Animal inflammation-based models of depression and their application to drug discovery

抗抑郁药 小胶质细胞 萧条(经济学) 神经科学 发病机制 免疫系统 机制(生物学) 医学 炎症 斑马鱼 药品 生物信息学 药物发现 焦虑 生物 免疫学 精神科 基因 宏观经济学 经济 哲学 认识论 生物化学
作者
Li Ma,Konstantin A. Demin,Т. А. Колесникова,Sergey L. Khatsko,Xiaolin Zhu,Xiaodong Yuan,Cai Song,Darya A. Meshalkina,Brian E. Leonard,Li Tian,Allan V. Kalueff
出处
期刊:Expert Opinion on Drug Discovery [Taylor & Francis]
卷期号:12 (10): 995-1009 被引量:57
标识
DOI:10.1080/17460441.2017.1362385
摘要

Introduction: Depression, anxiety and other affective disorders are globally widespread and severely debilitating human brain diseases. Despite their high prevalence and mental health impact, affective pathogenesis is poorly understood, and often remains recurrent and resistant to treatment. The lack of efficient antidepressants and presently limited conceptual innovation necessitate novel approaches and new drug targets in the field of antidepressant therapy.Areas covered: Herein, the authors discuss the emerging role of neuro-immune interactions in affective pathogenesis, which can become useful targets for CNS drug discovery, including modulating neuroinflammatory pathways to alleviate affective pathogenesis.Expert opinion: Mounting evidence implicates microglia, polyunsaturated fatty acids (PUFAs), glucocorticoids and gut microbiota in both inflammation and depression. It is suggested that novel antidepressants can be developed based on targeting microglia-, PUFAs-, glucocorticoid- and gut microbiota-mediated cellular pathways. In addition, the authors call for a wider application of novel model organisms, such as zebrafish, in studying shared, evolutionarily conserved (and therefore, core) neuro-immune mechanisms of depression.

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