Department of Pharmaceutical Sciences, School of Pharmaceutical Sciences, University of São Paulo , Ribeirão Preto, São Paulo 14040-903, Brazil.
Department of Internal Medicine, Division of Nephrology and Hypertension, Mayo Clinic College of Medicine , Rochester, Minnesota 55905, United States.
J Med Chem. 2018 Feb 22;61(4):1609-1621. doi: 10.1021/acs.jmedchem.7b01566. Epub 2018 Feb 13.
The plant metabolite 3,4,5-tri-O-galloylquinic acid methyl ester (TGAME, compound 6) was synthesized, and its potential effect on calcium oxalate monohydrate (COM) crystal binding to the surface of Madin-Darby canine kidney cells type I (MDCKI) and crystal growth in a Drosophila melanogaster Malpighian tubule (MT) model were investigated. Membrane, cytosolic, and total annexin A1 (AxA1), α-enolase, and heat shock protein 90 (HSP90) amounts were examined by Western blot analysis after subcellular fractionation, then confirmed by immunofluorescence staining of cultured cells. Pretreatment of MDCKI cells with TGAME for up to 6 h significantly diminished COM crystal binding in a concentration-dependent manner. TGAME significantly inhibited AxA1 surface expression by immunofluorescence microscopy, whereas intracellular AxA1 increased. Western blot analysis confirmed AxA1 expression changes in the membrane and cytosolic fractions of compound-treated cells, whereas whole cell AxA1 remained unchanged. TGAME also significantly decreased the size, number, and growth of calcium oxalate (CaOx) crystals induced in a Drosophila melanogaster MT model and possessed a potent antioxidant activity in a DPPH assay.
植物代谢产物 3,4,5-三-O-没食子酰基奎宁酸甲酯(TGAME,化合物 6)被合成,并研究了其对一水合草酸钙(COM)晶体与 Madin-Darby 犬肾细胞 I 型(MDCKI)表面结合以及在黑腹果蝇马尔皮基氏管(MT)模型中晶体生长的潜在影响。通过亚细胞分级分离后进行 Western blot 分析,检查膜、胞质和总膜联蛋白 A1(AxA1)、α-烯醇酶和热休克蛋白 90(HSP90)的含量,然后通过培养细胞的免疫荧光染色进行确认。用 TGAME 预处理 MDCKI 细胞长达 6 h 可显著降低 COM 晶体的浓度依赖性结合。免疫荧光显微镜观察显示,TGAME 显著抑制 AxA1 表面表达,而细胞内 AxA1 增加。Western blot 分析证实了化合物处理细胞的膜和胞质部分的 AxA1 表达变化,而整个细胞的 AxA1 保持不变。TGAME 还显著降低了黑腹果蝇 MT 模型中诱导的草酸钙(CaOx)晶体的大小、数量和生长,并在 DPPH 测定中具有很强的抗氧化活性。