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κ阿片受体对大鼠吗啡和可卡因自我给药行为的抑制作用

Kappa opioid inhibition of morphine and cocaine self-administration in rats.

作者信息

Glick S D, Maisonneuve I M, Raucci J, Archer S

机构信息

Department of Pharmacology and Neuroscience, Albany Medical College, NY 12208, USA.

出版信息

Brain Res. 1995 May 29;681(1-2):147-52. doi: 10.1016/0006-8993(95)00306-b.

Abstract

Two kappa agonists, U50,488 and spiradoline, produced dose-related acute decreases in both morphine and cocaine self-administration in rats; higher doses of both agents were required to decrease rates of bar-pressing for water. On the day after kappa agonist administration, both agents produced extinction-like patterns of responding in many rats self-administering morphine or cocaine but not in rats responding for water. Two days after their administration, both U50,488 and spiradoline produced significant decreases in both morphine and cocaine intake; some rats continued to show decreases in drug self-administration for 5-6 days. Although the kappa antagonist nor-binaltorphimine (10 mg/kg s.c.) had no effect itself on either morphine or cocaine self-administration, it fully antagonized the effects of U50,488 (10 m/kg i.p.). The results suggest that although endogenous kappa opioid systems may not tonically modulate mechanisms involved in drug reinforcement, pharmacological activation of kappa pathways may be a novel and effective pharmacological approach to treating both opioid and stimulant addiction.

摘要

两种κ阿片受体激动剂,U50,488和spiraoline,可使大鼠的吗啡和可卡因自身给药量出现与剂量相关的急性减少;两种药物都需要更高剂量才能降低按杠杆获取水的速率。给予κ阿片受体激动剂后的第二天,两种药物在许多自行给药吗啡或可卡因的大鼠中产生了类似消退的反应模式,但在为获取水而做出反应的大鼠中则没有。给药两天后,U50,488和spiraoline均使吗啡和可卡因摄入量显著减少;一些大鼠的药物自身给药量在5 - 6天内持续减少。尽管κ阿片受体拮抗剂去甲二氢吗啡酮(10毫克/千克,皮下注射)本身对吗啡或可卡因自身给药没有影响,但它完全拮抗了U50,488(10毫克/千克,腹腔注射)的作用。结果表明,虽然内源性κ阿片系统可能不会持续调节参与药物强化的机制,但κ途径的药理学激活可能是一种治疗阿片类药物成瘾和兴奋剂成瘾的新颖且有效的药理学方法。

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