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Year 2014 - Volume 34, Number 10
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Influence of Insulin-like Growth Factor I (IGF-I) on the survival and the in vitro development of caprine preantral follicles, 34(10):1037-1044
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ABSTRACT.- Costa S.L., Costa E.P., Pereira E.C.M., Benjamin L.A., Rodrigues M.T., Mendes V.R.A. & Silva T.F. 2014. Influence of Insulin-like Growth Factor I (IGF-I) on the survival and the in vitro development of caprine preantral follicles. Pesquisa Veterinária Brasileira 34(10):1037-1044. Programa de Pós-Graduação em Ciências Biológicas e da Saúde, Laboratório de Maturação de Ovócitos e Fertilização In Vitro, Universidade Federal de Viçosa, Avenida Peter Henry Rolfs s/n, Campus Universitário, Viçosa, MG 36570-900, Brazil. E-mail: sanelylc@hotmail.com
The aim of this study was to investigate the effects of the insulin-like growth factor -I (IGF-I) on survival, activation (transition from primordial to primary follicles) and growth of caprine preantral follicles cultured in vitro. Fragments of ovarian cortex were cultured for one and seven days in the absence or presence of IGF-I (0, 50 and 100ng/ml). The non-cultured and cultured tissues were processed and analyzed by histology and transmission electron microscopy. The culture for one day in a medium with 100ng/ml of IGF-I showed 86.7% of morphologically normal follicles. These results were similar (P>0.05) to the percentage of normal follicles found in the control (96.7%). It was also found that this medium increased the percentage of follicular activation (developing follicles) with one day of culture. The oocyte and follicular diameters remained similar to the control by culturing for one day in a medium containing 100ng/ml of IGF-I. The ultrastructural analysis did not confirm the integrity of the follicular fragments in a medium containing IGF-I (100ng/ml) after one and seven days of culture. In conclusion, this study demonstrated that the addition of 100 ng/ml of IGF-I in the culture medium enables the development of preantral follicles of goats with one day of culture. However, it is not sufficient to maintain the follicular integrity and the follicular survival rate after seven days of culture. |
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