Department of Obstetrics and Gynecology, School of Medicine, University of California, Davis, California, IVI-Madrid, Madrid, Spain.
Fertil Steril. 2013 Mar 1;99(3):889-96. doi: 10.1016/j.fertnstert.2012.11.006. Epub 2012 Nov 30.
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.
In vivo and in vitro studies.
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 μg/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.
评估来曲唑对体内卵巢大小和类固醇生成的影响,以及在体外单独培养和与颗粒细胞共培养时对间质细胞增殖和类固醇生成的影响,建立体外模型。
体内和体外研究。
研究实验室。
未成熟的 Sprague-Dawley 雌性大鼠。
来曲唑的体内作用在接受来曲唑(90 天持续释放 SC 微球,400μg/d)或安慰剂微球(对照组)的完整大鼠中进行研究。在体外实验中,单独培养或与颗粒细胞共培养时,培养间质细胞。
脱氧核糖核酸合成通过胸苷掺入测定法确定;类固醇生成通过质谱法确定;类固醇生成酶信使 RNA(mRNA)表达通过聚合酶链反应确定。
在体内,与对照组相比,来曲唑诱导卵巢大小增加,同时也诱导雄激素、LH 水平和 Cyp17a1mRNA 表达的显著增加。相反,在来曲唑暴露的大鼠中观察到 Star、Cyp11a1 和 Hsd3b1 转录本减少。在体外,来曲唑不会改变间质细胞增殖或 Cyp17a1mRNA 表达。同样,来曲唑也不会影响颗粒细胞-间质细胞共培养中的 Cyp17a1 转录本。
这些发现表明,来曲唑对大鼠卵巢的生长具有强大但间接的作用,并显著增加雄激素水平和 Cyp17a1mRNA 表达,这是调节雄激素生物合成途径的关键酶。本研究揭示了来曲唑在大鼠卵巢中的新作用机制。