Department of Pharmacology, Chongqing Key Laboratory of Biochemistry and Molecular Pharmacology, Chongqing Medical University, Chongqing 400016, China.
Evid Based Complement Alternat Med. 2013;2013:285489. doi: 10.1155/2013/285489. Epub 2013 Mar 20.
Rhizoma coptidis, the root of Coptis chinensis Franch, has been used in China as a folk medicine in the treatment of diabetes for thousands of years. Berberine, one of the active ingredients of Rhizoma coptidis, has been reported to improve symptoms of diabetes and to treat experimental cardiac hypertrophy, respectively. The objective of this study was to evaluate the potential effect of berberine on cardiomyocyte hypertrophy in diabetes and its possible influence on peroxisome proliferator-activated receptor- α (PPAR α )/nitric oxide (NO) signaling pathway. The cardiomyocyte hypertrophy induced by high glucose (25.5 mmol/L) and insulin (0.1 μ mol/L) (HGI) was characterized in rat primary cardiomyocyte by measuring the cell surface area, protein content, and atrial natriuretic factor mRNA expression level. Protein and mRNA expression were measured by western blot and real-time RT-PCR, respectively. The enzymatic activity of NO synthase (NOS) was measured using a spectrophotometric assay, and NO concentration was measured using the Griess assay. HGI significantly induced cardiomyocyte hypertrophy and decreased the expression of PPAR α and endothelial NOS at the mRNA and protein levels, which occurred in parallel with declining NOS activity and NO concentration. The effect of HGI was inhibited by berberine (0.1 to 100 μ mol/L), fenofibrate (0.3 μ mol/L), or L-arginine (100 μ mol/L). MK886 (0.3 μ mol/L), a selective PPAR α antagonist, could abolish the effects of berberine and fenofibrate. N (G) -nitro-L-arginine-methyl ester (100 μ mol/L), a NOS inhibitor, could block the effects of L-arginine, but only partially blocked the effects of berberine. These results suggest that berberine can blunt HGI-induced cardiomyocyte hypertrophy in vitro, through the activation of the PPAR α /NO signaling pathway.
黄连是毛茛科黄连属植物黄连的干燥根茎,在中国民间作为治疗糖尿病的药物已有数千年的历史。小檗碱是黄连的一种活性成分,已被报道可改善糖尿病的症状,并分别治疗实验性心肌肥厚。本研究旨在评估小檗碱对糖尿病心肌细胞肥大的潜在作用及其对过氧化物酶体增殖物激活受体-α(PPARα)/一氧化氮(NO)信号通路的可能影响。通过测量细胞表面积、蛋白含量和心钠素 mRNA 表达水平,来表征高葡萄糖(25.5mmol/L)和胰岛素(0.1μmol/L)(HGI)诱导的大鼠原代心肌细胞肥大。通过 Western blot 和实时 RT-PCR 分别测量蛋白和 mRNA 的表达。使用分光光度法测定一氧化氮合酶(NOS)的酶活性,使用格里斯测定法测定 NO 浓度。HGI 显著诱导心肌细胞肥大,并降低 PPARα 和内皮型 NOS 的 mRNA 和蛋白表达水平,同时 NOS 活性和 NO 浓度下降。小檗碱(0.1 至 100μmol/L)、非诺贝特(0.3μmol/L)或 L-精氨酸(100μmol/L)可抑制 HGI 的作用。MK886(0.3μmol/L),一种选择性的 PPARα 拮抗剂,可消除小檗碱和非诺贝特的作用。NOS 抑制剂 N(G)-硝基-L-精氨酸甲酯(100μmol/L)可阻断 L-精氨酸的作用,但仅部分阻断小檗碱的作用。这些结果表明,小檗碱可通过激活 PPARα/NO 信号通路,减弱体外 HGI 诱导的心肌细胞肥大。