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组胺H2受体激动剂对豚鼠离体心脏的抗过敏作用。

The antianaphylactic action of histamine H2-receptor agonists in the guinea-pig isolated heart.

作者信息

Blandina P, Brunelleschi S, Fantozzi R, Giannella E, Mannaioni P F, Masini E

出版信息

Br J Pharmacol. 1987 Mar;90(3):459-66. doi: 10.1111/j.1476-5381.1987.tb11195.x.

Abstract

The effects of histamine and of H1- and H2-receptor agonists on the response to specific antigen were studied in isolated hearts taken from actively sensitized guinea-pigs. Histamine and H2-receptor agonists (dimaprit, impromidine) dose-dependently decrease the positive chronotropic and inotropic effects, and the severity of arrhythmias evoked by the challenge of sensitized hearts with specific antigen. Nordimaprit and the selective H1-receptor agonist 2-pyridyl-ethyl-amine (2-PEA) did not modify the patterns of cardiac anaphylaxis. The positive inotropic and chronotropic responses of the isolated heart to exogenous histamine appear to be partly reduced in the presence of dimaprit. The H2-receptor agonists decrease the amount of histamine released during cardiac anaphylaxis which is increased by cimetidine, while nordimaprit and PEA were ineffective, indicating an inhibitory function afforded by H2-receptors in cardiac anaphylaxis.

摘要

在取自主动致敏豚鼠的离体心脏中,研究了组胺以及H1和H2受体激动剂对特异性抗原反应的影响。组胺和H2受体激动剂(二甲双胍、英普咪定)剂量依赖性地降低了阳性变时性和变力性作用,以及用特异性抗原激发致敏心脏所诱发的心律失常的严重程度。去甲双胍和选择性H1受体激动剂2-吡啶基乙胺(2-PEA)并未改变心脏过敏反应的模式。在存在二甲双胍的情况下,离体心脏对外源性组胺的阳性变力性和变时性反应似乎部分降低。H2受体激动剂减少了心脏过敏反应期间释放的组胺量,而西咪替丁会增加组胺释放量,而去甲双胍和PEA则无效,这表明H2受体在心脏过敏反应中具有抑制作用。

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