神经元可塑性、应激和抑郁:细胞骨架微管系统的参与?

M Bianchi, J J Hagan, C A Heidbreder
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引用次数: 73

摘要

在易受影响的个体中,压力源会增加患抑郁症的风险,最近的脑成像研究显示,受抑郁症影响的患者的边缘系统存在形态学改变。在抑郁个体的海马体中观察到的体积损失表明,抑郁症的发病机制可能涉及结构神经元的可塑性。动物的应激条件可导致海马结构神经元可塑性受损,其特征是顶端树突退缩和神经发生减少。细胞骨架微管系统固有的动态不稳定性对神经元的重塑和可塑性至关重要。我们最近的研究表明,急性和慢性应激都会降低大鼠海马中的微管动力学。其他作者已经证明,在啮齿类动物的海马体中,在功能上参与调节微管动力学的蛋白质可以被应激改变。此外,有证据表明,抗抑郁药物的急性和慢性治疗都可以影响微管蛋白的表达,这进一步加强了应激诱导的微管改变与抑郁症之间的联系。本综述将介绍越来越多的证据表明,应激诱导的神经元可塑性改变可能被认为是调节微管系统动力学的分子级联的激活和/或抑制的最终结果。此外,还将讨论靶向微管作为治疗情绪障碍的药物治疗方法的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuronal plasticity, stress and depression: involvement of the cytoskeletal microtubular system?

In susceptible individuals, stressors can increase the risk of onset of depression and recent brain imaging studies have shown morphometric alterations in the limbic system of patients affected by depression. The volume loss observed in the hippocampus of depressed individuals suggests a possible involvement of structural neuronal plasticity in the pathogenesis of depression. Stressful conditions in animals can result in impaired structural neuronal plasticity in the hippocampus, characterised by retraction of apical dendrites and decreased neurogenesis. The intrinsic dynamic instability of the cytoskeletal microtubular system is essential for neuronal remodelling and plasticity. We have recently shown that both acute and chronic stress decrease microtubular dynamics in the rat hippocampus. Other authors have demonstrated that proteins functionally involved in the regulation of microtubule dynamics can be altered by stress in the rodent hippocampus. Furthermore, the existence of a link between stress-induced microtubular changes and depression is further strengthened by evidence showing that both acute and chronic treatment with antidepressant drugs can affect the expression of microtubular proteins. The present review will introduce a growing body of evidence suggesting that stress-induced alterations in neuronal plasticity might be considered the final result of activation and/or inhibition of molecular cascades regulating the dynamics of the microtubular system. In addition, the prospect of targeting microtubules as a pharmacotherapeutic approach to treat mood disorders will be discussed.

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