Kenakin T P, Beek D
J Pharmacol Exp Ther. 1982 Feb;220(2):353-7.
The histamine-induced relaxation of bethanechol-contracted rabbit trachea was analyzed pharmacologically in experiments designed to determine whether this tissue contains relaxant histamine H2-receptors or an atypical histamine receptor. Relaxation to histamine was potentiated by inhibition of histamine H1-receptors with chlorpheniramine. A cimetidine-resistant relaxant effect of high concentrations of histamine was observed which correlated with concomitant decreases in organ bath pH upon addition of histamine. Neutralization of the histamine solution eliminated the cimetidine-resistant effects of histamine. Cimetidine, metiamide and burimamide were competitive antagonists of histamine-responses with pKB values of 6.6, 6.1 and 5.4, respectively. These estimates are not significantly different from literature values for antagonism of H2-receptors by these drugs in guinea-pig right atria. The potency ratio of histamine and 4-methylhistamine (a selective H2-receptor agonist) was not significantly different from that obtained in rabbit right atria, an H2-receptor-containing tissue. These data from studies with antagonists and agonists indicated that histamine produced relaxation of rabbit trachea by activation of histamine H2-receptors.
在旨在确定该组织是否含有组胺H2受体或非典型组胺受体的实验中,对组胺诱导的氨甲酰甲胆碱收缩的兔气管舒张进行了药理学分析。用氯苯那敏抑制组胺H1受体可增强对组胺的舒张作用。观察到高浓度组胺具有西咪替丁抗性的舒张作用,这与加入组胺后器官浴液pH值的相应降低相关。组胺溶液的中和消除了组胺的西咪替丁抗性作用。西咪替丁、甲硫米特和布立马胺是组胺反应的竞争性拮抗剂,其pKB值分别为6.6、6.1和5.4。这些估计值与这些药物在豚鼠右心房中对H2受体拮抗作用的文献值没有显著差异。组胺与4-甲基组胺(一种选择性H2受体激动剂)的效价比与在含H2受体的兔右心房中获得的效价比没有显著差异。这些来自拮抗剂和激动剂研究的数据表明,组胺通过激活组胺H2受体使兔气管舒张。