4.5 Article

Methylglyoxal reduces molecular responsiveness to 4 weeks of endurance exercise in mouse plantaris muscle

期刊

JOURNAL OF APPLIED PHYSIOLOGY
卷 132, 期 2, 页码 477-488

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.00539.2021

关键词

exercise resistance; glycation; insulin signaling; mitochondria; nonresponder

资金

  1. JSPS KAKENHI [18H03148, 19K22806, 21H03319, 19K20007, 20K19498, 18H03160, 19K22825, 19KK0254, 19K11520]
  2. Descente Foundation for the Promotion of Sports Science
  3. Uehara Memorial Foundation
  4. Science Research Promotion Fund from the Promotion and Mutual Aid Corporation for Private Schools of Japan
  5. Graduate School of Health Sciences, Toyohashi SOZO University
  6. Grants-in-Aid for Scientific Research [21H03319, 20K19498, 19K20007, 19K22806, 19K22825, 18H03148, 19KK0254, 19K11520, 18H03160] Funding Source: KAKEN

向作者/读者索取更多资源

This study investigated the effect of methylglyoxal on skeletal muscle adaptations following endurance exercise. The findings suggest that methylglyoxal is a factor deteriorating responsiveness to endurance exercise in primarily fast-twitch skeletal muscle.
Endurance exercise triggers skeletal muscle adaptations, including enhanced insulin signaling, glucose metabolism, and mitochondrial biogenesis. However, exercise-induced skeletal muscle adaptations may not occur in some cases, a condition known as exercise resistance. Methylglyoxal (MG) is a highly reactive dicarbonyl metabolite and has detrimental effects on the body such as causing diabetic complications, mitochondrial dysfunction, and inflammation. This study aimed to clarify the effect of methylglyoxal on skeletal muscle molecular adaptations following endurance exercise. Mice were randomly divided into four groups (n = 12/group): sedentary control group, voluntary exercise group, MG-treated group, and MG-treated with voluntary exercise group. Mice in the voluntary exercise group were housed in a cage with a running wheel, whereas mice in the MG-treated groups received drinking water containing 1% MG. Four weeks of voluntary exercise induced several molecular adaptations in the plantaris muscle, including increased expression of peroxisome proliferator-activated receptor gamma coactivator 1a (PGC1a), mitochondria complex proteins, Toll-like receptor 4 (TLR4), 72-kDa heat shock protein (HSP72), hexokinase II, and glyoxalase 1; this also enhanced insulin-stimulated Akt Ser473 phosphorylation and citrate synthase activity. However, these adaptations were suppressed with MG treatment. In the soleus muscle, the exercise-induced increases in the expression of TLR4, HSP72, and advanced glycation end products receptor 1 were inhibited with MG treatment. These findings suggest that MG is a factor that inhibits endurance exercise-induced molecular responses including mitochondrial adaptations, insulin signaling activation, and the upregulation of several proteins related to mitochondrial biogenesis, glucose handling, and glycation in primarily fast-twitch skeletal muscle. NEW & NOTEWORTHY This study investigated the effect of methylglyoxal, which is a highly reactive carbonyl metabolite and has detrimental effects on the body, on skeletal muscle adaptations following endurance exercise. Evidences from this study show that methylglyoxal is a factor deteriorating responsiveness to endurance exercise in primarily fast-twitch skeletal muscle.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据