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Chemoprevention by Pravastatin a 3‐Hydroxy‐3‐methylglutaryl‐coenzyme A Reductase Inhibitor of N‐Methyl‐N‐nitrosourea‐induced Colon Carcinogenesis in F344 Rats

机译:N-甲基-N-亚硝基脲诱导的F344大鼠中3-羟-3-甲基戊二酰辅酶A还原酶抑制剂普伐他汀的化学预防

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摘要

A potential chemopreventive action of pravastatin (Pr), a 3‐hydroxy‐3‐methylglutaryl‐coenzyme A redutase inhibitor, on colon carcinogenesis was evaluated in F344 rats. All rats at 7 weeks of age received an intrarectal dose of 2 mg of N‐methyl‐N‐nitrosourea 3 times weekly for 2 weeks in experiment I (2 groups of 16 rats each), and for 3 weeks in experiment II (4 groups of 30 rats each). They were given drinking water containing 0 ppm (control) or 200 ppm Pr during weeks 1 to 40 in experiment I, and containing 0 ppm (control), 25 ppm, 5 ppm and 1 ppm Pr during weeks 4 to 40 in experiment II. The body weight gains, and food and water intakes were similar in all the groups. The incidence of colon carcinomas at termination of the experiment at week 40 was not different in the 200 ppm Pr and control groups in experiment I (63% vs. 69%), while it was significantly lower in the 25 ppm and 5 ppm groups, but not in the 1 ppm Pr group, compared with the control group in experiment II (50%, 48%, and 77% vs. 80%). This inhibitory effect of Pr against colon carcinogenesis was not related to the cholesterol‐lowering effect of this agent. We postulate that Pr inhibits the promotion stage of colon carcinogenesis, perhaps through modulation of cholesterol synthesis in situ in the colonic mucosa, thereby suppressing farnesyl isoprenylation of growth‐regulating proteins such as p21 ras.
机译:在F344大鼠中评估了普伐他汀(Pr)(3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂)对结肠癌发生的潜在化学预防作用。在实验I中,所有7周大的大鼠每周3次接受直肠内剂量的N-甲基-N-亚硝基脲2 mg,共2周(实验组2组,每组16只大鼠),实验II的3周(4组)每只30只老鼠)。在实验I的第1至40周期间,给他们喝含0 ppm(对照)或200 ppm Pr的饮用水,在实验II的第4至40周期间,给它们含0 ppm(对照),25 ppm,5 ppm和1 ppm Pr的饮用水。在所有组中,体重增加,食物和水的摄入量相似。实验第40周时,实验结束时结肠癌的发生率在实验第一组的200 ppm Pr和对照组中没有差异(63%对69%),而在25 ppm和5 ppm组中则​​明显更低。而不是1 ppm Pr组,与实验II中的对照组相比(50%,48%和77%对80%)。 Pr对结肠癌的抑制作用与该药的降胆固醇作用无关。我们推测,Pr可能通过调节结肠粘膜中原位胆固醇的合成来抑制结肠癌发生的促进阶段,从而抑制了生长调节蛋白(例如p21 ras)的法呢基异戊二烯化。

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