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用单剂量吗啡处理豚鼠后,纳洛酮诱发的离体回肠运动活性和挛缩。

Locomotor activity and contracture of isolated ileum precipitated by naloxone following treatment of guinea-pigs with a single dose of morphine.

作者信息

Chahl L A, Thornton C A

出版信息

J Pharm Pharmacol. 1987 Jan;39(1):52-4. doi: 10.1111/j.2042-7158.1987.tb07163.x.

Abstract

Guinea-pigs treated with a single dose of morphine, 15 mg kg-1 s.c., exhibited an increase in locomotor activity 2 h later on injection of naloxone, 4 mg kg-1 i.p. At the same time, contracture of ileal preparations isolated from morphine-treated guinea-pigs occurred on addition of naloxone 1 microM. Contracture of the ileum was inhibited by the tachykinin antagonist, spantide, and was therefore presumably mediated by a substance P-like agent. This study has established a useful model for the parallel investigation of central and enteric nervous system mechanisms of opiate dependence.

摘要

用15毫克/千克皮下注射单剂量吗啡处理的豚鼠,在腹腔注射4毫克/千克纳洛酮2小时后,其运动活性增加。同时,从经吗啡处理的豚鼠分离出的回肠制剂在加入1微摩尔纳洛酮时发生挛缩。速激肽拮抗剂spantide抑制了回肠挛缩,因此推测其可能由一种P物质样介质介导。本研究建立了一个有用的模型,用于并行研究阿片类药物依赖的中枢和肠神经系统机制。

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