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Impairment of an Endothelial NAD+-H2S Signaling Network Is a Reversible Cause of Vascular Aging
Author(s) -
Abhirup Das,
George Huang,
Michael S. Bonkowski,
Alban Longchamp,
Catherine Li,
Michael Schultz,
LynnJee Kim,
Brenna Osborne,
Sanket Joshi,
Yuancheng Ryan Lu,
J. Humberto Treviño-Villarreal,
MyungJin Kang,
TzongTyng Hung,
Brendan Lee,
Eric O. Williams,
Masaki Igarashi,
James R. Mitchell,
Lindsay E. Wu,
Nigel Turner,
Zoltàn Arany,
Leonard Guarente,
David Sinclair
Publication year - 2018
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2018.02.008
Subject(s) - nad+ kinase , biology , sirtuin , sirtuin 1 , mediator , microbiology and biotechnology , endothelium , endothelial dysfunction , key (lock) , endocrinology , medicine , cancer research , biochemistry , enzyme , downregulation and upregulation , gene , ecology
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 + 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 2 S), a DR mimetic and regulator of endothelial NAD + 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.

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