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Antidepressants Impact Connexin 43 Channel Functions in Astrocytes

机译:抗抑郁药影响星形胶质细胞中的连接蛋白43通道功能。

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摘要

Glial cells, and in particular astrocytes, are crucial to maintain neuronal microenvironment by regulating energy metabolism, neurotransmitter uptake, gliotransmission, and synaptic development. Moreover, a typical feature of astrocytes is their high expression level of connexins, a family of membrane proteins that form gap junction channels allowing intercellular exchanges and hemichannels that provide release and uptake pathways for neuroactive molecules. Interestingly, several studies have revealed unexpected changes in astrocytes from depressive patients and rodent models of depressive-like behavior. Moreover, changes in the expression level of the astroglial connexin 43 (Cx43) have been reported in a depressive context. On the other hand, antidepressive drugs have also been shown to impact the expression of this connexin in astrocytes. However, so far there is little information concerning the functional consequence of these changes, i.e., the status of gap junctional communication and hemichannel activity in astrocytes exposed to antidepressants. In the present work we focused our attention on the action of seven antidepressants from four different therapeutic classes and tested their effects on Cx43 expression and on the two connexin-based channels functions studied in cultured astrocytes. We here report that when used at non-toxic and clinically relevant concentrations they have no effects on Cx43 expression but differential effects on Cx43 gap junction channels. Moreover, all tested antidepressants inhibit Cx43 hemichannel with different efficiency depending on their therapeutic classe. By studying the impact of antidepressants on the functional status of astroglial connexin channels, contributing to dynamic neuroglial interactions, our observations should help to better understand the mechanism by which these drugs provide their effect in the brain.
机译:胶质细胞,尤其是星形胶质细胞,通过调节能量代谢,神经递质的摄取,神经胶质的传递和突触的发育,对维持神经元的微环境至关重要。此外,星形胶质细胞的典型特征是其连接蛋白的高表达水平,连接蛋白是形成间隙连接通道的膜蛋白家族,允许细胞间交换和半通道为神经活性分子提供释放和摄取途径。有趣的是,一些研究发现抑郁症患者的星形胶质细胞发生了意想不到的变化,以及啮齿类动物的抑郁样行为。此外,在抑郁的背景下,星形胶质连接蛋白43(Cx43)的表达水平有所变化。另一方面,抗抑郁药也已显示出会影响星形胶质细胞中这种连接蛋白的表达。但是,到目前为止,关于这些改变的功能后果的信息很少,即暴露于抗抑郁药的星形胶质细胞中间隙连接通讯和半通道活性的状态。在目前的工作中,我们将注意力集中在来自四个不同治疗类别的七种抗抑郁药的作用上,并测试了它们对Cx43表达的影响以及在培养的星形胶质细胞中研究的两种基于连接蛋白的通道功能的影响。我们在此报告,当以无毒且临床上相关的浓度使用它们时,它们对Cx43表达没有影响,但对Cx43间隙连接通道有不同的影响。此外,所有测试的抗抑郁药根据其治疗类别均以不同的效率抑制Cx43半通道。通过研究抗抑郁药对星形胶质连接蛋白通道功能状态的影响,促进动态神经胶质相互作用,我们的观察结果应有助于更好地理解这些药物在大脑中发挥作用的机制。

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