Department of Pharmacy, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China.
Biol Pharm Bull. 2012;35(11):2050-3. doi: 10.1248/bpb.b12-00249. Epub 2012 Aug 31.
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 dependently decreased AGEs formation, with maximum inhibitory effects at 1 mM 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 1 mM were 84%. Overall, our present study provides the first evidence of the antiglycation effects of HSYA on AGEs formation in vitro.
研究羟基红花黄色素 A(HSYA)对体外蛋白质糖化的抑制作用。采用牛血清白蛋白(BSA)-葡萄糖法、BSA-甲基乙二醛(MGO)法和 N-乙酰甘氨酰-赖氨酸甲酯(G.K.)肽-核糖法,研究 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)评估晚期糖基化终产物(AGEs)的产生。在 BSA-葡萄糖法中,HSYA 浓度依赖性地降低 AGEs 的形成,在 1mM 时最大抑制率为 95%。此外,HSYA 还对 MGO 介导的蛋白质修饰及其随后的蛋白质交联具有显著的抑制作用。最后,当与 G.K.肽和核糖共孵育时,HSYA 表现出抗糖化作用,在 1mM 时最大抑制率为 84%。综上所述,本研究首次提供了 HSYA 在体外抑制 AGEs 形成的抗糖化作用的证据。