ALPHA(1)-ADRENOCEPTOR SUBTYPE(S) MEDIATING NORADRENALINE-INDUCED CONTRACTIONS OF THE GUINEA-PIG AORTA

被引:5
|
作者
ORIOWO, MA
机构
[1] Department of Pharmacology & Toxicology, Faculty of Medicine, Kuwait University, Safat, 13110
关键词
ALPHA(1)-ADRENOCEPTORS; SZL-49; CHLOROETHYLCLONIDINE; GUINEA-PIG AORTA; WB; 4101; NIFEDIPINE;
D O I
10.1111/j.1472-8206.1994.tb00801.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The effect of alpha(1)-adrenoceptor subtype selective antagonists, WB 4101, SZL-49 and chloroethylclonidine on noradrenaline-induced contractions of the guinea-pig aorta has been studied in an attempt to identify the alpha(1)-adrenoceptor subtype(s) involved in the response. Noradrenaline and SDZ NVI 085 induced contractions of the aorta. Noradrenaline-induced contractions were competitively antagonised by WB 4101 (pA(2) = 8.92, slope = 1.05). The contractions were significantly reduced by SZL-49 but not by chloroethylclonidine, indicating an action on alpha(1A)-adrenoceptor subtype. Noradrenaline-induced contractions of the aorta were not inhibited by nifedipine (10(-6) M). The results are interpreted to suggest that alpha(1A)-adrenoceptor subtype mediates noradrenaline-induced contractions of the guinea-pig aorta and that activation of alpha(1A)-adrenoceptor subtype in the guinea-pig aorta is probably linked to intracellular Ca++ release.
引用
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页码:214 / 219
页数:6
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