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首页> 外文期刊>The European Journal of Neuroscience >Performance of compulsive behavior in rats is not a unitary phenomenon - validation of separate functional components in compulsive checking behavior
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Performance of compulsive behavior in rats is not a unitary phenomenon - validation of separate functional components in compulsive checking behavior

机译:大鼠强迫行为的表现不是单一现象-强迫检查行为中各个功能组件的验证

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摘要

A previous analysis of the quinpirole sensitisation rat model of obsessive-compulsive disorder revealed that the behavioral pheno-type of compulsive checking consists of three constitutive components - vigor of checking performance, focus on the task of checking, and satiety following a bout of checking. As confirmation of this analysis, the aim of the present study was to reconstitute, without quinpirole treatment, each of the putative components, with the expectation that these would self-assemble into compulsive checking. To reconstitute vigor and satiety, the employed treatment was a bilateral lesion of the nucleus accumbens core (NAc), as this treatment was shown previously to exaggerate these components. To reconstitute focus, the employed treatment was a low dose of the serotonin-1A receptor agonist 8-hydroxy-2-(di-n-propylamino) tetralin hydrochloride (DPAT) (0.0625 mg/ kg), as high doses of this drug induce compulsive behavior and exacerbate focus. Results showed that injection of DPAT to NAc lesion rats did yield compulsive checking. Neither the drug alone nor the NAc lesion by itself produced compulsive checking. The demonstrated synthesis of compulsive checking by the combined treatment of low-dose DPAT and NAc lesion strengthened the previous fractionation of the model obsessive-compulsive disorder phenotype into three constitutive components, and suggested a role for serotonin-1A receptors outside the NAc in enhanced focus on the task of checking.
机译:先前对强迫症的喹吡罗致敏大鼠模型的分析显示,强迫检查的行为表型由三个组成部分组成:检查表现的活力,检查的重点和检查后的饱腹感。作为对该分析的证实,本研究的目的是在未经喹吡罗处理的情况下重构每个假定的成分,并期望这些成分会自动组装为强制性检查。为了恢复活力和饱腹感,采用的治疗方法是伏伏核的双侧病变(NAc),因为这种治疗方法先前已证明会夸大这些成分。为了重建焦点,采用的治疗方法是低剂量的5-羟色胺-1A受体激动剂8-羟基-2-(二-正丙基氨基)四氢化萘盐酸盐(DPAT)(0.0625 mg / kg),因为高剂量的该药物诱导强迫行为并加剧注意力。结果表明,向NAc损伤大鼠注射DPAT确实可以进行强迫检查。单独使用药物也不会对NAc病变本身进行强迫检查。通过低剂量DPAT和NAc病变的联合治疗,证实了强制检查的综合结果,将先前的模型强迫症表型分为三个组成部分,并提示了NAc之外的血清素1A受体在增强聚焦方面的作用在检查任务上。

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