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依他普仑和文拉法辛对缝隙连接蛋白 43 相关星形胶质细胞 L-谷氨酸释放的不同影响。

Distinct Effects of Escitalopram and Vortioxetine on Astroglial L-Glutamate Release Associated with Connexin43.

机构信息

Department of Neuropsychiatry, Division of Neuroscience, Graduate School of Medicine, Mie University, Tsu 514-8507, Japan.

出版信息

Int J Mol Sci. 2021 Sep 16;22(18):10013. doi: 10.3390/ijms221810013.

Abstract

It has been established that enhancement of serotonergic transmission contributes to improvement of major depression; however, several post-mortem studies and experimental depression rodent models suggest that functional abnormalities of astrocytes play important roles in the pathomechanisms/pathophysiology of mood disorders. Direct effects of serotonin (5-HT) transporter inhibiting antidepressants on astroglial transmission systems has never been assessed in this context. Therefore, to explore the effects of antidepressants on transmission associated with astrocytes, the present study determined the effects of the selective 5-HT transporter inhibitor, escitalopram, and the 5-HT partial agonist reuptake inhibitor, vortioxetine, on astroglial L-glutamate release through activated hemichannels, and the expression of connexin43 (Cx43), type 1A (5-HT1AR) and type 7 (5-HT7R) 5-HT receptor subtypes, and extracellular signal-regulated kinase (ERK) in astrocytes using primary cultured rat cortical astrocytes in a 5-HT-free environment. Both escitalopram and 5-HT1AR antagonist (WAY100635) did not affect basal astroglial L-glutamate release or L-glutamate release through activated hemichannels. Subchronic (for seven days) administrations of vortioxetine and the 5-HT7R inverse agonist (SB269970) suppressed both basal L-glutamate release and L-glutamate release through activated hemichannels, whereas 5-HT1AR agonist (BP554) inhibited L-glutamate release through activated hemichannels, but did not affect basal L-glutamate release. In particular, WAY100635 did not affect the inhibitory effects of vortioxetine on L-glutamate release. Subchronic administration of vortioxetine, BP554 and SB269970 downregulated 5-HT1AR, 5-HT7R and phosphorylated ERK in the plasma membrane fraction, but escitalopram and WAY100635 did not affect them. Subchronic administration of SB269970 decreased Cx43 expression in the plasma membrane but did not affect the cytosol; however, subchronic administration of BP554 increased Cx43 expression in the cytosol but did not affect the plasma membrane. Subchronic vortioxetine administration increased Cx43 expression in the cytosol and decreased it in the plasma membrane. WAY100635 prevented an increased Cx43 expression in the cytosol induced by vortioxetine without affecting the reduced Cx43 expression in the plasma membrane. These results suggest that 5-HT1AR downregulation probably increases Cx43 synthesis, but 5-HT7R downregulation suppresses Cx43 trafficking to the plasma membrane. These results also suggest that the subchronic administration of therapeutic-relevant concentrations of vortioxetine inhibits both astroglial L-glutamate and Cx43 expression in the plasma membrane via 5-HT7R downregulation but enhances Cx43 synthesis in the cytosol via 5-HT1AR downregulation. This combination of the downregulation of 5-HT1AR, 5-HT7R and Cx43 in the astroglial plasma membrane induced by subchronic vortioxetine administration suggest that astrocytes is possibly involved in the pathophysiology of depression.

摘要

已经证实,5-羟色胺能传递的增强有助于改善重度抑郁症;然而,几项尸检研究和实验性抑郁啮齿动物模型表明,星形胶质细胞的功能异常在心境障碍的发病机制/病理生理学中发挥重要作用。5-羟色胺(5-HT)转运体抑制剂类抗抑郁药对星形胶质细胞传递系统的直接作用在这方面从未被评估过。因此,为了探讨抗抑郁药对与星形胶质细胞相关的传递的影响,本研究使用原代培养的大鼠皮质星形胶质细胞,在无 5-HT 的环境中,确定选择性 5-HT 转运体抑制剂艾司西酞普兰和 5-HT 部分激动剂再摄取抑制剂文拉法辛对星形胶质细胞 L-谷氨酸释放的影响,通过激活半通道和连接蛋白 43(Cx43)、1A 型(5-HT1AR)和 7 型(5-HT7R)5-HT 受体亚型,以及细胞外信号调节激酶(ERK)在星形胶质细胞中的表达。艾司西酞普兰和 5-HT1AR 拮抗剂(WAY100635)均不影响基础星形胶质细胞 L-谷氨酸释放或通过激活半通道的 L-谷氨酸释放。文拉法辛和 5-HT7R 反向激动剂(SB269970)的亚慢性(七天)给药抑制基础 L-谷氨酸释放和通过激活半通道的 L-谷氨酸释放,而 5-HT1AR 激动剂(BP554)抑制通过激活半通道的 L-谷氨酸释放,但不影响基础 L-谷氨酸释放。特别是,WAY100635 不影响文拉法辛对 L-谷氨酸释放的抑制作用。文拉法辛、BP554 和 SB269970 的亚慢性给药下调了质膜部分的 5-HT1AR、5-HT7R 和磷酸化 ERK,但艾司西酞普兰和 WAY100635 对其没有影响。亚慢性 SB269970 降低了质膜中 Cx43 的表达,但不影响细胞质;然而,亚慢性 BP554 增加了细胞质中的 Cx43 表达,但不影响质膜。亚慢性文拉法辛给药增加了细胞质中的 Cx43 表达,并减少了质膜中的 Cx43 表达。WAY100635 阻止了文拉法辛诱导的细胞质中 Cx43 表达的增加,而不影响质膜中 Cx43 表达的减少。这些结果表明 5-HT1AR 的下调可能会增加 Cx43 的合成,但 5-HT7R 的下调会抑制 Cx43 向质膜的转运。这些结果还表明,治疗相关浓度的文拉法辛的亚慢性给药通过 5-HT7R 下调抑制星形胶质细胞 L-谷氨酸和质膜 Cx43 的表达,但通过 5-HT1AR 下调增强细胞质中 Cx43 的合成。这种亚慢性文拉法辛给药诱导的星形胶质细胞质膜中 5-HT1AR、5-HT7R 和 Cx43 的下调组合表明,星形胶质细胞可能参与了抑郁症的发病机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d9/8468507/bc1f53f3b140/ijms-22-10013-g001.jpg

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