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      NAD + intermediates: The biology and therapeutic potential of NMN and NR

      research-article
      1 , 2 , 3
      Cell metabolism

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          Abstract

          Research on the biology of NAD + has been gaining momentum, providing many critical insights into the pathogenesis of age-associated functional decline and diseases. In particular, two key NAD + intermediates, nicotinamide riboside (NR) and nicotinamide mononucleotide (NMN), have been extensively studied over the past several years. Supplementing these NAD + intermediates has shown preventive and therapeutic effects, ameliorating age-associated pathophysiologies and disease conditions. Although the pharmacokinetics and metabolic fates of NMN and NR are still under intensive investigation, these NAD + intermediates can exhibit distinct behavior and their fates appear to depend on the tissue distribution and expression levels of NAD + biosynthetic enzymes, nucleotidases, and presumptive transporters for each. A comprehensive concept that connects NAD + metabolism to the control of aging and longevity in mammals has been proposed, and the stage is now set to test whether these exciting preclinical results can be translated to improve human health.

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          Author and article information

          Journal
          101233170
          32527
          Cell Metab
          Cell Metab.
          Cell metabolism
          1550-4131
          1932-7420
          14 November 2017
          14 December 2017
          06 March 2018
          06 March 2019
          : 27
          : 3
          : 513-528
          Affiliations
          [1 ]Center for Human Nutrition, Division of Geriatrics and Nutritional Science, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA
          [2 ]Department of Physiology and Institute for Diabetes, Obesity, and Metabolism, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA
          [3 ]Department of Developmental Biology, Department of Medicine (Joint), Washington University School of Medicine, Campus Box 8103, 660 South Euclid Avenue, St. Louis, MO 63110, USA
          Author notes
          Contact Information: Jun Yoshino, MD., Ph.D., Assistant Professor of Medicine, Washington University School of Medicine, Campus Box 8103, 660 South Euclid Avenue, St. Louis, MO 63110, USA, Phone: (314) 362-8119, Fax: (314) 362-8230, jyoshino@ 123456wustl.edu , Joseph Baur, Ph.D., Associate Professor of Physiology, Perelman School of Medicine, University of Pennsylvania, 12-114 Smilow Center for Translational Research, 3400 Civic Center Blvd, Building 421, Philadelphia, PA 19104-5160, 215-746-4585 (office), 215-898-5408 (fax), baur@ 123456pennmedicine.upenn.edu , Shin-ichiro Imai, M.D., Ph.D. (Lead Contact), Professor, Department of Developmental Biology, Department of Medicine (Joint), Campus Box 8103, 660 South Euclid Avenue, St. Louis, MO 63110, USA, Tel: (314) 362-7228, Fax: (314) 362-7058, imaishin@ 123456wustl.edu
          [*]

          These three authors equally contributed to this work.

          Article
          PMC5842119 PMC5842119 5842119 nihpa919895
          10.1016/j.cmet.2017.11.002
          5842119
          29249689
          348f06b5-7f27-4ac8-8e61-a694f70a8b4d
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