4.6 Article

Subarachnoid hemorrhage enhances endothelin receptor expression and function in rat cerebral arteries

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NEUROSURGERY
卷 52, 期 5, 页码 1188-1194

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OXFORD UNIV PRESS INC
DOI: 10.1227/01.NEU.0000058467.82442.64

关键词

cerebral arteries; endothelin receptors; intracranial vasospasm; pharmacology; polymerase chain reaction; rats; subarachnoid hemorrhage

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OBJECTIVE: Inspired by organ culture-induced changes in the vascular endothelin (ET) receptor population, we investigated whether such changes occur in cerebral arteries in a rat subarachnoid hemorrhage (SAH) model. METHODS: SAH was induced with injection of 250 mul of blood into the prechiasmatic cistern. After 2 days, the middle cerebral artery, basilar artery, and posterior communicating artery were harvested. Pharmacological studies were performed in vitro, and 1; levels of messenger ribonucleic acid (mRNA) were quantified in real-time reverse transcriptase-polymerase chain reaction assays. RESULTS: In the middle cerebral artery and basilar artery from rats with induced SAH, enhanced biphasic responses to ET-1 were observed. The -log(50% effective concentration) value for the high-affinity phase was approximately 12, compared with approximately 8.5 for sham-operated animals. At a concentration of ET-1 of 10(-9) mmol/L (approximately equal to the physiological concentration of ET-1 in the plasma), submaximal contractions of 50 to 75% of the contraction obtained through stimulation with 60 mmol/L K+ were now observed. Quantitative mRNA studies with the same arteries demonstrated significant increases in the number of copies of ETB receptor mRNA but not ETA. receptor mRNA. Evidence of functional ETB receptors was provided in antagonist studies. The posterior communicating artery did not exhibit significant changes. CONCLUSION: The altered receptor profile observed may represent the final stage in i the series of events leading from SAH to actual spasm of the artery. The pharmacological data for the ETB receptor suggest complex interactions between normally present ETA receptors and up-regulated ETB receptors.

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