Rat testis 17β-estradiol: Identification by gas chromatography-mass spectrometry and age related cellular distribution

The aromatization of testosterone into 17β-estradiol (E 2) was assessed in purified Leydig and Sertoli cells from rats aged 10–80 days. E 2 was identified by gas chromatography-mass spectrometry (GC-MS) and measured both by radioimmunoassay (RIA) and GC-MS associated with stable isotope dilution. A...

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Veröffentlicht in:Journal of steroid biochemistry 1986-06, Vol.24 (6), p.1211-1216
Hauptverfasser: Papadopoulos, V., Carreau, S., Szerman-Joly, E., Drosdowsky, M.A., Dehennin, L., Scholler, R.
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Sprache:eng
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Zusammenfassung:The aromatization of testosterone into 17β-estradiol (E 2) was assessed in purified Leydig and Sertoli cells from rats aged 10–80 days. E 2 was identified by gas chromatography-mass spectrometry (GC-MS) and measured both by radioimmunoassay (RIA) and GC-MS associated with stable isotope dilution. A potent competitive inhibitor of the aromatase activity, 4-hydroxyandrostenedione (4-OH-A) was used to test the enzymatic specificity. The basal aromatase activity was present in both cell types whatever the age of the animals. The basal E 2 levels did not vary in Sertoli cells while a gradual increase was noted in Leydig cells until day 40, followed by a slight decrease in mature rats. In 10-day old animals, the aromatase activity was localized in Sertoli cells and highly stimulated by FSH; on day 20, both Sertoli and Leydig cells synthesized E 2 although E 2 from Sertoli cell origin was still predominant. Starting on day 20 until adulthood, the aromatase activity was under LH control in Leydig cells with a maximum around 40 days. The FSH and LH effects were mediated by cyclic AMP.
ISSN:0022-4731
DOI:10.1016/0022-4731(86)90385-7