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麻醉不会增加人类脑脊液中的阿片肽。

Anesthesia does not increase opioid peptides in cerebrospinal fluid of humans.

作者信息

Way W L, Hosobuchi Y, Johnson B H, Eger E I, Bloom F E

出版信息

Anesthesiology. 1984 Jan;60(1):43-5. doi: 10.1097/00000542-198401000-00009.

Abstract

One theory of narcosis postulates that inhaled anesthetics produce general anesthesia by causing the release of endogenous opioid peptides. In the present study, however, the concentration of immunoreactive beta-endorphin-like material (eight patients) or leu-enkephalin (four patients) did not increase in cerebrospinal fluid of patients 5 min after induction of anesthesia with thiopental, 2-5 mg/kg and N2O 70%; after an additional 10 min, during which halothane was added; at 5, 15, and 60 min after surgical incision; or after 30 min in the recovery room. Therefore, any contribution of the endorphin system to the production of general anesthesia does not appear to require the release of beta-endorphin.

摘要

一种麻醉理论假定,吸入性麻醉剂通过引起内源性阿片肽的释放而产生全身麻醉。然而,在本研究中,在用硫喷妥钠(2 - 5mg/kg)和70%氧化亚氮诱导麻醉5分钟后,8例患者脑脊液中免疫反应性β - 内啡肽样物质的浓度,以及4例患者脑脊液中亮氨酸脑啡肽的浓度均未升高;在额外添加氟烷的10分钟期间、手术切口后5分钟、15分钟和60分钟,或在恢复室30分钟后,这些浓度也未升高。因此,内啡肽系统对全身麻醉产生的任何作用似乎并不需要β - 内啡肽的释放。

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