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Effects of nipradilol on myocardial ischaemia produced by coronary stenosis in dogs.

机译:尼帕地洛对犬冠状动脉狭窄所致心肌缺血的影响。

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摘要

Effects of nipradilol which is a new beta-adrenoceptor blocking agent endowed with nitroglycerin-like vasodilator actions, its denitrated derivative (denitro nipradilol) and propranolol on abnormalities of regional myocardial shortening produced by partial occlusion of the left circumflex coronary artery (LCX) were studied in anaesthetized open-chest dogs. In the presence of LCX stenosis, nipradilol (0.1 mg kg-1, i.v.) produced marked decreases in heart rate and LVdP/dt without a significant increase in left ventricular end-diastolic pressure (LVEDP). It improved impaired myocardial segment shortening and restored normal cardiac lactate metabolism. Denitro nipradilol (0.2 mg kg-1 i.v.) and propranolol (0.2 mg kg-1 i.v.) both caused similar haemodynamic changes to nipradilol but also produced a significant increase in LVEDP. However, improvement by these two agents of regional dysfunction in the ischaemic myocardium was comparable to those seen with nipradilol. All three agents markedly inhibited isoprenaline-induced tachycardia, but vehicle did not. Atrial pacing abolished the beneficial effect of nipradilol on myocardial shortening in the ischaemic region without affecting other haemodynamic parameters. These results indicate that nipradilol alleviates acute myocardial ischaemia produced by coronary stenosis with similar efficacy to denitro nipradilol and propranolol suggesting, that a major part of the beneficial effect of nipradilol may be attributable to its beta-adrenoceptor blocking action.
机译:研究了尼帕地洛是一种新型的β-肾上腺素受体阻滞剂,具有硝化甘油样血管扩张剂作用,其反硝化衍生物(去硝基尼帕地洛尔)和普萘洛尔对部分闭塞左旋支冠状动脉(LCX)引起的局部心肌缩短异常的影响在麻醉的开胸犬中。在存在LCX狭窄的情况下,尼帕地洛(0.1 mg kg-1,i.v.)使心率和LVdP / dt明显降低,而左心室舒张末期压力(LVEDP)却没有明显增加。它改善了受损的心肌节段缩短,并恢复了正常的心脏乳酸代谢。硝基硝基尼泊洛尔(0.2 mg kg-1 i.v.)和普萘洛尔(0.2 mg kg-1 i.v.)都引起尼泊洛尔相似的血液动力学变化,但LVEDP显着增加。但是,这两种药物对缺血性心肌的局部功能障碍的改善与尼普地洛相似。所有这三种药物均显着抑制了异丙肾上腺素引起的心动过速,但赋形剂没有。心房起搏取消了尼帕地洛对缺血区域心肌缩短的有益作用,而没有影响其他血液动力学参数。这些结果表明,尼帕地洛减轻冠状动脉狭窄引起的急性心肌缺血,其功效与去硝基尼帕地洛和普萘洛尔相似,这表明尼帕地洛的主要有益作用可能归因于其β-肾上腺素受体的阻滞作用。

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    Noguchi, K.; Sakanashi, M.;

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  • 年度 1987
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