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NAD+ flux is maintained in aged mice despite lower tissue concentrations
Open accessAbstract
NAD+ is an essential coenzyme for all living cells. NAD+ concentrations decline with age, but whether this reflects impaired production or accelerated consumption remains unclear. We employed isotope tracing and mass spectrometry to probe age-related changes in NAD+ metabolism across tissues. In aged mice, we observed modest tissue NAD+ depletion (median decrease ∼30%). Circulating NAD+ precursors were not significantly changed, and isotope tracing showed the unimpaired synthesis of nicotinamide from tryptophan. In most tissues of aged mice, turnover of the smaller tissue NAD+ pool was modestly faster such that absolute NAD+ biosynthetic flux was maintained, consistent with more active NAD+-consuming enzymes. Calorie restriction partially mitigated age-associated NAD+ decline by decreasing consumption. Acute inflammatory stress induced by LPS decreased NAD+ by impairing synthesis in both young and aged mice. Thus, the decline in NAD+ with normal aging is relatively subtle and occurs despite maintained NAD+ production, likely due to increased consumption.
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“It is recognized the decrease of NAD+ levels in various tissues during aging [11, 13, 96, 97], playing a critical role in the pathophysiology of several diseases, including age-associated metabolic disorders, neurodegenerative diseases, and mental disorders [14].”
From NAD+ Precursors Nicotinamide Mononucleotide (NMN) and Nicotinamide Riboside (NR): Potential Dietary Contribution to Health (2023) · cites this paper as [96]
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1 retracted
Age 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
RetractedGomes, 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
NAD + in aging, metabolism, and neurodegeneration
Verdin, E. (2015) · Science · doi:10.1126/science.aac4854 · Cited by 1,319
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
Someya, S., Yu, W., Hallows, W. C., Xu, J., Vann, J. M., Leeuwenburgh, C., Tanokura, M., Denu, J. M., & Prolla, T. A. (2010) · Cell · doi:10.1016/j.cell.2010.10.002 · Cited by 1,150
NAD+ 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
Self-citationRegulation of mammalian nucleotide metabolism and biosynthesis
Lane, A. N., & Fan, T. W.-M. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv047 · Cited by 959
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-citationMills, K. F., Yoshida, S., Stein, L. R., Grozio, A., Kubota, S., Sasaki, Y., Redpath, P., Migaud, M. E., Apte, R. S., Uchida, K., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.09.013 · Cited by 930
Self-citationNampt/PBEF/Visfatin Regulates Insulin Secretion in β Cells as a Systemic NAD Biosynthetic Enzyme
Revollo, J. R., Körner, A., Mills, K. F., Satoh, A., Wang, T., Garten, A., Dasgupta, B., Sasaki, Y., Wolberger, C., Townsend, R. R., et al. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.09.003 · Cited by 911
Camacho-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
Fulco, M., Cen, Y., Zhao, P., Hoffman, E. P., McBurney, M. W., Sauve, A. A., & Sartorelli, V. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.02.004 · Cited by 843
Caloric restriction improves health and survival of rhesus monkeys
Mattison, J. A., Colman, R. J., Beasley, T. M., Allison, D. B., Kemnitz, J. W., Roth, G. S., Ingram, D. K., Weindruch, R., de Cabo, R., & Anderson, R. M. (2017) · Nature Communications · doi:10.1038/ncomms14063 · Cited by 838
