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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):一种新型强效长效抗心律失常药物。

N-(2,6-Dimethylphenyl)-8-pyrrolizidineacetamide hydrochloride hemihydrate (SUN 1165): a new potent and long-acting antiarrhythmic agent.

作者信息

Aisaka K, Hidaka T, Inomata N, Hamasaki S, Ishihara T, Morita M

出版信息

Arzneimittelforschung. 1985;35(8):1239-45.

PMID:4074441
Abstract

N-(2,6-Dimethylphenyl)-8-pyrrolizidineacetamide hydrochloride hemihydrate (SUN 1165) at the doses of 2.5 mg/kg i.v. and 3-10 mg/kg i.d. or p.o. restored sinus rhythm from ventricular multifocal arrhythmias induced by two-stage ligation of the coronary artery in the conscious dogs, Harris model, without causing gastrointestinal and central nervous system side effects. The onset of antiarrhythmic action was 1-2 min after i.v. injection and 15-30 min after an oral administration, and this action lasted longer than 1 h after i.v. and 6 h after oral administration, respectively. SUN 1165 was also effective in suppressing ouabain-and halothane-epinephrine-induced ventricular arrhythmias at the doses of 1.7 and 1.2 mg/kg i.v. and 1-10 mg/kg i.d. It did not impair parasympathetic nerve activity. SUN 1165 showed a local anesthetic or membrane stabilizing activity comparable to lidocaine and disopyramide. In conscious dogs without arrhythmia, SUN 1165 had no deleterious cardiohemodynamic effect and no gross behavioral effect at the oral doses of 3 and 10 mg/kg. Thus, it is concluded that SUN 1165 is an orally effective, potent and long-acting class I type antiarrhythmic agent without serious side effects common to other antiarrhythmic drugs.

摘要

N-(2,6-二甲基苯基)-8-吡咯烷乙酰胺盐酸盐半水合物(SUN 1165),静脉注射剂量为2.5毫克/千克,皮下或口服剂量为3 - 10毫克/千克,可使清醒犬(哈里斯模型)在冠状动脉两阶段结扎诱导的室性多灶性心律失常恢复窦性心律,且不引起胃肠道和中枢神经系统副作用。静脉注射后抗心律失常作用的起效时间为1 - 2分钟,口服给药后为15 - 30分钟,静脉注射后该作用持续超过1小时,口服给药后持续6小时。SUN 1165在静脉注射剂量为1.7毫克/千克和皮下剂量为1 - 10毫克/千克时,对哇巴因和氟烷 - 肾上腺素诱导的室性心律失常也有效。它不损害副交感神经活动。SUN 1165显示出与利多卡因和丙吡胺相当的局部麻醉或膜稳定活性。在无心律失常的清醒犬中,口服剂量为3和10毫克/千克时,SUN 1165没有有害的心脏血流动力学效应和明显的行为影响。因此,得出结论,SUN 1165是一种口服有效的、强效且长效的I类抗心律失常药物,没有其他抗心律失常药物常见的严重副作用。

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