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Letrozole increases ovarian growth and Cyp17a1 gene expression in the rat ovary

机译:来曲唑增强大鼠卵巢的卵巢生长和Cyp17a1基因表达

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Objective: To evaluate the effects of letrozole on ovarian size and steroidogenesis in vivo, as well as on proliferation and steroidogenesis of theca-interstitial cells alone and in coculture with granulosa cells using an in vitro model. Design: In vivo and in vitro studies. Setting: Research laboratory. Animal(s): Immature Sprague-Dawley female rats. Intervention(s): In vivo effects of letrozole were studied in intact rats receiving either letrozole (90-day continuous-release SC pellets, 400 ??g/d) or placebo pellets (control group). In in vitro experiments, theca cells were cultured alone or in coculture with granulosa cells in the absence or presence of letrozole. Main Outcome Measure(s): Deoxyribonucleic acid synthesis was determined by thymidine incorporation assay; steroidogenesis by mass spectrometry; and steroidogenic enzyme messenger RNA (mRNA) expression by polymerase chain reaction. Result(s): In vivo, letrozole induced an increase in ovarian size compared with the control group and also induced a profound increase of androgen, LH levels, and Cyp17a1 mRNA expression. Conversely, a decrease in Star, Cyp11a1, and Hsd3b1 transcripts was observed in letrozole-exposed rats. In vitro, letrozole did not alter either theca cell proliferation or Cyp17a1 mRNA expression. Similarly, letrozole did not affect Cyp17a1 transcripts in granulosa-theca cocultures. Conclusion(s): These findings suggest that letrozole exerts potent, but indirect, effect on growth of rat ovary and dramatically increases androgen levels and Cyp17a1 mRNA expression, the key enzyme regulating the androgen biosynthesis pathway. The present findings reveal novel mechanisms of action of letrozole in the rat ovary. ?2013 by American Society for Reproductive Medicine.
机译:目的:使用体外模型,评价来曲唑对体内卵巢大小和类固醇生成的影响,以及对单独的ca-间质细胞和与颗粒细胞共培养的细胞增殖和类固醇生成的影响。设计:体内和体外研究。地点:研究实验室。动物:Sprague-Dawley未成年雌性大鼠。干预措施:在接受来曲唑(90天连续释放SC药丸,400μg/ d)或安慰剂药丸(对照组)的完整大鼠中研究了来曲唑的体内作用。在体外实验中,在不存在或存在来曲唑的情况下,单独培养theca细胞或与颗粒细胞共培养。主要指标:通过胸苷掺入法测定脱氧核糖核酸的合成;质谱法测定类固醇生成;聚合酶链反应表达类固醇酶信使RNA(mRNA)。结果:在体内,来曲唑与对照组相比,卵巢大小增加,并且还引起雄激素,LH水平和Cyp17a1 mRNA表达的大幅增加。相反,在来曲唑暴露的大鼠中观察到Star,Cyp11a1和Hsd3b1转录物的减少。在体外,来曲唑不会改变细胞的增殖或Cyp17a1 mRNA的表达。同样,来曲唑在颗粒-鞘膜共培养中也不影响Cyp17a1转录本。结论:这些发现表明,来曲唑对大鼠卵巢的生长具有有效但间接的作用,并显着增加了雄激素水平和Cyp17a1 mRNA表达,这是调节雄激素生物合成途径的关键酶。本发现揭示了来曲唑在大鼠卵巢中的新作用机理。 ?2013年美国生殖医学学会。

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