首页> 美国卫生研究院文献>The Journal of Neuroscience >Effort-Related Motivational Effects of the VMAT-2 Inhibitor Tetrabenazine: Implications for Animal Models of the Motivational Symptoms of Depression
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Effort-Related Motivational Effects of the VMAT-2 Inhibitor Tetrabenazine: Implications for Animal Models of the Motivational Symptoms of Depression

机译:VMAT-2抑制剂Tetrabenazine的与工作有关的动机效果:对抑郁症动机症状的动物模型的影响

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摘要

Motivated behaviors are often characterized by a high degree of behavioral activation, and work output and organisms frequently make effort-related decisions based upon cost/benefit analyses. Moreover, people with major depression and other disorders often show effort-related motivational symptoms such as anergia, psychomotor retardation, and fatigue. It has been suggested that tasks measuring effort-related choice behavior could be used as animal models of the motivational symptoms of depression, and the present studies characterized the effort-related effects of the vesicular monoamine transport (VMAT) inhibitor tetrabenazine. Tetrabenazine produces depressive symptoms in humans and, because of its selective inhibition of VMAT-2, it preferentially depletes dopamine (DA). Rats were assessed using a concurrent fixed-ratio 5/chow feeding choice task that is known to be sensitive to dopaminergic manipulations. Tetrabenazine shifted response choice in rats, producing a dose-related decrease in lever pressing and a concomitant increase in chow intake. However, it did not alter food intake or preference in parallel free-feeding choice studies. The effects of tetrabenazine on effort-related choice were reversed by the adenosine A2A antagonist MSX-3 and the antidepressant bupropion. A behaviorally active dose of tetrabenazine decreased extracellular DA in nucleus accumbens and increased expression of DARPP-32 in accumbens medium spiny neurons in a pattern indicative of reduced transmission at both D1 and D2 DA receptors. These experiments demonstrate that tetrabenazine, which is used in animal models to produce depression-like effects, can alter effort-related choice behavior. These studies have implications for the development of animal models of the motivational symptoms of depression and related disorders.
机译:动机行为通常以高度的行为激活为特征,工作输出和有机体经常基于成本/收益分析做出与工作相关的决策。此外,患有严重抑郁症和其他疾病的人经常表现出与努力相关的动机症状,如无痛,精神运动迟缓和疲劳。已经提出,测量与努力相关的选择行为的任务可以用作抑郁的动机症状的动物模型,并且本研究表征了水泡单胺转运(VMAT)抑制剂丁苯那嗪与努力相关的作用。四苯那嗪在人体内会产生抑郁症状,并且由于其对VMAT-2的选择性抑制,它优先消耗多巴胺(DA)。使用并发的固定比率5 /慢食选择任务对大鼠进行评估,已知该任务对多巴胺能操作敏感。 Tetrabenazine改变了大鼠的反应选择,产生了与剂量相关的杠杆压低和食物摄取量增加。然而,在平行自由进食选择研究中,它并没有改变食物的摄入量或偏好。腺苷A2A拮抗剂MSX-3和抗抑郁药安非他酮逆转了丁苯那嗪对与努力相关的选择的作用。行为有效剂量的丁苯那嗪降低伏隔核中的细胞外DA,并增加伏伏中棘状神经元中DARPP-32的表达,这表明在D1和D2 DA受体处的传输均减少。这些实验证明,在动物模型中使用的丁苯那嗪可以产生类似抑郁的效果,可以改变与努力相关的选择行为。这些研究对于抑郁症和相关疾病的动机症状的动物模型的发展具有重要意义。

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