PARP-1 inhibition increases mitochondrial metabolism through SIRT1 activation
Bai, P., Cantó, C., Oudart, H., Brunyánszki, A., Cen, Y., Thomas, C., Yamamoto, H., Huber, A., Kiss, B., Houtkooper, R. H., et al. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.03.004 · Cited by 837
The power to reduce: pyridine nucleotides—small molecules with a multitude of functions
Pollak, N., Dölle, C., & Ziegler, M. (2007) · Biochemical Journal · doi:10.1042/bj20061638 · Cited by 730
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
Data Conversion with ProteoWizard msConvert
Adusumilli, R., & Mallick, P. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6747-6_23 · Cited by 609
Tissue-specific regulation of SIRT1 by calorie restriction
Chen, D., Bruno, J., Easlon, E., Lin, S.-J., Cheng, H.-L., Alt, F. W., & Guarente, L. (2008) · Genes & Development · doi:10.1101/gad.1650608 · Cited by 567
Quantitative Analysis of NAD Synthesis-Breakdown Fluxes
Liu, L., Su, X., Quinn, W. J., Hui, S., Krukenberg, K., Frederick, D. W., Redpath, P., Zhan, L., Chellappa, K., White, E., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.03.018 · Cited by 564
Self-citationAge-Associated Changes In Oxidative Stress and NAD+ Metabolism In Human Tissue
Massudi, H., Grant, R., Braidy, N., Guest, J., Farnsworth, B., & Guillemin, G. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042357 · Cited by 545
NAD + metabolism: Bioenergetics, signaling and manipulation for therapy
Yang, Y. J., & Sauve, A. A. (2016) · Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics · doi:10.1016/j.bbapap.2016.06.014 · Cited by 509
Macrophage 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
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
Determination of confidence intervals of metabolic fluxes estimated from stable isotope measurements
Antoniewicz, M. R., Kelleher, J. K., & Stephanopoulos, G. N. (2006) · Metabolic Engineering · doi:10.1016/j.ymben.2006.01.004 · Cited by 451
Senescent cells promote tissue NAD+ decline during ageing via the activation of CD38+ macrophages
Covarrubias, A. J., Kale, A., Perrone, R., Lopez-Dominguez, J. A., Pisco, A. O., Kasler, H. G., Schmidt, M. S., Heckenbach, I., Kwok, R., Wiley, C. D., et al. (2020) · Nature Metabolism · doi:10.1038/s42255-020-00305-3 · Cited by 420
Increase in Activity During Calorie Restriction Requires Sirt1
Chen, D., Steele, A. D., Lindquist, S., & Guarente, L. (2005) · Science · doi:10.1126/science.1118357 · Cited by 419
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
Tarragó, M. G., Chini, C. C. S., Kanamori, K. S., Warner, G. M., Caride, A., de Oliveira, G. C., Rud, M., Samani, A., Hein, K. Z., Huang, R., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.03.016 · Cited by 384
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
CD38 ecto-enzyme in immune cells is induced during aging and regulates NAD+ and NMN levels
Chini, C. C. S., Peclat, T. R., Warner, G. M., Kashyap, S., Espindola-Netto, J. M., de Oliveira, G. C., Gomez, L. S., Hogan, K. A., Tarragó, M. G., Puranik, A. S., et al. (2020) · Nature Metabolism · doi:10.1038/s42255-020-00298-z · Cited by 349
Self-citationSirtuins mediate mammalian metabolic responses to nutrient availability
Chalkiadaki, A., & Guarente, L. (2012) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2011.225 · Cited by 344
Nicotinamide Improves Aspects of Healthspan, but Not Lifespan, in Mice
Mitchell, S. J., Bernier, M., Aon, M. A., Cortassa, S., Kim, E. Y., Fang, E. F., Palacios, H. H., Ali, A., Navas-Enamorado, I., Di Francesco, A., et al. (2018) · Cell Metabolism · doi:10.1016/j.cmet.2018.02.001 · Cited by 338
