安普克
衰老
生酮饮食
内分泌学
内科学
细胞生物学
蛋白激酶A
生物
AMP活化蛋白激酶
基因剔除小鼠
激酶
医学
神经科学
生物化学
受体
表型
癫痫
基因
作者
Sung-Jen Wei,Joseph Schell,E. Sandra Chocrón,Mahboubeh Varmazyad,Guogang Xu,Wan Hsi Chen,Gloria Martı́nez,Felix F. Dong,Prethish Sreenivas,Rolando Trevino,Haiyan Jiang,Yan Du,Afaf Saliba,Wei Qian,Brandon Lorenzana,Alia Nazarullah,Jenny C. Chang,Kumar Sharma,Erin Munkácsy,Nobuo Horikoshi,David Gius
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-05-17
卷期号:10 (20)
被引量:11
标识
DOI:10.1126/sciadv.ado1463
摘要
A ketogenic diet (KD) is a high-fat, low-carbohydrate diet that leads to the generation of ketones. While KDs improve certain health conditions and are popular for weight loss, detrimental effects have also been reported. Here, we show mice on two different KDs and, at different ages, induce cellular senescence in multiple organs, including the heart and kidney. This effect is mediated through adenosine monophosphate-activated protein kinase (AMPK) and inactivation of mouse double minute 2 (MDM2) by caspase-2, leading to p53 accumulation and p21 induction. This was established using p53 and caspase-2 knockout mice and inhibitors to AMPK, p21, and caspase-2. In addition, senescence-associated secretory phenotype biomarkers were elevated in serum from mice on a KD and in plasma samples from patients on a KD clinical trial. Cellular senescence was eliminated by a senolytic and prevented by an intermittent KD. These results have important clinical implications, suggesting that the effects of a KD are contextual and likely require individual optimization.
科研通智能强力驱动
Strongly Powered by AbleSci AI