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Nicotinamide riboside is uniquely and orally bioavailable in mice and humans
Nicotinamide riboside (NR) is in wide use as an NAD(+) precursor vitamin. Here we determine the time and dose-dependent effects of NR on blood NAD(+) metabolism in humans. We report that human blood NAD(+) can rise as much as 2.7-fold with a single oral dose of NR in a pilot study of one individual,...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062546/ https://www.ncbi.nlm.nih.gov/pubmed/27721479 http://dx.doi.org/10.1038/ncomms12948 |
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author | Trammell, Samuel A. J. Schmidt, Mark S. Weidemann, Benjamin J. Redpath, Philip Jaksch, Frank Dellinger, Ryan W. Li, Zhonggang Abel, E. Dale Migaud, Marie E. Brenner, Charles |
author_facet | Trammell, Samuel A. J. Schmidt, Mark S. Weidemann, Benjamin J. Redpath, Philip Jaksch, Frank Dellinger, Ryan W. Li, Zhonggang Abel, E. Dale Migaud, Marie E. Brenner, Charles |
author_sort | Trammell, Samuel A. J. |
collection | PubMed |
description | Nicotinamide riboside (NR) is in wide use as an NAD(+) precursor vitamin. Here we determine the time and dose-dependent effects of NR on blood NAD(+) metabolism in humans. We report that human blood NAD(+) can rise as much as 2.7-fold with a single oral dose of NR in a pilot study of one individual, and that oral NR elevates mouse hepatic NAD(+) with distinct and superior pharmacokinetics to those of nicotinic acid and nicotinamide. We further show that single doses of 100, 300 and 1,000 mg of NR produce dose-dependent increases in the blood NAD(+) metabolome in the first clinical trial of NR pharmacokinetics in humans. We also report that nicotinic acid adenine dinucleotide (NAAD), which was not thought to be en route for the conversion of NR to NAD(+), is formed from NR and discover that the rise in NAAD is a highly sensitive biomarker of effective NAD(+) repletion. |
format | Online Article Text |
id | pubmed-5062546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50625462016-10-27 Nicotinamide riboside is uniquely and orally bioavailable in mice and humans Trammell, Samuel A. J. Schmidt, Mark S. Weidemann, Benjamin J. Redpath, Philip Jaksch, Frank Dellinger, Ryan W. Li, Zhonggang Abel, E. Dale Migaud, Marie E. Brenner, Charles Nat Commun Article Nicotinamide riboside (NR) is in wide use as an NAD(+) precursor vitamin. Here we determine the time and dose-dependent effects of NR on blood NAD(+) metabolism in humans. We report that human blood NAD(+) can rise as much as 2.7-fold with a single oral dose of NR in a pilot study of one individual, and that oral NR elevates mouse hepatic NAD(+) with distinct and superior pharmacokinetics to those of nicotinic acid and nicotinamide. We further show that single doses of 100, 300 and 1,000 mg of NR produce dose-dependent increases in the blood NAD(+) metabolome in the first clinical trial of NR pharmacokinetics in humans. We also report that nicotinic acid adenine dinucleotide (NAAD), which was not thought to be en route for the conversion of NR to NAD(+), is formed from NR and discover that the rise in NAAD is a highly sensitive biomarker of effective NAD(+) repletion. Nature Publishing Group 2016-10-10 /pmc/articles/PMC5062546/ /pubmed/27721479 http://dx.doi.org/10.1038/ncomms12948 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Trammell, Samuel A. J. Schmidt, Mark S. Weidemann, Benjamin J. Redpath, Philip Jaksch, Frank Dellinger, Ryan W. Li, Zhonggang Abel, E. Dale Migaud, Marie E. Brenner, Charles Nicotinamide riboside is uniquely and orally bioavailable in mice and humans |
title | Nicotinamide riboside is uniquely and orally bioavailable in mice and humans |
title_full | Nicotinamide riboside is uniquely and orally bioavailable in mice and humans |
title_fullStr | Nicotinamide riboside is uniquely and orally bioavailable in mice and humans |
title_full_unstemmed | Nicotinamide riboside is uniquely and orally bioavailable in mice and humans |
title_short | Nicotinamide riboside is uniquely and orally bioavailable in mice and humans |
title_sort | nicotinamide riboside is uniquely and orally bioavailable in mice and humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5062546/ https://www.ncbi.nlm.nih.gov/pubmed/27721479 http://dx.doi.org/10.1038/ncomms12948 |
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