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双苄基异喹啉生物碱衍生物的心血管药理作用

Cardiovascular pharmacological effects of bisbenzylisoquinoline alkaloid derivatives.

作者信息

Qian Jia-Qing

机构信息

Faculty of Pharmacology, Tongji Medical College of Huazhong University of Science and Technology, Wuhan 430030, China.

出版信息

Acta Pharmacol Sin. 2002 Dec;23(12):1086-92.

Abstract

Tetrandrine, dauricine, daurisoline and neferine are bisbenzylisoquinoline alkaloid derivatives isolated from Chinese traditional medicine and herbs. The cardiovascular pharmacological effects and the mechanism of actions of these compounds were reviewed. Tetrandrine isolated from Stephania tetrandra S Moore possesses antihypertensive and antiarrhythmic effects. The antihypertensive effects of tetrandrine have been demonstrated in experimental hypertensive animals and in hypertensive patients. Recent studies showed that in addition to its calcium antagonistic effect, tetrandrine interacted with M receptors. Modulation by M receptor is one of the pharmacological mechanisms of cardiovascular effects of tetrandrine. Dauricine and daurisoloine were isolated from Menispermum dauricum DC. The antiarrhythmic effects of dauricine have been verified in different experimental arrhythmic models and in cardiac arrhythmic patients. Dauricine blocked the cardiac transmembrane Na+,K+ and Ca2+ ion currents. Differing from quinidine and sotalol, which exhibited reverse use-dependent effect, dauricine prolonged APD in a normal use-dependent manner in experimental studies. The antiarrhythmic effect of daurisoline and neferine which is an alkaloid isolated from Nelumbo nucifera Gaertn, and their mechanisms of actions have also been studied. The antiarrhythmic effect of daurisoline is more potent than that of dauricine.

摘要

粉防己碱、蝙蝠葛碱、蝙蝠葛苏林碱和甲基莲心碱是从中国传统中草药中分离得到的双苄基异喹啉生物碱衍生物。本文综述了这些化合物的心血管药理作用及其作用机制。从防己科植物粉防己中分离得到的粉防己碱具有降压和抗心律失常作用。粉防己碱的降压作用已在实验性高血压动物和高血压患者中得到证实。最近的研究表明,粉防己碱除具有钙拮抗作用外,还可与M受体相互作用。M受体调节是粉防己碱心血管效应的药理机制之一。蝙蝠葛碱和蝙蝠葛苏林碱是从蝙蝠葛中分离得到的。蝙蝠葛碱的抗心律失常作用已在不同的实验性心律失常模型和心律失常患者中得到证实。蝙蝠葛碱可阻断心脏跨膜Na+、K+和Ca2+离子电流。与奎尼丁和索他洛尔表现出的反向使用依赖性效应不同,蝙蝠葛碱在实验研究中以正常的使用依赖性方式延长动作电位时程(APD)。对蝙蝠葛苏林碱和从莲中分离得到的生物碱甲基莲心碱的抗心律失常作用及其作用机制也进行了研究。蝙蝠葛苏林碱的抗心律失常作用比蝙蝠葛碱更强。

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