Myostatin expression is not altered by insulin deficiency and replacement in streptozotocin-diabetic rat skeletal muscles

Clin Nutr. 2004 Dec;23(6):1413-7. doi: 10.1016/j.clnu.2004.06.007.

Abstract

Background and aims: Insulin is a major post-prandial muscle-anabolic hormone. A substantial loss of skeletal muscle mass occurs in insulin-deprived diabetes and is reversed by insulin treatment. Myostatin is a negative regulator of muscle mass upregulated in several chronic catabolic conditions. Whether myostatin expression is altered in insulin-deprived diabetes is unknown. In spite of opposite effects on muscle mass the potential role of basal circulating insulin in the regulation of myostatin expression is also undetermined.

Methods: We measured (Northern Blot) myostatin transcript levels in muscle groups with different fiber composition in streptozotocin-diabetic male rats receiving one of the following treatments for eight weeks: (1) control (C); (2) diabetes without treatment (DM); (3) diabetes with once-daily slow-acting insulin treatment (INS).

Results: INS normalized plasma insulin and prevented weight reduction observed in DM. In fast-twitch gastrocnemius muscle myostatin transcript levels were unchanged (P>0.4) in both DM and INS compared to C. Myostatin transcripts were not measurable in any group in slow-twitch soleus muscle.

Conclusions: Muscle-specific myostatin expression is not increased under catabolic conditions in insulin-deprived diabetes. Insulin treatment also does not change myostatin transcript levels. The data provide the first assessment of potential interplay between insulin and myostatin and they do not support a major role of circulating insulin in the in vivo regulation of myostatin gene expression. A role of myostatin in muscle catabolism in chronic insulin-deprived diabetes is also not indicated by the current results.

MeSH terms

  • Animals
  • Blotting, Northern
  • Diabetes Mellitus, Experimental / drug therapy*
  • Gene Expression Regulation
  • Hypoglycemic Agents / therapeutic use*
  • Insulin / deficiency*
  • Insulin / therapeutic use*
  • Male
  • Muscle, Skeletal / metabolism*
  • Myostatin
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Streptozocin
  • Transforming Growth Factor beta / genetics
  • Transforming Growth Factor beta / metabolism*
  • Weight Loss / physiology

Substances

  • Hypoglycemic Agents
  • Insulin
  • Mstn protein, rat
  • Myostatin
  • Transforming Growth Factor beta
  • Streptozocin