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二甲双胍与黄连素对高糖诱导的脂肪生成的协同作用。

Synergistic Effect of Metformin and Berberine on High Glucose-induced Lipogenesis.

作者信息

Babaei Khorzoughi Reyhaneh, Namvarjah Fatemeh, Teimouri Maryam, Hosseini Hossein, Meshkani Reza

机构信息

Department of Clinical Biochemistry, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Pharm Res. 2019 Fall;18(4):1921-1930. doi: 10.22037/ijpr.2019.15085.12867.

Abstract

Metformin and berberine have been reported to have lipid lowering effects. This study aims to investigate lipid lowering effects of berberine and Metformin, alone and in combination, in HepG2 cells to determine whether berberine and Metformin work synergistically and elucidate their mechanisms. HepG2 cells were treated with 33 mM glucose in the presence of various concentrations of berberine and Metformin, alone and in combination, for 24 h. The cytotoxic effects of these compounds were determined by MTT assay. Oil red O staining, triglyceride measurement, and gene expression analyses were performed to evaluate the effects of these compounds on hepatocytes lipogenesis. Berberine at doses 20 µM and 40 µM and Metformin at doses 1 mM and 2 mM reduced total lipid content and triglyceride level in HepG2 cells. Metformin (mM) and berberine (µM) at combination ratios of 2:40, 1:20, 0.5:10, and 0.25:5 exhibited a synergistic lipid-lowering effect on HepG2 cells. These ratios could significantly decrease total lipid content and triglyceride level in HepG2 cells. The lowest dose of the combination [Metformin (0.25 mM) and berberine (5 μM)] also synergistically reduced the expression of the FAS and SREBP-1c genes in HepG2 cells treated with high glucose. The combination of Metformin and berberine exerted synergistic lipid-lowering effects on HepG2 cells by reducing total lipid content, triglyceride level, and the expression of the genes involved in lipogenesis.

摘要

据报道,二甲双胍和黄连素具有降脂作用。本研究旨在探讨黄连素和二甲双胍单独及联合使用对HepG2细胞的降脂作用,以确定黄连素和二甲双胍是否协同作用,并阐明其作用机制。在存在不同浓度的黄连素和二甲双胍单独及联合使用的情况下,用33 mM葡萄糖处理HepG2细胞24小时。通过MTT法测定这些化合物的细胞毒性作用。进行油红O染色、甘油三酯测量和基因表达分析,以评估这些化合物对肝细胞脂肪生成的影响。20 μM和40 μM剂量的黄连素以及1 mM和2 mM剂量的二甲双胍降低了HepG2细胞中的总脂质含量和甘油三酯水平。二甲双胍(mM)与黄连素(μM)以2:40、1:20、0.5:10和0.25:5的组合比例对HepG2细胞表现出协同降脂作用。这些比例可显著降低HepG2细胞中的总脂质含量和甘油三酯水平。最低剂量的组合[二甲双胍(0.25 mM)和黄连素(5 μM)]也协同降低了高糖处理的HepG2细胞中FAS和SREBP-1c基因的表达。二甲双胍和黄连素的组合通过降低总脂质含量、甘油三酯水平以及参与脂肪生成的基因的表达,对HepG2细胞发挥协同降脂作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bae2/7059038/771d6ad2150e/ijpr-18-1921-g001.jpg

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