Cell · 2018
Impairment of an Endothelial NAD+-H2S Signaling Network Is a Reversible Cause of Vascular Aging.
СтатьяПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Das Abhirup, Huang George X, Bonkowski Michael S, Longchamp Alban, Li Catherine, Schultz Michael B, Kim Lynn-Jee, Osborne Brenna, Joshi Sanket, Lu Yuancheng, Treviño-Villarreal Jose Humberto, Kang Myung-Jin, Hung Tzong-Tyng, Lee Brendan, Williams Eric O, Igarashi Masaki, Mitchell James R, Wu Lindsay E, Turner Nigel, Arany Zolt, Guarente Leonard, Sinclair David A
Аннотация
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.
Предметные рубрики MeSH
AgingAnimalsEndothelial CellsHumansHydrogen SulfideMiceMice, KnockoutMicrovesselsMitochondriaMuscle, SkeletalNADNeovascularization, PhysiologicPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPhysical Conditioning, AnimalRNA InterferenceRNA, Small InterferingReceptors, NotchSignal TransductionSirtuin 1Vascular Endothelial Growth Factor A