Korsak Z, Hermanowicz G, Fijałkowska I
Acta Physiol Pol. 1983 May-Jun;34(3):383-91.
Imidazole (IM) exerts a positive inotropic effect on the guinea pig heart in a dose-dependent manner. This effect is not controlled by any of histamine receptors. Both, mepyramine - a H1-histamine receptor blocker, and cimetidine - a H2-histamine receptor blocker have no influence on IM responses. A positive inotropic action of IM on the heart has been shown in both, normal Ringer-Locke solution and in solutions with calcium deficit, however, the relative increase in contraction amplitude was higher at lower calcium concentrations than in solutions with normal calcium content. In calcium - free solution IM produces a marked delay of heart arrest, but fails to restore the heart action stopped by absence of calcium in the perfusion medium. The effects of IM and theophylline are additive. It is concluded that the action of IM on the guinea pig heart is not connected with histamine receptors, and a possible role of IM as a regulator of free calcium ions is suggested.
咪唑(IM)对豚鼠心脏具有剂量依赖性的正性肌力作用。这种作用不受任何组胺受体的控制。H1组胺受体阻滞剂美吡拉敏和H2组胺受体阻滞剂西咪替丁对IM的反应均无影响。在正常林格 - 洛克溶液和缺钙溶液中,IM对心脏均显示出正性肌力作用,然而,在较低钙浓度下,收缩幅度的相对增加高于正常钙含量的溶液。在无钙溶液中,IM可显著延迟心脏停搏,但无法恢复因灌注介质中缺钙而停止的心脏活动。IM和茶碱的作用是相加的。得出的结论是,IM对豚鼠心脏的作用与组胺受体无关,并提示IM可能作为游离钙离子调节剂发挥作用。