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(2RS,3SR)-2-氨甲基-2,3,7,8-四氢-2,3,5,8,8-五甲基-6H-呋喃并[2,3-e]吲哚-7-酮盐酸盐(UK-1745)的心血管效应,一种具有血管舒张和抗心律失常特性的新型强心剂。

Cardiovascular effects of (2RS,3SR)- 2-aminomethyl-2,3,7,8-tetrahydro-2,3,5,8,8-pentamethyl-6H-furo- [2,3-e]indol-7-one hydrochloride (UK-1745), a novel cardiotonic agent with vasodilatory and antiarrhythmic properties.

作者信息

Uchida Y, Kawada M, Sawanobori K, Sonoki H, Inoue K, Mizuno K, Itou T, Tabunoki Y, Tsukamoto M, Ohashi Y, Kyotani Y, Shimizu N, Fujii M, Nakamura M

机构信息

Clinical Physiology and Cardiovascular Center, Toho University Hospital at Sakura, Chiba, Japan.

出版信息

Arzneimittelforschung. 1998 Mar;48(3):219-31.

PMID:9553677
Abstract

The cardiovascular effects of (2RS,3SR)-2-aminomethyl-2,3,7,8- tetrahydro-2,3,5,8,8-pentamethyl-6H-furo[2,3-e]indol-7-one hydrochloride (CAS 170684-14-7, UK-1745), a novel cardiotonic agent, were investigated using in vitro and in vivo preparations. In paced left atria isolated from guinea pigs, both UK-1745 and vesnarinone (CAS 81840-15-5) showed a concentration-dependent positive inotropic effect. In spontaneously beating guinea pig right atria, both agents caused only a minimal chronotropic effect. In isolated, blood-perfused canine papillary muscle preparations, UK-1745 and vesnarinone injected intra-arterially into the anterior septal artery (ASA) increased the developed tension in a dose-dependent manner. In isolated, blood-perfused canine sinoatrial node preparations, both agents injected into the right coronary artery (RCA) did not cause any appreciable changes in the sinus rate. UK-1745 increased the blood flow through the ASA and the RCA in a dose-dependent manner, whereas vesnarinone did not. In anesthetized open-chest dogs, UK-1745 injected intravenously increased cardiac contractility and cardiac output, and decreased left ventricular end-diastolic pressure, systemic vascular resistance and heart rate. In experimentally induced acute heart failure in anesthetized open-chest dogs, intravenously injected UK-1745 effectively improved hemodynamic functions. In conscious instrumented dogs, orally administered UK-1745 increased LV dP/dtmax with insignificant changes in systemic blood pressure and heart rate. In mice, orally administered UK-1745 protected the development of ventricular fibrillation induced by chloroform inhalation, whereas vesnarinone did not. Thus, in respect of inotropic and chronotropic effects, UK-1745 closely resembled vesnarinone, but differed from vesnarinone in respect of coronary vasodilating and antiarrhythmic effects. The results suggest that UK-1745 is a novel positive inotropic agent with vasodilatory and antiarrhythmic properties, without significant chronotropic action, and may be beneficial for the treatment of congestive heart failure.

摘要

使用体外和体内实验制剂,对新型强心剂(2RS,3SR)-2-氨甲基-2,3,7,8-四氢-2,3,5,8,8-五甲基-6H-呋喃并[2,3-e]吲哚-7-酮盐酸盐(CAS 170684-14-7,UK-1745)的心血管效应进行了研究。在从豚鼠分离的起搏左心房中,UK-1745和维司力农(CAS 81840-15-5)均呈现浓度依赖性正性肌力作用。在自发搏动的豚鼠右心房中,两种药物仅引起最小的变时作用。在分离的、血液灌注的犬乳头肌制剂中,经动脉注射到前间隔动脉(ASA)中的UK-1745和维司力农以剂量依赖性方式增加了收缩张力。在分离的、血液灌注的犬窦房结制剂中,注入右冠状动脉(RCA)的两种药物均未引起窦性心率的任何明显变化。UK-1745以剂量依赖性方式增加了通过ASA和RCA的血流量,而维司力农则没有。在麻醉的开胸犬中,静脉注射UK-1745可增加心脏收缩力和心输出量,并降低左心室舒张末期压力、全身血管阻力和心率。在麻醉的开胸犬实验性诱导的急性心力衰竭中,静脉注射UK-1745有效改善了血流动力学功能。在清醒的仪器化犬中,口服UK-1745可增加左心室dp/dtmax,而全身血压和心率无明显变化。在小鼠中,口服UK-1745可保护吸入氯仿诱导的心室颤动的发生,而维司力农则不能。因此,就正性肌力和变时作用而言,UK-1745与维司力农非常相似,但在冠状动脉扩张和抗心律失常作用方面与维司力农不同。结果表明,UK-1745是一种新型的具有血管舒张和抗心律失常特性的正性肌力药物,无明显的变时作用,可能对治疗充血性心力衰竭有益。

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