Carroll P R, Glover W E
Br J Pharmacol. 1977 Feb;59(2):333-41. doi: 10.1111/j.1476-5381.1977.tb07497.x.
1 Histamine produced dose-dependent contractile responses on both isolated perfused ear arteries and aortic strips of the rabbit. These responses were blocked by mepyramine and potentiated by both metiamide and dithiothreitol. 2 In the presence of maximum potentiation by metiamide, dithiothreitol still potentiated the contractile response to histamine of both preparations. 3 In the presence of mepyramine, histamine produced dose-dependent reductions in the contractile response to noradrenaline. This vasodilator action of histamine was abolished by metiamide but was unaffected by dithiothreitol. 4 The vasodilator action of histamine on the human isolated perfused temporal artery and the positive inotropic effect of histamine on the isolated spontaneously beating atria of the rabbit were blocked by metiamide but unaffected by dithiothreitol. 5 It is concluded that the rabbit aorta, like the ear artery, contains both H1 and H2 histamine receptors and that dithiothreitol potentiates cardiovascular responses mediated by H1-receptors but not by H2-receptors.
1 组胺对兔离体灌注耳动脉和主动脉条均产生剂量依赖性的收缩反应。这些反应被美吡拉敏阻断,而被甲硫米特和二硫苏糖醇增强。2 在甲硫米特最大程度增强作用存在的情况下,二硫苏糖醇仍能增强两种制剂对组胺的收缩反应。3 在美吡拉敏存在的情况下,组胺使对去甲肾上腺素的收缩反应产生剂量依赖性降低。组胺的这种血管舒张作用被甲硫米特消除,但不受二硫苏糖醇影响。4 组胺对人离体灌注颞动脉的血管舒张作用以及组胺对兔离体自发搏动心房的正性变力作用被甲硫米特阻断,但不受二硫苏糖醇影响。5 得出结论,兔主动脉与耳动脉一样,含有H1和H2组胺受体,且二硫苏糖醇增强由H1受体介导的心血管反应,而不增强由H2受体介导的反应。