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Behavioral sensitization to quinpirole is not associated with increased nucleus accumbens dopamine overflow.

机译:对喹吡罗的行为敏感性与伏伏核多巴胺溢流增加无关。

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This study assessed the relationship between extracellular nucleus accumbens (NAc) dopamine (DA) concentrations and sensitized locomotor activation following repeated administration of the DA D2-like receptor agonist quinpirole. Locomotor activity measures and nucleus accumbens microdialysis samples were collected concurrently in response to the first (acute) and tenth (repeated) quinpirole injection (0.5 mg/kg s.c., every other day). Results indicate that acute quinpirole produced locomotor activation and that repeated quinpirole resulted in locomotor sensitization. Acute quinpirole significantly decreased the detection of extracellular concentrations of DA and the DA metabolites dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) in the NAc. Following repeated quinpirole, basal NAc DA levels were decreased, whereas basal DOPAC levels were increased. Nevertheless, quinpirole challenge elicited a significant decrease in DA, DOPAC and HVA following repeated treatment. In addition, although acute quinpirole did not affect NAc levels of the serotonin metabolite 5-hydroxyindolacetic acid (5-HIAA), quinpirole challenge produced a significant increase in 5-HIAA levels following repeated treatment. Taken together, these data indicate that functional DA autoreceptor subsensitivity is not a necessary condition for the expression of behavioral sensitization to quinpirole. Instead, it appears that behavioral sensitization to quinpirole occurs predominantly as a consequence of neuroadaptations that are post-synaptic to DA release.
机译:这项研究评估了重复给予DA D2样受体激动剂喹吡罗后细胞外伏隔核(NAc)多巴胺(DA)浓度与致敏自发激活之间的关系。响应于第一次(急性)和第十次(重复)喹吡罗注射(0.5 mg / kg s.c.,隔天一次),同时收集运动活动性指标和伏隔核微透析样品。结果表明,急性喹吡罗产生运动活化,重复喹吡罗导致运动致敏。急性喹吡咯显着降低了NAc中DA和DA代谢物二羟基苯基乙酸(DOPAC)和高香草酸(HVA)的细胞外浓度检测。反复服用喹吡罗后,基础NAc DA水平降低,而基础DOPAC水平升高。然而,在重复治疗后,喹吡罗激发导致DA,DOPAC和HVA显着降低。另外,尽管急性喹吡罗不影响5-羟色胺乙酸5-羟色胺代谢产物(5-HIAA)的NAc水平,但在重复治疗后,喹吡罗激发使5-HIAA水平显着增加。综上所述,这些数据表明功能性DA自身受体亚敏感性不是表达对喹吡罗的行为敏感性的必要条件。相反,似乎对喹吡罗的行为敏化主要是由于对DA释放进行突触后神经适应而引起的。

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