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花青素对葡萄糖和甲基乙二醛诱导的蛋白质糖基化及氧化性DNA损伤的保护作用。

Protective effect of cyanidin against glucose- and methylglyoxal-induced protein glycation and oxidative DNA damage.

作者信息

Suantawee Tanyawan, Cheng Henrique, Adisakwattana Sirichai

机构信息

Program in Biomedical Sciences, Graduate School, Chulalongkorn University, Bangkok 10330, Thailand.

Department of Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803, USA.

出版信息

Int J Biol Macromol. 2016 Dec;93(Pt A):814-821. doi: 10.1016/j.ijbiomac.2016.09.059. Epub 2016 Sep 16.

DOI:10.1016/j.ijbiomac.2016.09.059
PMID:27645922
Abstract

Cyanidin, a natural anthocyanin abundant in fruits and vegetables, has shown the health benefits due to its pharmacological properties. However, there was no evidence regarding anti-glycation activity of cyanidin. The aim of the study was to investigate the inhibitory effect of cyanidin on methylglyoxal (MG)- and glucose-induced protein glycation in bovine serum albumin (BSA) as well as oxidative DNA damage. Free radical scavenging activity and the MG-trapping ability of cyanidin were also investigated. The results demonstrated that cyanidin (0.125-1mM) significantly inhibited the formation of fluorescent and non-fluorescent AGEs in BSA/MG and BSA/glucose systems. There was a significantly improved protein thiol in BSA/MG and BSA/glucose when incubated with cyanidin. Correspondingly, cyanidin decreased the level of protein carbonyl content in BSA/glucose system. Moreover, cyanidin (0.5-1mM) prevented lysine/MG-mediated oxidative DNA damage in the absence or presence of copper ion. The results demonstrated that cyanidin showed the MG-trapping ability in a concentration-dependent manner. Cyanidin also reduced superoxide anion and hydroxyl radical generation in lysine/MG system. The mechanism by which cyanidin inhibited protein glycation was the MG-trapping ability and the free radical scavenging activity. The present study suggests that cyanidin might be a promising antiglycation agent for preventing or ameliorating AGEs-mediated diabetic complications.

摘要

花青素是一种在水果和蔬菜中大量存在的天然花青素,因其药理特性而具有健康益处。然而,没有关于花青素抗糖基化活性的证据。本研究的目的是研究花青素对甲基乙二醛(MG)和葡萄糖诱导的牛血清白蛋白(BSA)蛋白糖基化以及氧化DNA损伤的抑制作用。还研究了花青素的自由基清除活性和MG捕获能力。结果表明,花青素(0.125 - 1mM)显著抑制了BSA/MG和BSA/葡萄糖体系中荧光和非荧光晚期糖基化终产物(AGEs)的形成。与花青素一起孵育时,BSA/MG和BSA/葡萄糖中的蛋白质巯基有显著改善。相应地,花青素降低了BSA/葡萄糖体系中蛋白质羰基含量的水平。此外,花青素(0.5 - 1mM)在有无铜离子的情况下均能防止赖氨酸/MG介导的氧化DNA损伤。结果表明,花青素以浓度依赖的方式表现出MG捕获能力。花青素还减少了赖氨酸/MG体系中超氧阴离子和羟基自由基的产生。花青素抑制蛋白质糖基化的机制是MG捕获能力和自由基清除活性。本研究表明,花青素可能是一种有前途的抗糖基化剂,用于预防或改善AGEs介导的糖尿病并发症。

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