Neuroscience Research Center, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Institute for Cognitive Science Studies (ICSS), Tehran, Iran.
Physiology Research Center, Kashan University of Medical Sciences, Kashan, Iran.
Peptides. 2018 Mar;101:25-31. doi: 10.1016/j.peptides.2017.12.017. Epub 2017 Dec 19.
Orexinergic system is involved in reward processing and drug addiction. Objectives here, we investigated the effect of intra-hippocampal CA1 administration of orexin-1 receptor (OX1r) antagonist on the expression, and extinction of morphine-induced place preference in rats. Conditioned place preference (CPP) was induced by subcutaneous injection of morphine (5 mg/kg) during a 3-day conditioning phase. Two experimental plots were designed; SB334867 as a selective OX1r antagonist was dissolved in 12% DMSO, prepared in solutions with different concentrations (3, 30, and 300 nM), and microinjected into the CA1 and some neighboring regions (0.5 μl/side), bilaterally. CPP score and locomotor activity were recorded during the CPP test. Results demonstrated that intra-CA1 administration of the OX1r antagonist attenuates the expression of morphine-induced CPP. Furthermore, higher concentrations of SB334867 facilitated the extinction period of morphine-induced CPP and reduced its latency. Nevertheless, solely administration of DMSO did not have any influence on the CPP scores and locomotion in both phases. Our findings suggest that OX1rs in the CA1 region of the hippocampus are involved in the expression of morphine CPP. Moreover, blockade of OX1rs could facilitate extinction and may extinguish the ability of drug-related cues. It seems that the antagonist might be considered as a propitious therapeutic agent in suppressing drug-seeking behaviors.
食欲素能系统参与奖赏处理和药物成瘾。目的是研究海马 CA1 内注射食欲素-1 受体 (OX1r) 拮抗剂对吗啡诱导的大鼠位置偏爱表达和消退的影响。条件性位置偏爱 (CPP) 通过皮下注射吗啡 (5mg/kg) 在 3 天的适应阶段诱导。设计了两个实验方案;SB334867 是一种选择性 OX1r 拮抗剂,溶解在 12% DMSO 中,制备成不同浓度 (3、30 和 300 nM) 的溶液,双侧微量注射到 CA1 和一些相邻区域 (0.5 μl/侧)。在 CPP 测试期间记录 CPP 评分和运动活动。结果表明,CA1 内注射 OX1r 拮抗剂可减弱吗啡诱导的 CPP 的表达。此外,较高浓度的 SB334867 促进了吗啡诱导的 CPP 的消退期,并减少了其潜伏期。然而,单独给予 DMSO 在两个阶段均未对 CPP 评分和运动产生任何影响。我们的研究结果表明,海马 CA1 区的 OX1rs 参与了吗啡 CPP 的表达。此外,阻断 OX1rs 可能促进消退,并可能削弱与药物相关线索的能力。该拮抗剂似乎可以被认为是抑制觅药行为的一种有前途的治疗药物。