H3 RECEPTOR-MEDIATED INHIBITION OF THE NEUROGENIC VASOPRESSOR RESPONSE IN PITHED RATS

被引:51
作者
MALINOWSKA, B
SCHLICKER, E
机构
[1] UNIV BONN,INST PHARMACOL & TOXIKOL,REUTERSTR 2B,W-5300 BONN 1,GERMANY
[2] MED ACAD BIALYSTOK,DEPT PHARMACODYNAM,PL-15062 BIALYSTOK,POLAND
关键词
HISTAMINE-H3 RECEPTORS (PRESYNAPTIC); R-(-)-ALPHA-METHYLHISTAMINE; SYMPATHETIC NERVES; (PITHED RAT);
D O I
10.1016/0014-2999(91)90915-D
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In pithed rats, the H-3 agonist R-(-)-alpha-methylhistamine (R-alpha-MeHA) inhibited the electrically induced increase in blood pressure without affecting the vasopressor response to exogenous noradrenaline. The effect of R-alpha-MeHA was not affected by the H-1 and H-2 antagonists dimetindene and ranitidine, but attenuated by the H-3 antagonist thioperamide. At higher doses, R-alpha-MeHA itself increased basal blood pressure; this effect was not affected by the H-1, H-2 and H-3 antagonists. In conclusion, the neurogenic vasopressor response can be modulated via H-3 receptors, probably located presynaptically on postganglionic sympathetic nerve fibres.
引用
收藏
页码:307 / 310
页数:4
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