Dietary fiber down-regulates colonic tumor necrosis factor α and nitric oxide production in trinitrobenzenesulfonic acid-induced colitic rats

被引:98
作者
Rodríguez-Cabezas, ME
Gálvez, J [1 ]
Lorente, MD
Concha, A
Camuesco, D
Azzouz, S
Osuna, A
Redondo, L
Zarzuelo, A
机构
[1] Univ Granada, Dept Pharmacol, Sch Pharm, E-18071 Granada, Spain
[2] Univ Granada, Sch Sci, Dept Parasitol, E-18071 Granada, Spain
[3] Hosp Univ Virgen de las Nieves, Dept Pathol, Granada, Spain
[4] Madaus Labs SA, Barcelona, Spain
关键词
dietary fiber; rat colitis; tumor necrosis factor; nitric oxide synthase; short chain fatty acids;
D O I
10.1093/jn/132.11.3263
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Previous studies have revealed the beneficial effects exerted by dietary fiber in human inflammatory bowel disease, which were associated with an increased production of SCFA in distal colon. The aim of the present study was to elucidate the probable mechanisms involved in the beneficial effects of a fiber-supplemented diet (5% Plantago ovata seeds) in the trinitrobenzenesulfonic acid (TNBS) model of rat colitis, with special attention to its effects on the production of some of the mediators involved in the inflammatory response, such as tumor necrosis factor alpha (TNFalpha) and nitric oxide (NO). Rats were fed the fiber-supplemented diet for 2 wk before TNBS colitis induction and thereafter until colonic evaluation 1 wk later. The results obtained showed that dietary fiber supplementation facilitated recovery from intestinal insult as evidenced both histologically, by a preservation of intestinal cytoarchitecture, and biochemically, by a significant reduction in colonic myeloperoxidase activity and by restoration of colonic glutathione levels. This intestinal anti-inflammatory effect was associated with lower TNFa levels and lower NO synthase activity in the inflamed colon, showing significant differences when compared with nontreated colitic rats. Moreover, the intestinal contents from fiber-treated colitic rats showed a significantly higher production of SCFA, mainly butyrate and propionate. We conclude that the increased production of these SCFA may contribute to recovery of damaged colonic mucosa because they constitute substrates for the colonocyte and, additionally, that they can inhibit the production of proinflammatory mediators, such as TNFalpha and NO.
引用
收藏
页码:3263 / 3271
页数:9
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