Self-citationSLC25A51 is a mammalian mitochondrial NAD(+) transporter
Luongo, T. S., Eller, J. M., Lu, M.-J., Niere, M., Raith, F., Perry, C., Bornstein, M. R., Oliphint, P., Wang, L., McReynolds, M. R., et al. (2020) · Nature · doi:10.1038/s41586-020-2741-7 · Cited by 308
Self-citationMetabolite Spectral Accuracy on Orbitraps
Su, X., Lu, W., & Rabinowitz, J. D. (2017) · Analytical Chemistry · doi:10.1021/acs.analchem.7b00396 · Cited by 270
Self-citationStein, L. R., & Imai, S. (2014) · The EMBO Journal · doi:10.1002/embj.201386917 · Cited by 265
P7C3 Neuroprotective Chemicals Function by Activating the Rate-Limiting Enzyme in NAD Salvage
Wang, G., Han, T., Nijhawan, D., Theodoropoulos, P., Naidoo, J., Yadavalli, S., Mirzaei, H., Pieper, A. A., Ready, J. M., & McKnight, S. L. (2014) · Cell · doi:10.1016/j.cell.2014.07.040 · Cited by 243
Guan, Y., Wang, S.-R., Huang, X.-Z., Xie, Q.-H., Xu, Y.-Y., Shang, D., & Hao, C.-M. (2017) · Journal of the American Society of Nephrology · doi:10.1681/asn.2016040385 · Cited by 238
Ubaida‐Mohien, C., Lyashkov, A. E., González‐Freire, M., Tharakan, R., Shardell, M. D., Moaddel, R., Semba, R. D., Chia, C. W., Gorospe, M., Sen, R., et al. (2019) · eLife · doi:10.7554/elife.49874 · Cited by 234
Sauve, A. A., & Schramm, V. L. (2003) · Biochemistry · doi:10.1021/bi034959l · Cited by 213
NAD and the aging process: role in life, death and everything in between
Chini, C. C. S., Tarragó, M. G., & Chini, E. N. (2017) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2016.11.003 · Cited by 208
The Plasma NAD + Metabolome Is Dysregulated in “Normal” Aging
Clement, J., Wong, M. W. K., Poljak, A., Sachdev, P. S., & Braidy, N. (2018) · Rejuvenation Research · doi:10.1089/rej.2018.2077 · Cited by 206
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Kory, N., uit de Bos, J., van der Rijt, S., Jankovic, N., Güra, M., Arp, N., Pena, I. A., Prakash, G., Chan, S. H., Kunchok, T., et al. (2020) · Science Advances · doi:10.1126/sciadv.abe5310 · Cited by 205
CD38 Is Robustly Induced in Human Macrophages and Monocytes in Inflammatory Conditions
Amici, S. A., Young, N. A., Miranda, J. N., Jablonski, K., Arcos, J., Rosas, L. E., Papenfuss, T. L., Torrelles, J. B., Jarjour, W. N., & Guerau‐de‐Arellano, M. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01593 · Cited by 203
Emerging therapeutic roles for NAD+ metabolism in mitochondrial and age‐related disorders
Srivastava, S. (2016) · Clinical and Translational Medicine · doi:10.1186/s40169-016-0104-7 · Cited by 200
NAD + metabolism: A therapeutic target for age-related metabolic disease
Mouchiroud, L., Houtkooper, R. H., & Auwerx, J. (2013) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.3109/10409238.2013.789479 · Cited by 193
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
Extraction and Quantitation of Nicotinamide Adenine Dinucleotide Redox Cofactors
Lu, W., Wang, L., Chen, L., Hui, S. T., & Rabinowitz, J. D. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7014 · Cited by 189
Self-citationMcReynolds, M. R., Chellappa, K., & Baur, J. A. (2020) · Experimental Gerontology · doi:10.1016/j.exger.2020.110888 · Cited by 179
Self-citationAksoy, P., Escande, C., White, T. A., Thompson, M., Soares, S. M., Benech, J. C., & Chini, E. N. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.08.066 · Cited by 178
Caloric restriction: From soup to nuts
Spindler, S. R. (2009) · Ageing Research Reviews · doi:10.1016/j.arr.2009.10.003 · Cited by 169
