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McN-4130在几种动物模型中的抗心律失常和抗纤颤特性。

Antiarrhythmic and antifibrillatory properties of McN-4130 in several animal models.

作者信息

Damiano B P, Sit S P, Fortunato M A, Stranieri M T, Brannan M D

机构信息

Department of Biological Research, McNeil Pharmaceutical, Spring House, Pennsylvania 19477.

出版信息

J Cardiovasc Pharmacol. 1988 May;11(5):581-90. doi: 10.1097/00005344-198805000-00011.

Abstract

McN-4130 is an experimental compound having antiarrhythmic and antifibrillatory activity in several animal models. In anesthetized, open-chest pigs subjected to total occlusion and subsequent reperfusion of the left anterior descending coronary artery, McN-4130 dose-dependently (2.5-10.0 mg/kg i.v.) protected against fibrillation and death. Mean arterial pressure was not significantly affected, but heart rate was dose-dependently reduced. In anesthetized normal dogs, McN-4130 increased ventricular fibrillation threshold for up to 45 min. This increase in fibrillation threshold was associated with concurrent increases in ventricular conduction time and ventricular effective refractory period. In conscious dogs subjected to occlusion of the left anterior descending coronary artery 24 h previously, McN-4130, 2.5 and 5.0 mg/kg i.v., significantly reduced the rate of ventricular arrhythmias for up to 45 min. McN-4130 was more effective and had a longer duration of action than comparable doses of lidocaine and disopyramide. McN-4130 was orally effective in this model at 10 mg/kg. These results indicate that McN-4130, a structurally unique experimental antiarrhythmic compound, may be useful as a ventricular antiarrhythmic agent with antifibrillatory properties.

摘要

McN - 4130是一种实验性化合物,在多种动物模型中具有抗心律失常和抗纤颤活性。在麻醉的、开胸的猪身上,对其左前降支冠状动脉进行完全闭塞并随后再灌注,McN - 4130呈剂量依赖性(静脉注射2.5 - 10.0 mg/kg)地预防纤颤和死亡。平均动脉压未受到显著影响,但心率呈剂量依赖性降低。在麻醉的正常犬中,McN - 4130使心室纤颤阈值提高达45分钟。这种纤颤阈值的升高与心室传导时间和心室有效不应期的同时增加相关。在24小时前左前降支冠状动脉已被闭塞的清醒犬中,静脉注射2.5和5.0 mg/kg的McN - 4130可使室性心律失常发生率显著降低达45分钟。McN - 4130比同等剂量的利多卡因和丙吡胺更有效且作用持续时间更长。在该模型中,McN - 4130以10 mg/kg口服有效。这些结果表明,McN - 4130是一种结构独特的实验性抗心律失常化合物,可能作为一种具有抗纤颤特性的室性抗心律失常药物有用。

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