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Inhibitory effects of hydroxysafflor yellow A on the formation of advanced glycation end products in vitro

机译:羟基红花黄色素A对体外晚期糖基化终产物形成的抑制作用

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摘要

To investigate the inhibitory effects of hydroxysafflor yellow A (HSYA) on the protein glycation in vitro. Using bovine serum albumin (BSA)-glucose assay, BSA-methylglyoxal (MGO) assay, and N-acetylglycyl-lysine methyl ester (G.K.) peptide-ribose assay, inhibitory effects of HSYA were investigated. Advanced glycation end products (AGEs) production was assessed by AGEs-specific fluorescence and sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). In BSA-glucose assay, HSYA concentration dependency decreased AGEs formation, with maximum inhibitory effects at 1mM by 95%. Further more, HSYA also showed significant inhibitory effects on MGO-medicated protein modification and subsequent cross-linking of proteins. Finally, when co-incubated with G.K. peptide and ribose, HSYA exhibited its antiglycation effects, and the maximum inhibitory effects of HSYA at 1mM were 84%. Overall, our present study provides the first evidence of the antiglycation effects of HSYA on AGEs formation in vitro.
机译:为了研究羟基红花黄A(HSYA)对体外蛋白质糖基化的抑制作用。使用牛血清白蛋白(BSA)-葡萄糖测定法,BSA-甲基乙二醛(MGO)测定法和N-乙酰基甘氨酰赖氨酸甲酯(G.K.)肽核糖测定法,研究了HSYA的抑制作用。通过AGEs特异性荧光和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)评估了高级糖基化终产物(AGEs)的产生。在BSA-葡萄糖测定中,HSYA浓度依赖性降低了AGEs的形成,在1mM处的最大抑制作用达到95%。此外,HSYA还显示出对MGO药物修饰的蛋白质和随后的蛋白质交联具有明显的抑制作用。最后,与G.K.共同孵化时肽和核糖中,HSYA表现出其抗糖基化作用,并且在1mM时HSYA的最大抑制作用为84%。总体而言,我们的研究提供了HSYA对体外AGEs形成的抗糖基化作用的第一个证据。

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