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日本传统药物 yokukansan 增强培养的大鼠皮质星形胶质细胞中谷氨酸转运体 GLT-1 的功能。

Yokukansan, a Traditional Japanese Medicine, Enhances the Glutamate Transporter GLT-1 Function in Cultured Rat Cortical Astrocytes.

作者信息

Ueki Toshiyuki, Kawakami Zenji, Kanno Hitomi, Omiya Yuji, Mizoguchi Kazushige, Yamamoto Masahiro

机构信息

Tsumura Kampo Research Laboratories, Kampo Research & Development Division, Tsumura & Co., 3586 Yoshiwara, Ami-machi, Inashiki-gun, Ibaraki 300-1192, Japan.

出版信息

Evid Based Complement Alternat Med. 2018 May 6;2018:6804017. doi: 10.1155/2018/6804017. eCollection 2018.

Abstract

Astrocytes carry two glutamate transporters-GLAST and GLT-1-the latter of which is responsible for >90% of glutamate uptake activity in the brain; however, under culture conditions, the GLT-1 expression in astrocytes is exceedingly low, as is the glutamate uptake activity mediated by GLT-1. This study aimed to elucidate the effects of yokukansan (YKS) in relation to the GLT-1-mediated regulation of extracellular glutamate concentrations. Thus, we treated cultured astrocytes with tumor necrosis factor- (TNF-) and dibutyryl-cAMP (dBcAMP) (hereinafter, referred to as "TA") to increase GLT-1 expression and then functionally examined how YKS would affect glutamate uptake ability derived from GLT-1. Contrary to expectations, although the TA treatments did not affect the uptake activity, YKS significantly augmented it. Conversely, GLAST-derived glutamate uptake was significantly reduced by TA treatments but was unaffected by YKS. Subsequently, we analyzed the GLT-1 protein and mRNA levels and found that TA treatments had significantly increased them, which were then further augmented by YKS. These findings suggest that YKS enhances GLT-1-derived glutamate transport functions in TA-treated cultured astrocytes and that this process entails increased GLT-1 protein and mRNA levels. This type of mechanism may contribute to the YKS-mediated regulation of extracellular glutamate concentrations.

摘要

星形胶质细胞携带两种谷氨酸转运体——谷氨酸天冬氨酸转运体(GLAST)和谷氨酸转运体1(GLT-1),其中后者负责大脑中90%以上的谷氨酸摄取活性;然而,在培养条件下,星形胶质细胞中GLT-1的表达极低,由GLT-1介导的谷氨酸摄取活性也很低。本研究旨在阐明逍遥散(YKS)对GLT-1介导的细胞外谷氨酸浓度调节的影响。因此,我们用肿瘤坏死因子-α(TNF-α)和二丁酰环磷腺苷(dBcAMP)(以下简称“TA”)处理培养的星形胶质细胞以增加GLT-1表达,然后从功能上研究YKS如何影响源自GLT-1的谷氨酸摄取能力。与预期相反,尽管TA处理不影响摄取活性,但YKS显著增强了它。相反,TA处理显著降低了源自GLAST的谷氨酸摄取,但YKS对其没有影响。随后,我们分析了GLT-1蛋白和mRNA水平,发现TA处理显著增加了它们,然后YKS进一步增强了它们。这些发现表明,YKS增强了TA处理的培养星形胶质细胞中源自GLT-1的谷氨酸转运功能,并且这一过程需要增加GLT-1蛋白和mRNA水平。这种机制可能有助于YKS介导的细胞外谷氨酸浓度调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6439/5960509/9c45d067a95a/ECAM2018-6804017.001.jpg

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