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N-(2,6-二甲基苯基)-8-吡咯烷乙酰胺盐酸盐半水合物(SUN 1165),一种新型抗心律失常药物:对心脏传导的影响

N-(2,6-dimethylphenyl)-8-pyrrolizidineacetamide hydrochloride hemihydrate (SUN 1165), a new antiarrhythmic agent: effects on cardiac conduction.

作者信息

Hidaka T, Hamasaki S, Aisaka K, Ishihara T, Morita M, Toyama J, Yamada K

出版信息

Arzneimittelforschung. 1985;35(9):1381-6.

PMID:4084339
Abstract

Effects of N-(2,6-dimethylphenyl)-8-pyrrolizidineacetamide hydrochloride hemihydrate (SUN 1165) on cardiac conduction were studied in anesthetized, anesthetized open-chest and conscious dogs and rabbit Langendorff hearts following either intravenous (i.v.) bolus injection and continuous infusion or intraarterial injection. SUN 1165 at antiarrhythmic doses (or concentrations), prolonged PQ interval in dogs inherently showing broad QRS complex without affecting QRS duration, but prolonged both PQ interval and QRS duration in dogs showing narrow QRS complex, in a dose-dependent manner. At higher doses (or plasma concentrations), SUN 1165 caused a marked prolongation of PQ interval together with QRS duration and subsequently, in most cases, elicited conduction block within the atrial muscle as evidenced by disappearance of P wave. SUN 1165 caused the dose-related prolongations of atrio-ventricular conduction time and intra-atrial conduction time, and at the highest dose it blocked conduction within the atrial muscle in some cases. In the rabbit Langendorff hearts, SUN 1165 tended to prolong intraatrial and His-Purkinje-ventricular conduction time in preference to atrio-ventricular one. At higher concentrations, SUN 1165 produced conduction block in the Purkinje-ventricular system. These results suggest that SUN 1165, at the antiarrhythmic doses (or plasma concentrations), causes a delay of cardiac conduction by acting on the atrial muscle and His-Purkinje-ventricular system without affecting conduction through A-V node region, and at higher doses (or concentrations) produces conduction block by acting again on the atrial muscle or on His-Purkinje-ventricular system without impairing conduction in the A-V node.

摘要

在麻醉、开胸麻醉和清醒的犬以及兔Langendorff心脏中,通过静脉推注和持续输注或动脉内注射,研究了盐酸N-(2,6-二甲基苯基)-8-吡咯烷乙酰胺半水合物(SUN 1165)对心脏传导的影响。在抗心律失常剂量(或浓度)下,SUN 1165可使固有QRS波群增宽的犬的PQ间期延长,而不影响QRS时限,但可使QRS波群狭窄的犬的PQ间期和QRS时限均延长,且呈剂量依赖性。在更高剂量(或血浆浓度)下,SUN 1165可使PQ间期和QRS时限显著延长,随后在大多数情况下,可引起心房肌内传导阻滞,表现为P波消失。SUN 1165可使房室传导时间和心房内传导时间呈剂量依赖性延长,在最高剂量时,在某些情况下可阻断心房肌内传导。在兔Langendorff心脏中,SUN 1165倾向于优先延长心房内和希氏-浦肯野-心室传导时间,而不是房室传导时间。在更高浓度下,SUN 1165可在浦肯野-心室系统中产生传导阻滞。这些结果表明,在抗心律失常剂量(或血浆浓度)下,SUN 1165通过作用于心房肌和希氏-浦肯野-心室系统而导致心脏传导延迟,而不影响通过房室结区域的传导,在更高剂量(或浓度)下,通过再次作用于心房肌或希氏-浦肯野-心室系统而产生传导阻滞,而不损害房室结内的传导。

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