Octacosanol Attenuates Inflammation in Both RAW264.7 Macrophages and a Mouse Model of Colitis

被引:169
作者
Guo, Tianyi [1 ]
Lin, Qinlu [1 ]
Li, Xinhua [2 ]
Nie, Ying [1 ]
Wang, Long [1 ]
Shi, Limin [1 ]
Xu, Wei [1 ]
Hu, Tao [1 ]
Guo, Ting [1 ]
Luo, Feijun [1 ]
机构
[1] Cent South Univ Forestry & Technol, Coll Food Sci & Engn, Natl Engn Lab Rice & Byprod, Lab Mol Nutr, Changsha 410004, Hunan, Peoples R China
[2] Cent S Univ, Xiangya Hosp, Dept Gastroenterol, Changsha 410008, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
octacosanol; colitis; inflammation factor; MAPK; NF-kappa B; AP-1; NF-KAPPA-B; CHRONIC ULCERATIVE-COLITIS; ACID-INDUCED COLITIS; BOWEL-DISEASE; NITRIC-OXIDE; OXIDATIVE STRESS; MOLECULAR-BASIS; CROHNS-DISEASE; P38; MAPK; MICE;
D O I
10.1021/acs.jafc.6b05465
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Octacosanol has multiple biological functions. In this study, the anti-inflammatory effect and molecular mechanism of octacosanol were evaluated by using dextran sulfate sodium (DSS)-induced ulcerative colitis model in mice and lipopolysaccharide (LPS)-stimulated mouse macrophage RAW264.7 cells. The colitis mouse model was induced by 3.0% DSS in 8-week ICR mice and octacosanol orally administered with 100 mg/kg/day. The results showed that octacosanol significantly improved the health status of mice and reduced DSS-induced pathological damage in the colonic tissues. Octacosanol obviously inhibited the mRNA and protein expression levels of pro-inflammatory factors of colonic tissues. In vitro, octacosanol administration significantly reduced the expression of mRNA or protein of pro-inflammatory cytokines and the phosphorylation of c-Jun N-terminal kinase and p38, and it also partly prevented LPS-induced translocations of NF-kappa B and AP-1. Octacosanol has anti-inflammatory effect, and its molecular mechanism may be involved in downregulating the expression of inflammatory factors and blocking of MAPK/NF-KB/AP-1 signaling pathway.
引用
收藏
页码:3647 / 3658
页数:12
相关论文
共 51 条
[1]   iNOS-mediated nitric oxide production and its regulation [J].
Aktan, F .
LIFE SCIENCES, 2004, 75 (06) :639-653
[2]   A 12-MONTH STUDY OF POLICOSANOL ORAL TOXICITY IN SPRAGUE-DAWLEY RATS [J].
ALEMAN, CL ;
MAS, R ;
HERNANDEZ, C ;
RODEIRO, I ;
CEREJIDO, E ;
NOA, M ;
CAPOTE, A ;
MENENDEZ, R ;
AMOR, A ;
FRAGA, V ;
SOTOLONGO, V ;
JIMENEZ, S .
TOXICOLOGY LETTERS, 1994, 70 (01) :77-87
[3]   Activation of AMP-kinase by Policosanol Requires Peroxisomal Metabolism [J].
Banerjee, Subhashis ;
Ghoshal, Sarbani ;
Porter, Todd D. .
LIPIDS, 2011, 46 (04) :311-321
[4]   Conventional drug therapy for inflammatory bowel disease [J].
Bryant, Robert V. ;
Brain, Oliver ;
Travis, Simon P. L. .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2015, 50 (01) :90-112
[5]   Gamma-irradiated resveratrol negatively regulates LPS-induced MAPK and NF-κB signaling through TLR4 in macrophages [J].
Byun, Eui-Baek ;
Sung, Nak-Yun ;
Park, Jae-Nam ;
Yang, Mi-So ;
Park, Sang-Hyun ;
Byun, Eui-Hong .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2015, 25 (02) :249-259
[6]   Macrophage-mediated inflammation in metabolic disease [J].
Chawla, Ajay ;
Nguyen, Khoa D. ;
Goh, Y. P. Sharon .
NATURE REVIEWS IMMUNOLOGY, 2011, 11 (11) :738-749
[7]  
Chen Fang Chen Fang, 2006, Acta Nutrimenta Sinica, V28, P269
[8]   Anti-inflammatory effects of Huangqin tang extract in mice on ulcerative colitis [J].
Chen, Peidong ;
Zhou, Xi ;
Zhang, Li ;
Shan, Mingqiu ;
Bao, Beihua ;
Cao, Yudan ;
Kang, An ;
Ding, Anwei .
JOURNAL OF ETHNOPHARMACOLOGY, 2015, 162 :207-214
[9]   Germinated brown rice and its bio-functional compounds [J].
Cho, Dong-Hwa ;
Lim, Seung-Taik .
FOOD CHEMISTRY, 2016, 196 :259-271
[10]   Signal transduction pathways involving p38 MAPK, JNK, NFκB and AP-1 influences the response of chondrocytes cultured in agarose constructs to IL-1β and dynamic compression [J].
Chowdhury, T. T. ;
Salter, D. M. ;
Bader, D. L. ;
Lee, D. A. .
INFLAMMATION RESEARCH, 2008, 57 (07) :306-313