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Studies on the hepatoprotective effect of fucoidans from brown algae Kjellmaniella crassifolia

•The fucoidan content from brown algae Kjellmaniella crassifolia was about 3.3 times of that from Saccharina japonica.•The structural characteristics, including sulfate and fucose contents, correlated with their hepatoprotective effects.•There was a positive correlation between dose and efficacy.•Th...

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Bibliographic Details
Published in:Carbohydrate polymers 2018-08, Vol.193, p.298-306
Main Authors: Liu, Shu, Wang, Qiukuan, Song, Yuefan, He, Yunhai, Ren, Dandan, Cong, Haihua, Wu, Long
Format: Article
Language:English
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Summary:•The fucoidan content from brown algae Kjellmaniella crassifolia was about 3.3 times of that from Saccharina japonica.•The structural characteristics, including sulfate and fucose contents, correlated with their hepatoprotective effects.•There was a positive correlation between dose and efficacy.•The fucoidans of K. crassifolia have the potential as ingredients for functional food for protecting liver damage. For illustrating the relation of different structural characteristics correlated with the hepatoprotective effect, studies of fucoidan from algae Kjellmaniella crassifolia, a brown alga distributed in north Japan, were carried out. The fucoidan fractions of K. crassifolia were extracted, separated, and purified using a combinatorial procedure consisting of enzymolysis, ethanol precipitation, DEAE and size-exclusion chromatographies. The fundamental characteristics of the four enriched fucoidan fractions (KF1-KF4), including their sulphate content and monosaccharide composition, were investigated. The fucose was the main composition of monosaccharide for KF1-KF4, that of KF4 was up to 91.4%. The Glu-UA was the special composition of monosaccharide. FTIR and NMR spectroscopy were employed to elucidate the structural features of all fractions which further illustrated that fucose was the main monosaccharide. It was found all the four fractions showed antioxidative activity against hydroxyl radical and had the bioactive effects on CCl4-induced liver injury.
ISSN:0144-8617
1879-1344
DOI:10.1016/j.carbpol.2018.03.077