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In vitro steroid-induced meiosis in Rhinella arenarum oocytes: role of pre-MPF activation

Published online by Cambridge University Press:  26 May 2015

Ana Josefina Arias Torres
Affiliation:
Instituto de Biología, Facultad de Bioqca, Qca. y Farmacia, INSIBIO-UNT, Chacabuco 461, Tucumán, Argentina
Marta Inés Bühler
Affiliation:
Instituto de Biología, Facultad de Bioqca, Qca. y Farmacia, INSIBIO-UNT, Chacabuco 461, Tucumán, Argentina
Liliana Isabel Zelarayán*
Affiliation:
Instituto de Biología, Facultad de Bioqca, Qca. y Farmacia, INSIBIO-UNT, Chacabuco 461, 4000 San Miguel de Tucumán, Tucumán, Argentina
*
All correspondence to: Liliana Isabel Zelarayán. Instituto de Biología, Facultad de Bioqca, Qca. y Farmacia, INSIBIO-UNT, Chacabuco 461, 4000 San Miguel de Tucumán, Tucumán, Argentina. Tel: +549 381 4247752 Int. 7093. Fax: +549 381 4247752 Int. 7004. E-mail: [email protected]

Summary

In this work we showed the relationship between seasonal periods and the response of R. arenarum follicles and oocytes to different steroids. Using in vitro germinal vesicle breakdown (GVBD) assays, we demonstrated that P4 is the main steroid capable of inducing maturation in R. arenarum oocytes and follicles. In the second part of this work we showed that androgens can activate pre-maturation promoting factors (pre-MPFs) such as P4, by cytoplasm microinjection experiments. The results indicated that the steroids assayed induced oocyte and follicle maturation in a dose- and time-dependent manner. In oocytes, P4 was the most efficient steroid as a maturation inducer (EC50 of the reproductive period, 6 nM, EC50 of the non-reproductive period ≅ 30 nM). Androgens (DHEA, dehydroepiandrosterone; T, testosterone; and AD, androstenedione) were less efficient maturation inducers than P4 (EC50 reproductive period ≅ 50, 120 and 600 nM respectively). Similar results were obtained with intact follicles in both seasonal periods. Although the response of follicles to the different androgens was variable, in no case was it above the above the response induced by P4. Independently of the season, oocytes and follicles incubated in P4, P5 and T underwent GVBD after 6–10 h while oocytes and follicles incubated in DHEA and AD matured more slowly. Furthermore, we demonstrated that microinjection of mature cytoplasm from androgen-treated oocytes is sufficient to promote GVBD in immature recipient oocytes (DHEA, 57 ± 12%; AD, 60 ± 8%; T, 56 ± 13%). Thus, androgens such as DHEA, T and AD are as competent as P4 to activate pre-MPF.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2015 

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