Department of Rheumatology and Allergy, IMSUT Hospital, The Institute of Medical Science, The University of Tokyo, Shirokanedai, Minato-ku, Tokyo, Japan.
Division of Rheumatology, Center for Antibody and Vaccine Therapy, IMSUT Hospital, The Institute of Medical Science, The University of Tokyo, Shirokanedai, Minato-ku, Tokyo, Japan.
Am J Physiol Endocrinol Metab. 2021 Feb 1;320(2):E346-E358. doi: 10.1152/ajpendo.00184.2020. Epub 2020 Nov 23.
Age-related sarcopenia is associated with a variety of changes in skeletal muscle. These changes are interrelated with each other and associated with systemic metabolism, the details of which, however, are largely unknown. Eicosapentaenoic acid (EPA) is a promising nutrient against sarcopenia and has multifaceted effects on systemic metabolism. In this study, we hypothesized that the aging process in skeletal muscle can be intervened by the administration of EPA. Seventy-five-week-old male mice were assigned to groups fed an EPA-deprived diet (EPA-) or an EPA-enriched diet with 1 wt% EPA (EPA+) for 12 wk. Twenty-four-week-old male mice fed with normal chow were also analyzed. At baseline, the grip strength of the aging mice was lower than that of the young mice. After 12 wk, EPA+ showed similar muscle mass but increased grip strength compared with EPA-. EPA+ displayed higher insulin sensitivity than EPA-. Immunohistochemistry and gene expression analysis of myosin heavy chains (MyHCs) revealed fast-to-slow fiber type transition in aging muscle, which was partially inhibited by EPA. RNA sequencing (RNA-Seq) analysis suggested that EPA supplementation exerts pathway-specific effects in skeletal muscle including the signatures of slow-to-fast fiber type transition. In conclusion, we revealed that aging skeletal muscle in male mice shows lower grip strength and fiber type changes, both of which can be inhibited by EPA supplementation irrespective of muscle mass alteration. This study demonstrated that the early phenotype of skeletal muscle in aging male mice is characterized by muscle weakness with fast-to-slow fiber type transition, which could be ameliorated by feeding with EPA-enriched diet. EPA induced metabolic changes such as an increase in systemic insulin sensitivity and altered muscle transcriptome in the aging mice. These changes may be related to the fiber type transition and influence muscle quality.
年龄相关性肌肉减少症与骨骼肌的多种变化有关。这些变化相互关联,并与全身代谢有关,但细节在很大程度上尚不清楚。二十碳五烯酸(EPA)是一种有前途的抗肌肉减少症的营养物质,对全身代谢有多种影响。在这项研究中,我们假设 EPA 的给药可以干预骨骼肌的衰老过程。75 周龄雄性小鼠被分为两组,分别喂食缺乏 EPA 的饮食(EPA-)或富含 1wt% EPA 的饮食(EPA+)12 周。还分析了喂食正常饲料的 24 周龄雄性小鼠。在基线时,衰老小鼠的握力低于年轻小鼠。12 周后,EPA+显示出与 EPA-相似的肌肉质量,但握力增加。EPA+显示出比 EPA-更高的胰岛素敏感性。肌球蛋白重链(MyHCs)的免疫组织化学和基因表达分析显示,衰老肌肉中出现快肌向慢肌纤维类型转变,而 EPA 部分抑制了这种转变。RNA 测序(RNA-Seq)分析表明,EPA 补充对骨骼肌具有特定的通路效应,包括慢肌向快肌纤维类型转变的特征。总之,我们揭示了雄性小鼠衰老骨骼肌表现出较低的握力和纤维类型变化,这两种变化都可以通过 EPA 补充来抑制,而与肌肉质量变化无关。本研究表明,衰老雄性小鼠骨骼肌的早期表型特征为肌肉无力伴快肌向慢肌纤维类型转变,通过喂食富含 EPA 的饮食可以改善这种情况。EPA 诱导的代谢变化,如全身胰岛素敏感性增加和衰老小鼠肌肉转录组改变,可能与纤维类型转变有关,并影响肌肉质量。