Doctoral Programs of Medical Science, Faculty of Medicine, Universitas Airlangga, Surabaya 60113, Indonesia.
Department of Physiology, Faculty of Medicine, Universitas Muhammadiyah Surabaya, Surabaya 60132, Indonesia.
Nutrients. 2024 Sep 15;16(18):3112. doi: 10.3390/nu16183112.
Fasting potentially alters the aging process induced by obesity by regulating telomere integrity, which is related to longevity genes. However, the impact of periodic fasting (PF) on the expression of longevity genes, particularly Forkhead Box O Transcription Factors (FOXO3a) and the Human Telomerase Reverse Transcriptase (hTERT), is not fully understood. This study aimed to analyze the effects of PF, specifically on FOXO3a, hTERT expression, and other associated factors.
A quasi-experimental 10-day study was conducted in Surabaya, East Java, Indonesia. This study consisted of an intervention group (PFG), which carried out PF for ten days using a daily 12 h time-restricted eating protocol, and a control group (CG), which had daily meals as usual. FOXO3a and hTERT expression were analyzed by quantitative real-time qPCR. A paired -test/Wilcoxon test, independent -test/Mann-Whitney U-test, and Spearman's correlation test were used for statistical analysis.
Thirty-six young men participated in this study. During the post-test period, FOXO3a expression in the PFG increased 28.56 (±114.05) times compared to the pre-test, but the difference was not significant. hTERT expression was significantly higher in both the CG and PFG. The hTERT expression in the PFG was 10.26 (±8.46) times higher than in the CG, which was only 4.73 (±4.81) times higher. There was also a positive relationship between FOXO and hTERT in the CG.
PF significantly increased hTERT expression in the PFG; however, no significant increase was found in FOXO3a expression. PF regimens using the 12 h time-restricted eating approach may become a potential strategy for preventing obesity-induced premature aging by regulating longevity gene expression.
禁食通过调节端粒完整性来改变肥胖引起的衰老过程,而端粒完整性与长寿基因有关。然而,周期性禁食(PF)对长寿基因,特别是叉头框 O 转录因子(FOXO3a)和人类端粒酶逆转录酶(hTERT)的表达的影响尚未完全阐明。本研究旨在分析 PF 对 FOXO3a、hTERT 表达和其他相关因素的影响。
在印度尼西亚泗水进行了一项为期 10 天的准实验研究。该研究包括干预组(PFG)和对照组(CG)。干预组在 10 天内进行 PF,采用每天 12 小时限时进食方案,而对照组则照常进食。通过定量实时 qPCR 分析 FOXO3a 和 hTERT 的表达。使用配对检验/Wilcoxon 检验、独立检验/Mann-Whitney U 检验和 Spearman 相关检验进行统计分析。
36 名年轻男性参与了这项研究。在测试后期间,PFG 中的 FOXO3a 表达增加了 28.56(±114.05)倍,与测试前相比差异无统计学意义。CG 和 PFG 中的 hTERT 表达均显著升高。PFG 中的 hTERT 表达比 CG 高 10.26(±8.46)倍,仅高 4.73(±4.81)倍。CG 中还存在 FOXO 与 hTERT 之间的正相关关系。
PF 显著增加了 PFG 中的 hTERT 表达,但 FOXO3a 表达没有显著增加。采用 12 小时限时进食方法的 PF 方案可能成为通过调节长寿基因表达预防肥胖引起的早衰的潜在策略。