Boosting NAD+ with a small molecule that activates NAMPT
Gardell, S. J., Hopf, M., Khan, A., Dispagna, M., Hampton Sessions, E., Falter, R., Kapoor, N., Brooks, J., Culver, J., Petucci, C., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11078-z · Cited by 169
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
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
Regulation Analysis Of Energy Metabolism
Brand, M. D. (1997) · Journal of Experimental Biology · doi:10.1242/jeb.200.2.193 · Cited by 132
The caloric restriction paradigm: Implications for healthy human aging
Anderson, R. M., & Weindruch, R. (2012) · American Journal of Human Biology · doi:10.1002/ajhb.22243 · Cited by 125
Epistasis-driven identification of SLC25A51 as a regulator of human mitochondrial NAD import
Girardi, E., Agrimi, G., Goldmann, U., Fiume, G., Lindinger, S., Sedlyarov, V., Srndic, I., Gürtl, B., Agerer, B., Kartnig, F., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-19871-x · Cited by 123
Sauve, A. A., Munshi, C. B., Lee, H. C., & Schramm, V. L. (1998) · Biochemistry · doi:10.1021/bi981248s · Cited by 120
Peak Annotation and Verification Engine for Untargeted LC–MS Metabolomics
Wang, L., Xing, X., Chen, L., Yang, L., Su, X., RABITZ, H. A., Lu, W., & Rabinowitz, J. D. (2018) · Analytical Chemistry · doi:10.1021/acs.analchem.8b03132 · Cited by 120
Self-citationMatalonga, J., Glaría, E., Bresque, M., Escande, C., Carbo, J. M. C. I., Kiefer, K., Vicente, R., León, T. E., Beceiro, S., Pascual-García, M., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.01.007 · Cited by 118
SIRT3 and mitochondrial metabolism in neurodegenerative diseases
Salvatori, I., Valle, C., Ferri, A., & Carrì, M. T. (2017) · Neurochemistry International · doi:10.1016/j.neuint.2017.04.012 · Cited by 110
Musso, T., Deaglio, S., Franco, L., Calosso, L., Badolato, R., Garbarino, G. M., Dianzani, U., & Malavasi, F. (2001) · PubMed · Cited by 95
Musso, T., Deaglio, S., Franco, L., Calosso, L., Badolato, R., Garbarino, G. M., Dianzani, U., & Malavasi, F. (2001) · Journal of Leukocyte Biology · doi:10.1189/jlb.69.4.605 · Cited by 94
NMNAT2‐mediated NAD + generation is essential for quality control of aged oocytes
Wu, X., Hu, F., Zeng, J., Han, L., Qiu, D., Wang, H., Ge, J., Ying, X., & Wang, Q. (2019) · Aging Cell · doi:10.1111/acel.12955 · Cited by 92
Frederick, D. W., Davis, J. G., Dávila, A., Agarwal, B., Michán, S., Puchowicz, M. A., Nakamaru‐Ogiso, E., & Baur, J. A. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.579565 · Cited by 91
Self-citationSong, J., Ke, S.-F., Zhou, C.-C., Zhang, S.-L., Guan, Y.-F., Xu, T.-Y., Sheng, C., Wang, P., & Miao, C. (2013) · The Journals of Gerontology Series A · doi:10.1093/gerona/glt122 · Cited by 79
Kang, B., Tirumurugaan, K. G., Deshpande, D. A., Amrani, Y., Panettieri, R. A., Walseth, T. F., & Karman, M. S. (2006) · The FASEB Journal · doi:10.1096/fj.05-4585fje · Cited by 70
Dölle, C., Niere, M., Lohndal, E., & Ziegler, M. (2009) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-0190-4 · Cited by 70
Sims, C. A., Guan, Y., Mukherjee, S., Singh, K., Botolin, P., Dávila, A., & Baur, J. A. (2018) · JCI Insight · doi:10.1172/jci.insight.120182 · Cited by 67
Self-citationMoreno‐Vinasco, L., Quijada, H., Sammani, S., Siegler, J. H., Letsiou, E., Deaton, R. J., Saadat, L., Zaidi, R., Messana, J., Gann, P. H., et al. (2014) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2012-0519oc · Cited by 49
Roles of interleukin-1 and tumor necrosis factor in lipopolysaccharide-induced hypoglycemia
