Increase in cardiac muscle fructose content in streptozotocin-induced diabetic rats

Metabolism. 1992 Oct;41(10):1041-6. doi: 10.1016/0026-0495(92)90283-g.

Abstract

To evaluate the activation of the sorbitol pathway in cardiac muscle in diabetic rats, we measured sorbitol, fructose, and myo-inositol content in cardiac tissue obtained from control and streptozotocin-diabetic rats, with or without an 8-week insulin treatment, using gas chromatography-mass spectrometry (GC-MS). Cardiac fructose and sorbitol content in 10-week diabetic rats increased by 60-fold and 3.9-fold of those of control rats, respectively (P less than .001). In contrast, cardiac myo-inositol content in 10-week diabetic rats decreased to 56% (P less than .025) of the control value. The abnormalities in cardiac fructose, sorbitol, and myo-inositol content were completely normalized by the 8-week insulin treatment, which was initiated 2 weeks after the induction of diabetes. There was no difference in cardiac aldose reductase activity between control and diabetic rats. However, cardiac sorbitol dehydrogenase activity in diabetic rats was 151% (P less than .005) higher than that of control rats, although hepatic sorbitol dehydrogenase activity was not different between the two groups. These results indicate that the sorbitol pathway is significantly activated in cardiac tissue obtained from streptozotocin-induced diabetic rats, which results in the marked cardiac accumulation of fructose.

MeSH terms

  • Aldehyde Reductase / metabolism
  • Animals
  • Diabetes Mellitus, Experimental / metabolism*
  • Fructose / analysis*
  • Fructose / metabolism
  • Gas Chromatography-Mass Spectrometry
  • Inositol / analysis
  • Inositol / metabolism
  • L-Iditol 2-Dehydrogenase / metabolism
  • Male
  • Papillary Muscles / chemistry*
  • Papillary Muscles / enzymology
  • Papillary Muscles / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Sorbitol / analysis
  • Sorbitol / metabolism
  • Streptozocin

Substances

  • Fructose
  • Inositol
  • Sorbitol
  • Streptozocin
  • L-Iditol 2-Dehydrogenase
  • Aldehyde Reductase