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纳洛酮可逆转活的大肠杆菌败血症的组织效应。

Naloxone reverses tissue effects of live Escherichia coli sepsis.

作者信息

Rees M, Payne J G, Bowen J C

出版信息

Surgery. 1982 Jan;91(1):81-6.

PMID:6275563
Abstract

Hypoxia of the superficial gastric epithelium induced by a systemic infusion of live Escherichia coli organisms was mimicked by a local intra-arterial infusion of the naturally occurring opiate beta-endorphin. Naloxone, a specific opiate antagonist, reversed the gastric epithelial hypoxia induced by sepsis and also prevented the development of systemic acidosis. The mean blood pH of septic dogs had declined during the experiment from 7.42 +/- 0.06 to 6.88 +/- 0.17, whereas corresponding values for the naloxone-treated group were 7.38 +/- 0.06 and 7.32 +/- 0.08. These experiments, which support the concept of beta-endorphin involvement in the pathogenesis of septic shock, indicate a direct tissue response to circulatory beta-endorphin and highlight a further beneficial effect of naloxone in the management of sepsis.

摘要

通过局部动脉内输注天然存在的阿片类物质β-内啡肽,可模拟全身输注活大肠杆菌诱导的胃浅表上皮缺氧。纳洛酮是一种特异性阿片拮抗剂,可逆转脓毒症诱导的胃上皮缺氧,并预防全身酸中毒的发生。在实验过程中,脓毒症犬的平均血液pH值从7.42±0.06降至6.88±0.17,而纳洛酮治疗组的相应值分别为7.38±0.06和7.32±0.08。这些实验支持了β-内啡肽参与脓毒症休克发病机制的概念,表明组织对循环β-内啡肽有直接反应,并突出了纳洛酮在脓毒症治疗中的进一步有益作用。

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