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J Nutr. 2002 Jan;132(1):11-9.  

 

Dietary polyunsaturated fatty acids improve histological and biochemical

alterations in rats with experimental ulcerative colitis.

 

Nieto N, Torres MI, Rios A, Gil A.
 

Department of Biochemistry and Molecular Biology, University of Granada, 18071

Granada, Spain.

 

The aim of the present study was to determine whether dietary intake of

monounsaturated (MUFA) and/or polyunsaturated fatty acids (PUFA) of the (n- 3)

and (n-6) series could improve intestinal damage and reduce inflammation in

experimental ulcerative colitis (UC). Rats were treated with 80 mg/kg body of

2,4,6-trinitrobenzenesulfonic acid and fed for 1 or 2 wk diets enriched in olive

oil (OO), fish oil (FO), or purified pig brain phospholipids (BPL), as sources

of monounsaturated and PUFA of the (n-3) and (n-3) + (n-6) series. Evaluation of

macroscopic and microscopic colonic damage was assessed. Ultrastructural and

histologic changes were analyzed as well as plasma and colonic mucosa fatty acid

profiles and some biochemical markers of injury and inflammation [alkaline

phosphatase (AP), mieloperoxidase (MPO), prostaglandin E(2) (PGE(2)) and

leukotriene B(4)]. Fatty acid profiles of both plasma and mucosa mostly

reflected the dietary fatty acid composition. Plasma MUFA proportions were

higher in UC animals fed the OO diet compared with FO or BPL groups 1 and 2 wk

and (n-3) long chain PUFA (LC-PUFA) were higher in the FO than in the OO and BPL

groups. At 1 wk, UC led to lower MUFA mucosa levels and (n-3)LC-PUFA were higher

in the FO group compared with the OO and BPL groups. Rats with UC fed FO at 1 wk

showed significantly less macroscopic and microscopic colonic damage. They also

have lower AP and MPO activities and PGE(2) levels compared with the OO and BPL

groups and showed enhanced histological repair, less necrotic areas within the

mucosa, and more goblet cells with mature mucin granules. These results suggest

that the use of balanced diets containing (n-3) LC-PUFA could ameliorate the

inflammation and mucosal damage in UC.