甲基乙二醛
糖基化
化学
氧化应激
体外
生物化学
牛血清白蛋白
酶
受体
作者
His Lin,Ting‐Yun Lin,Jer‐An Lin,Kuan‐Chen Cheng,Shella Permatasari Santoso,Chun-Hsu Chou,Chang‐Wei Hsieh
出处
期刊:Antioxidants
[MDPI AG]
日期:2021-10-10
卷期号:10 (10): 1589-1589
被引量:8
标识
DOI:10.3390/antiox10101589
摘要
Advanced glycation end products (AGEs) can induce oxidative stress and inflammation. AGEs are major risk factors for the development of many aging-related diseases, such as cancer and diabetes. In this study, Pholiota nameko polysaccharides (PNPs) were prepared from water extract of P. nameko via graded alcohol precipitation (40%, 60%, and 80% v/v). We explored the in vitro antiglycation ability of the PNPs and inhibition of methylglyoxal (MG)-induced Hs68 cell damage. In a bovine serum albumin (BSA) glycation system, PNPs significantly inhibited the formation of Amadori products. Fluorescence spectrophotometry revealed that the PNPs trapped MG and reduced MG-induced changes in functional groups (carbonyl and ε-NH2) in the BSA. Pretreating Hs68 cells with PNPs enhanced the cell survival rate and protected against MG-induced cell damage. This was due to decreased intracellular ROS content. PNPs thus mitigate skin cell damage and oxidative stress resulting from glycation stress, making them a potential raw material for antiaging-related skincare products.
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