Cerebral ischemia upregulates vascular endothelin ET(B) receptors in rat

Stroke. 2002 Sep;33(9):2311-6. doi: 10.1161/01.str.0000028183.04277.32.

Abstract

Background and purpose: Elevated levels of endothelin-1 (ET-1) have been reported in cerebral ischemia. A role for ET may prove more important if the vascular receptors were changed. We addressed whether there is any change in ET receptor expression in cerebral ischemia.

Methods: The right middle cerebral artery (MCA) was occluded in male Wistar rats for 2 hours with the intraluminal filament method. The basilar artery and both MCAs were removed after 46 hours of recirculation. The contractile responses to ET-1, a combined ET(A) and ET(B) receptor agonist, and sarafotoxin 6c (S6c), a selective ET(B) receptor agonist, were examined in vitro, and ET receptor mRNA was quantified by real-time polymerase chain reaction.

Results: S6c, which had no contractile effect per se on fresh or sham-operated rat cerebral arteries, induced a marked contraction in the occluded MCA (E(max) [maximum contraction, calculated as percentage of the contractile capacity of 63.5 mmol/L K+]=68+/-68%; P<0.0001), while there was no difference in the responses to ET-1 after cerebral ischemia. Real-time polymerase chain reaction revealed a significant upregulation of both the ET(A) and ET(B) receptors (both P<0.05) in the occluded MCA compared with the nonoccluded MCA from the same rats.

Conclusions: Focal cerebral ischemia in rat induces increased transcription of both ET(A) and ET(B) receptors, which results in the appearance of a contractile response to the ET(B) receptor agonist S6c. These results suggest a role for ET receptors in the pathogenesis of a vascular component after cerebral ischemia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basilar Artery / drug effects
  • Basilar Artery / physiopathology
  • Brain Ischemia / etiology
  • Brain Ischemia / physiopathology*
  • Disease Models, Animal
  • Endothelin-1 / pharmacology
  • In Vitro Techniques
  • Infarction, Middle Cerebral Artery / complications
  • Infarction, Middle Cerebral Artery / physiopathology
  • Male
  • Middle Cerebral Artery / drug effects
  • Middle Cerebral Artery / physiopathology
  • Peptide Elongation Factor 1 / genetics
  • Peptide Elongation Factor 1 / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Receptors, Endothelin / agonists
  • Receptors, Endothelin / genetics
  • Receptors, Endothelin / metabolism*
  • Up-Regulation
  • Vasoconstriction / drug effects
  • Vasoconstrictor Agents / pharmacology
  • Viper Venoms / pharmacology

Substances

  • Endothelin-1
  • Peptide Elongation Factor 1
  • RNA, Messenger
  • Receptor, Endothelin A
  • Receptor, Endothelin B
  • Receptors, Endothelin
  • Vasoconstrictor Agents
  • Viper Venoms
  • sarafotoxins s6