Protection of 4-hydroxybenzyl-chitooligomers against inflammatory responses in Chang liver cells

被引:12
作者
Mai Duy Luu Trinh [1 ]
Minh-Hiep Dinh
Ngo, Dai-Hung [2 ]
Dang-Khoa Tran [1 ]
Quoc-Tuan Tran [1 ]
Vo, Thanh-Sang [2 ]
Dai-Nghiep Ngo [1 ]
机构
[1] Vietnam Natl Univ Ho Chi Minh City, Univ Sci, Fac Biol, Dept Biochem, Ho Chi Minh City, Vietnam
[2] Pukyong Natl Univ, Specialized Grad Sch Sci & Technol Convergence, Dept Marinebio Convergence Sci, Pusan 608737, South Korea
关键词
Anti-inflammation; 4-Hydroxybenzyl-chitooligomers; Chang liver cells; iNOS; COX-2; NITRIC-OXIDE SYNTHASE; AMINOETHYL-CHITOOLIGOSACCHARIDES; CHITOSAN OLIGOSACCHARIDES; OXIDATIVE STRESS; INHIBIT; CYCLOOXYGENASE-2; EXPRESSION; PROTEIN;
D O I
10.1016/j.ijbiomac.2014.01.064
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The aim of this study was to investigate anti-inflammatory activity of 4-hydroxybenzyl-chitooligomers (HB-COS) in Chang liver cells stimulated by a cytokine mixture. It was revealed that HB-COS decreased the level of nitric oxide and prostaglandin E-2 (PGE(2)) production by diminishing the expressions of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) without significant cytotoxicity. Moreover, HB-COS exerted inhibitory effects on the production of pro-inflammatory mediator (interleukin-6) in Chang liver cells. Notably, HB-COS exhibited anti-inflammatory activities via blocking degradation of inhibitory kappa B alpha (I kappa B-alpha), translocation of nuclear factor kappa B (NF-kappa B), and phosphorylation of mitogen-activated protein kinases (MAPKs) in a dose-dependent manner. Collectively, these findings indicated that HB-COS possessed potential anti-inflammatory effects in Chang liver cells, and could be a useful therapeutic agent for the treatment of hepatic inflammatory diseases. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
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