Norozpour Yaser, Zarrabian Shahram, Rezaee Laleh, Haghparast Abbas
Department of Cognitive Neuroscience, Institute for Cognitive Science Studies.
Department of Anatomical Sciences and Cognitive Neuroscience, Faculty of Medicine, Tehran Medical Sciences, Islamic Azad University.
Behav Neurosci. 2019 Dec;133(6):545-555. doi: 10.1037/bne0000335. Epub 2019 Aug 15.
Addiction to opioids is an important global problem. Published research has indicated the powerful rewarding effects of drug use, which in the case of opiates like morphine may lead to drug addiction and maladaptive decision making with negative social consequences. In-depth comprehension of the role of responsible mechanisms in addiction can lead us to better and more effective treatments for drug dependence. Continuing previous work in our laboratory, in this study we aimed to investigate the role of dopamine D1- and D2-like receptors in the dentate gyrus (DG) on the reinstatement of drug-seeking behavior induced by the combination of forced swim stress and a subthreshold dose of morphine on extinguished morphine-conditioned place preference in rats. The rats were bilaterally implanted with 2 separate cannulas into the DG region. After the extinction phase of morphine-conditioned place preference, the animals received different doses (0.5, 2, and 4 μg per 0.5 μL vehicle/side) of SCH-23390 or sulpiride on the reinstatement day and were tested for the combination of forced swim stress and a subthreshold dose of morphine in discrete groups. Our findings indicated that D1- and D2-like receptor antagonists attenuated the reinstatement induced by the combination of FSS and the subthreshold dose of morphine. The reduction was more robust in groups of animals that received sulpiride as compared with SCH-23390. Our results showed a role for DG dopamine receptors in relapse to drugs of abuse, the activity of which may be induced by exposure to a stressor like forced swim stress. (PsycINFO Database Record (c) 2019 APA, all rights reserved).
阿片类药物成瘾是一个重要的全球性问题。已发表的研究表明了药物使用的强大奖赏效应,就吗啡等阿片类药物而言,这可能导致药物成瘾以及产生具有负面社会后果的适应不良决策。深入理解成瘾相关机制的作用能够引导我们找到更好、更有效的药物依赖治疗方法。延续我们实验室之前的工作,在本研究中,我们旨在探究齿状回(DG)中的多巴胺D1样和D2样受体在强迫游泳应激与亚阈值剂量吗啡联合诱导的觅药行为恢复中所起的作用,该行为恢复是针对大鼠中已消退的吗啡条件性位置偏爱而言。大鼠双侧植入2根独立的套管至DG区域。在吗啡条件性位置偏爱的消退阶段之后,动物在恢复日接受不同剂量(每0.5 μL溶媒/侧0.5、2和4 μg)的SCH-23390或舒必利,并在不同分组中接受强迫游泳应激与亚阈值剂量吗啡联合测试。我们的研究结果表明,D1样和D2样受体拮抗剂减弱了由强迫游泳应激与亚阈值剂量吗啡联合诱导的恢复。与接受SCH-23390的动物组相比,接受舒必利的动物组中这种减弱更为显著。我们的结果显示了DG多巴胺受体在滥用药物复发中的作用,其活性可能由暴露于强迫游泳应激等应激源所诱导。(PsycINFO数据库记录(c)2019美国心理学会,保留所有权利)