Yoshie Toshihiro, Saito Chiharu, Kawano Fuminori
Department of Sports and Health Science, Faculty of Human Health and Science, Matsumoto University, 2095-1 Niimura, Matsumoto City, Nagano 390-1295 Japan.
Graduate School of Health Sciences, Matsumoto University, 2095-1 Niimura, Matsumoto City, Nagano 390-1295 Japan.
Lab Anim Res. 2020 Aug 8;36:25. doi: 10.1186/s42826-020-00060-2. eCollection 2020.
The purpose of the present study was to investigate how the effects of high-fat diet feeding on the skeletal muscle persisted during aging using mice. Post-weaned male mice were fed a high-fat diet between 1- and 3-mo-old followed by return to supply a normal diet until 13-mo-old. Monthly physical tests demonstrated that age-related glucose intolerance that was generally developed after 10-mo-old in the control mice was significantly improved in mice fed a high-fat diet. Interestingly, mRNA expressions of , , and were up-regulated by high-fat feeding and persisted in the tibialis anterior muscle until 13-mo-old. At and loci, enhanced distributions of active histone modifications were noted in the high-fat-fed mice at 13-mo-old. In contrast, age-related accumulation of histone variant H3.3 at these loci was suppressed. These results indicated that epigenetic modifications caused by early nutrition mediated the changes in skeletal muscle gene expression during aging.
本研究的目的是利用小鼠研究高脂饮食喂养对骨骼肌的影响在衰老过程中是如何持续存在的。断奶后的雄性小鼠在1至3月龄期间喂食高脂饮食,随后恢复供应正常饮食直至13月龄。每月进行的体能测试表明,对照小鼠通常在10月龄后出现的与年龄相关的葡萄糖不耐受在喂食高脂饮食的小鼠中得到了显著改善。有趣的是,高脂喂养上调了[具体基因名称未给出]、[具体基因名称未给出]和[具体基因名称未给出]的mRNA表达,并且在胫前肌中持续至13月龄。在13月龄的高脂喂养小鼠中,在[具体基因座未给出]和[具体基因座未给出]位点观察到活性组蛋白修饰的分布增强。相反,这些位点上组蛋白变体H3.3与年龄相关的积累受到抑制。这些结果表明,早期营养引起的表观遗传修饰介导了衰老过程中骨骼肌基因表达的变化。