西妥因1
生物
锡尔图因
调解人
内分泌学
内科学
内皮功能障碍
钥匙(锁)
细胞生物学
NAD+激酶
内皮
生物化学
癌症研究
下调和上调
酶
基因
医学
生态学
作者
Abhirup Das,George Huang,Michael S. Bonkowski,Alban Longchamp,Catherine Li,Michael Schultz,Lynn‐Jee Kim,Brenna Osborne,Sanket Joshi,Yuancheng Ryan Lu,J. Humberto Treviño-Villarreal,Myung‐Jin Kang,Tzong‐Tyng Hung,Brendan Lee,Eric O. Williams,Masaki Igarashi,James R. Mitchell,Lindsay E. Wu,Nigel Turner,Zoltàn Arany
出处
期刊:Cell
[Cell Press]
日期:2018-03-01
卷期号:173 (1): 74-89.e20
被引量:433
标识
DOI:10.1016/j.cell.2018.02.008
摘要
Summary
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 (H2S), 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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