Glucose modifies the cross-talk between insulin and the beta-adrenergic signalling system in vascular smooth muscle cells

J Hypertens. 2000 Oct;18(10):1457-64. doi: 10.1097/00004872-200018100-00014.

Abstract

Background: Abnormalities in the vascular function of insulin are observed in insulin resistance, and hyperglycaemia is one of the important factors inducing insulin resistance.

Objective: To investigate the role of glucose in the interaction of insulin and beta-adrenergic signalling systems in vascular smooth muscle cells (VSMC).

Methods: After cells were treated with D-glucose (525 mmol/l) and insulin (100 nmol/l), adenylyl cyclase activity was measured in the presence of isoproterenol, forskolin, and cholera toxin. Assays for insulin-induced activities of insulin receptor substrate (IRS)-1, phosphoinositide 3-kinase (PI3-K) and mitogen-activated protein kinase (MAPK) were performed.

Results: In the presence of low glucose concentrations (5 mmol/l), insulin enhanced isoproterenol-, forskolin- and cholera toxin-stimulated adenylyl cyclase activities. This stimulatory effect was abolished by PI3-K inhibitors, wortmannin, or LY294002. In contrast, in the presence of high glucose concentrations (25 mmol/l), insulin attenuated isoproterenol-stimulated activity but not cholera toxin- or forskolin-stimulated activity. Insulin-stimulated activities of IRS-1 and PI3-K, but not MAPK activity, were also attenuated in the presence of high concentrations of glucose. The MAPK kinase inhibitor, PD98059, abolished the inhibitory effect of insulin on the beta-adrenergic signalling system. Troglitazone and pioglitazone prevented this inhibitory effect of insulin by restoring IRS-1 and PI3-K activities.

Conclusions: In the presence of low glucose concentrations, insulin stimulates the beta-adrenergic signalling system through the IRS-1/PI3-K pathway. However, in the presence of high glucose concentrations, the effect of insulin is switched to an inhibitory one, through the MAPK pathway. Our finding suggests that high glucose concentrations modify the cross-talk between insulin and the beta-adrenergic signalling systems in VSMC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Chromans / pharmacology
  • Glucose / pharmacology*
  • Insulin / pharmacology*
  • Insulin Receptor Substrate Proteins
  • Insulin Resistance
  • Isoproterenol / pharmacology
  • Mitogen-Activated Protein Kinases / physiology
  • Muscle, Smooth, Vascular / cytology
  • Muscle, Smooth, Vascular / metabolism*
  • Phosphatidylinositol 3-Kinases / physiology
  • Phosphoproteins / physiology
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Adrenergic, beta / physiology*
  • Thiazoles / pharmacology
  • Thiazolidinediones*
  • Troglitazone

Substances

  • Chromans
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, rat
  • Phosphoproteins
  • Receptors, Adrenergic, beta
  • Thiazoles
  • Thiazolidinediones
  • Phosphatidylinositol 3-Kinases
  • Mitogen-Activated Protein Kinases
  • Troglitazone
  • Glucose
  • Isoproterenol