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NAD(+) oscillation and hypothalamic neuronal functions

A substantial body of evidence shows the importance of nicotinamide adenine dinucleotide (NAD(+)) biosynthesis and its regulation in a wide range of cellular metabolism. The expression of nicotinamide phosphoribosyltransferase (NAMPT) is regulated in a circadian manner by the core clock mechanism an...

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Autores principales: Tokizane, Kyohei, Imai, Shin-ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Faculty Opinions Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130408/
https://www.ncbi.nlm.nih.gov/pubmed/34046646
http://dx.doi.org/10.12703/r/10-42
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author Tokizane, Kyohei
Imai, Shin-ichiro
author_facet Tokizane, Kyohei
Imai, Shin-ichiro
author_sort Tokizane, Kyohei
collection PubMed
description A substantial body of evidence shows the importance of nicotinamide adenine dinucleotide (NAD(+)) biosynthesis and its regulation in a wide range of cellular metabolism. The expression of nicotinamide phosphoribosyltransferase (NAMPT) is regulated in a circadian manner by the core clock mechanism and NAD(+)-dependent sirtuins, producing the circadian oscillation of NAD(+). The hypothalamus is a critical center for the homeostatic regulation of metabolism, circadian rhythm, and age-associated physiology. The dysfunction of systemic NAD(+) biosynthesis over age affects the functions of hypothalamic neurons, causing age-associated metabolic pathophysiologies, including obesity and age-associated diseases. These recent studies suggest that NAD(+) oscillation contributes to the hypothalamic function, and its disruption produces circadian and aging-related metabolic disorders. Furthermore, new studies have demonstrated a novel intertissue NAD(+)-dependent communication as a potential target for preventing and treating such disorders and for extending the health span of humans.
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spelling pubmed-81304082021-05-26 NAD(+) oscillation and hypothalamic neuronal functions Tokizane, Kyohei Imai, Shin-ichiro Fac Rev Review Article A substantial body of evidence shows the importance of nicotinamide adenine dinucleotide (NAD(+)) biosynthesis and its regulation in a wide range of cellular metabolism. The expression of nicotinamide phosphoribosyltransferase (NAMPT) is regulated in a circadian manner by the core clock mechanism and NAD(+)-dependent sirtuins, producing the circadian oscillation of NAD(+). The hypothalamus is a critical center for the homeostatic regulation of metabolism, circadian rhythm, and age-associated physiology. The dysfunction of systemic NAD(+) biosynthesis over age affects the functions of hypothalamic neurons, causing age-associated metabolic pathophysiologies, including obesity and age-associated diseases. These recent studies suggest that NAD(+) oscillation contributes to the hypothalamic function, and its disruption produces circadian and aging-related metabolic disorders. Furthermore, new studies have demonstrated a novel intertissue NAD(+)-dependent communication as a potential target for preventing and treating such disorders and for extending the health span of humans. Faculty Opinions Ltd 2021-04-27 /pmc/articles/PMC8130408/ /pubmed/34046646 http://dx.doi.org/10.12703/r/10-42 Text en Copyright: © 2021 Imai S et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Tokizane, Kyohei
Imai, Shin-ichiro
NAD(+) oscillation and hypothalamic neuronal functions
title NAD(+) oscillation and hypothalamic neuronal functions
title_full NAD(+) oscillation and hypothalamic neuronal functions
title_fullStr NAD(+) oscillation and hypothalamic neuronal functions
title_full_unstemmed NAD(+) oscillation and hypothalamic neuronal functions
title_short NAD(+) oscillation and hypothalamic neuronal functions
title_sort nad(+) oscillation and hypothalamic neuronal functions
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130408/
https://www.ncbi.nlm.nih.gov/pubmed/34046646
http://dx.doi.org/10.12703/r/10-42
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