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氨基酯类局部麻醉药的神经阻滞差异活性。

Differential nerve blocking activity of amino-ester local anaesthetics.

作者信息

Wildsmith J A, Gissen A J, Gregus J, Covino B G

出版信息

Br J Anaesth. 1985 Jun;57(6):612-20. doi: 10.1093/bja/57.6.612.

Abstract

The in vitro sensitivities to local anaesthetic blockade of A, B and C nerve fibres in rabbit vagus nerves were examined using a series of structurally similar amino-ester agents which varied in lipid solubility and anaesthetic potency. A fibres were found to be the most sensitive and C fibres the least sensitive to conduction blockade with all the agents, provided that equilibrium blockade was allowed to develop. A correlation existed between the intrinsic anaesthetic potency of the various agents and their lipid solubilities. Equipotent concentrations of the drugs blocked C fibres at approximately the same rate, but there were marked variations in the rate at which A fibres were blocked. Amethocaine, an agent of high lipid solubility, blocked A fibres more quickly than C. As lipid solubility decreased through the series studied, so the onset of conduction blockade of A fibres was prolonged. It is suggested that this related to decreasing ability to penetrate the lipid diffusion barriers around A fibres. The traditional view that C fibres were more sensitive to block may have arisen because of confusion between absolute sensitivity and rate of development of conduction blockade.

摘要

使用一系列结构相似、脂溶性和麻醉效能各异的氨基酯类药物,研究了兔迷走神经中A、B和C神经纤维对局部麻醉阻滞的体外敏感性。结果发现,只要达到平衡阻滞,所有药物对A纤维的传导阻滞最为敏感,对C纤维最不敏感。各种药物的固有麻醉效能与其脂溶性之间存在相关性。等效浓度的药物对C纤维的阻滞速率大致相同,但对A纤维的阻滞速率存在显著差异。高脂溶性药物丁卡因对A纤维的阻滞速度比对C纤维快。在所研究的系列药物中,随着脂溶性降低,A纤维传导阻滞的起效时间延长。这表明这与穿透A纤维周围脂质扩散屏障的能力下降有关。传统观点认为C纤维对阻滞更敏感,可能是由于绝对敏感性和传导阻滞发展速率之间的混淆所致。

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