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硝酸N-(2-羟乙基)烟酰胺(SG-75)对完整麻醉大鼠中乙酰甲胆碱诱导的心电图变化的影响。

Effects of N-(2-hydroxyethyl)nicotinamide nitrate (SG-75) on methacholine-induced ECG changes in intact anesthetized rats.

作者信息

Aono J, Akima M, Sakai K

出版信息

Jpn J Pharmacol. 1981 Oct;31(5):823-30. doi: 10.1254/jjp.31.823.

Abstract

The effects of a newly developed nicotinamide derivative, N-(2-hydroxyethyl)nicotinamide nitrate (SG-75, Nicorandil), were examined in an experimental model of angina pectoris, utilizing methacholine-induced ECG changes as main parameter in intact anesthetized rats. The right carotid artery was exposed and through it a special cannula was inserted to a point near the right and left coronary ostium. Such a device made it possible to inject drugs more selectively into the coronary artery. Single intra-aortic injections of 4 to 8 micrograms of methacholine caused a transient elevation of the ST segment and T wave of the electrocardiogram (ECG). SG-75 (3 mg/kg i.v. or 10 mg/kg p.o.) prevented these changes in the ECG, while a potent vasodilator, papaverine, failed to do so. In the isolated, donor-perfused rat heart, SG-75 (1-30 micrograms) injected into the coronary perfusion system caused dose-dependent vasodilation, while 0.1-0.8 micrograms acetylcholine as well as methacholine produced marked vasoconstriction. SG-75 (10 mg/kg) administered orally to the donor rat inhibited the coronary vasoconstriction produced by the cholinomimetic drugs, whereas papaverine (30 micrograms i.a.) failed to prevent it. The inhibitory effects of SG-75 on methacholine-induced ECG changes in intact rats seemed to be due to its spasmolytic action.

摘要

利用乙酰甲胆碱诱导的心电图变化作为主要参数,在完整麻醉大鼠的心绞痛实验模型中,研究了一种新开发的烟酰胺衍生物N-(2-羟乙基)烟酰胺硝酸盐(SG-75,尼可地尔)的作用。暴露右颈动脉,并通过它插入一根特殊的套管至左右冠状动脉口附近的一点。这种装置使更有选择性地向冠状动脉内注射药物成为可能。单次主动脉内注射4至8微克乙酰甲胆碱会导致心电图(ECG)的ST段和T波短暂升高。SG-75(静脉注射3毫克/千克或口服10毫克/千克)可预防这些心电图变化,而一种强效血管扩张剂罂粟碱则不能。在离体的、供体灌注的大鼠心脏中,向冠状动脉灌注系统注射SG-75(1至30微克)会引起剂量依赖性血管舒张,而0.1至0.8微克乙酰胆碱以及乙酰甲胆碱则会产生明显的血管收缩。给供体大鼠口服SG-75(10毫克/千克)可抑制拟胆碱药物引起的冠状动脉收缩,而罂粟碱(动脉内注射30微克)则不能预防。SG-75对完整大鼠中乙酰甲胆碱诱导的心电图变化的抑制作用似乎归因于其解痉作用。

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