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