Vogel, S. N., Henricson, B. E., & Neta, R. (1991) · Infection and Immunity · doi:10.1128/iai.59.7.2494-2498.1991 · Cited by 46
Deuterium isotope effects on initial rates of the liver alcohol dehydrogenase reaction. V
Bush, K., SHINER, V. J. J., & Mahler, H. R. (1973) · Biochemistry · doi:10.1021/bi00747a037 · Cited by 42
NAD SYNTHESIS IN ANIMAL TISSUES
Dietrich, L. S., Muniz, O. E., & Powanda, M. C. (1968) · THE JOURNAL OF VITAMINOLOGY · doi:10.5925/jnsv1954.14.supplement_123 · Cited by 40
Alterations in energy substrate metabolism in mice with different degrees of sepsis
Irahara, T., Sato, N., Otake, K., Matsumura, S., Inoue, K., Ishihara, K., Fushiki, T., & Yokota, H. (2018) · Journal of Surgical Research · doi:10.1016/j.jss.2018.01.021 · Cited by 37
Nicotinamide adenine dinucleotide replenishment rescues colon degeneration in aged mice
Zhu, X., Shen, W., Wang, Y., Jaiswal, A., Ju, Z., & Sheng, Q. (2017) · Signal Transduction and Targeted Therapy · doi:10.1038/sigtrans.2017.17 · Cited by 31
Shibata, K. (2018) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.64.90 · Cited by 30
Wei, X., Jia, R., Wang, G., Hong, S., Song, L., Sun, B., Chen, K., Wang, N., Wang, Q., Luo, X. M., et al. (2020) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2020.108377 · Cited by 29
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Self-citationBehr, A., Taguchi, H., & Gholson, R. K. (1981) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(81)91817-9 · Cited by 8
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Metadata
- Authors
- McReynolds, M. R., Chellappa, K., Chiles, E., Jankowski, C., Shen, Y., Chen, L., Descamps, H. C., Mukherjee, S., Bhat, Y. R., Lingala, S. R., Chu, Q., Botolin, P., Hayat, F., Doke, T., Susztak, K., Thaiss, C. A., Lu, W., Migaud, M. E., Su, X., Rabinowitz, J. D., & Baur, J. A.
- Affiliations
- Princeton University (US)
- University of Pennsylvania (US)
- Rutgers, The State University of New Jersey (US)
- USA Mitchell Cancer Institute (US)
- Corresponding author
- Rabinowitz, Joshua D.
- Baur, Joseph A.
- ORCID
- Venue
- Cell Systems
- Publisher
- Elsevier BV
- Published
- 2021-12
- Volume
- 12
- Issue
- 12
- Pages
- 1160-1172.e4
- ISSN
- 2405-4712 (ISSN-L)
- PMC
- PMC8678178
- OpenAlex
- W3199408799
- Cited by
- 112
- References
- 79
- Citations by year
- 2026: 19 · 2025: 21 · 2024: 25 · 2023: 28 · 2022: 17 · 2021: 2
- FWCI
- 9.92
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- journal article
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- en
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- www.elsevier.com/legal/tdmrep-license (tdm)
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- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell Systems (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIDDK (R01DK098656, DP1DK113643)
- Crohn's and Colitis Foundation of America
- National Institutes of Health
- Princeton University
- Children's Hospital of Philadelphia
- Rutgers Cancer Institute of New Jersey
- Diabetes Research Center (P30-DK19525)
- Burroughs Wellcome Fund
- NIA (R01AG043483)
- Howard Hughes Medical Institute
- NCI (CA211437, -CCSG P30CA072720-5923)
- 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
- NAD+ metabolism, aging, NAD biosynthesis, NAD+ consumption, tryptophan, NAD+ precursors, caloric restriction, lipopolysaccharide, inflammation, aged mice
- MeSH terms
- Aging, Animals, NAD, Niacinamide, Caloric Restriction, Mice
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.
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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