Joo J, Cox C C, Kindred E D, Lashinger L M, Young M E, Bray M S
Department of Nutritional Sciences, University of Texas at Austin, Austin, TX, USA.
Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.
Int J Obes (Lond). 2016 Sep;40(9):1444-51. doi: 10.1038/ijo.2016.80. Epub 2016 May 2.
Both circadian disruption and timing of feeding have important roles in the development of metabolic disease. Despite growing acceptance that the timing of food consumption has long-term impact on metabolic homeostasis, little is known regarding the immediate influence on whole body metabolism, or the mechanisms involved. We aimed to examine the acute effects of time-of-day-dependent high fat feeding on whole body substrate metabolism and metabolic plasticity, and to determine the potential contribution of the adipocyte circadian clock.
Mice were fed a regimen of 4-h meal at the beginning and end of the dark (waking) cycle, separated by 4 h of fasting. Daily experimental conditions consisted of either an early very high fat or high fat (EVHF or EHF, 60 or 45% kcals from fat, respectively) or late (LVHF or LHF) meal, paired with a low fat (LF, 10% kcals from fat) meal. Metabolic parameters, glucose tolerance, body fat composition and weight were assessed. To determine the role of the adipocyte circadian clock, an aP2-CLOCK mutant (ACM) mouse model was used.
Mice in the EVHF or EHF groups showed a 13.2 or 8.84 higher percentage of caloric intake from fat and had a 0.013 or 0.026 lower daily average respiratory exchange ratio, respectively, compared with mice eating the opposite feeding regime. Changes in glucose tolerance, body fat composition and weight were not significant at the end of the 9-day restricted feeding period. ACM mice did not exhibit different metabolic responses to the feeding regimes compared with wild-type littermates. Circadian clock disruption did not influence the short-term response to timed feeding.
Both the total fat composition of diet and the timing of fat intake may differentially mediate the effect of timed feeding on substrate metabolism, but may not induce acute changes in metabolic flexibility.
昼夜节律紊乱和进食时间在代谢性疾病的发生发展中均起着重要作用。尽管人们越来越认可食物摄入时间对代谢稳态具有长期影响,但对于其对全身代谢的即时影响或相关机制却知之甚少。我们旨在研究昼夜节律依赖性高脂喂养对全身底物代谢和代谢可塑性的急性影响,并确定脂肪细胞昼夜节律钟的潜在作用。
在黑暗(清醒)周期开始和结束时给小鼠喂食4小时,中间间隔4小时禁食。每日实验条件包括早期极高脂或高脂(分别为EVHF或EHF,脂肪提供60%或45%的千卡热量)或晚期(LVHF或LHF)进食,同时搭配低脂(LF,脂肪提供10%的千卡热量)进食。评估代谢参数、葡萄糖耐量、体脂组成和体重。为确定脂肪细胞昼夜节律钟的作用,使用了aP2-CLOCK突变体(ACM)小鼠模型。
与采用相反喂养方式的小鼠相比,EVHF或EHF组小鼠从脂肪中摄入的热量百分比分别高出13.2%或8.84%,每日平均呼吸交换率分别低0.013或0.026。在9天的限制喂养期结束时,葡萄糖耐量、体脂组成和体重的变化不显著。与野生型同窝小鼠相比,ACM小鼠对喂养方式未表现出不同的代谢反应。昼夜节律钟紊乱未影响对定时喂养的短期反应。
饮食中的总脂肪组成和脂肪摄入时间可能以不同方式介导定时喂养对底物代谢的影响,但可能不会引起代谢灵活性的急性变化。