Modifying effect of tuna orbital oil rich in docosahexaenoic acid and vitamin D-3 on azoxymethane-induced colonic aberrant crypt foci in rats

Citation
H. Kohno et al., Modifying effect of tuna orbital oil rich in docosahexaenoic acid and vitamin D-3 on azoxymethane-induced colonic aberrant crypt foci in rats, ONCOL REP, 7(5), 2000, pp. 1069-1074
Citations number
47
Categorie Soggetti
Oncology
Journal title
ONCOLOGY REPORTS
ISSN journal
1021335X → ACNP
Volume
7
Issue
5
Year of publication
2000
Pages
1069 - 1074
Database
ISI
SICI code
1021-335X(200009/10)7:5<1069:MEOTOO>2.0.ZU;2-T
Abstract
The modifying effect of dietary tuna (Thunnus thynnus orientalis) orbital o il rich in docosahexaenoic acid (DHA) and vitamin D-3 (VD3) on the developm ent of azoxymethane (AOM)-induced colonic aberrant crypt foci (ACF) was inv estigated in male F344 rats. Animals were given three weekly subcutaneous i njections of AOM (15 mg/kg body weight) to induce ACF. The rats were fed th e experimental diet containing 5% tuna orbital oil (low fish oil), 23.5% tu na orbital oil (high fish oil), 5% corn oil (low corn oil) or 23.5% corn oi l (high corn oil) for 5 weeks, starting 1 week before the first dose of AOM . Animals were sacrificed 2 weeks after the last AOM injection to count col onic ACF and assay the expression of cyclooxygenase (COX)-1 and -2. High co rn oil diet significantly increased the development of ACF, when compared w ith low corn oil diet (P<0.005). High fish oil diet also increased ACF form ation compared with low fish oil diet (P<0.01), but the increase was smalle r than high corn oil diet. The frequency of ACF was significantly lower in the rats fed high fish oil diet than high corn oil diet (P<0.02). Moreover, frequency of ACF consisted of 4 or more crypts in rats fed the high fish o il diet was significantly lower than that of rats given high corn oil diet. COX-1 and COX-2 expression did not significantly differ among the groups. These results suggest that fish oil derived from tuna, which contains high amounts of DHA and VD3, suppresses the formation and growth of ACF without affecting COX-1 and COX-2 expression, and may have a preventive effect on c olon carcinogenesis.