Differential muscle gene expression as a function of disease progression in Goto-Kakizaki diabetic rats

Mol Cell Endocrinol. 2011 May 16;338(1-2):10-7. doi: 10.1016/j.mce.2011.02.016. Epub 2011 Feb 26.

Abstract

The Goto-Kakizaki (GK) rat, a polygenic non-obese model of type 2 diabetes, is a useful surrogate for study of diabetes-related changes independent of obesity. GK rats and appropriate controls were killed at 4, 8, 12, 16 and 20 weeks post-weaning and differential muscle gene expression along with body and muscle weights, plasma hormones and lipids, and blood cell measurements were carried out. Gene expression analysis identified 204 genes showing 2-fold or greater differences between GK and controls in at least 3 ages. Array results suggested increased oxidative capacity in GK muscles, as well as differential gene expression related to insulin resistance, which was also indicated by HOMA-IR measurements. In addition, potential new biomarkers in muscle gene expression were identified that could be either a cause or consequence of T2DM. Furthermore, we demonstrate here the presence of chronic inflammation evident both systemically and in the musculature, despite the absence of obesity.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blood Cell Count
  • Blood Glucose
  • Body Weights and Measures
  • Diabetes Mellitus, Experimental / genetics*
  • Energy Metabolism / genetics
  • Fatty Acids / blood
  • Gene Expression Profiling*
  • Genes
  • Inflammation / genetics
  • Insulin / blood
  • Male
  • Muscle, Skeletal / growth & development
  • Muscle, Skeletal / metabolism*
  • Oligonucleotide Array Sequence Analysis
  • Organ Size
  • Rats
  • Rats, Inbred WKY
  • Rats, Transgenic
  • Signal Transduction / genetics
  • Transcription, Genetic*

Substances

  • Blood Glucose
  • Fatty Acids
  • Insulin