Effects of UV/H2O2 degradation and step gradient ethanol precipitation on Sargassum fusiforme polysaccharides: Physicochemical characterization and protective effects against intestinal epithelial injury.
Effects of UV/H2O2 degradation and step gradient ethanol precipitation on Sargassum fusiforme polysaccharides: Physicochemical characterization and protective effects against intestinal epithelial injury.
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DOI:
10.1016/j.foodres.2022.111093
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发表时间:
2022-03
影响因子:
8.1
通讯作者:
Wanzi Yao;Mengyuan Liu;Xiaoyong Chen;Lijun You;Yongxuan Ma;K. Hileuskaya
中科院分区:
文献类型:
--
作者:
Wanzi Yao;Mengyuan Liu;Xiaoyong Chen;Lijun You;Yongxuan Ma;K. Hileuskaya
In this study, the degraded purified fraction fromSargassum fusiformepolysaccharides (SFP), named DSFP, was produced by the treatment of ultraviolet/hydrogen peroxide (UV/H2O2) degradation and step gradient ethanol precipitation. Results showed that the treatment significantly reduced the molecular weight of polysaccharides, from 282.83 kDa to 18.54 kDa, and influenced their surface morphology and roughness. SFP and DSFP were typical sulfated polysaccharides, mainly composed of fucose, galacturonic acid, glucuronic acid, galactose, and mannose. Both SFP and DSFP increased cell migration during intestinal epithelial wound healing and stimulated the cell cycle progression by promoting the transition from G0/G1 to S phase in the rat intestine epithelium cells (IEC-6). But DSFP had a stronger positive effect on wound healing and cell migration than SFP. It reinforced the intestinal barrier function and attenuated lipopolysaccharides-induced intestinal inflammation. DSFP significantly downregulated the expression ofToll-like receptor 4,tumor necrosis factor-α,interleukin-6,interleukin-1β, andinducible nitric oxide synthaseby 53.14%, 92.41%, 66.01%, 68.24%, and 78.09%, respectively, and upregulated that ofinterleukin-10by 2.48 folds when compared to the model. Therefore, the treatment (UV/H2O2degradation and step gradient ethanol precipitation) could effectively improve the protective effects against intestinal epithelial injury.