首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >RODENT MODELS OF OBSESSIVE COMPULSIVE DISORDER: EVALUATING VALIDITY TO INTERPRET EMERGING NEUROBIOLOGY
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RODENT MODELS OF OBSESSIVE COMPULSIVE DISORDER: EVALUATING VALIDITY TO INTERPRET EMERGING NEUROBIOLOGY

机译:诱惑强迫症的啮齿动物模型:评估诠释新兴神经生物学的有效性

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摘要

Obsessive Compulsive Disorder (OCD) is a common neuropsychiatric disorder with unknown molecular underpinnings. Identification of genetic and non genetic risk factors has largely been elusive, primarily because of a lack of power. In contrast, neuroimaging has consistently implicated the cortico-striatal-thalamo-cortical circuits in OCD. Pharmacological treatment studies also show specificity, with consistent response of OCD symptoms to chronic treatment with serotonin reuptake inhibitors; although most patients are left with residual impairment. In theory, animal models could provide a bridge from the neuroimaging and pharmacology data to an understanding of pathophysiology at the cellular and molecular level. Several mouse models have been proposed using genetic, immunological, pharmacological, and optogenetic tools. These experimental model systems allow testing of hypotheses about the origins of compulsive behavior. Several models have generated behavior that appears compulsive-like, particularly excessive grooming, and some have demonstrated response to chronic serotonin reuptake inhibitors, establishing both face validity and predictive validity. Construct validity is more difficult to establish in the context of a limited understanding of OCD risk factors. Our current models may help us to dissect the circuits and molecular pathways that can elicit OCD-relevant behavior in rodents. We can hope that this growing understanding, coupled with developing technology, will prepare us when robust OCD risk factors are better understood.
机译:强迫症(OCD)是一种常见的神经精神障碍具有未知分子基础。遗传和非遗传风险因素的鉴定在很大程度上是难以实现的,主要是因为缺乏动力。相比之下,神经影像学一贯牵连在OCD的皮质 - 纹状体 - 丘脑 - 皮质电路。药物治疗的研究还表明特异性,与强迫症的症状与五羟色胺再摄取抑制剂治疗慢性乙型肝炎一致的响应;虽然大多数患者会留下残余的损害。从理论上讲,动物模型可以提供从影像学和药理学数据的桥梁,在细胞和分子水平的病理生理学的理解。一些小鼠模型已利用遗传,免疫学,药理学,和光遗传学工具建议。这些实验模型系统允许测试有关的强迫行为起源的假说。几个模型已经产生显示强迫状,特别是过度梳理行为,并且一些已经证明了响应于慢性血清素再摄取抑制剂,建立两个表面效度和预测效度。构想效度是比较困难的强迫症的风险因素了解有限的背景下建立的。我们目前的模型可以帮助我们来剖析,可以在啮齿动物诱发强迫症有关的行为的电路和分子途径。我们希望这个人们越来越认识到,再加上开发的技术,将准备我们,当强大的强迫症的危险因素得到更好的理解。

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