Dénes B, Greeff K
Eur J Pharmacol. 1979 Aug 15;57(4):417-22. doi: 10.1016/0014-2999(79)90504-1.
Experiments were carried out in order to study the interaction between cardioactive glycosides and histamine or histamine H1- AND/OR H2-receptor antagonists in anaesthetized cats or guinea pigs. The toxicity of ouabain or digoxin was tested by infusing the glycosides until idioventricular rhythm or death occurred. Histamine increased the toxicity of ouabain, but the histamine H1- and/or H2-receptor antagonists (metiamide and mepyramine)did not influence the toxicity of digitalis. In cats the increase in pulmonary arterial blood pressure caused by digoxin was not affectedby histamine H1- and/or H2-receptor antagonism in spite of the fact that the increase of pulmonary blood pressure caused by histamine could be abolished by H1-receptor antagonists. Our results indicate that histamine is not involved in the toxic effect of cardiac glycosides.
为了研究强心苷与组胺或组胺H1和/或H2受体拮抗剂在麻醉猫或豚鼠体内的相互作用,进行了实验。通过输注糖苷直至出现心室自主节律或死亡来测试哇巴因或地高辛的毒性。组胺增加了哇巴因的毒性,但组胺H1和/或H2受体拮抗剂(甲硫米特和美吡拉敏)并未影响洋地黄的毒性。在猫中,尽管组胺H1受体拮抗剂可消除组胺引起的肺血压升高,但地高辛引起的肺动脉血压升高不受组胺H1和/或H2受体拮抗作用的影响。我们的结果表明,组胺不参与强心苷的毒性作用。