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苄基异喹啉类肌松药的未来。

The future of the benzylisoquinolinium relaxants.

作者信息

Savarese J J, Wastila W B

机构信息

New York Hospital-Cornell University Medical Center, New York, USA.

出版信息

Acta Anaesthesiol Scand Suppl. 1995;106:91-3. doi: 10.1111/j.1399-6576.1995.tb04317.x.

Abstract

The benzylisoquinolinium relaxants currently include the intermediate-acting agent, atracurium, and the short-acting agent, mivacurium. This class of relaxants has always retained the distinct advantages of rapid degradation, enzymatic metabolism, or both in the plasma, resulting in short half-lives and fast, complete recovery, unrelated to dose or duration of administration. Any improvements in this class of relaxants must focus on retaining this property at the same time as decreasing or eliminating histamine release, which has always been the major disadvantage of the benzylisoquinoliniums. The introduction of 51W89, an isomer of atracurium, may represent an advance in the development of this class of relaxants.

摘要

苄基异喹啉类肌松药目前包括中效的阿曲库铵和短效的米库氯铵。这类肌松药始终保留着在血浆中快速降解、酶代谢或两者兼具的显著优势,从而导致半衰期短以及快速、完全恢复,与给药剂量或持续时间无关。这类肌松药的任何改进都必须在保留这一特性的同时,减少或消除组胺释放,而组胺释放一直是苄基异喹啉类药物的主要缺点。阿曲库铵的异构体51W89的推出可能代表了这类肌松药发展的一个进步。

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