作者
Cameron G McCarthy, Saroj Chakraborty, Gagandeep Singh, Beng San Yeoh, Zachary J Schreckenberger, Avinash Singh, Blair Mell, Nicole R Bearss, Tao Yang, Xi Cheng, Matam Vijay-Kumar, Camilla F Wenceslau, Bina Joe
发表日期
2021/10/10
期刊
JCI insight
卷号
6
期号
20
出版商
American Society for Clinical Investigation
简介
Autophagy has long been associated with longevity, and it is well established that autophagy reverts and prevents vascular deterioration associated with aging and cardiovascular diseases. Currently, our understanding of how autophagy benefits the vasculature is centered on the premise that reduced autophagy leads to the accumulation of cellular debris, resulting in inflammation and oxidative stress, which are then reversed by reconstitution or upregulation of autophagic activity. Evolutionarily, autophagy also functions to mobilize endogenous nutrients in response to starvation. Therefore, we hypothesized that the biosynthesis of the most physiologically abundant ketone body, β-hydroxybutyrate (βHB), would be autophagy dependent and exert vasodilatory effects via its canonical receptor, Gpr109a. To the best of our knowledge, we have revealed for the first time that the biosynthesis of βHB can be impaired by …
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