内分泌学
内科学
合成代谢
安普克
卡路里
脂肪变性
生物
脂肪生成
高胰岛素血症
昼夜节律
营养感应
肥胖
医学
脂肪组织
胰岛素抵抗
信号转导
酶
蛋白激酶A
生物化学
作者
Megumi Hatori,Christopher Vollmers,Amir Zarrinpar,Luciano DiTacchio,Eric A. Bushong,Shubhroz Gill,Mathias Leblanc,Amandine Chaix,Matthew S. Joens,James A. J. Fitzpatrick,Mark H. Ellisman,Satchidananda Panda
出处
期刊:Cell Metabolism
[Cell Press]
日期:2012-05-17
卷期号:15 (6): 848-860
被引量:1785
标识
DOI:10.1016/j.cmet.2012.04.019
摘要
While diet-induced obesity has been exclusively attributed to increased caloric intake from fat, animals fed a high-fat diet (HFD) ad libitum (ad lib) eat frequently throughout day and night, disrupting the normal feeding cycle. To test whether obesity and metabolic diseases result from HFD or disruption of metabolic cycles, we subjected mice to either ad lib or time-restricted feeding (tRF) of a HFD for 8 hr per day. Mice under tRF consume equivalent calories from HFD as those with ad lib access yet are protected against obesity, hyperinsulinemia, hepatic steatosis, and inflammation and have improved motor coordination. The tRF regimen improved CREB, mTOR, and AMPK pathway function and oscillations of the circadian clock and their target genes' expression. These changes in catabolic and anabolic pathways altered liver metabolome and improved nutrient utilization and energy expenditure. We demonstrate in mice that tRF regimen is a nonpharmacological strategy against obesity and associated diseases.
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