4.6 Review

An astroglial basis of major depressive disorder? An overview

期刊

GLIA
卷 65, 期 8, 页码 1227-1250

出版社

WILEY
DOI: 10.1002/glia.23143

关键词

gap junctions; gliotransmitter; glucose metabolism; glutamate transporter; neurotrophin

资金

  1. National Natural Science Foundation of China [81329003, 31430032, 81671356, U1201225]
  2. Program for Changjiang Scholars and Innovative Research Team in University [IRT_16R37]
  3. Specialized Research Fund for the Doctoral Program of Higher Education of China [20134433130002]

向作者/读者索取更多资源

Depression is a chronic, recurring, and serious mood disorder that afflicts up to 20% of the global population. The monoamine hypothesis has dominated our understanding of the pharmacotherapy of depression for more than half a century; however, our understanding of the pathophysiology and pathogenesis of major depression has lagged far behind. Astrocytes are the most abundant and versatile cells in the brain, participating in most, if not all, of brain functions as both a passive housekeeper and an active player. Mounting evidence from clinical, preclinical and post-mortem studies has revealed a decrease in the number or density of astrocytes and morphological and functional astroglial atrophy in patients with major depressive disorder (MDD) and in animal models of depression. Furthermore, currently available antidepressant treatments at least partially exert their therapeutic effects on astrocytes. More importantly, dysfunctional astrocytes lead to depressive-like phenotypes in animals. Together, current studies point to astroglial pathology as the potential root cause of MDD. Thus, a shift from a neuron-centric to an astrocyte-centric cause of MDD has gained increasing attention during the past two decades. Here we will summarize the current evidence supporting the hypothesis that MDD is a disease of astrocyte pathology and highlight previous studies on promising strategies that directly target astrocytes for the development of novel antidepressant treatments.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据