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Carcinogenicity of Captafol in F344/DuCrj Rats

机译:卡他福在F344 / DuCrj大鼠中的致癌性

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摘要

Captafol was administered at dietary levels of 0 (control), 750 and 1,500 parts per million (ppm) to groups of 50 male and 50 female F344/DuCrj rats for 104 weeks, and then all animals were maintained without captafol for a further 8 weeks, and killed in week 113. Renal cell carcinoma was found in eight of 50 male rats treated with 1,500 ppm and in one of 50 male rats treated with 750 ppm of captafol. The incidences of renal adenomas, including micro‐adenomas, and basophilic altered cell tubules were significantly higher in both sexes treated with captafol than in controls, and the increases were apparently dose‐dependent except that of adenomas in females. The incidences of neoplastic and preneoplastic lesions of the kidney in captafol‐treated animals were higher in males than in females. Captafol also induced hepatocellular carcinomas in four of 50 female rats in the 1,500 ppm group. The incidences of hyperplastic (neoplastic) nodules and foci of cellular alterations in the liver were also significantly increased in both sexes treated with captafol, the increases being dose‐dependent. In conclusion, captafol induced renal cell carcinomas in male rats and hepatocellular carcinomas in female rats.
机译:分别向50只雄性和50只雌性F344 / DuCrj大鼠的组中以饮食水平0(对照组),750和百万分之1500和百万分之1500施用卡他福,持续104周,然后将所有动物在无卡他酚的情况下再维持8周,并在第113周被杀死。在用1500 ppm处理的50只雄性大鼠中有8只在用750 ppm卡他氟治疗的50只雄性大鼠中有1只发现了肾细胞癌。卡他福治疗的两性患者的肾腺瘤(包括微腺瘤和嗜碱细胞改变的肾小管)的发生率均显着高于对照组,并且除雌性腺瘤外,明显与剂量有关。经卡他福治疗的动物中,肾脏的肿瘤性和肿瘤性病变的发生率在雄性中高于雌性。 Captafol还在1,500 ppm组的50只雌性大鼠中的4只中诱发了肝细胞癌。在使用卡他福治疗的两性中,增生性(瘤性)结节的发生率和肝脏细胞改变的发生率也显着增加,增加是剂量依赖性的。综上所述,卡他福诱导雄性大鼠的肾细胞癌和雌性大鼠的肝细胞癌。

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