Recombinant insulin-like growth factor I normalizes expression of renal glucose transporters in diabetic rats

Am J Physiol. 1997 Jul;273(1 Pt 2):F27-37. doi: 10.1152/ajprenal.1997.273.1.F27.

Abstract

By immunocytochemistry we have studied the effect of recombinant human insulin-like growth factor I (rhIGF-I) on expression of renal GLUT-1, -2, and -5 in rats with streptozotocin (STZ)-induced diabetes. In the renal tubules of these rats, expression of GLUT-1 was reduced and that of GLUT-2 was increased. GLUT-1 expression was restored, and GLUT-2 expression was normalized by 2-wk administration of rhIGF-I. We have shown that GLUT-5 was expressed at the brush-border membrane of the proximal convoluted tubules (PCT) of the cortex and at the glomerular mesangial cells (GMC) in normal rat kidney. In the diabetic rats, GLUT-5 expression was increased at both sites, along with an increase of GLUT-2 expression at the basolateral membrane of PCT, and was decreased to normal level at both sites by treatment with rhIGF-I. Thus, like GLUT-2, GLUT-5 is suggested to regulate glucose reabsorption in PCT. The relationship between overexpression of GLUT-5 in GMC and accumulation of sorbitol and advanced glycosylation end products are discussed. Regulation of GLUT expression may play an important role on renal glucose homeostasis.

MeSH terms

  • Analysis of Variance
  • Animals
  • Body Weight / drug effects
  • Cell Membrane / metabolism
  • Diabetes Mellitus, Experimental / metabolism*
  • Diabetes Mellitus, Experimental / physiopathology
  • Diabetic Nephropathies / physiopathology
  • Gene Expression / drug effects
  • Glomerular Mesangium / metabolism
  • Glucose Transporter Type 1
  • Glucose Transporter Type 2
  • Glucose Transporter Type 4
  • Glycogen / metabolism
  • Humans
  • Immunohistochemistry
  • Insulin / pharmacology
  • Insulin-Like Growth Factor I / pharmacology*
  • Kidney / drug effects
  • Kidney / metabolism*
  • Kidney / physiopathology
  • Kidney Cortex / metabolism
  • Kidney Tubules, Proximal / metabolism
  • Male
  • Microvilli / metabolism
  • Models, Biological
  • Monosaccharide Transport Proteins / biosynthesis*
  • Muscle Proteins*
  • Organ Size / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins / pharmacology
  • Reference Values
  • Weight Gain / drug effects

Substances

  • Glucose Transporter Type 1
  • Glucose Transporter Type 2
  • Glucose Transporter Type 4
  • Insulin
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • Recombinant Proteins
  • SLC2A1 protein, human
  • SLC2A4 protein, human
  • Slc2a1 protein, rat
  • Slc2a4 protein, rat
  • Insulin-Like Growth Factor I
  • Glycogen