共 50 条
Ketogenic diet induces p53-dependent cellular senescence in multiple organs
被引:18
|作者:
Wei, Sung-Jen
[1
,2
]
Schell, Joseph R.
[1
,2
]
Chocron, E. Sandra
[1
,2
]
Varmazyad, Mahboubeh
[1
,2
]
Xu, Guogang
[1
,2
]
Chen, Wan Hsi
[1
,2
]
Martinez, Gloria M.
[1
,2
]
Dong, Felix F.
[1
,2
]
Sreenivas, Prethish
[1
,2
]
Trevino, Rolando
[1
,2
]
Jiang, Haiyan
[1
,2
]
Du, Yan
[3
,4
]
Saliba, Afaf
[3
]
Qian, Wei
[5
,6
]
Lorenzana, Brandon
[1
,2
]
Nazarullah, Alia
[1
,2
]
Chang, Jenny
[5
,6
]
Sharma, Kumar
[3
,7
]
Munkacsy, Erin
[1
,2
]
Horikoshi, Nobuo
[1
,2
]
Gius, David
[1
,2
]
机构:
[1] UT Hlth San Antonio MD Anderson, Joe R & Teresa Lozano Long Sch Med, Dept Radiat Oncol, Mays Canc Ctr, San Antonio, TX 78229 USA
[2] UT Hlth San Antonio, Barshop Inst Longev & Aging Studies, San Antonio, TX 78229 USA
[3] UT Hlth San Antonio, Ctr Precis Med, San Antonio, TX USA
[4] UT Hlth San Antonio, Sch Nursing, San Antonio, TX USA
[5] Houston Methodist Canc Ctr, Houston, TX USA
[6] Houston Methodist Res Inst, Houston, TX USA
[7] UT Hlth San Antonio, Dept Med, Div Nephrol, San Antonio, TX USA
来源:
关键词:
BETA-HYDROXYBUTYRATE;
OXIDATIVE STRESS;
PROTEIN;
P53;
CELLS;
MICE;
METABOLISM;
LONGEVITY;
COMPLEX;
HEALTH;
D O I:
10.1126/sciadv.ado1463
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
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.
引用
收藏
页数:17
相关论文