Impairment of an Endothelial NAD<sup>+</sup>-H<sub>2</sub>S Signaling Network Is a Reversible Cause of Vascular Aging.

Détails

ID Serval
serval:BIB_B144D581C7C5
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Impairment of an Endothelial NAD<sup>+</sup>-H<sub>2</sub>S Signaling Network Is a Reversible Cause of Vascular Aging.
Périodique
Cell
Auteur⸱e⸱s
Das A., Huang G.X., Bonkowski M.S., Longchamp A., Li C., Schultz M.B., Kim L.J., Osborne B., Joshi S., Lu Y., Treviño-Villarreal J.H., Kang M.J., Hung T.T., Lee B., Williams E.O., Igarashi M., Mitchell J.R., Wu L.E., Turner N., Arany Z., Guarente L., Sinclair D.A.
ISSN
1097-4172 (Electronic)
ISSN-L
0092-8674
Statut éditorial
Publié
Date de publication
22/03/2018
Peer-reviewed
Oui
Volume
173
Numéro
1
Pages
74-89.e20
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
A decline in capillary density and blood flow with age is a major cause of mortality and morbidity. Understanding why this occurs is key to future gains in human health. NAD precursors reverse aspects of aging, in part, by activating sirtuin deacylases (SIRT1-SIRT7) that mediate the benefits of exercise and dietary restriction (DR). We show that SIRT1 in endothelial cells is a key mediator of pro-angiogenic signals secreted from myocytes. Treatment of mice with the NAD <sup>+</sup> booster nicotinamide mononucleotide (NMN) improves blood flow and increases endurance in elderly mice by promoting SIRT1-dependent increases in capillary density, an effect augmented by exercise or increasing the levels of hydrogen sulfide (H <sub>2</sub> S), a DR mimetic and regulator of endothelial NAD <sup>+</sup> levels. These findings have implications for improving blood flow to organs and tissues, increasing human performance, and reestablishing a virtuous cycle of mobility in the elderly.
Mots-clé
Aging, Animals, Endothelial Cells/cytology, Endothelial Cells/metabolism, Humans, Hydrogen Sulfide/metabolism, Mice, Mice, Knockout, Microvessels/metabolism, Mitochondria/metabolism, Muscle, Skeletal/metabolism, NAD/metabolism, Neovascularization, Physiologic, Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha/metabolism, Physical Conditioning, Animal, RNA Interference, RNA, Small Interfering/metabolism, Receptors, Notch/metabolism, Signal Transduction, Sirtuin 1/antagonists & inhibitors, Sirtuin 1/genetics, Sirtuin 1/metabolism, Vascular Endothelial Growth Factor A/metabolism, NAD(+), aging, angiogenesis, endurance, exercise, hydrogen sulfide, ischemia, nicotinamide mononucleotide, sirtuins, skeletal muscle capillaries
Pubmed
Web of science
Open Access
Oui
Financement(s)
Fonds national suisse / Carrières / P1LAP3_158895
Création de la notice
07/03/2021 13:38
Dernière modification de la notice
08/03/2021 7:26
Données d'usage