Anti-inflammatory effects of orally administered glucosamine oligomer in an experimental model of inflammatory bowel disease

被引:67
作者
Azuma, Kazuo [1 ]
Osaki, Tomohiro [1 ]
Kurozumi, Seiji [2 ]
Kiyose, Masatoshi [2 ]
Tsuka, Takeshi [1 ]
Murahata, Yusuke [1 ]
Imagawa, Tomohiro [1 ]
Itoh, Norihiko [1 ]
Minami, Saburo [1 ]
Sato, Kimihiko [2 ]
Okamoto, Yoshiharu [1 ]
机构
[1] Tottori Univ, Sch Vet Med, Dept Vet Clin Med, Tottori 6808553, Japan
[2] Koyo Chem Co Ltd, Chiyoda Ku, Tokyo 1020072, Japan
关键词
Glucosamine oligomers; Inflammatory bowel disease; Anti-inflammatory; Functional food; Nuclear factor-kappa B; SODIUM-INDUCED COLITIS; NF-KAPPA-B; NITRIC-OXIDE; ULCERATIVE-COLITIS; CHITIN NANOFIBRILS; EPITHELIAL-CELLS; MECHANISMS; ANTITUMOR; MICE; CHITOOLIGOSACCHARIDES;
D O I
10.1016/j.carbpol.2014.09.012
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
Anti-inflammatory effects of oral administration of the glucosamine oligomers (chito-oligosaccharides: COS) were evaluated in an experimental model of inflammatory bowel disease (IBD). Oral administration of COS improved shortening of colon length and tissue injury (as assessed by histology) in mice. Oral administration of COS inhibited inflammation in the colonic mucosa by suppression of myeloperoxidase activation in inflammatory cells, as well as activation of nuclear factor-kappa B, cyclooxygenase-2, and inducible nitric oxide synthase. Oral administration of COS also reduced serum levels of pro-inflammatory cytokines (tumor necrosis factor-alpha and interleukin-6). Moreover, it prolonged survival time in mice. These data suggest that COS have anti-inflammatory effects in an experimental model of IBD, and could be new functional foods for IBD patients. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:448 / 456
页数:9
相关论文
共 38 条
[31]
Tokoro A., 1989, Biotherapy, V3, P51
[32]
Glucosamine Inhibits IL-1β-Mediated IL-8 Production in Prostate Cancer Cells by MAPK Attenuation [J].
Tsai, Cheng-Yen ;
Lee, Tzong-Shyuan ;
Kou, Yu Ru ;
Wu, Yuh-Lin .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2009, 108 (02) :489-498
[33]
Mechanisms of Probiotic Action: Implications for Therapeutic Applications in Inflammatory Bowel Diseases [J].
Vanderpool, Charles ;
Yan, Fang ;
Polk, D. Brent .
INFLAMMATORY BOWEL DISEASES, 2008, 14 (11) :1585-1596
[34]
Reclamation of chitinous materials by bromelain for the preparation of antitumor and antifungal materials [J].
Wang, San-Lang ;
Lin, Hue-Tin ;
Liang, Tzu-Wen ;
Chen, Yu-Jen ;
Yen, Yue-Horng ;
Guo, Shian-Pin .
BIORESOURCE TECHNOLOGY, 2008, 99 (10) :4386-4393
[35]
Chitosan oligosaccharides suppress production of nitric oxide in lipopolysaccharide-induced N9 murine microglial cells in vitro [J].
Wei, Peng ;
Ma, Pan ;
Xu, Qing-Song ;
Bai, Qun-Hua ;
Gu, Jian-Guo ;
Xi, Hao ;
Du, Yu-Guang ;
Yu, Chao .
GLYCOCONJUGATE JOURNAL, 2012, 29 (5-6) :285-295
[36]
Glucosamine regulation of LPS-mediated inflammation in human bronchial epithelial cells [J].
Wu, Yuh-Lin ;
Kou, Yu Ru ;
Ou, Hui-Ling ;
Chien, Han-Yun ;
Chuang, Kun-Han ;
Liu, Han-Hsun ;
Lee, Tzong-Shyuan ;
Tsai, Cheng-Yen ;
Lu, Meng-Lun .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2010, 635 (1-3) :219-226
[37]
Glucosamine, a naturally occurring amino monosaccharide, suppresses dextran sulfate sodium-induced colitis in rats [J].
Yomogida, Shin ;
Kojima, Yuko ;
Tsutsumi-Ishii, Yuko ;
Hua, Jian ;
Sakamoto, Koji ;
Nagaoka, Isao .
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE, 2008, 22 (03) :317-323
[38]
Chitosan oligosaccharide as potential therapy of inflammatory bowel disease: Therapeutic efficacy and possible mechanisms of action [J].
Yousef, Mohammad ;
Pichyangkura, Rath ;
Soodvilai, Sunhapas ;
Chatsudthipong, Varanuj ;
Muanprasat, Chatchai .
PHARMACOLOGICAL RESEARCH, 2012, 66 (01) :66-79