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The carcinogenicity of polycyclic hydrocarbon epoxides in newborn mice

机译:多环烃环氧化物对新生小鼠的致癌性

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Benz(a)anthracene injected subcutaneously during the first 3 days of life caused a dose related increase in the incidence of liver and lung tumours in Swiss mice but over a similar dose range, the K region epoxide of benz(a)anthracene was less effective. Neonatally injected 7-methylbenz(a) was considerably more active than its K region epoxide in increasing the incidence of liver tumours in males. Both the parent compound and the epoxide slightly raised the incidence of lung tumours. Both chrysene and its K region epoxide increased liver tumour incidence but not lung tumour incidence. The K region epoxides of dibenz(a,h)-anthracene and 3-methylcholanthrene were without apparent effect on the incidence of liver, lung or other tumours despite indications from previously reported studies that the parent hydrocarbons are active at the same dose levels. The K region epoxide of phenanthrene had no effect on the incidence of any kind of neoplasm.
机译:在生命的前3天皮下注射苯并(a)蒽引起剂量相关的瑞士小鼠肝脏和肺部肿瘤的发生率增加,但在相似的剂量范围内,苯并(a)蒽的K区环氧化物的疗效较差。新生儿注射的7-甲基苯并(a)在增加男性肝脏肿瘤发生率方面比其K区环氧化物更具活性。母体化合物和环氧化物都略微增加了肺肿瘤的发生率。 ry及其K区环氧化物均会增加肝肿瘤的发生率,但不会增加肺肿瘤的发生率。尽管先前报道的研究表明母体烃在相同剂量水平下具有活性,但联苯(a,h)-蒽和3-甲基胆碱的K区环氧化物对肝,肺或其他肿瘤的发生率没有明显影响。菲的K区环氧对任何种类的肿瘤的发生率都没有影响。

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