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Animal models of obsessive-compulsive disorder: Exploring pharmacology and neural substrates

机译:强迫症动物模型:探索药理学和神经基质

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During the last 30 years there have been many attempts to develop animal models of obsessive-compulsive disorder (OCD). Most models have not been studied further following the original publication, and in the past few years, most papers present studies employing a few established animal models, exploring the neural basis of compulsive behavior and developing new treatment strategies. Here we summarize findings from the five most studied animal models of OCD: 8-OHDPAT (8-hydroxy-2-(di-n-propylamino)-tetralin hydrobromide) induced decreased alternation, quinpirole-induced compulsive checking, marble burying, signal attenuation and spontaneous stereotypy in deer mice. We evaluate each model's face validity, derived from similarity between the behavior in the model and the specific symptoms of the human condition, predictive validity, derived from similarity in response to treatment (pharmacological or other), and construct validity, derived from similarity in the mechanism (physiological or psychological) that induces behavioral symptoms and in the neural systems involved. We present ideas regarding future clinical research based on each model's findings, and on this basis, also emphasize possible new approaches for the treatment of OCD.
机译:在过去的30年中,已经进行了许多尝试来开发强迫症动物模型(OCD)。在最初的出版物发布之后,大多数模型都没有得到进一步的研究,并且在过去的几年中,大多数论文采用了一些已建立的动物模型,探索强迫行为的神经基础并开发了新的治疗策略来进行研究。在这里,我们总结了来自五个最受研究的强迫症动物模型的发现:8-OHDPAT(8-羟基-2-(二-正丙基氨基)-氢溴酸四氢萘)引起的交替减少,喹吡罗引起的强迫检查,大理石掩埋,信号衰减和自发的刻板印象在鹿老鼠。我们评估每个模型的脸部有效性,该模型的面部行为源自模型行为与人类状况的特定症状之间的相似性,预测有效性,源自针对治疗(药理或其他)的相似性,以及构造有效性,源自于模型中的相似性诱发行为症状并涉及神经系统的机制(生理或心理)。我们根据每个模型的发现提出有关未来临床研究的想法,并在此基础上还强调可能的新方法来治疗强迫症。

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