雌性大鼠肝微粒体体外合成16α-羟孕酮及其在乳腺癌发病中的可能作用

C.J.M. Arts , J.W.G.M. Wilmer , A.Th.H.J. De Bie , H. Van Den Berg
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引用次数: 4

摘要

雌性大鼠菌株(Sprague-Dawley, Wistar和Fisher)的肝脏匀浆在NADPH再生培养基中孵育,存在标记和未标记的雌酮。以雄性大鼠和雌性小鼠肝微粒体为阳性对照。采用高效液相色谱法和纸层析法,在实验条件下发现雌性大鼠肝脏匀浆能够将雌酮转化为16α-羟孕酮等多种代谢物。在以16α-羟雄酮为试验物质的致突变性试验(Ames试验)中,5株被试菌株中TA98和ta1538两株的his+瘤体数量较对照增加了2 ~ 3倍。在所使用的试验中,雌酮没有引起任何突变。由此可见,雌性大鼠能够体外合成16α-羟孕酮。这种化合物是否是乳腺癌的危险因素尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro synthesis of 16α-hydroxyestrone by female rat liver microsomes: Its possible role in the etiology of breast cancer

Liver homogenates from female rat strains (Sprague-Dawley, Wistar and Fisher) were incubated in a NADPH regenerating medium in the presence of labelled and unlabelled estrone. Liver microsomes isolated from male rats and female mice were used as positive controls. Using HPLC and paper chromatography, under the experimental conditions used it was found that liver homogenates from female rats were able to convert estrone to various metabolites such as 16α-hydroxyestrone. In a mutagenicity assay (Ames test), with 16α-hydroxyestrone as test substance, two strains (TA98 and TA 1538) of the five strains tested showed a 2–3-fold increase in the number of his+ revenants relative to the control values. Estrone did not cause any mutagens in the test used.

It is concluded that female rats are able to synthesize 16α-hydroxyestrone in vitro. Whether this compound is risk factor for breast cancer remains unclear.

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