Hyperglycemia activates glucose transport in rat skeletal muscle via a Ca(2+)-dependent mechanism

Diabetes. 1995 Nov;44(11):1345-8. doi: 10.2337/diab.44.11.1345.

Abstract

We investigated the acute effect of hyperglycemia on 3-O-methylglucose transport in isolated rat epitrochlearis muscles. High levels of glucose (20 mmol/l) induced an approximately twofold increase in the rate of glucose transport when compared with muscles exposed to a low level of glucose (8 mmol/l) (P < 0.001). The hyperglycemic effect was additive to the effects of both insulin and exercise on the glucose transport rates. Dantrolene (25 mumol/l), a potent inhibitor of Ca2+ release from the sarcoplasmic reticulum, blocked the ability of hyperglycemia to increase glucose transport by 73% (P < 0.01). Although dantrolene had no effect on the non-insulin-stimulated or the insulin-stimulated glucose transport rates during normoglycemic conditions, the effect of exercise was completely blocked in the presence of dantrolene (P < 0.01). Inhibition of phosphatidylinositol (PI) 3-kinase by wortmannin (500 nmol/l) had no effect on the activation of glucose transport by hyperglycemia, whereas the insulin-stimulated glucose transport was completely abolished (P < 0.001). These findings suggest that hyperglycemia activates glucose transport by a Ca(2+)-dependent activation of glucose transport does not involve the activation of PI 3-kinase and is separate from the mass-action effect of glucose on glucose transport.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3-O-Methylglucose
  • Androstadienes / pharmacology
  • Animals
  • Biological Transport / drug effects
  • Calcium / metabolism*
  • Dantrolene / pharmacology*
  • Enzyme Inhibitors / pharmacology
  • Glucose / metabolism*
  • Hyperglycemia / metabolism*
  • In Vitro Techniques
  • Insulin / pharmacology*
  • Male
  • Methylglucosides / metabolism*
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / metabolism*
  • Phosphatidylinositol 3-Kinases
  • Phosphotransferases (Alcohol Group Acceptor) / antagonists & inhibitors
  • Physical Exertion*
  • Rats
  • Rats, Wistar
  • Sarcoplasmic Reticulum / drug effects
  • Sarcoplasmic Reticulum / metabolism
  • Wortmannin

Substances

  • Androstadienes
  • Enzyme Inhibitors
  • Insulin
  • Methylglucosides
  • 3-O-Methylglucose
  • Phosphatidylinositol 3-Kinases
  • Phosphotransferases (Alcohol Group Acceptor)
  • Dantrolene
  • Glucose
  • Calcium
  • Wortmannin