Gould Todd D, Einat Haim
Mood and Anxiety Program, Department of Psychiatry, University of Maryland School of Medicine, 701 West Pratt Street, Suite 388, Baltimore, Maryland 21201, USA.
Neurosci Biobehav Rev. 2007;31(6):825-31. doi: 10.1016/j.neubiorev.2007.05.007. Epub 2007 May 31.
The limited number of suitable animal models of bipolar disorder available for in-depth behavioral, biochemical, histological, and pharmacological analysis is a rate-limiting step in the process of understanding the relevant neurobiology of the disorder, as well as the development of novel medications. In the search for new models, both new and old approaches hold promise for future discoveries. Clinical studies regarding the underlying genetics and pathophysiology of bipolar disorder are providing important clues. In particular, the identification of susceptibility genes for bipolar disorder will help to define specific neurobiological processes, and associated behaviors, that are unquestionably involved in the pathways connecting genes and distal symptoms. These endophenotypes will hold great value in further enhancing the validity of animal models and will strongly complement symptom-based models and models of medication efficacy. Regardless of the path taken by different researchers to develop better models, we believe that this area of work requires additional attention not only from researchers but also from funding agencies.
可用于深入行为、生化、组织学和药理学分析的双相情感障碍合适动物模型数量有限,这是理解该疾病相关神经生物学以及开发新型药物过程中的一个限速步骤。在寻找新模型的过程中,新旧方法都有望带来未来的发现。关于双相情感障碍潜在遗传学和病理生理学的临床研究正在提供重要线索。特别是,双相情感障碍易感基因的鉴定将有助于确定特定的神经生物学过程以及相关行为,这些无疑参与了连接基因和远端症状的途径。这些内表型对于进一步提高动物模型的有效性具有重要价值,并将有力地补充基于症状的模型和药物疗效模型。无论不同研究人员采用何种途径来开发更好的模型,我们认为这一工作领域不仅需要研究人员,也需要资助机构给予更多关注。