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利多卡因、布比卡因、2-氯普鲁卡因以及2-氯普鲁卡因与布比卡因混合物局部神经毒性的体内比较研究。

A comparative in vivo study of local neurotoxicity of lidocaine, bupivacaine, 2-chloroprocaine, and a mixture of 2-chloroprocaine and bupivacaine.

作者信息

Barsa J, Batra M, Fink B R, Sumi S M

出版信息

Anesth Analg. 1982 Dec;61(12):961-7.

PMID:7149299
Abstract

This study was undertaken because of several recent reports of adverse neurologic reactions following the use of 2-chloroprocaine. Carotid sheaths containing undisturbed vagus nerve were surgically exposed in rabbits and bathed in situ for up to 1 hour in one of the following-isotonic solutions: physiologic salt solution, lidocaine 2%, bupivacaine 0.75%, 2-chloroprocaine 3%, or a mixture of 2-chloroprocaine 1.5% and bupivacaine 0.375%. Each solution contained epinephrine, 5 micrograms/ml, (1:200,000). In other animals the carotid sheaths were bathed in physiologic salt solution, or 2-chloroprocaine 3% without epinephrine. The nerves were excised 10 to 12 days later. C-fiber impulse conduction was normal in nerves that had been exposed to physiologic salt solution with or without epinephrine, to lidocaine, or to bupivacaine. Conduction was absent or markedly impaired in several nerve specimens following exposure to 2-chloroprocaine. Histologic sections revealed the presence of epineurial cellular infiltration and fibrosis, perineurial fibrosis, and axonal degeneration in nerves that had been exposed to 2-chloroprocaine or the mixture of 2-chloroprocaine and bupivacaine. Histologic abnormalities were minor or absent following exposure to lidocaine, to bupivacaine, or to physiologic salt solution. These findings suggest that, under the conditions of the experiments, 2-chloroprocaine is more neurotoxic than lidocaine or bupivacaine.

摘要

开展这项研究是因为最近有几份关于使用2 - 氯普鲁卡因后出现不良神经反应的报告。在兔子身上手术暴露含有未受干扰迷走神经的颈动脉鞘,并在以下等渗溶液之一中进行长达1小时的原位浸泡:生理盐溶液、2%利多卡因、0.75%布比卡因、3% 2 - 氯普鲁卡因,或1.5% 2 - 氯普鲁卡因与0.375%布比卡因的混合物。每种溶液均含有肾上腺素,5微克/毫升(1:200,000)。在其他动物中,颈动脉鞘用生理盐溶液或不含肾上腺素的3% 2 - 氯普鲁卡因浸泡。10至12天后切除神经。暴露于含或不含肾上腺素的生理盐溶液、利多卡因或布比卡因的神经中,C纤维冲动传导正常。暴露于2 - 氯普鲁卡因后,几个神经标本的传导消失或明显受损。组织学切片显示,暴露于2 - 氯普鲁卡因或2 - 氯普鲁卡因与布比卡因混合物的神经中存在神经外膜细胞浸润和纤维化、神经束膜纤维化以及轴突变性。暴露于利多卡因、布比卡因或生理盐溶液后,组织学异常轻微或不存在。这些发现表明,在实验条件下,2 - 氯普鲁卡因比利多卡因或布比卡因具有更强的神经毒性。

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