Ciccocioppo Roberto, Economidou Daina, Fedeli Amalia, Angeletti Stefania, Weiss Friedbert, Heilig Markus, Massi Maurizio
Department of Pharmacological Sciences and Experimental Medicine, University of Camerino, Via Scalzino 3, 62032 Camerino, Italy.
Psychopharmacology (Berl). 2004 Mar;172(2):170-8. doi: 10.1007/s00213-003-1645-1. Epub 2003 Nov 18.
Nociceptin/orphanin FQ (N/OFQ), the endogenous ligand of the opioid-like orphan receptor NOP, was shown to reduce home-cage ethanol consumption, ethanol-induced conditioned place preference and stress-induced reinstatement of alcohol-seeking behaviour.
The present study, using genetically selected Marchigian Sardinian alcohol-preferring (msP) rats, was designed to evaluate the effect of this opioid peptide on 10% ethanol and 10% sucrose self-administration, under a fixed-ratio 1 (FR 1) or a progressive-ratio (PR) schedule of reinforcement. Furthermore, using an experimental model of relapse in which rats were trained to lever press for ethanol in the presence of the discriminative stimulus of an orange odour (S(+)) and a 1-s cue light (CS(+)) or for water in the presence of anise odour (S(-)) and 1-s white noise (CS(-)), the effect of N/oFQ on cue-induced reinstatement of extinguished ethanol responding was investigated.
Sub-chronic (6 days) intracerebroventricular (i.c.v.) injection of 0.5 microg or 1.0 microg N/OFQ per rat significantly reduced alcohol self-administration under both the FR 1 and PR schedules of reinforcement. Conversely, i.c.v. administration of 0.5, 1.0 or 4.0 microg of the peptide per rat did not affect sucrose self-administration. In addition, i.c.v. N/OFQ (1.0-2.0 microg per rat) significantly inhibited the reinstatement of extinguished ethanol responding under an S(+)/CS(+) condition, whereas lever pressing under S(-)/CS(-) was not altered.
The present study demonstrates that the reinforcing effects of ethanol are markedly blunted by activation of the opioidergic N/OFQ receptor system. Moreover, the data provide evidence of the efficacy of N/OFQ to prevent reinstatement of ethanol-seeking behaviour elicited by environmental conditioned stimuli.
痛敏肽/孤啡肽(N/OFQ)是阿片样孤儿受体NOP的内源性配体,已被证明可减少笼内乙醇消耗量、乙醇诱导的条件性位置偏爱以及应激诱导的觅酒行为恢复。
本研究使用基因筛选的马尔基安撒丁岛嗜酒(msP)大鼠,旨在评估这种阿片肽在固定比率1(FR 1)或渐进比率(PR)强化程序下对10%乙醇和10%蔗糖自我给药的影响。此外,使用复发实验模型,其中大鼠在橙色气味(S(+))和1秒提示光(CS(+))的辨别性刺激下训练按压杠杆获取乙醇,或在茴芹气味(S(-))和1秒白噪声(CS(-))下训练按压杠杆获取水,研究N/OFQ对线索诱导的已消退乙醇反应恢复的影响。
每只大鼠脑室内(i.c.v.)亚慢性(6天)注射0.5微克或1.0微克N/OFQ,在FR 1和PR强化程序下均显著减少乙醇自我给药。相反,每只大鼠脑室内注射0.5、1.0或4.0微克该肽不影响蔗糖自我给药。此外,脑室内注射N/OFQ(每只大鼠1.0 - 2.0微克)在S(+)/CS(+)条件下显著抑制已消退乙醇反应的恢复,而在S(-)/CS(-)条件下的杠杆按压未改变。
本研究表明,激活阿片样N/OFQ受体系统可显著减弱乙醇的强化作用。此外,数据提供了证据,证明N/OFQ可有效预防环境条件刺激引发的觅酒行为恢复。