Department of Molecular Physiology and Neurobiology, University of Wrocław, Sienkiewicza 21, 50-335 Wrocław, Poland.
Cells. 2020 Mar 16;9(3):727. doi: 10.3390/cells9030727.
Glycogen synthase kinase 3β (GSK3β), originally described as a negative regulator of glycogen synthesis, is a molecular hub linking numerous signaling pathways in a cell. Specific GSK3β inhibitors have anti-depressant effects and reduce depressive-like behavior in animal models of depression. Therefore, GSK3β is suggested to be engaged in the pathogenesis of major depressive disorder, and to be a target and/or modifier of anti-depressants' action. In this review, we discuss abnormalities in the activity of GSK3β and its upstream regulators in different brain regions during depressive episodes. Additionally, putative role(s) of GSK3β in the pathogenesis of depression and the influence of anti-depressants on GSK3β activity are discussed.
糖原合酶激酶 3β(GSK3β)最初被描述为糖原合成的负调节剂,是一个分子枢纽,可将细胞中的许多信号通路联系起来。特定的 GSK3β 抑制剂具有抗抑郁作用,并可减少抑郁症动物模型中的抑郁样行为。因此,GSK3β 被认为参与了重性抑郁症的发病机制,是抗抑郁药作用的靶点和/或调节剂。在这篇综述中,我们讨论了在抑郁发作期间不同脑区 GSK3β及其上游调节因子活性的异常。此外,还讨论了 GSK3β 在抑郁症发病机制中的潜在作用以及抗抑郁药对 GSK3β 活性的影响。