Levi R, Allan G, Zavecz J H
Fed Proc. 1976 Jun;35(8):1942-7.
Current evidence pertinent to the identification of cardiac histamine receptors in the guinea pig is reviewed. Pharmacological characterization has been aided by the use of selective agonists and antagonists for both types of histamine receptors. It appears that both H1 and H2 receptors mediate the cardiac effects of histamine. Histamine H2 receptors mediate the positive chronotropic and ventricular inotropic effects. H1 receptors mediate the negative dromotropic effect of histamine and possibly the atrial inotropic effect. Histamine-induced arrhythmias involve H1 receptors (arrhythmias of conduction) or H2 receptors (arrhythmias of automaticity), or both. The receptors mediating the histamine-induced increase in coronary flow are not as clearly defined: both H1 and H2 receptors might be implicated.
本文综述了目前与豚鼠心脏组胺受体鉴定相关的证据。对两种类型组胺受体的选择性激动剂和拮抗剂的使用有助于进行药理学特性分析。似乎H1和H2受体均介导组胺对心脏的作用。组胺H2受体介导正性变时性和心室变力性作用。H1受体介导组胺的负性变传导性作用以及可能的心房变力性作用。组胺诱导的心律失常涉及H1受体(传导性心律失常)或H2受体(自律性心律失常),或两者皆有。介导组胺诱导的冠状动脉血流量增加的受体尚未明确界定:H1和H2受体可能均与之有关。