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穿心莲内酯通过蛋白激酶C途径促进L6细胞对葡萄糖的摄取及葡萄糖转运蛋白4的转运。

Andrographolide Promotes Uptake of Glucose and GLUT4 Transport through the PKC Pathway in L6 Cells.

作者信息

Liao Jingya, Yang Ziwei, Yao Yanhong, Yang Xinzhou, Shen Jinhua, Zhao Ping

机构信息

Institute for Medical Biology & Hubei Provincial Key Laboratory for Protection and Application of Special Plants in the Wuling Area of China, College of Life Sciences, South-Central Minzu University, Wuhan 430074, China.

School of Pharmaceutical Sciences, South-Central Minzu University, Min-Zu Road, Wuhan 430074, China.

出版信息

Pharmaceuticals (Basel). 2022 Oct 31;15(11):1346. doi: 10.3390/ph15111346.

Abstract

Glucose transporter 4 (GLUT4) is a membrane protein that regulates blood glucose balance and is closely related to type 2 diabetes. Andrographolide (AND) is a diterpene lactone extracted from herbal medicine Andrographis paniculata, which has a variety of biological activities. In this study, the antidiabetic effect of AND in L6 cells and its mechanism were investigated. The uptake of glucose of L6 cells was detected by a glucose assay kit. The expression of GLUT4 and phosphorylation of protein kinase B (PKB/Akt), AMP-dependent protein kinase (AMPK), and protein kinase C (PKC) were detected by Western blot. At the same time, the intracellular Ca levels and GLUT4 translocation in myc-GLUT4-mOrange-L6 cells were detected by confocal laser scanning microscopy. The results showed that AND enhanced the uptake of glucose, GLUT4 expression and fusion with plasma membrane in L6 cells. Meanwhile, AND also significantly activated the phosphorylation of AMPK and PKC and increased the concentration of intracellular Ca. AND-induced GLUT4 expression was significantly inhibited by a PKC inhibitor (Gö6983). In addition, in the case of 0 mM extracellular Ca and 0 mM extracellular Ca + 10 μM BAPTA-AM (intracellular Ca chelator), AND induced the translocation of GLUT4, and the uptake of glucose was significantly inhibited. Therefore, we concluded that AND promoted the expression of GLUT4 and its fusion with plasma membrane in L6 cells through PKC pathways in a Ca-dependent manner, thereby increasing the uptake of glucose.

摘要

葡萄糖转运蛋白4(GLUT4)是一种调节血糖平衡的膜蛋白,与2型糖尿病密切相关。穿心莲内酯(AND)是从草药穿心莲中提取的二萜内酯,具有多种生物活性。本研究探讨了AND对L6细胞的抗糖尿病作用及其机制。用葡萄糖检测试剂盒检测L6细胞的葡萄糖摄取。通过蛋白质免疫印迹法检测GLUT4的表达以及蛋白激酶B(PKB/Akt)、AMP依赖的蛋白激酶(AMPK)和蛋白激酶C(PKC)的磷酸化。同时,通过共聚焦激光扫描显微镜检测myc-GLUT4-mOrange-L6细胞内的钙离子水平和GLUT4转位情况。结果表明,AND增强了L6细胞对葡萄糖的摄取、GLUT4的表达及其与质膜的融合。同时,AND还显著激活了AMPK和PKC的磷酸化,并增加了细胞内钙离子浓度。PKC抑制剂(Gö6983)显著抑制了AND诱导的GLUT4表达。此外,在细胞外钙离子浓度为0 mM以及细胞外钙离子浓度为0 mM并添加10 μM BAPTA-AM(细胞内钙离子螯合剂)的情况下,AND诱导了GLUT4的转位,且葡萄糖摄取显著受到抑制。因此,我们得出结论,AND通过PKC途径以钙离子依赖的方式促进L6细胞中GLUT4的表达及其与质膜的融合,从而增加葡萄糖的摄取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ec4/9698946/e7e384d2ca60/pharmaceuticals-15-01346-g001.jpg

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