Protective effect of cyanidin against glucose- and methylglyoxal-induced protein glycation and oxidative DNA damage
Document Type
Article
Publication Date
12-1-2016
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.
Publication Source (Journal or Book title)
International journal of biological macromolecules
First Page
814
Last Page
821
Recommended Citation
Suantawee, T., Cheng, H., & Adisakwattana, S. (2016). Protective effect of cyanidin against glucose- and methylglyoxal-induced protein glycation and oxidative DNA damage. International journal of biological macromolecules, 93 (Pt A), 814-821. https://doi.org/10.1016/j.ijbiomac.2016.09.059