Mest H J, Hörhold I, Rein T, Riedel A, Broquet C
Department of Pharmacology and Toxicology, School of Medicine, Martin Luther University Halle-Wittenberg, Germany.
Pharmacol Res. 1992 Feb-Mar;25(2):173-80. doi: 10.1016/1043-6618(92)91385-t.
Different mediators released by anaphylaxis seem to be involved in different pathophysiological conditions, including cardiac arrhythmia. Histamine, 5-HT and platelet-activating factor (PAF) could participate in the enhanced arrhythmogenicity during anaphylaxis in guinea-pigs. The threshold dose of ouabain-induced arrhythmia is decreased in actively sensitized guinea-pigs by i.p. administration of ovalbumin. The purpose of the present paper was to investigate the effect of different mediator antagonists. Antagonists of PAF (WEB 2170), histamine (clemastine) and 5-HT (cyproheptadine) in doses of 5.0 mg/kg, 5.0 mg/kg and 0.5 mg/kg, respectively, can increase the threshold dose of ouabain-induced arrhythmias signalling an antiarrhythmic effect. A combination of WEB 2170 and clemastine, each of them in inactive doses (2.0 mg/kg and 1.0 mg/kg, respectively) showed a statistically significant antiarrhythmic effect. A combination of the same dose of WEB 2170 and cyproheptadine (0.1 mg/kg) under the same conditions induced an antiarrhythmic effect, too. BN 52256 is a new antiallergic drug synthesized on the basis of a novel concept of combining inhibitory activity against various inflammatory mediators in one molecule. BN 52256 in doses of 20-80 micrograms/kg exhibited a statistically significant antiarrhythmic effect. BN 52256 needed a 12.5-125 fold lower dose to induce the same antiarrhythmic effect compared to the antagonists of PAF, histamine or 5-HT investigated in this study. Depending on the pathophysiological conditions, different mediators seem to be involved in the occurrence of cardiac arrhythmia. A complex inhibition of these mediators could induce a more specific influence on such kinds of cardiac arrhythmias.
过敏反应释放的不同介质似乎参与了不同的病理生理状况,包括心律失常。组胺、5-羟色胺和血小板活化因子(PAF)可能参与了豚鼠过敏反应期间心律失常的增强。通过腹腔注射卵清蛋白,主动致敏的豚鼠哇巴因诱导的心律失常阈值剂量降低。本文的目的是研究不同介质拮抗剂的作用。PAF拮抗剂(WEB 2170)、组胺拮抗剂(氯马斯汀)和5-羟色胺拮抗剂(赛庚啶)的剂量分别为5.0mg/kg、5.0mg/kg和0.5mg/kg,可增加哇巴因诱导的心律失常阈值剂量,表明具有抗心律失常作用。WEB 2170和氯马斯汀各以无活性剂量(分别为2.0mg/kg和1.0mg/kg)联合使用显示出统计学上显著的抗心律失常作用。相同剂量的WEB 2170和赛庚啶(0.1mg/kg)在相同条件下联合使用也诱导了抗心律失常作用。BN 52256是一种基于将对各种炎症介质的抑制活性结合在一个分子中的新概念合成的新型抗过敏药物。20-80微克/千克剂量的BN 52256表现出统计学上显著的抗心律失常作用。与本研究中研究的PAF、组胺或5-羟色胺拮抗剂相比,BN 52256诱导相同抗心律失常作用所需的剂量低12.5-125倍。根据病理生理状况,不同的介质似乎参与了心律失常的发生。对这些介质的复杂抑制可能会对这类心律失常产生更特异性的影响。