/ddy356 · Cited by 62
Stein, L. R., Wozniak, D. F., Dearborn, J. T., Kubota, S., Apte, R. S., Izumi, Y., Zorumski, C. F., & Imai, S. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.4730-13.2014 · Cited by 58
Johnson, S., Wozniak, D. F., & Imai, S. (2018) · npj Aging and Mechanisms of Disease · doi:10.1038/s41514-018-0029-z · Cited by 57
Flagged first, then by citations
5 of the 233 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Birkmayer, 1995, Nicotinamide adenine dinucleotide (NADH)- a new therapeutic approach: preliminary results with cancer patients and patients with dementia of the Alzheimer type, J. Tumor Marker Oncol., 10, 1
Cited by
Sorted by citations
Hallmarks of neurodegenerative diseases
Wilson, D. M., Cookson, M. R., Van Den Bosch, L., Zetterberg, H., Holtzman, D. M., & Dewachter, I. (2023) · Cell · doi:10.1016/j.cell.2022.12.032 · Cited by 1,789
Aging and aging-related diseases: from molecular mechanisms to interventions and treatments
Guo, J., Huang, X., Dou, L., Yan, M., Shen, T., Tang, W., & Li, J. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01251-0 · Cited by 1,976
NAD+ metabolism and its roles in cellular processes during ageing
Covarrubias, A. J., Perrone, R., Grozio, A., & Verdin, E. (2021) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-00313-x · Cited by 1,617
Autophagy in healthy aging and disease
Aman, Y., Schmauck-Medina, T., Hansen, M., Morimoto, R. I., Simon, A. K., Bjedov, I., Palikaras, K., Simonsen, A., Johansen, T., Tavernarakis, N., et al. (2021) · Nature Aging · doi:10.1038/s43587-021-00098-4 · Cited by 1,313
Self-citationNAD+ metabolism: pathophysiologic mechanisms and therapeutic potential
Xie, N., Zhang, L., Gao, W. Q., Huang, C., Huber, P., Zhou, X., Li, C. L., Shen, G., & Zou, B. (2020) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-020-00311-7 · Cited by 1,147
Metadata
- Authors
- Lautrup, S., Sinclair, D. A., Mattson, M. P., & Fang, E. F.
- Affiliations
- University of Oslo (NO)
- Harvard University (US)
- Johns Hopkins University (US)
- Corresponding author
- Fang, Evandro F.
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2019-10
- Volume
- 30
- Issue
- 4
- Pages
- 630-655
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC6787556
- OpenAlex
- W2977367243
- Cited by
- 790
- References
- 233
- Citations by year
- 2026: 140 · 2025: 130 · 2024: 126 · 2023: 115 · 2022: 123 · 2021: 100 · 2020: 52 · 2019: 4
- FWCI
- 8.51
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- NORA - Norwegian Open Research Archives (submittedVersion, other-oa)
- Funders
- Mayo Clinic
- Glenn Foundation for Medical Research
- Harvard Medical School
- National Natural Science Foundation of China (207819, 269901, 81971327)
- Akershus Universitetssykehus
- Zhengzhou University
- Norges Forskningsråd (262175, 277813)
- Norges Idrettshøgskole (R01 AG019719, R01 DK100263, R37 AG028730)
- Sun Yat-sen University
- Jinan University
- Topics
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Receptors and Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Molecular Research
- Keywords
- NAD+, brain aging, neurodegenerative diseases, neuronal resilience, NAD+ metabolism, neurological disease treatment
- MeSH terms
- Aging, Animals, Brain, Cell Line, Humans, NAD, Neurons, Neurodegenerative Diseases, Mice, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
A language model drew the claims from the paper on 2026-10-05, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-05 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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