Cerebral ischemia upregulates vascular endothelin ETB receptors in rat

被引:124
作者
Stenman, E
Malmsjo, M
Uddman, E
Gido, G
Wieloch, T
Edvinsson, L
机构
[1] Univ Lund Hosp, Wallenberg Neurocentrum, Div Expt Vasc Res, Dept Internal Med, S-22184 Lund, Sweden
[2] Univ Lund Hosp, Dept Clin Neurosci, Div Expt Brain Res, S-22185 Lund, Sweden
关键词
cerebral ischemia; endothelins; middle cerebral artery; receptors endothelin; rats;
D O I
10.1161/01.STR.0000028183.04277.32
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 ETA and ETB receptor agonist and sarafotoxin 6c (S6c) a selective ETB 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-m [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 ETA and ETB 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 ETA and ETB receptors which results in the appearance of a contractile response to the ETB receptor agonist S6c These results suggest a role for ET receptors in the pathogenesis of a vascular component after cerebral ischemia.
引用
收藏
页码:2311 / 2316
页数:6
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