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κ-阿片受体激动剂U50,488H可诱导豚鼠产生急性身体依赖性。

The kappa-opioid receptor agonist U50,488H induces acute physical dependence in guinea-pigs.

作者信息

Brent P J, Chahl L A, Cantarell P A, Kavanagh C

机构信息

Neuropharmacology Laboratory, Faculty of Medicine, University of Newcastle, NSW, Australia.

出版信息

Eur J Pharmacol. 1993 Sep 14;241(2-3):149-56. doi: 10.1016/0014-2999(93)90196-o.

Abstract

The present study was undertaken to determine whether acute physical dependence occurred in guinea-pigs in vivo and guinea-pig isolated ileum following a single dose of the kappa-opioid receptor agonist U50,488H. Administration of naloxone hydrochloride, 15 and 30 mg/kg s.c., to guinea-pigs treated 1 h before with U50,488H, 10 mg/kg s.c., induced increased locomotor activity accompanied by behavioural responses which differed from those previously found in this species with morphine withdrawal. Nor-binaltorphimine, 10 mg/kg s.c., given 1 h after administration of U50,488H, 10 mg/kg s.c., produced a small but significant increase in locomotor activity but no other withdrawal behaviours. The morphine withdrawal response was not significantly affected by U50,488H, 1 or 10 mg/kg s.c. On the guinea-pig isolated ileum, nor-binaltorphimine, 1 microM, produced a withdrawal contracture following 2 min contact of the ileum with U50,488H 1 microM. U50,488H, 1 microM, abolished the [Met5]enkephalin withdrawal response of the ileum. It is concluded that dependence occurs following activation of kappa-opioid receptors, which is largely non-morphine-like in the central nervous system, but which is morphine-like in the enteric nervous system.

摘要

本研究旨在确定单次给予κ-阿片受体激动剂U50,488H后,豚鼠体内及豚鼠离体回肠是否会出现急性身体依赖性。给预先皮下注射10mg/kg U50,488H 1小时后的豚鼠皮下注射15mg/kg和30mg/kg盐酸纳洛酮,会导致运动活性增加,并伴有与该物种先前吗啡戒断反应不同的行为反应。在皮下注射10mg/kg U50,488H 1小时后给予10mg/kg皮下注射的去甲二氢吗啡酮,会使运动活性出现小幅但显著的增加,但未出现其他戒断行为。皮下注射1mg/kg或10mg/kg U50,488H对吗啡戒断反应无显著影响。在豚鼠离体回肠上,1μM去甲二氢吗啡酮在回肠与1μM U50,488H接触2分钟后会产生戒断性挛缩。1μM U50,488H消除了回肠的[Met5]脑啡肽戒断反应。结论是,κ-阿片受体激活后会产生依赖性,这在中枢神经系统中很大程度上不像吗啡,但在肠神经系统中像吗啡。

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