Salk Institute for Biological Studies, La Jolla, CA 92037, USA.
Cell Metab. 2012 Jun 6;15(6):848-60. doi: 10.1016/j.cmet.2012.04.019. Epub 2012 May 17.
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.
虽然饮食诱导的肥胖症仅归因于脂肪摄入热量的增加,但自由进食高脂肪饮食(HFD)的动物会日夜频繁进食,扰乱正常的进食周期。为了测试肥胖症和代谢疾病是由 HFD 还是代谢周期的破坏引起的,我们让老鼠每天接受自由进食或限时进食(tRF)HFD8 小时。接受 tRF 的老鼠从 HFD 中摄入的热量与自由进食的老鼠相同,但它们可以预防肥胖症、高胰岛素血症、肝脂肪变性和炎症,并改善运动协调能力。tRF 方案改善了 CREB、mTOR 和 AMPK 通路的功能以及昼夜节律钟及其靶基因表达的波动。这些分解代谢和合成代谢途径的变化改变了肝脏代谢组,提高了营养物质的利用和能量消耗。我们在老鼠身上证明,tRF 方案是对抗肥胖症和相关疾病的非药物策略。