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MG 8926(一种潜在的抗心律失常和抗心绞痛药物)的血流动力学和代谢效应

The haemodynamic and metabolic effects of MG 8926, a prospective antidysrhythmic and antianginal agent.

作者信息

Marshall R J, Parratt J R

出版信息

Br J Pharmacol. 1977 Feb;59(2):311-22. doi: 10.1111/j.1476-5381.1977.tb07494.x.

Abstract

1 The antidysrhythmic, haemodynamic and metabolic effects of a new prospective antianginal and antidysrhythmic agent, N-(3-3-dipenylpropyl)-alpha-methyl-beta-cyclohexylethylamine hydrochloride (MG 8926), have been compared with the chemically related substance, prenylamine, in anaesthetized greyhounds and guinea-pigs. 2 When given intravenously 20 min beforehand, both MG 8926 and prenylamine (5 mg/kg) significantly suppressed the early dysrhythmias induced by coronary artery ligation in anaesthetized greyhounds. At a dose of 1 mg/kg, MG 8926 also protected anaesthetized guinea-pigs from dysrhythmias induced by ouabain infusions. 3 In dogs pretreated with MG 8926, metabolic changes indicative of myocardial ischaemia (increased PCO2 and potassium efflux, decreased oxygen content and pH) were less marked than those occurring in control animals. 4 Evidence was obtained that MG 8926, when given either before or after coronary occlusion, was capable of decreasing the severity of myocardial ischaemia as assessed by ST-segment changes in epicardial electrocardiograms.

摘要
  1. 一种新型潜在抗心绞痛和抗心律失常药物N-(3,3-二苯基丙基)-α-甲基-β-环己基乙胺盐酸盐(MG 8926)的抗心律失常、血流动力学及代谢作用,已在麻醉的灵缇犬和豚鼠身上与化学相关物质普尼拉明进行了比较。2. 若提前20分钟静脉给药,MG 8926和普尼拉明(5毫克/千克)均能显著抑制麻醉灵缇犬冠状动脉结扎诱发的早期心律失常。剂量为1毫克/千克时,MG 8926还能保护麻醉豚鼠免受哇巴因输注诱发的心律失常。3. 在预先用MG 8926处理的犬中,提示心肌缺血的代谢变化(二氧化碳分压升高、钾外流增加、氧含量和pH值降低)比对照动物中出现的变化不那么明显。4. 有证据表明,无论在冠状动脉闭塞前还是闭塞后给予MG 8926,通过心外膜心电图ST段变化评估,它都能够减轻心肌缺血的严重程度。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0285/1667736/068f88a67385/brjpharm00498-0099-a.jpg

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