Heat-shock-induced glucose transporter 4 in the slow-twitch muscle of rats
Language English Country Czech Republic Media print-electronic
Document type Journal Article
PubMed
25470523
DOI
10.33549/physiolres.932757
PII: 932757
Knihovny.cz E-resources
- MeSH
- Cell Line MeSH
- Muscle, Skeletal physiology MeSH
- Rats MeSH
- Rats, Sprague-Dawley MeSH
- Glucose Transporter Type 4 metabolism MeSH
- HSP70 Heat-Shock Proteins metabolism MeSH
- Heat-Shock Response physiology MeSH
- Muscle Fibers, Slow-Twitch physiology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Glucose Transporter Type 4 MeSH
- HSP70 Heat-Shock Proteins MeSH
- Slc2a4 protein, rat MeSH Browser
In this study, lipoic acid and heat shock treatments were applied to C(2)C(12) myotubes and Sprague-Dawley rats to investigate changes in the heat shock protein 70 (HSP70) and glucose transporter 4 (GLUT4) in 4 different skeletal muscle groups. The results of western blotting indicated that treatment of lipoic acid for 24 h, heat-shock and combined lipoic acid and heat-shock which all increased the level of HSP70 substantially in C(2)C(12) myotubes. However, either lipoic acid or heat-shock did not increase the level of GLUT4 in C(2)C(12) myotubes. In an in vitro migration assay, lipoic acid increased wound migration only when it was applied for 3 h. Moreover, our in vivo results revealed that lipoic acid did not increase HSP70 and GLUT4 in all 4 different skeletal muscles. Furthermore, heat-shock increased HSP70 in all 4 different muscle groups, and heat-shock treatment alone increased the GLUT4 in the soleus muscle only, suggesting that the GLUT4 increased by heat-shock was slow-twitch muscle specific. Collectively, our results indicated that heat-shock is critical factor that modulates GLUT4 and HSP70 in the skeletal muscle of rats.
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