Department of Molecular Neuroscience, Centre for Addiction and Mental Health, Campbell Family Mental Health Research Institute , Toronto, ON , Canada ; Department of Pharmacology, Faculty of Medicine, University of Toronto , Toronto, ON , Canada.
Department of Molecular Neuroscience, Centre for Addiction and Mental Health, Campbell Family Mental Health Research Institute , Toronto, ON , Canada ; Department of Pharmacology, Faculty of Medicine, University of Toronto , Toronto, ON , Canada ; Department of Psychiatry, Faculty of Medicine, University of Toronto , Toronto, ON , Canada.
Front Psychiatry. 2015 Feb 18;6:13. doi: 10.3389/fpsyt.2015.00013. eCollection 2015.
Patients with schizophrenia are at an increased risk for the development of depression. Overlap in the symptoms and genetic risk factors between the two disorders suggests a common etiological mechanism may underlie the presentation of comorbid depression in schizophrenia. Understanding these shared mechanisms will be important in informing the development of new treatments. Rodent models are powerful tools for understanding gene function as it relates to behavior. Examining rodent models relevant to both schizophrenia and depression reveals a number of common mechanisms. Current models which demonstrate endophenotypes of both schizophrenia and depression are reviewed here, including models of CUB and SUSHI multiple domains 1, PDZ and LIM domain 5, glutamate Delta 1 receptor, diabetic db/db mice, neuropeptide Y, disrupted in schizophrenia 1, and its interacting partners, reelin, maternal immune activation, and social isolation. Neurotransmission, brain connectivity, the immune system, the environment, and metabolism emerge as potential common mechanisms linking these models and potentially explaining comorbid depression in schizophrenia.
精神分裂症患者发生抑郁的风险增加。两种疾病的症状和遗传风险因素存在重叠,这表明共病性抑郁在精神分裂症中的表现可能存在共同的病因机制。了解这些共同的机制对于新的治疗方法的发展很重要。啮齿动物模型是研究与行为相关的基因功能的有力工具。研究与精神分裂症和抑郁症都相关的啮齿动物模型揭示了许多共同的机制。本文综述了目前同时具有精神分裂症和抑郁症表型的模型,包括 CUB 和 SUSHI 多结构域 1、PDZ 和 LIM 结构域 5、谷氨酸 δ1 受体、糖尿病 db/db 小鼠、神经肽 Y、精神分裂症 1 及其相互作用伙伴、reelin、母体免疫激活和社会隔离。神经传递、大脑连接、免疫系统、环境和代谢被认为是将这些模型联系起来并可能解释精神分裂症共病性抑郁的潜在共同机制。