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首页> 外文期刊>The Journal of Reproduction and Development >Differential expression of 3 beta -hydroxysteroid dehydrogenase mRNA in rat testes exposed to endocrine disruptors.
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Differential expression of 3 beta -hydroxysteroid dehydrogenase mRNA in rat testes exposed to endocrine disruptors.

机译:3β-羟类固醇脱氢酶mRNA在暴露于内分泌干扰物的大鼠睾丸中的差异表达。

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摘要

Expression of 3 beta -hydroxysteroid dehydrogenase (3 beta -HSD) is mainly found in the Leydig cells from which steroid hormones are biosynthesized in the testes. To investigate whether endocrine disruptors affect the microenvironment of the testes, the mRNA expression of 3 beta -HSD as a molecular marker for androgen biosynthesis was analysed in rat testes exposed to several endocrine disruptors using a reverse transcription-polymerase chain reaction technique. Testosterone [50, 200 and 1000 micro g/kg body weight (BW)], flutamide (1, 5 and 25 mg/kg BW), ketoconazole (0.2, 1, 5 and 25 mg/kg BW), diethylhexyl phthalate (10, 50 and 250 mg/kg BW), nonylphenol (10, 50, 100 and 250 mg/kg BW), octylphenol (10, 50 and 250 mg/kg BW), and diethylstilbestrol (10, 20 and 40 micro g/kg BW) were orally administered to 4-week-old Sprague-Dawley rats for 3 weeks daily. Although testosterone at a low dose (50 micro g/kg/day) increased the expression of 3 beta -HSD mRNA, it was significantly decreased in the rats treated with 200 or 1000 micro g/kg/day testosterone compared with the control group (P<0.05). Furthermore, ketoconazole, diethylhexyl phthalate, nonylphenol, octylphenol and diethylstilbestrol caused significant downregulation of 3 beta -HSD mRNA in the testes at all doses (P<0.05). However, flutamide remarkably increased the level of 3 beta -HSD mRNA in the testes (P<0.05). These results suggest that endocrine disruptors may influence androgen biosynthesis in the testes by alteration of 3 beta -HSD mRNA expression..
机译:3β-羟基类固醇脱氢酶(3β-HSD)的表达主要存在于Leydig细胞中,在睾丸中生物合成了类固醇激素。为了研究内分泌干扰物是否影响睾丸的微环境,使用逆转录-聚合酶链反应技术分析了暴露于数种内分泌干扰物的大鼠睾丸中3β-HSD的mRNA表达,作为雄激素生物合成的分子标记。睾丸激素[50、200和1000 micro g / kg体重(BW)],氟他酰胺(1、5和25 mg / kg BW),酮康唑(0.2、1、5和25 mg / kg BW),邻苯二甲酸二乙基己酯(10 ,50和250 mg / kg体重,壬基酚(10、50、100和250 mg / kg体重),辛基苯酚(10、50和250 mg / kg体重)和己烯雌酚(10、20和40 micro g / kg将BW)口服给予4周大的Sprague-Dawley大鼠,每天3周。尽管低剂量(50 micro g / kg / day)的睾丸激素可增加3 beta -HSD mRNA的表达,但与对照组相比,在200或1000 micro g / kg / day的睾丸激素治疗的大鼠中,睾丸激素的表达显着降低( P <0.05)。此外,在所有剂量下,酮康唑,邻苯二甲酸二乙基己酯,壬基酚,辛基酚和己烯雌酚引起睾丸中3β-HSD mRNA的显着下调(P <0.05)。然而,氟他胺显着增加了睾丸中3β-HSD mRNA的水平(P <0.05)。这些结果表明,内分泌干扰物可能通过改变3β-HSD mRNA表达来影响睾丸中雄激素的生物合成。

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