Occurrence and in vitro biosynthesis of 11-ketotestosterone in Siberian sturgeon, Acipenser baeri Brandt maturing females

[Departement_IRSTEA]GMA [TR1_IRSTEA]GMA4-Ressources aquatiques vivantes exploitées [Departement_IRSTEA]GMA [TR1_IRSTEA]GMA4-Ressources aquatiques vivantes exploitées [Departement_IRSTEA]GMA [TR1_IRSTEA]GMA4-Ressources aquatiques vivantes exploitées [Departement_IRSTEA]GMA [TR1_IRSTEA]GMA4-Ressources...

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Bibliographic Details
Published in:Fish Physiology and Biochemistry
Main Authors: Cuisset, B., Fostier, Alexis, Williot, Patrick, Bennetau-Pelissero, C., Le Menn, F.
Other Authors: Université de Bordeaux (UB), Station de physiologie des poissons, Institut National de la Recherche Agronomique (INRA), Centre national du machinisme agricole, du génie rural, des eaux et forêts (CEMAGREF)
Format: Article in Journal/Newspaper
Language:English
Published: HAL CCSD 1995
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Online Access:https://hal.inrae.fr/hal-02715087
https://doi.org/10.1007/BF00004069
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Summary:[Departement_IRSTEA]GMA [TR1_IRSTEA]GMA4-Ressources aquatiques vivantes exploitées [Departement_IRSTEA]GMA [TR1_IRSTEA]GMA4-Ressources aquatiques vivantes exploitées [Departement_IRSTEA]GMA [TR1_IRSTEA]GMA4-Ressources aquatiques vivantes exploitées [Departement_IRSTEA]GMA [TR1_IRSTEA]GMA4-Ressources aquatiques vivantes exploitées International audience High levels of 11-ketotestosterone (11KT) were found (49 to 160 ng ml(-1)) in plasma of Siberian sturgeon females during the end of their reproductive cycle. These levels were measured either by specific radioimmunoassay, or both by specific radioimmunoassay and by UV absorption after HPLC (isocratic conditions, 33% methanol, 26% acetonitrile, 41% water). In order to find the origin of 11KT synthesis, ovaries were incubated (30 min and 2h at 20 degrees C) with tritiated 17-hydroxyprogesterone (17OHP) or with tritiated androstenedione (A4). Testosterone (conversion rate from tritiated 17OHP: 4%) and 11-ketotestosterone (conversion rate from tritiated A4: 1.6%) were identified as metabolites of respectively 17OHP and A4 (TLC, HPLC and crystallization). 11 beta-hydroxyandrostenedione (11 beta OHA4) and 11 beta-hydroxytestosterone (11 beta OHT) were suggested to be intermediate metabolites. Besides interrenal and blood cells were incubated respectively with tritiated cortisol and tritiated A4. 11 beta OHA4 was identified in interrenal incubation (yield from tritiated cortisol: 1.2%). 11KT in interrenal (yield from tritiated cortisol: 0.14%), and 11 beta OHA4 and 11KT in blood cells (yield from tritiated A4: 1.6%), were suspected to be synthesized (TLC, HPLC, acetylation). No significant metabolization of tritiated cortisol could be found in liver. The possible contribution of each of these tissues to high 11KT levels found in plasma is discussed.