Protective effect of polysaccharides from Sargassum fusiforme against UVB-induced oxidative stress in HaCaT human keratinocytes
•A polysaccharide fraction (SFP-P1) was purified from Sargassum fusiform.•The composition and structural characteristics of SFP-P1 were investigated.•SFP-P1 increased the activities of SOD, GSH-PX and decreased the level of ROS.•SFP-P1 suppressed the UVB-induced expression of MMP-1 and MMP-9. In thi...
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Published in | Journal of functional foods Vol. 36; pp. 332 - 340 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Ltd
01.09.2017
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | •A polysaccharide fraction (SFP-P1) was purified from Sargassum fusiform.•The composition and structural characteristics of SFP-P1 were investigated.•SFP-P1 increased the activities of SOD, GSH-PX and decreased the level of ROS.•SFP-P1 suppressed the UVB-induced expression of MMP-1 and MMP-9.
In this study, Sargassum fusiforme polysaccharide was purified using a DEAE-Sepharose fast-flow column to obtain Sargassum fusiforme polysaccharides fraction (SFP-P1). As expected, the SFP-P1 contains mainly carbohydrates (87%) with less than 1% protein. Within the carbohydrate, it contains about 10% sulfate and 18% uronic acids. SFP-P1 consisted of l-fucose (13.17%), galactose (4.28%), glucose (1.95%), xylose (5.50%), and mannose (75.10%) with an average molecular weight of 113kDa. Mannose and l-fucose were two predominant monosaccharides. In addition, (1→)-linked or (1→6)-linked, (1→2)-linked or (1→4)-linked and (1→3)-linked glycosyl linkages accounted for 1.62%, 60.69% and 37.69% of all linkages in the molecule, respectively. The glycosidic linkage types of SFP-P1 were proven to be→3,6)-α-d-Manp(1→,→4)-α-d-GalAp(1→,→4)-β-d-Xylp(1→and→3,4)-α-d-GlcAp(1→. The results indicated the SFP-P1 had cytoprotective activity against UVB-induced oxidative stress in HaCaT cells through stimulation of SOD, GSH-PX enzymes activities and ROS. Also SFP-P1 suppressed the UVB-induced expression of MMP-1 & MMP-9. |
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ISSN: | 1756-4646 2214-9414 |
DOI: | 10.1016/j.jff.2017.06.051 |