Abstract | BACKGROUND: Galacto- oligosaccharides potentially attenuate colonic inflammation by two mechanisms: through beneficial effects on intestinal microflora and by increasing the colonic short-chain fatty acid concentration. The purpose of this study was to investigate the effects of galacto- oligosaccharides on the development of inflammation and on the growth of bifidobacteria in trinitrobenzene sulphonic acid (TNBS)-induced colitis, a model that has been shown to benefit from short-chain fatty acid administration and to be associated with alterations in the colonic microflora. METHODS: Rats were given daily either whey-derived or lactose-derived galacto- oligosaccharides (4 g kg(-1) day(-1), p.o.); starting 10 days before colitis induction, or dexamethasone (2 mg kg(-1) day(-1), s.c., a positive control), starting at colitis induction. Colon wet weight, macroscopic damage and myeloperoxidase activity were assessed 72 h after the induction of colitis. Faecal bifidobacteria were counted at the beginning of the study, and immediately before and 72 h after colitis induction. RESULTS: CONCLUSIONS:
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Authors | R Holma, P Juvonen, M Z Asmawi, H Vapaatalo, R Korpela |
Journal | Scandinavian journal of gastroenterology
(Scand J Gastroenterol)
Vol. 37
Issue 9
Pg. 1042-7
(Sep 2002)
ISSN: 0036-5521 [Print] England |
PMID | 12374229
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Galactans
- Glucocorticoids
- Oligosaccharides
- Dexamethasone
- Trinitrobenzenesulfonic Acid
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Topics |
- Animals
- Bifidobacterium
(physiology)
- Body Weight
- Colitis
(chemically induced, microbiology, prevention & control)
- Colon
(drug effects, microbiology)
- Colony Count, Microbial
- Dexamethasone
(administration & dosage)
- Galactans
(administration & dosage)
- Glucocorticoids
(administration & dosage)
- Intestinal Mucosa
(drug effects, microbiology)
- Male
- Models, Animal
- Oligosaccharides
(administration & dosage)
- Rats
- Trinitrobenzenesulfonic Acid
(toxicity)
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