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纳洛酮对犬低血容量性休克的逆转作用。

Naloxone reversal of hypovolemic shock in dogs.

作者信息

Vargish T, Reynolds D G, Gurll N J, Lechner R B, Holaday J W, Faden A I

出版信息

Circ Shock. 1980;7(1):31-8.

PMID:6248264
Abstract

The endogenous opiate ligand, beta-endorphin, is released during stress. We tested the hypothesis that endorphins may be involved in the pathophysiology of hemorrhagic shock by using the opiate receptor blocking agent, naloxone. Two groups of five anesthetized dogs were instrumented to monitor cardiovascular performance and subjected to a protocol in which they were bled into a reservoir to lower mean arterial pressure to 45 mmHg and maintained at that pressure for one hour. At that time the reservoir was clamped and on group of dogs received an intravenous bolus of naloxone (2 mg/kg) and an infusion at 2 mg/kg-hr. These dogs demonstrated a prompt increase in arterial pressure, left ventricular dp/dtmax and cardiac output. The shed blood was returned at t = 2 hr and drug infusion continued for 2 hours. The control group of dogs received saline in equivalent volume. The control dogs died within 30 minutes of clamping the reservoir while all five treated dogs survived beyond 72 hours (P less than 0.02). These data suggest the involvement of endorphins acting on opiate receptors as part of the pathophysiology in this shock model.

摘要

内源性阿片样配体β-内啡肽在应激期间释放。我们通过使用阿片受体阻断剂纳洛酮,来检验内啡肽可能参与失血性休克病理生理学的这一假说。两组各五只麻醉犬被安装监测心血管功能的仪器,并按照如下方案进行实验:将它们的血液放至一个贮血器中,使平均动脉压降至45 mmHg,并维持此压力一小时。此时夹住贮血器,一组犬静脉注射一剂纳洛酮(2 mg/kg),并以2 mg/kg·小时的速度持续输注。这些犬的动脉压、左心室dp/dtmax和心输出量迅速升高。在t = 2小时时回输放出的血液,并继续输注药物2小时。对照组犬接受等量的生理盐水。对照组犬在夹住贮血器后30分钟内死亡,而所有五只接受治疗的犬存活超过72小时(P < 0.02)。这些数据表明,在这个休克模型中,作用于阿片受体的内啡肽参与了病理生理学过程。

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