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D1 receptors in the nucleus accumbens-shell, but not the core, are involved in mediating ethanol-seeking behavior of alcohol-preferring (P) rats

机译:伏隔核壳中的D1受体(而不是核心)中的D1受体参与介导偏好酒精的(P)大鼠的寻乙醇行为

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摘要

Clinical and preclinical research suggest that activation of the mesolimbic dopamine (DA) system is involved in mediating the rewarding actions of drugs of abuse, as well as promoting drug-seeking behavior. Inhibition of DA D1 receptors in the nucleus accumbens (Acb) can reduce ethanol (EtOH)-seeking behavior of non-selective rats triggered by environmental context. However, to date, there has been no research on the effects of D1 receptor agents on EtOH- seeking behavior of high alcohol-preferring (P) rats following prolonged abstinence. The objective of the present study was to examine the effects of microinjecting the D1 antagonist SCH 23390 or the D1 agonist A-77636 into the Acb shell or Acb core on spontaneous recovery of EtOH-seeking behavior. After 10 weeks of concurrent access to EtOH and water, P rats underwent seven extinction sessions (EtOH and water withheld), followed by 2 weeks in their home cages without access to EtOH or operant sessions. In the 2nd week of the home cage phase, rats were bilaterally implanted with guide cannula aimed at the Acb shell or Acb core; rats were allowed 7d ays to recover before EtOH-seeking was assessed by the Pavlovian Spontaneous Recovery (PSR) model. Administration of SCH23390 (1μg/side) into the Acb shell inhibited responding on the EtOH lever, whereas administration of A-77636 (0.125μg/side) increased responding on the EtOH lever. Microinfusion of D1 receptor agents into the Acb core did not alter responding on the EtOH lever. Responses on the water lever were not altered by any of the treatments. The results suggest that activation of D1 receptors within the Acb shell, but not Acb core, are involved in mediating PSR of EtOH-seeking behavior of P rats.
机译:临床和临床前研究表明,中脑边缘多巴胺(DA)系统的激活与调解滥用药物的奖励作用以及促进药物寻找行为有关。伏伏核(Acb)中DA D1受体的抑制作用可降低由环境引起的非选择性大鼠对乙醇(EtOH)的寻求行为。然而,迄今为止,尚未有关于D1受体药物对禁酒时间长的高酒精偏爱(P)大鼠EtOH寻求行为的影响的研究。本研究的目的是研究将D1拮抗剂SCH 23390或D1激动剂A-77636微注射到Acb壳或Acb核中对寻求EtOH行为自发恢复的影响。在同时接触EtOH和水10周后,P大鼠经历了7次灭绝阶段(EtOH和禁水),随后在其家中饲养了2周而无法接触EtOH或未进行手术。在笼养阶段的第二周,将大鼠的双侧导向套管植入针对Acb壳或Acb核的双环。通过巴甫洛夫自发恢复(PSR)模型评估寻求EtOH的大鼠后7天ays恢复。将SCH23390(1μg/侧)注入Acb壳会抑制EtOH杠杆的响应,而A-77636(0.125μg/侧)则增强EtOH杠杆的响应。 D1受体试剂微注入Acb核心不会改变对EtOH杠杆的反应。对水杠杆的反应未因任何处理而改变。结果表明,Acb壳内D1受体的激活而不是Acb核心,参与了P大鼠EtOH寻求行为的PSR介导。

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