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首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Role of dopamine neurotransmission in the long-term effects of repeated social defeat on the conditioned rewarding effects of cocaine
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Role of dopamine neurotransmission in the long-term effects of repeated social defeat on the conditioned rewarding effects of cocaine

机译:多巴胺神经递质在重复社会失败中对可卡因有益奖励作用的长期影响的作用

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摘要

Numerous studies report that social defeat stress alters dopamine (DA) neurotransmission in several areas of the brain. Alterations of the mesolimbic dopaminergic pathway are believed to be responsible for the increased vulnerability to drug use observed as a result of social stress. In the present study, we evaluated the influence of DA receptors on the long-term effect of repeated social defeat (RSD) on the conditioned rewarding and reinstating effects of cocaine. For this purpose, the D1R antagonist SCH 23390 and the D1R antagonist raclopride were administered 30 min before each social defeat and a cocaine-induced CPP procedure was initiated three weeks later. The expression of the D1R and D2R was also measured in the cortex and hippocampus throughout the entire procedure. Mice exposed to RSD showed an increase in the conditioned rewarding effects of cocaine thatwas blocked by both DA receptors antagonists when a subthreshold dose of cocaine was employed. However, while the vulnerability to reinstatement of the preference induced by 25 mg/kg cocaine-induced CPP was abolished by the D1R antagonist, it was practically unaffected by raclopride. Increases in D2R receptor levels were observed in the cortex of defeated animals after the first and fourth social defeats and in the hippocampus 3-weeks later. Nevertheless, D1R receptor levels in the hippocampus decreased only after the last social defeat. Our results confirm that RSD enhances the conditioned rewarding effects of cocaine and that both DA receptors are involved in this enduring effect of social stress. (C) 2016 Elsevier Inc. All rights reserved.
机译:众多研究报告称,社会失败胁迫改变了大脑的几个地区的多巴胺(DA)神经递质。培养的多巴胺能途径的改变被认为是由于社会压力所观察到的药物用量增加的脆弱性。在本研究中,我们评估了DA受体对重复社会失败(RSD)对可卡因的条件奖励和恢复效果的长期影响的影响。为此目的,在每次社会失败之前30分钟给予D1R拮抗剂SCH 23390和D1R拮抗剂丙酮,并在三个星期后启动了可卡因诱导的CPP程序。在整个过程中,还在皮质和海马中测量D1R和D2R的表达。暴露于RSD的小鼠表明,当使用亚替斯卡尔的亚替代剂量时,Cocaine拮抗剂阻断的可卡因的条件奖励作用的增加。然而,虽然D1R拮抗剂废除了对25mg / kg可卡因诱导的CPP诱导的偏好的脆弱性,但其实际上不受丙烯普雷的影响。在第一个和第四个社会失败和海马在3周后,在击败动物的皮质中观察到D2R受体水平的增加。然而,海马的D1R受体水平只有在最后一次社会失败后才会减少。我们的结果证实,RSD增强了可卡因的调节奖励效果,并且两种DA受体都参与了这种社会压力的持久影响。 (c)2016年Elsevier Inc.保留所有权利。

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