EVIDENCE FOR A NORADRENERGIC INNERVATION TO ALPHA-1A-ADRENOCEPTORS IN RAT-KIDNEY

被引:37
作者
BLUE, DR
VIMONT, RL
CLARKE, DE
机构
[1] Institute of Pharmacology, Syntex Research, Palo Alto, California, 94304
关键词
ALPHA-1A-ADRENOCEPTORS; 5-METHYL-URAPIDIL; CHLOROETHYLCLONIDINE; DIHYDROPYRIDINE-SENSITIVE CALCIUM CHANNELS; INNERVATION; KIDNEY;
D O I
10.1111/j.1476-5381.1992.tb12760.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 Experiments were undertaken to characterize the alpha1-adrenoceptor subtype mediating vasoconstrictor responses to periarterial noradrenergic nerve stimulation (PNS) in the isolated perfused kidney of the rat. 2 Vasoconstrictor responses to nerve stimulation were inhibited by prazosin (10 nM), 5-methyl-urapidil (30 nM), and nitrendipine (1 muM) but were resistant to inhibition by chloroethylclonidine (100 muM). 3 5-Methyl-urapidil (30 nM), chloroethylclonidine (100 muM) and nitrendipine (1 muM) did not inhibit the neuronal release of tritium from nerves loaded with [H-3]-noradrenaline. 4 The results suggest that renovascular alpha1A-adrenoceptors receive a noradrenergic innervation and that the innervated receptors are coupled to dihydropyridine-sensitive calcium channels.
引用
收藏
页码:414 / 417
页数:4
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