Antioxidant effect of phospholipids on the oxidation of refined perilla oil (PO;α‐18:3, 54.5%; 16:0, 7.2%; 18:0, 2.6%; 18:1, 18.6%; 18:2, 15.5%), tocopherol‐free (POF) and tocopherol‐enriched (POR) perilla oil were investigated by measuring weight‐gains and by the oven test at 37°C. The oxidative stability of PO was especially increased by additions of phosphatidylethanolamine (PE) and phosphatidylserine (PS), but phosphatidylcholine (PC) scarcely showed an antioxidant effect. The oxidative stability of POF was markedly low, and none of the phospholipids (PC, PE, PS) showed an antioxidant effect on the oxidation of POF. The stability of POR was lower than that of PO regardless of its higher tocopherol contents. However, the oxidation of POR was significantly suppressed by additions of PE and PS, as was observed with PO. PC showed a small antioxidant effect on the oxidation of POR. Therefore, it seems that the antioxidant effects of phospholipids, especially of PE and PS, was due to the presence of tocopherols in the perilla oil.

The inhibitory effect of dietary perilla oil rich in the n‐3 polyunsaturated fatty acid α‐linolenic acid against colon carcinogenesis was investigated in rats. Four groups of 26 F344 rats each received an intrarectal dose of 2 mg of N‐methyl‐N‐nitrosourea 3 times a week for 2 weeks, and received a diet containing 12% perilla oil, 6% or 12% safflower oil (rich in the n‐6 polyunsaturated fatty acid linoleic acid), or 12% palm oil (rich in saturated and monounsaturated fatty acids). At week 35, the incidence of colon cancer was significantly lower in perilla oil‐fed rats than in other dietary groups; 19% vs. 46%, 56% and 58%. When examined at week 10, the concentration of fecal bile acids, known to be tumor promoters, was not significantly different among the dietary groups, and the intrarectal deoxycholic acid‐induced colonic mucosal ornithine decarboxylase activity, a marker of tumor promotion, was significantly lower in perilla oil‐fed group than in other groups. The serum and colonic mucosal fatty acid compositions and the blood plasma prostaglandin E2 level directly reflected the fatty acid composition of each dietary fat. The results suggest that the anti‐tumor‐promoting effect of dietary perilla oil was a result of a decreased sensitivity of colonic mucosa to tumor promoters arising from the altered fatty acid composition in membrane phospholipid of colonic epithelial cells, and was not a consequence of a decrease of promoters such as bile acids.

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