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[里氏有限公司对神经肌肉阻滞剂的研究]

[Investigation of neuromuscular blocking agents at Richter Ltd].

作者信息

Kárpáti Egon, Bíró Katalin, Kukorelli Tibor

机构信息

Richter Gedeon Vegyészeti Gyár Rt., Budapest.

出版信息

Acta Pharm Hung. 2002;72(1):37-48.

Abstract

Investigation of new neuromuscular blocking agents was started 30 years ago in Richter Ltd. This paper presents the results obtained by Richter's scientists. 2 compounds out of 100 bisquaternary ammonio steroid having androstane skeleton were selected for further pharmacological study. One of these agents, pipecuronium bromide (Arduan) elicited long-lasting block of neuromuscular transmission without cardiovascular side effects in both animal experiments and clinical studies. Arduan is a powerful competitive antagonist of acetylcholine, since it can bind pre- and postsynaptic (N1) receptors of the transmitters. It has no remarkable cumulative effect. Neostigmine rapidly and completely antagonized the neuromuscular blockade caused by pipecuronium. Arduan was introduced into clinical practice. The second compound, RGH-4201 (Duador) evoked a neuromuscular block of short duration. It showed slight atropin-like cardio-vagolytic effect in animal experiments. In the clinical studies, however, the cardiovascular side effects were found to be too strong. Therefore, it was not introduced in clinical practice.

摘要

30年前,里奇特有限公司就开始了新型神经肌肉阻滞剂的研究。本文介绍了里奇特公司科学家们所取得的研究成果。在100种具有雄甾烷骨架的双季铵甾体化合物中,挑选出2种化合物进行进一步的药理学研究。其中一种药物,哌库溴铵(阿端)在动物实验和临床研究中均能引起持久的神经肌肉传递阻滞,且无心血管副作用。阿端是一种强效的乙酰胆碱竞争性拮抗剂,因为它能与递质的突触前和突触后(N1)受体结合。它没有明显的累积效应。新斯的明能迅速且完全地拮抗哌库溴铵引起的神经肌肉阻滞。阿端已被应用于临床实践。第二种化合物,RGH - 4201(杜阿多)引起的神经肌肉阻滞持续时间较短。在动物实验中,它表现出轻微的类似阿托品的迷走神经解作用。然而,在临床研究中,发现其心血管副作用过大。因此,它未被应用于临床实践。

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