Enteral diets enriched with medium-chain triglycerides and N-3 fatty acids prevent chemically induced experimental colitis in rats

被引:35
作者
Kono, Hiroshi [1 ]
Fujii, Hideki [1 ]
Ogiku, Masahito [1 ]
Tsuchiya, Masato [1 ]
Ishii, Kenichi [1 ]
Hara, Michio [1 ]
机构
[1] Univ Yamanashi, Dept Surg 1, Fac Med, Yamanashi 4093898, Japan
关键词
INFLAMMATORY-BOWEL-DISEASE; CROHNS-DISEASE; TNF-ALPHA; NUTRITION; ENDOTOXIN; LIVER; MANAGEMENT; CYTOKINES; DIAGNOSIS; ENTERITIS;
D O I
10.1016/j.trsl.2010.07.012
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The specific purpose of this study was to evaluate the significant effects of medium-chain triglycerides (MCTs) and N-3 fatty acids on chemically induced experimental colitis induced by 2,4,6-trinitrobenzene sulphonic acid (TNBS) in rats. Male Wistar rats were fed liquid diets enriched with N-6 fatty acid (control diets), N-3 fatty acid (MCT-diets), and N-3 fatty acid and MCT (MCT+ diets) for 2 weeks and then were given an intracolonic injection of TNBS. Serum and tissue samples were collected 5 days after ethanol or TNBS enema. The severity of colitis was evaluated pathologically, and tissue myeloperoxidase activity was measured in colonic tissues. Furthermore, protein levels for inflammatory cytokines and a chemokine were assessed by an enzyme-linked immunosorbent assay in colonic tissues. Induction of proinflammatory cytokines tumor necrosis factor-a and interleukin-1 beta in the colon by TNBS enema was markedly attenuated by the MCT+ diet among the 3 diets studied. Furthermore, the induction of chemokines macrophage inflammatory protein-2 and monocyte chemotactic protein-1 also was blunted significantly in animals fed the MCT+ diets. As a result, MPO activities in the colonic tissue also were blunted significantly in animals fed the MCT+ diets compared with those fed the control diets or the MCT - diets. Furthermore, the MCT+ diet improved chemically induced colitis significantly among the 3 diets studied. Diets enriched with both MCTs and N-3 fatty acids may be effective for the therapy of inflammatory bowel disease as antiinflammatory immunomodulating nutrients. (Translational Research 2010;156:282-291)
引用
收藏
页码:282 / 291
页数:10
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