Carter C A, Milholland R J, Shea W, Ip M M
Cancer Res. 1983 Aug;43(8):3559-62.
The effect of the prostaglandin synthetase inhibitor indomethacin on the dietary fat enhancement of 7,12-dimethylbenz(a)anthracene-induced mammary tumorigenesis has been examined in female Sprague-Dawley rats. Rats were fed either a normal-fat or high-fat diet (5 or 18% corn oil, respectively) with or without 0.004% indomethacin, starting 3 days after a single intragastric intubation of 5 mg 7,12-dimethylbenz(a)anthracene. Results of this experiment demonstrated that indomethacin completely blocked the stimulatory effect of fat on tumorigenesis, as measured by a decreased tumor incidence, a decreased number of tumors per group, a decreased tumor size, and an increased latency. No effect of indomethacin was observed in rats fed the normal-fat diet. These data suggest that at least part of the stimulatory effect of polyunsaturated fat on 7,12-dimethylbenz(a)anthracene-induced mammary tumorigenesis may be mediated through an increased synthesis of prostaglandins.
在雌性斯普拉格-道利大鼠中,研究了前列腺素合成酶抑制剂吲哚美辛对饮食脂肪增强7,12-二甲基苯并(a)蒽诱导的乳腺肿瘤发生的影响。在单次胃内插管给予5mg 7,12-二甲基苯并(a)蒽3天后,给大鼠分别喂食含或不含0.004%吲哚美辛的正常脂肪或高脂肪饮食(分别为5%或18%玉米油)。该实验结果表明,通过降低肿瘤发生率、每组肿瘤数量、肿瘤大小以及延长潜伏期来衡量,吲哚美辛完全阻断了脂肪对肿瘤发生的刺激作用。在喂食正常脂肪饮食的大鼠中未观察到吲哚美辛的作用。这些数据表明,多不饱和脂肪对7,12-二甲基苯并(a)蒽诱导的乳腺肿瘤发生的刺激作用至少部分可能是通过前列腺素合成增加介导的。