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Effects of the NOP agonist SCH221510 on producing and attenuating reinforcing effects as measured by drug self-administration in rats

机译:NOP激动剂SCH221510对大鼠自我给药所产生的增强作用和减弱的增强作用

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Nociceptinlorphanin FQ peptide (NOP) receptor agonists attenuate morphine-induced conditioned place preference in rodents. However, it is not known whether NOP agonists have reinforcing properties or can inhibit mu opioicl receptor (MOP)-mediated reinforcement as measured by drug self-administration in rodents. Further understanding the behavioral effects of NOP agonists could suggest them as having potential in attenuating reinforcing effects of opioids. In the first part of the study, reinforcing properties of selective NOP agonist SCH221510 were determined and compared with the full MOP agonist remilentanil under fixed-ratio 5 (FR5) and progressive-ratio (PR) schedules of drug self-administration. In the second part, effects of systemic and intracisternal pretreatment of SCH221510 were determined and compared with MOP antagonist naltrexone in attenuating reinforcing effects of remifentanil and a non-drug reinforcer (sucrose pellets). Remifentanil self-administration (0.3-10 Jig/kg/infusion) generated a biphasic dose-response curve, characteristic of drugs with reinforcing properties. SCH221510 (3-300 Jig/kg/ infusion) self-administration resulted in flat dose-response curves and early break-points under the PR, indicative of drugs lacking reinforcing value. Intracisternally, but not systemically, administered SCH221510 (0.3-3 Jig) attenuated remifentanil self-administration, comparable with systemic naltrexone (0.03-0.3 mg/kg). SCH221510 (1-3 jig), unlike naltrexone (0.03-1 mg/kg), attenuated responding for sucrose pellets. Both effects of SC1-1221510 were reversed by the NOP antagonist J-113397 (0.3-3 jig), These results suggest that SCH221510 does not function as a reinforcer in rats, and that it can attenuate the reinforcing value of MOP agonists; therefore, the potential utility of NOP agonists for the treatment of drug addiction warrants further evaluation. (C) 2014 Elsevier B.V. All rights reserved.
机译:Nociceptinlorphanin FQ肽(NOP)受体激动剂减弱了吗啡诱导的啮齿类动物条件性位置偏爱。但是,尚不知道NOP激动剂是否具有增强特性或是否可以抑制啮齿类动物药物自我给药所测得的μopicicic receptor(MOP)介导的增强作用。进一步了解NOP激动剂的行为效应可能表明它们具有减弱阿片类药物增强作用的潜力。在研究的第一部分中,确定了选择性NOP激动剂SCH221510的增强性能,并将其与完全MOP激动剂瑞芬太尼在固定比例5(FR5)和渐进比率(PR)药物自我给药方案下进行比较。在第二部分中,确定了SCH221510的全身和脑池内预处理的效果,并将其与MOP拮抗剂纳曲酮在减弱瑞芬太尼和非药物增强剂(蔗糖颗粒)的增强效果上进行了比较。瑞芬太尼自我给药(0.3-10 Jig / kg /输液)可产生两相剂量反应曲线,这是具有增强特性的药物的特征。 SCH221510(3-300 Jig / kg /输注)自我给药导致PR下的剂量反应曲线和早期断裂点平坦,表明药物缺乏增强价值。与全身性纳曲酮(0.03-0.3 mg / kg)相比,腹腔内(而非全身)施用的SCH221510(0.3-3 Jig)可减缓瑞芬太尼的自用。与纳曲酮(0.03-1 mg / kg)不同,SCH221510(1-3夹具)对蔗糖颗粒的响应减弱。 NOP拮抗剂J-113397(0.3-3 jig)逆转了SC1-1221510的两种作用。这些结果表明SCH221510不能在大鼠中起增强剂的作用,并且可以减弱MOP激动剂的增强作用。因此,NOP激动剂在治疗药物成瘾方面的潜在效用值得进一步评估。 (C)2014 Elsevier B.V.保留所有权利。

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