17 beta-Estradiol modulation of glucose transporter 1 expression in blood-brain barrier

Am J Physiol. 1997 Jun;272(6 Pt 1):E1016-22. doi: 10.1152/ajpendo.1997.272.6.E1016.

Abstract

The present study was designed to evaluate 17 beta-estradiol (E2) modulation of glucose transporter 1 (GLUT-1) protein and mRNA expression in blood-brain barrier (BBB) endothelium. Female rats were ovariectomized (OVX) for 12-14 days, then E2 was injected at dosages of 1-100 micrograms/kg sc at 2-16 h before sampling. Glucose transport into BBB endothelial cells was assessed using 2-deoxy-[14C]glucose (2-[14C]DG) uptake. GLUT-1 protein and mRNA samples were analyzed by Western and Northern blotting, respectively. E2 treatment caused dose- and time-dependent increases in 2-[14C]DG uptake and GLUT-1 protein expression by microvessels. The peak responses were induced by 10 micrograms/kg E2 dose at the 4-h sampling time (36.0 and 31.3% increases, P < 0.05, respectively). GLUT-1 mRNA demonstrated a transient increase at 15 min (55%, P < 0.05), then decreased to basal level by 2 h. This study shows that in vivo treatment with E2 increases 2-[14C]DG uptake into the BBB endothelial cells and suggests this E2 effect is due to its modulation of GLUT-1 mRNA and protein.

Publication types

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

MeSH terms

  • Animals
  • Blood-Brain Barrier / physiology*
  • Brain / blood supply
  • Deoxyglucose / metabolism
  • Dose-Response Relationship, Drug
  • Endothelium, Vascular / drug effects
  • Endothelium, Vascular / metabolism*
  • Estradiol / blood
  • Estradiol / pharmacology*
  • Female
  • Glucose Transporter Type 1
  • Kinetics
  • Microcirculation / drug effects
  • Microcirculation / metabolism*
  • Monosaccharide Transport Proteins / biosynthesis*
  • Ovariectomy
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Transcription, Genetic / drug effects*
  • von Willebrand Factor / analysis

Substances

  • Glucose Transporter Type 1
  • Monosaccharide Transport Proteins
  • RNA, Messenger
  • Slc2a1 protein, rat
  • von Willebrand Factor
  • Estradiol
  • Deoxyglucose