کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1992328 | 1541080 | 2007 | 4 صفحه PDF | دانلود رایگان |

Lung maturation is delayed in male fetuses compared to females and androgens are responsible of this delay. On the other hand, a normal role was proposed for androgens in the developing lung based on a correlation between expression of type 5 17β-hydroxysteroid dehydrogenase (HSD), which catalyzes testosterone synthesis, and the emergence of mature type II pneumonocytes, a developmental event associated with the surge of surfactant synthesis. All these observations underline the importance of the metabolism of androgens in the developing lung. Here, we report a study on the expression of genes involved in the metabolism of the most potent androgen, 5α-dihydrotestosterone, in the mouse fetal lung between gestation days 15.5 and 18.5. Synthesis and inactivation of 5α-dihydrotestosterone occur through 5α-reductase and 3α-HSD activities, respectively. Type 1 5α-reductase was expressed throughout the gestation time window analyzed at fairly constant levels with no gender difference, except that a slight decrease was observed on gestation day 18.5. In contrast, expression of m3α-HSD presented a marked increase on gestation day 17.5, when the maturation of type II pneumonocytes occurs, and followed its progression at least until gestation day 18.5. In conclusion, our data show that m3α-HSD mRNA is a reliable marker of lung maturity in normal pregnancy.
Journal: The Journal of Steroid Biochemistry and Molecular Biology - Volume 103, Issue 1, January 2007, Pages 61–64