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利多卡因在过敏反应中的抑制作用。

The inhibitory action of lidocaine in anaphylaxis.

作者信息

Weiss E B, Hargraves W A, Viswanath S G

出版信息

Am Rev Respir Dis. 1978 May;117(5):859-69. doi: 10.1164/arrd.1978.117.5.859.

Abstract

The action of lidocaine, a local anesthetic, was investigated during anaphylaxis in guinea pigs after passive sensitization in vitro of lung tissue and trachealis muscle. Pretreatment of the trachealis muscle with 8.54 mM lidocaine resulted in the total inhibition of anaphylactic isometric tension. Full reversal of anaphylactic-induced contractures was rapidly achieved with concentrations of 4.27 mM lidocaine. Release of histamine from both lung tissue and trachealis muscle was inhibited by 73 to 82 per cent, respectively, over concentration ranges of 2.13 to 8.54 mM lidocaine. A bimodal effect on sensitized tissues was noted, with lidocaine causing a slight release of histamine in the trachealis muscle of 1.6 per cent at a concentration of 8.54 mM. Lidocaine did not impair the initial passive sensitization process, nor did it appear to elute antibody once it was cell bound. The dual inhibitory effect on mast-cell release of mediators and on muscle contraction by lidocaine may be related in part to common processes involving the binding or flux of calcium.

摘要

在豚鼠体外被动致敏肺组织和平滑肌后发生过敏反应期间,对局部麻醉药利多卡因的作用进行了研究。用8.54 mM利多卡因预处理平滑肌可导致过敏反应等长张力的完全抑制。浓度为4.27 mM的利多卡因能迅速使过敏诱导的挛缩完全逆转。在2.13至8.54 mM利多卡因的浓度范围内,肺组织和平滑肌中组胺的释放分别被抑制73%至82%。观察到利多卡因对致敏组织有双峰效应,在浓度为8.54 mM时,利多卡因会使平滑肌中组胺轻微释放1.6%。利多卡因不损害初始被动致敏过程,且一旦抗体与细胞结合,它似乎也不会洗脱抗体。利多卡因对肥大细胞介质释放和肌肉收缩的双重抑制作用可能部分与涉及钙结合或通量的共同过程有关。

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