Angiotensin II increases glucose uptake and glucose transporter-1 mRNA levels in astroglia

Am J Physiol. 1995 Mar;268(3 Pt 1):E384-90. doi: 10.1152/ajpendo.1995.268.3.E384.

Abstract

In this study, we have investigated the effects of angiotensin II (ANG II) on glucose uptake into astroglia cultured from adult rat hypothalamus and brain stem. ANG II (30 min to 4 h; 10(-9) to 10(-6) M) stimulated time- and concentration-dependent increases in the uptake of 2-deoxy-D-[3H]glucose into cultured astroglia. This effect of ANG II (10(-7) M) is via AT1 receptors and protein kinase C (PKC), since it was inhibited by losartan (10(-6) M) and staurosporine (10(-6) M), respectively. Furthermore, this ANG II action was inhibited by both cycloheximide (1 microgram/ml) and actinomycin D (10(-6) M), indicating that synthesis of new glucose transporters is involved. This was confirmed by the finding that ANG II (30 min to 4 h; 10(-9) to 10(-5) M) stimulated time- and concentration-dependent increases in the steady-state levels of glucose transporter-1 (GLUT-1) mRNA in these cultures. In addition, the increase in steady-state levels of GLUT-1 mRNA elicited by ANG II was mediated by AT1 receptors and PKC. These data suggest that ANG II stimulates glucose uptake into cultured astroglia via a pathway that involves AT1 receptors, PKC, and increased steady-state levels of GLUT-1 mRNA.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Angiotensin II / pharmacology*
  • Animals
  • Astrocytes / drug effects
  • Astrocytes / metabolism*
  • Biological Transport / drug effects
  • Cells, Cultured
  • Cycloheximide / pharmacology
  • Deoxyglucose / metabolism
  • Glucose / metabolism*
  • Glucose Transporter Type 1
  • Kinetics
  • Monosaccharide Transport Proteins / genetics*
  • Protein Kinase C / metabolism
  • RNA, Messenger / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Tritium

Substances

  • Glucose Transporter Type 1
  • Monosaccharide Transport Proteins
  • RNA, Messenger
  • Slc2a1 protein, rat
  • Tritium
  • Angiotensin II
  • Cycloheximide
  • Deoxyglucose
  • Protein Kinase C
  • Glucose