130 Flavanoid Increases the in Vitro Developmental Ability of Cloned and Parthenogenetic Porcine Embryos

Abstract

Flavonoid has anti-oxidant properties and has been shown to protect cells against oxygen radical damage. This study therefore, evaluated the effect of flavonoid on the in vitro development ability of porcine embryos produced by parthenogenesis (PA) or somatic cell nuclear transfer (SCNT). Porcine embryos were produced from abattoir-derived prepubertal oocytes either by PA or SCNT of fetal fibroblast into enucleated oocytes essentially as we described earlier (Gupta et al. 2008 Mol. Reprod. Dev. 75, 588–597). One-cell embryos were subsequently cultured in NCSU23 + 0.4% polyvinyl alcohol supplemented with or without 10 μm flavanoid for 7 days at 39°C in a humidified atmosphere of 5% CO2 in air. Results showed that the presence of flavonoid in the culture medium increased (v. controls) the rate of blastocyst in both PA (31.7 ± 4.0 v. 20.4 ± 2.0%) and SCNT (20.6 ± 2.5 v. 12.2 ± 2.9%) groups, respectively (P < 0.05). These blastocysts also had higher ability to hatch (PA: 53.7 ± 3.6 v. 34.0 ± 2.4%; SCNT: 70.9 ± 2.5 v. 45.7 ± 2.9%) and contained higher cell number (PA: 38.9 ± 2.0 v. 31.3 ± 2.1; SCNT: 37.5 ± 2.0 v. 29.7 ± 2.5) than those of control groups (P < 0.05). Western blot analysis of parthenogenetic blastocysts showed that, flavonoid also reduced the expression of caspase-3 and p38 mitogen-activated protein kinase (MAPK) proteins by 3.1 ± 0.1 and 7.7 ± 0.2 fold, respectively while expression of ERK1/2 protein was increased by 4.7 ± 2.3 fold. The 2′,7′-dichlorofluorescene fluorescence staining of embryos further revealed that the activity of reactive oxygen species (ROS) was significantly reduced in flavonoid treated embryos by 2 fold(P < 0.05). These data therefore, suggest that flavonoid may improve the in vitro development rate and quality of porcine embryos by reducing ROS activity and change in protein expression.