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中枢给予吗啡或蛙皮素后大鼠搔抓反应的特征

Characterization of scratching responses in rats following centrally administered morphine or bombesin.

作者信息

Lee H, Naughton N N, Woods J H, Ko M C H

机构信息

Department of Anesthesiology, College of Medicine, Ewha Womans University, Seoul, South Korea.

出版信息

Behav Pharmacol. 2003 Nov;14(7):501-8. doi: 10.1097/01.fbp.0000095082.80017.0f.

Abstract

The aim of this study was to characterize scratching behavior elicited by central administration of morphine or bombesin in rats, and to determine the role of opioid receptors in scratching induced by both pruritogenic agents. Central administration included intracisternal (i.c.), intrathecal (i.t.), and intracerebroventricular (i.c.v.) routes. Scratching events made with hind paws were counted by observers blinded to treatment conditions. Intracisternal morphine (0.01-0.1 microg) produced dose-dependent increases in scratching; the maximum response to i.c. morphine 0.1 microg was approximately 500 scratches within a 1-hour period. Neither i.t. nor i.c.v. morphine significantly increased scratching. Bombesin (0.01-0.32 microg) elicited robust scratching following i.c. administration. The maximum response to i.c. bombesin 0.32 microg was approximately 4000 scratches within a 1-hour period. Both i.t. and i.c.v. bombesin produced profound scratching at similar doses. Antagonist studies confirmed that mu-opioid receptors selectively mediate i.c. morphine-induced scratching. However, selective mu-, kappa-, and delta-opioid antagonists did not attenuate i.c. bombesin-induced scratching. These results demonstrate that morphine and bombesin elicit scratching through different receptor mechanisms, at different central sites, and to different degrees.

摘要

本研究的目的是描述大鼠经中枢给予吗啡或蛙皮素所引发的抓挠行为特征,并确定阿片受体在这两种致痒剂诱发抓挠中的作用。中枢给药途径包括脑池内(i.c.)、鞘内(i.t.)和脑室内(i.c.v.)注射。由对治疗条件不知情的观察者对后爪的抓挠次数进行计数。脑池内注射吗啡(0.01 - 0.1微克)可使抓挠次数呈剂量依赖性增加;脑池内注射0.1微克吗啡的最大反应是在1小时内约500次抓挠。鞘内或脑室内注射吗啡均未显著增加抓挠次数。蛙皮素(0.01 - 0.32微克)经脑池内注射后可引发强烈的抓挠。脑池内注射0.32微克蛙皮素的最大反应是在1小时内约4000次抓挠。鞘内和脑室内注射蛙皮素在相似剂量下均可引发强烈的抓挠。拮抗剂研究证实,μ-阿片受体选择性介导脑池内注射吗啡诱发的抓挠。然而,选择性的μ-、κ-和δ-阿片拮抗剂并未减弱脑池内注射蛙皮素诱发的抓挠。这些结果表明,吗啡和蛙皮素通过不同的受体机制、在不同的中枢部位以及以不同的程度引发抓挠。

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