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Prevention of H2O2-induced oxidative stress in Chang liver cells by 4-hydroxybenzyl-chitooligomers
•Intracellular free radicals scavenging activities of 4-hydroxybenzyl-chitooligomers (HB-COS) were determined in Chang liver cells.•HB-COS exerted protective effects against reactive oxygen species and DNA oxidation.•HB-COS increased the gene and protein expressions of intracellular antioxidant enzy...
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Published in: | Carbohydrate polymers 2014-03, Vol.103, p.502-509 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •Intracellular free radicals scavenging activities of 4-hydroxybenzyl-chitooligomers (HB-COS) were determined in Chang liver cells.•HB-COS exerted protective effects against reactive oxygen species and DNA oxidation.•HB-COS increased the gene and protein expressions of intracellular antioxidant enzymes.•Antioxidant effects are due to suppression of NF-κB signaling pathway.•Collectively, HB-COS can be used as a free radicals scavenger in cellular system.
In this study, a bioactive derivative of chitooligomers (1.0–3.0kDa), 4-hydroxybenzyl-COS (HB-COS), was synthesized to enhance antioxidant activity. Hence, HB-COS was evaluated for its capabilities against H2O2-induced oxidative stress in human Chang liver cells. It was found that HB-COS possessed the free radical scavenging activity via decreasing the intracellular reactive oxygen species production. Furthermore, HB-COS significantly reduced the oxidation of DNA in a dose-dependent manner. Notably, HB-COS treatment upregulated the gene and protein expressions of antioxidative enzymes and thereby enhancing the intracellular antioxidant mechanisms. In addition, HB-COS treatment caused a remarkable blockade on degradation of inhibitory kappa B alpha (IκB-α) protein and translocation of nuclear factor kappa B (NF-κB). The current study demonstrated that HB-COS effectively attenuated hydrogen peroxide-induced oxidative stress in Chang liver cells by increasing levels of antioxidant enzymes and inhibiting reactive oxygen species generation, DNA oxidation and the NF-κB signaling pathway. |
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ISSN: | 0144-8617 1879-1344 |
DOI: | 10.1016/j.carbpol.2013.12.061 |