Abstract

This study was conducted to determine the effect of Papaver rhoeas L. extract on in vitro maturation (IVM) of sheep oocytes. Sheep ovaries collected from a local abattoir were transported to the laboratory within 2h after slaughter. The cumulus–oocyte complexes (COCs) were aspirated from follicles (2–6mm in diameter). Good quality COCs were selected and cultured in TCM 199 supplemented with 0 (control), 25, 50, 100 and 200μg/ml of P. rhoeas extract. The COCs were incubated at 38.5°C in humidified atmosphere of 5% CO2 in air for 24h. After the incubation period, expansion of cumulus cells and the nuclear status of the oocytes were assessed by phase contrast microscopy and Hoechst 33258, respectively. There were no significant differences between treatments in the percentage of cumulus expansion (P>0.05). The percentage of arrested oocytes at germinal vesicle (GV) stage in the control group was significantly (P<0.05) higher than other treatments. There were significant (P<0.05) differences between all concentrations of extract and the control group in the percentage of in vitro maturated oocytes to metaphase II (MII) stage. The oocytes treated with 50μg/ml extract achieved the highest percentage of MII stage compared to the control (P<0.05); however, no significant difference observed between 25, 50 and 100μg/ml extract. In conclusion, the results of this study show that supplementation of appropriate concentrations of P. rhoeas extract (50μg/ml) in maturation medium improve the sheep oocyte maturation rate. Moreover, effects of P. rhoeas extract on oocyte maturation were dependent on the extract concentration in the maturation medium.

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