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泮库溴铵、Org NC 45及其他泮库溴铵类似物在猫体内的神经肌肉和自主神经阻滞活性。

The neuromuscular and autonomic blocking activities of pancuronium, Org NC 45, and other pancuronium analogues, in the cat.

作者信息

Durant N N, Marshall I G, Savage D S, Nelson D J, Sleigh T, Carlyle I C

出版信息

J Pharm Pharmacol. 1979 Dec;31(12):831-6. doi: 10.1111/j.2042-7158.1979.tb13675.x.

Abstract

Twenty-six mono- or bis-quaternary salts of 3,17-dioxy-2 beta, 16 beta-dipiperidino-5 alpha-androstanes (including pancuronium) and one 17-desoxy congener were tested for neuromuscular blocking and autonomic blocking activities in the chloralose-anaesthetized cat. The 17 beta-acetoxy series, all the members of which contain an acetylcholine-like fragment in the steroidal D-ring, was most selective for effecting neuromuscular blockade. The salient member of this series is 3 alpha, 17 beta-diacetoxy-2 beta, 16 beta-dipiperidino-5 alpha-androstane 16 beta-N-monomethobromide (Org NC 45) which is highly selective in blocking neuromuscular transmission in that a dose approximately sixty times greater than the neuromuscular blocking dose was required to block responses to vagal stimulation. In contrast, in doses sufficient to produce neuromuscular block, pancuronium simultaneously blocked responses to vagal stimulation. Moreover, pancuronium and Org NC 45 exhibited the same order of neuromuscular blocking activity and therefore the latter potentially represents a useful addition to the armamentarium of neuromuscular blocking agents currently in clinical use.

摘要

在水合氯醛麻醉的猫身上,对26种3,17 - 二氧代 - 2β,16β - 二哌啶基 - 5α - 雄甾烷的单季铵盐或双季铵盐(包括泮库溴铵)以及1种17 - 去氧类似物进行了神经肌肉阻滞和自主神经阻滞活性测试。17β - 乙酰氧基系列的所有成员在甾体D环中都含有一个类似乙酰胆碱的片段,对产生神经肌肉阻滞最具选择性。该系列的显著成员是3α,17β - 二乙酰氧基 - 2β,16β - 二哌啶基 - 5α - 雄甾烷16β - N - 一甲基溴化物(Org NC 45),它在阻断神经肌肉传递方面具有高度选择性,即阻断迷走神经刺激反应所需的剂量比神经肌肉阻滞剂量大约大60倍。相比之下,在足以产生神经肌肉阻滞的剂量下,泮库溴铵同时阻断了对迷走神经刺激的反应。此外,泮库溴铵和Org NC 45表现出相同顺序的神经肌肉阻滞活性,因此后者可能是目前临床使用的神经肌肉阻滞剂药物库中的一个有用补充。

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