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[苯氧苄胺对麦角新碱诱导的家兔冠状动脉阻力增加的拮抗作用]

[Phenoxybenzamine antagonism of ergometrine-induced increase of coronary artery resistance in rabbits].

作者信息

Bongrani S, Raddino R, Ferrari R, Rodelli P

出版信息

Boll Soc Ital Biol Sper. 1980 Jul 30;56(14):1445-51.

PMID:7448041
Abstract

Ergometrine is currently used as a test for Prinzmetal variant angina, causing specifically a coronary artery spasm in these patients, even if the mechanism of this drug on coronaries is still unclear. In isolated rabbit heart perfused at constant flow the administration of ergometrine at the concentration of 2.2 x 10(-5) M evoked a marked and longlasting increase of coronary resistance which was revealed by a rise in perfusion pressure from 68.2 +/- 12.9 to 124.4 +/- 21.7 (m +/- SD; n=21). This increase appears only with repeated perfusions of the drug and moreover it was not reproducible in the same preparation after its maximal response. The vasoconstriction was not significantly affected either by atropine or mepyramine, but it was strongly reduced by the phenoxybenzamine pretreatment (2.9 x 10(-6) M; n=8). It is evident the role of alpha-adrenergic receptors in ergometrine effect, but our results do not allow to understand its true mechanism, in fact the noradrenaline release can not be completely excluded.

摘要

麦角新碱目前被用作普萘洛尔变异型心绞痛的一种检测药物,即使该药物对冠状动脉的作用机制仍不清楚,但它能在这些患者中特异性地引发冠状动脉痉挛。在以恒定流量灌注的离体兔心脏中,给予浓度为2.2×10⁻⁵ M的麦角新碱会引发冠状动脉阻力显著且持久的增加,这可通过灌注压力从68.2±12.9升高至124.4±21.7(平均值±标准差;n = 21)得以体现。这种增加仅在重复灌注该药物时出现,而且在同一制剂达到最大反应后无法再现。血管收缩不受阿托品或美吡拉敏的显著影响,但苯氧苄胺预处理(2.9×10⁻⁶ M;n = 8)可使其显著降低。显然,α-肾上腺素能受体在麦角新碱的作用中发挥了作用,但我们的结果无法明确其真正机制,实际上,去甲肾上腺素的释放不能被完全排除。

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