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Research Communication

Consumption of Fish Oil Leads to Prompt Incorporation of Eicosapentaenoic Acid into Colonic Mucosa of Patients Prior to Surgery for Colorectal Cancer, But Has No Detectable Effect on Epithelial Cytokinetics¹

Institute of Food Research, Norwich Research Park, Colney, Norwich, NR4 7UA, United Kingdom, and Norfolk and Norwich Hospital, Brunswick Road, Norwich, NR1 3SR, United Kingdom

² To whom correspondence should be addressed.

Fish oil (FO) was previously reported to partially normalize colorectal crypt cell cytokinetics in patients with colorectal neoplasms. We determined the effect of FO on the fatty acid composition of colonic mucosa and mesenteric adipose tissue and on rectal crypt cell proliferation in patients undergoing surgery for colonic carcinoma. Patients (49—28 males; 21 females) were randomly assigned to consume FO capsules (2 g b.d.; FO group) containing 1.4 g eicosapentaenoic acid (EPA) and 1.0 g docosahexaenoic acid per day, or safflower oil capsules (2 g b.d.; placebo group) for an average of 12.3 ± 0.5 d prior to surgery. Rectal biopsies were obtained at entry, at surgery, and 8–12 wk postsurgery. Colonic biopsies and samples of mesenteric adipose tissue were analyzed for fatty acids by gas–liquid chromatography. Mitosis was determined in whole crypt mounts. The proportion of EPA (g/100 g total fatty acids) in mucosal lipids was significantly greater in FO patients compared to the placebo group, but there was no effect on mesenteric adipose tissue. However self-reported use of FO supplements prior to surgery was associated with higher levels of EPA in adipose tissue. There was no significant effect of FO on the frequency or spatial distribution of crypt cell mitosis. EPA from marine oil supplements is rapidly incorporated into the colonic mucosal lipids of humans, but the levels achieved in the present study did not modify colorectal cytokinetics.

KEY WORDS: • fish oil • lipids • colon • crypt • cancer • proliferation • humans

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