3.9 Article

Lipid content and cryotolerance of in vitro-produced bovine embryos treated with forskolin before vitrification

Journal

PESQUISA VETERINARIA BRASILEIRA
Volume 37, Issue 4, Pages 395-400

Publisher

REVISTA PESQUISA VETERINARIA BRASILEIRA
DOI: 10.1590/S0100-736X2017000400015

Keywords

Lipid content; cryotolerance; forskolin; vitrification; in vitro production; embryo; bovine; intracytoplasmic lipid accumulation

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The aim of the present study was to evaluate the intracytoplasmic lipid content, development and cryotolerance of in vitro-produced bovine embryos treated with different concentrations of forskolin before vitrification. Embryos were produced from abattoir-derived ovaries and allocated into four groups. In the treatment groups, forskolin was added to the in vitro culture medium on Day 6 and incubated for 24 hours in one of the following concentrations: 2.5 mu M (Forsk 2.5 group), 5.0 mu M (Forsk 5.0 group) or 10.0 mu M (Forsk 10.0 group). Embryos from the control group were cultured without forskolin. On Day 7 of culture, the expanded blastocysts were stained with the lipophilic dye Sudan Black B for determination of the intracytoplasmic lipid content or were cryopreserved via the Vitri-Inga (R) procedure. Although there were no significant differences (P>0.05) in the blastocyst rates between the Control group (44.9%) and the other treatments, the embryo production was lower (P<0.05) in Forsk 10.0 group (38.8%) compared to Forsk 2.5 (50.5%) and Forsk 5.0 (54.7%) groups. The intracytoplasmic lipid content (expressed in arbitrary units of pixels) in blastocysts from the Control group (1.00 +/- 0.03) was similar (P>0.05) to that found in Forsk 2.5 (0.92 +/- 0.03) and Forsk 10.0 groups (1.06 +/- 0.03) groups; however the lipid accumulation in blastocysts from Forsk 5.0 group (0.82 +/- 0.04) was lower than in the Control group (P<0.05). Based on these results, Forsk 5.0 treatment was tested for cryotolerance and it was observed that the blastocoel re-expansion rate evaluated 24 hours after warming was greater (P<0.05) in Forsk 5.0 group (72.2%) compared to the Control group (46.2%). In conclusion, pre-treatment with forskolin at a concentration of 5.0 mu M for 24 hours before vitrification is effective in reducing the intracytoplasmic lipid content and, consequently, improves cryotolerance of IVP bovine embryos.

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