SIRT1 Deacetylase in SF1 Neurons Protects against Metabolic Imbalance

被引:141
作者
Ramadori, Giorgio [1 ]
Fujikawa, Teppei [1 ]
Anderson, Jason [1 ]
Berglund, Eric D. [1 ]
Frazao, Renata [1 ]
Michan, Shaday [2 ,3 ]
Vianna, Claudia R. [1 ]
Sinclair, David A. [2 ]
Elias, Carol F. [1 ]
Coppari, Roberto [1 ,4 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Div Hypothalam Res, Dallas, TX 75390 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Paul F Glenn Labs, Boston, MA 02115 USA
[3] Inst Nacl Salud, Inst Geriatria, Mexico City 04510, DF, Mexico
[4] Univ Politecn Marche, Dipartimento Med Sperimentale & Clin, I-60020 Ancona, Italy
基金
美国国家卫生研究院;
关键词
VENTROMEDIAL HYPOTHALAMIC NUCLEUS; DIET-INDUCED OBESITY; GLUCOSE-HOMEOSTASIS; MITOCHONDRIAL-FUNCTION; CALORIE RESTRICTION; ARCUATE NUCLEUS; GENE-EXPRESSION; POMC NEURONS; BODY-WEIGHT; DISEASE;
D O I
10.1016/j.cmet.2011.06.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chronic feeding on high-calorie diets causes obesity and type 2 diabetes mellitus (T2DM), illnesses that affect hundreds of millions. Thus, understanding the pathways protecting against diet-induced metabolic imbalance is of paramount medical importance. Here, we show that mice lacking SIRT1 in steroidogenic factor 1 (SF1) neurons are hypersensitive to dietary obesity owing to maladaptive energy expenditure. Also, mutant mice have increased susceptibility to developing dietary T2DM due to insulin resistance in skeletal muscle. Mechanistically, these aberrations arise, in part, from impaired metabolic actions of the neuropeptide orexin-A and the hormone leptin. Conversely, mice overexpressing SIRT1 in SF1 neurons are more resistant to diet-induced obesity and insulin resistance due to increased energy expenditure and enhanced skeletal muscle insulin sensitivity. Our results unveil important protective roles of SIRT1 in SF1 neurons against dietary metabolic imbalance.
引用
收藏
页码:301 / 312
页数:12
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