Suppr超能文献

小檗碱通过下调 miR-106b 激活 β-catenin/TCF4 信号通路,促进肠 L 细胞 GLP-1 的产生。

Berberine activates the β-catenin/TCF4 signaling pathway by down-regulating miR-106b to promote GLP-1 production by intestinal L cells.

机构信息

Department of Endocrinology, The First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, PR China.

Department of Endocrinology, The First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, PR China.

出版信息

Eur J Pharmacol. 2021 Nov 15;911:174482. doi: 10.1016/j.ejphar.2021.174482. Epub 2021 Sep 2.

Abstract

Berberine facilitates the production of glucagon-like peptide-1 (GLP-1) by intestinal L cells. Here, we aimed to reveal the mechanism of berberine facilitating the production of GLP-1 by intestinal L cells. In this study, we confirmed that the 100 mg/kg berberine daily through diet decreased the miR-106b expression and elevated the expressions of β-catenin and T-cell factor 4 (TCF4) in colon tissues of high-fat diet mice; berberine decreased the concentrations of triglycerides, total cholesterol and the ratio of low-density lipoprotein cholesterol and high-density lipoprotein cholesterol in mouse serum samples; berberine decreased the blood glucose in the mouse tail vein blood and promoted GLP-1 production by intestinal L cells in mouse serum samples and elevated the GLP-1 expression in mouse colon tissues. Meanwhile, the mechanism analysis demonstrated that a dose of 100 μM berberine down-regulated the miR-106b expression by elevating the methylation levels of miR-106b in STC-1 cells and miR-106b bound to TCF4 in 293T cells. Moreover, the 100 mg/kg berberine daily through diet activated the β-catenin/TCF4 signaling pathway by decreasing miR-106b, thereby facilitating GLP-1 production in intestinal L cells through the in vivo assays. Conclusively, our experimental data illustrated that berberine decreased miR-106b expression by increasing its methylation levels and then activated the β-catenin/TCF4 signaling pathway, thereby facilitating GLP-1 production by intestinal L cells.

摘要

小檗碱促进肠 L 细胞产生胰高血糖素样肽-1(GLP-1)。在这里,我们旨在揭示小檗碱促进肠 L 细胞产生 GLP-1 的机制。在这项研究中,我们通过饮食证实每天 100mg/kg 小檗碱可降低高脂肪饮食小鼠结肠组织中 miR-106b 的表达,同时升高β-catenin 和 T 细胞因子 4(TCF4)的表达;小檗碱降低了小鼠血清样本中甘油三酯、总胆固醇和低密度脂蛋白胆固醇与高密度脂蛋白胆固醇比值的浓度;小檗碱降低了小鼠尾静脉血中的血糖,并促进了小鼠血清样本中肠 L 细胞 GLP-1 的产生,同时升高了小鼠结肠组织中 GLP-1 的表达。与此同时,机制分析表明,100μM 小檗碱通过增加 STC-1 细胞中 miR-106b 的甲基化水平和 miR-106b 在 293T 细胞中与 TCF4 结合,下调了 miR-106b 的表达。此外,饮食中每天 100mg/kg 小檗碱通过降低 miR-106b 激活了 β-catenin/TCF4 信号通路,从而通过体内实验促进肠 L 细胞中 GLP-1 的产生。总而言之,我们的实验数据表明,小檗碱通过增加其甲基化水平降低 miR-106b 的表达,然后激活β-catenin/TCF4 信号通路,从而促进肠 L 细胞中 GLP-1 的产生。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验