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Poster Presentation : Oocyte Maturation / Embryonic Development

Melatonin Supplementation during Prolonged In Vitro Maturation Improves the Quality and Development of Poor-quality Porcine Oocytes

초록

영어

Poor-quality oocytes (those with 1 to 2 layers of cumulus cells) typically possess low meiotic competence and development. Prolonging the duration of in vitro maturation (IVM; 52 h) can enhance the maturation rate of poor-quality oocytes, but it does not improve subsequent embryonic development. This likely reflects the increased reactive oxygen species (ROS) production and apoptosis seen in these oocytes compared with the non-prolonged IVM (44 h) group. Melatonin is a free radical scavenger, anti-oxidant and anti-apoptotic agent that has been reported to enhance the quality of embryos by inhibiting ROS generation and apoptosis. Therefore, we herein investigated whether melatonin combined with prolonged IVM (52 h) could improve the quality and development of poor-quality oocytes. We supplemented IVM and/or in vitro culture (IVC) media with various concentrations (0, 10-7, 10-6 and 10-5 M) of melatonin, and estimated parameters related to oocyte quality and development. The addition of melatonin (10-6 M) to a prolonged IVM system improved the oocyte quality and development compared to those of the melatonin-free oocytes group, and that this was due to decreases in ROS generation, apoptosis, and DNA damage. When melatonin was added during both IVM (10-6 M) and IVC (10-6 M), we observed a cumulative positive influence on embryonic development and quality; this treatment enhanced the expression level of Oct4, and decreased the levels of ROS, DNA damage and apoptosis. Together, these findings suggest that the combination of melatonin plus prolonged IVM can improve the quality and development of poor-quality porcine oocytes via anti-oxidative and anti-apoptotic effects.

저자정보

  • Tao Lin Department of Animal Science & Biotechnology, Research Center for Transgenic Cloned Pigs, Chungnam National University, Daejeon 34134, Republic of Korea
  • Jae Eun Lee Department of Animal Science & Biotechnology, Research Center for Transgenic Cloned Pigs, Chungnam National University, Daejeon 34134, Republic of Korea
  • Jeong Won Kang Department of Animal Science & Biotechnology, Research Center for Transgenic Cloned Pigs, Chungnam National University, Daejeon 34134, Republic of Korea
  • Joo Bin Lee Department of Animal Science & Biotechnology, Research Center for Transgenic Cloned Pigs, Chungnam National University, Daejeon 34134, Republic of Korea
  • So Yeon Kim Department of Animal Science & Biotechnology, Research Center for Transgenic Cloned Pigs, Chungnam National University, Daejeon 34134, Republic of Korea
  • Dong Il Jin Department of Animal Science & Biotechnology, Research Center for Transgenic Cloned Pigs, Chungnam National University, Daejeon 34134, Republic of Korea

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