Hardiany Novi Silvia, Remifta Putra Muhammad Alifian, Penantian Raya Makarim, Antarianto Radiana Dhewayani
Department of Biochemistry & Molecular Biology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Heliyon. 2023 Jan 21;9(2):e13144. doi: 10.1016/j.heliyon.2023.e13144. eCollection 2023 Feb.
Aging is a multifactorial degenerative process that can be modulated by fasting through activation of the Fork-head transcription factor of the O class 3 (), which plays an important role in increasing lifespans. However, the effects of different fasting durations on the expression of in the liver has not yet been reported.
This study analyzed the effects of different fasting durations on the expression and its pathway by measuring sirtuin1 (), insulin-like growth factor-1 (), and superoxide dismutase (SOD) activity in the liver.
New Zealand white rabbits were used to mimic the effects of fasting on humans. The rabbits were divided into the control, intermittent fasting (IF), and prolonged fasting (PF) groups. Both fasting groups were interspersed with the non-fasting phase for 8 h. This treatment was conducted for 6 days. On Day 7, all the rabbits were sacrificed, and their livers were taken to measure the and mRNA expressions the protein level, and the SOD activity level. ANOVA, multiple comparison, and Pearson's correlation were performed for statistical analysis.
The and mRNA expressions were significantly higher in the IF group than in the control group. The expression was also 2.5 times higher in the IF group than in the PF group. There was a positive correlation between the and mRNA expressions. The protein level was significantly lower in the IF and PF groups than in the control group. The SOD-specific activity level was significantly higher in the IF group than in the control and PF groups.
Intermittent fasting significantly increased the and mRNA expressions and the SOD activity level in the livers of the rabbits and significantly decreased the circulating and hepatic Therefore, intermittent fasting may give a protective intervention effect towards aging.
衰老为多因素导致的退行性过程,可通过禁食激活O类3型叉头转录因子(FOXO3)进行调节,该因子在延长寿命方面发挥重要作用。然而,不同禁食时长对肝脏中FOXO3表达的影响尚未见报道。
本研究通过检测肝脏中沉默调节蛋白1(SIRT1)、胰岛素样生长因子1(IGF-1)及超氧化物歧化酶(SOD)活性,分析不同禁食时长对FOXO3表达及其通路的影响。
采用新西兰白兔模拟禁食对人体的影响。将兔子分为对照组、间歇性禁食(IF)组和延长禁食(PF)组。两个禁食组均穿插8小时非禁食期。此处理持续6天。第7天,处死所有兔子,取肝脏检测FOXO3和SIRT1 mRNA表达、SIRT1蛋白水平及SOD活性水平。采用方差分析、多重比较及Pearson相关性分析进行统计学分析。
IF组FOXO3和SIRT1 mRNA表达显著高于对照组。IF组SIRT1表达也比PF组高2.5倍。FOXO3和SIRT1 mRNA表达之间呈正相关。IF组和PF组SIRT1蛋白水平显著低于对照组。IF组SOD比活性水平显著高于对照组和PF组。
间歇性禁食显著增加了兔子肝脏中FOXO3和SIRT1 mRNA表达及SOD活性水平,并显著降低了循环和肝脏中的IGF-1。因此,间歇性禁食可能对衰老具有保护性干预作用。