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In Vitro Sex Steroid Metabolism in Red Spotted Grouper, Epinephelus akaara during Oocyte Maturation

We studied steroid metabolites produced from red-spotted grouper ovarian follicles during maturation. Oocytes with 350–500 μm diameter were in vitro incubated in the presence of [(3)H] 17α-hydroxyprogesterone as a precursor. Steroid metabolites were extracted from incubated media and oocytes. The ex...

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Detalles Bibliográficos
Autores principales: Hwang, In Joon, Baek, Hea Ja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Developmental Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8328477/
https://www.ncbi.nlm.nih.gov/pubmed/34386642
http://dx.doi.org/10.12717/DR.2021.25.2.75
Descripción
Sumario:We studied steroid metabolites produced from red-spotted grouper ovarian follicles during maturation. Oocytes with 350–500 μm diameter were in vitro incubated in the presence of [(3)H] 17α-hydroxyprogesterone as a precursor. Steroid metabolites were extracted from incubated media and oocytes. The extracts were separated and identified using thin layer chromatography, high performance liquid chromatography and gas chromatography-mass spectrometry. The identified metabolites were androstenedione (A(4)), testosterone (T) and estrone (E(1)). The metabolites of A(4) was dominant in all size of oocytes and it was the highest in 480 μm diameter oocytes. The metabolites of two progestins, 17α,20β-dihydroxy-4-pregnen-3-one and 17α,20α-dihydroxy-4-pregnen-3-one were detected in the oocytes less than 480 μm diameter although they were not identified definitely. In the oocytes of 480 μm diameter, metabolite of progestin was the highest, and germinal vesicle (GV) was still in the middle of cytoplasm. In the oocytes of 500 μm diameter, GV was began to migrate and the major metabolites were A(4) and E(1). The metabolite of E(1) was detected in all size of oocytes and it was higher than that of E(2). These results suggest that oocytes of 480 μm diameter are the transitional stage involving steroidogenic shift to final oocyte maturation and potential function of E(1) during maturation process.