Author/Authors :
Farahavar، Abbas نويسنده Department of Animal Science, Faculty of Agriculture and Natural Resources, University of Tehran , , Shirazi، Abolfazl نويسنده Research Institute of Animal Embryo Technology, Shahrekord University Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR , , Khoram، Hamid نويسنده Department of Animal Science, Faculty of Agriculture and Natural Resources, University of TehranDepartment of Clinical Sciences, Faculty of Veterinary Medicine, University of Shahid Chamran , , Zareh Shahneh، Ahmad نويسنده Department of Animal Science, Faculty of Agriculture and Natural Resources, University of Tehran , , Sarvari، Ali نويسنده Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR , , Naderi، Mohammad Mehdi نويسنده Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR , , Borjian Boroujeni، Sara نويسنده Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR , , Zhandi، Mahdi نويسنده Department of Animal Science, Faculty of Agriculture and Natural Resources, University of Tehran ,
Abstract :
Background: The basal medium that supports Isolated Mouse Oviduct (IMO) is important for supporting embryo development and quality.
Methods: The culture of ovine IVM/IVF zygotes was done in IMO using SOFaaciBSA and SOFaaBSA as basal medium of IMO and in SOFaaBSA alone as control. For preparation of IMO mature inbred strain C57BL/6 female mice were synchronized and mated with vasectomized males. The females with vaginal plug were sacrificed and the zygotes were transferred in to the isolated oviduct at 20 hpi. The oviducts were cultured with SOFaaciBSA and SOFaaBSA for 6 days. Another group of zygotes were cultured in SOFaaBSA alone as control.
Results: Culture of zygotes in the IMO with SOFaaciBSA and SOFaaBSA, did not significantly affect the development and quality of embryos (p>0.05). The hatching rate, total and trophectoderm cells number in IMO groups’ blastocysts were significantly higher than SOFaaBSA alone. The morphological appearance of IMO blastocysts was superior to SOFaaBSA alone. When the quality of oocytes was poor, IMO could better support ovine embryo development either with SOFaaBSA or SOFaaciBSA than SOFaaBSA alone and there was a significant difference in blastocyst formation at day 6 with SOFaaBSA alone.
Conclusion: The culture of ovine IVM/IVF zygotes in IMO using two highly efficient ruminant embryo culture media not only could support development of ovine embryos similar to the level in non IMO culture system (SOFaaBSA alone) but also could improve the quality of resulting embryos. Additionally, IMO could better support the development of ovine embryos derived from poor quality oocytes compared to the SOFaaBSA alone.
