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Why NAD + Declines during Aging: It’s Destroyed
Open accessAbstract
NAD(+) is required not only for life but for a long life. In this issue, Camacho-Pereira et al. (2016) implicate CD38 in the decline of NAD(+) during aging, with implications for combating age-related diseases.
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“Senescent cells can decrease NAD+ through SASP activation of the NAD-degrading enzyme CD38 on the surface of macrophages and, remarkably, senolytics partially restore tissue NAD+ levels139,140.”
From Cellular senescence and senolytics: the path to the clinic (2022) · cites this paper as [140]
Experimental — accuracy not yet measuredIn the citing paper
“Sirtuin activity and NAD levels both decline with age116,117.”
From Ageing and rejuvenation of tissue stem cells and their niches (2023) · cites this paper as [117]
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NAD + repletion improves mitochondrial and stem cell function and enhances life span in mice
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“Observed effects include increased insulin sensitivity, reversal of mitochondrial dysfunction, reduced stem cell senescence, and extension of lifespan (Bai et al., 2011; Gomes et al., 2013; Yoshino et al., 2011; Zhang et al., 2016).”
BackgroundNutrient-Sensitive Mitochondrial NAD+ Levels Dictate Cell Survival
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Flavonoid Apigenin Is an Inhibitor of the NAD+ase CD38
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Metadata
- Authors
- Schultz, M. B., & Sinclair, D. A.
- Affiliations
- Harvard University (US)
- Corresponding author
- Sinclair, David A.
- ORCID
- Sinclair, David A.
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2016-06
- Volume
- 23
- Issue
- 6
- Pages
- 965-966
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC5088772
- OpenAlex
- W2423823537
- Cited by
- 126
- References
- 10
- Citations by year
- 2026: 9 · 2025: 4 · 2024: 14 · 2023: 14 · 2022: 22 · 2021: 25 · 2020: 16 · 2019: 12 · 2018: 6 · 2017: 3 · 2016: 1
- FWCI
- 4.21
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute on Aging (R37AG028730)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK100263)
- Topics
- Health Sciences › Medicine › Geriatrics and Gerontology › Sirtuins and Resveratrol in Medicine
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Molecular Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Keywords
- aging, CD38, NAD+ metabolism, age-related diseases, sirtuins, NAD+ salvage pathway
- MeSH terms
- Aging, Animals, Mitochondria, Models, Biological, NAD, Mice, ADP-ribosyl Cyclase 1
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