...
首页> 外文期刊>Behavioural pharmacology >The nucleus accumbens shell and the dorsolateral striatum mediate the reinforcing effects of cocaine through a serial connection
【24h】

The nucleus accumbens shell and the dorsolateral striatum mediate the reinforcing effects of cocaine through a serial connection

机译:伏伏核壳和背外侧纹状体通过串联连接介导可卡因的增强作用

获取原文
获取原文并翻译 | 示例
           

摘要

The reinforcing and addictive properties of cocaine are thought to rely on the dopaminergic innervation of the striatum. The ventromedial [i.e. nucleus accumbens shell (NAcc) shell] and dorsolateral [dorsolateral striatum (DLS)] regions of the striatum are serially connected, and it is thought that slowly developing neuroadaptations are responsible for the recruitment of the DLS in mediating habitual drug use after extended drug experience. Remarkably, we have recently shown that the DLS is also involved in cocaine self-administration after limited use, to modulate the reinforcing properties of the drug, a function usually ascribed to the NAcc shell. Here, we investigated whether the involvement of the DLS in cocaine reinforcement requires dopaminergic activity within the NAcc shell, by performing a pharmacological disconnection study. We infused the dopamine receptor antagonist alpha-flupenthixol unilaterally into the NAcc shell and infused this same antagonist into the contralateral DLS, thereby disrupting dopaminergic interconnectivity within the striatum. We show that this disconnection results in increased responding for cocaine under a fixed ratio-1 schedule of reinforcement in rats with limited cocaine experience. These data suggest that a functional dopaminergic interaction between the NAcc shell and the DLS mediates cocaine reinforcement during the early stages of drug use. Copyright (C) 2015 Wolters Kluwer Health, Inc. All rights reserved.
机译:可卡因的增强和成瘾性被认为依赖于纹状体的多巴胺能神经支配。腹侧[即纹状体的伏隔核壳(NAcc)和背外侧[dorslateral striatum(DLS)]区域是串联连接的,并且认为长期发展的神经适应作用是缓慢发展的神经适应负责DLS的募集,以在长期吸毒后介导习惯性吸毒。值得注意的是,我们最近表明,在有限使用后,DLS还参与了可卡因的自我给药,以调节药物的增强特性,这种功能通常归因于NAcc壳。在这里,我们通过进行药理学断开研究,调查了DLS参与可卡因强化是否需要NAcc壳内的多巴胺能活性。我们将多巴胺受体拮抗剂α-氟哌丁醇单侧注入NAcc壳中,并将该相同拮抗剂注入对侧DLS中,从而破坏纹状体内的多巴胺能互连性。我们表明,这种分离导致可卡因经验有限的大鼠在固定比例-1强化强化下对可卡因的反应增加。这些数据表明,在药物使用的早期阶段,NAcc壳层和DLS之间的功能性多巴胺能相互作用介导了可卡因的强化作用。版权所有(C)2015 Wolters Kluwer Health,Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号