Caffeine and oocyte vitrification: Sheep as an animal model

Oocyte cryopreservation is valuable way of preserving the female germ line. Vitrification of immature ovine oocytes decreased the levels of both maturation promoting factor (MPF) and mitogen-activated protein kinase (MAPK) in metaphase II (MII) oocytes after IVM. Our aims were 1) to evaluate the eff...

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Main Authors: Adel R. Moawad, Inchul Choi, Jie Zhu, Abou Bakr A. EL-Wishy, Dasari Amarnath, Wenchao Chen, Keith H.S. Campbell
Format: Article
Language:English
Published: Taylor & Francis Group 2018-01-01
Series:International Journal of Veterinary Science and Medicine
Online Access:http://www.sciencedirect.com/science/article/pii/S2314459917301539
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spelling doaj-889d43ef437a41d2a0b16c671c1bd4ad2020-11-24T22:01:38ZengTaylor & Francis GroupInternational Journal of Veterinary Science and Medicine2314-45992018-01-016S41S48Caffeine and oocyte vitrification: Sheep as an animal modelAdel R. Moawad0Inchul Choi1Jie Zhu2Abou Bakr A. EL-Wishy3Dasari Amarnath4Wenchao Chen5Keith H.S. Campbell6Department of Theriogenology, Faculty of Veterinary Medicine, Cairo University, PO BOX 12211, Giza, Egypt; Animal Development and Biotechnology Group, School of Biosciences, The University of Nottingham, Sutton Bonington Campus, Loughborough, Leicestershire LE12 5RD, UK; Corresponding author at: Department of Theriogenology, Faculty of Veterinary Medicine, Cairo University, PO BOX 12211, Giza, Egypt.Animal Development and Biotechnology Group, School of Biosciences, The University of Nottingham, Sutton Bonington Campus, Loughborough, Leicestershire LE12 5RD, UK; Department of Animal Biosystem Sciences, College of Agriculture and Life Sciences Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon 305-764, Republic of KoreaAnimal Development and Biotechnology Group, School of Biosciences, The University of Nottingham, Sutton Bonington Campus, Loughborough, Leicestershire LE12 5RD, UK; College of Life Sciences, The University of Inner Mongolia, 1010070, People’s Republic of ChinaDepartment of Theriogenology, Faculty of Veterinary Medicine, Cairo University, PO BOX 12211, Giza, EgyptAnimal Development and Biotechnology Group, School of Biosciences, The University of Nottingham, Sutton Bonington Campus, Loughborough, Leicestershire LE12 5RD, UK; College of Life Sciences, The University of Inner Mongolia, 1010070, People’s Republic of China; Taconic Farms Inc., Five University Place Rensselaer, NY 12144-3439, USAAnimal Development and Biotechnology Group, School of Biosciences, The University of Nottingham, Sutton Bonington Campus, Loughborough, Leicestershire LE12 5RD, UKAnimal Development and Biotechnology Group, School of Biosciences, The University of Nottingham, Sutton Bonington Campus, Loughborough, Leicestershire LE12 5RD, UKOocyte cryopreservation is valuable way of preserving the female germ line. Vitrification of immature ovine oocytes decreased the levels of both maturation promoting factor (MPF) and mitogen-activated protein kinase (MAPK) in metaphase II (MII) oocytes after IVM. Our aims were 1) to evaluate the effects of vitrification of ovine GV-oocytes on spindle assembly, MPF/MAP kinases activities, and preimplantation development following IVM and IVF, 2) to elucidate the impact of caffeine supplementation during IVM on the quality and development of vitrified/warmed ovine GV-oocytes. Cumulus-oocyte complexes (COCs) from mature ewes were divided into vitrified, toxicity and control groups. Oocytes from each group were matured in vitro for 18 h in caffeine free IVM medium and denuded oocytes were incubated in maturation medium supplemented with 10 mM (+) or without (−) caffeine for another 6 h. At 24 h.p.m., oocytes were evaluated for spindle configuration, MPF/MAP kinases activities or fertilized and cultured in vitro for 7 days. Caffeine supplementation did not significantly affect the percentages of oocytes with normal spindle assembly in all the groups. Caffeine supplementation during IVM did not increase the activities of both kinases in vitrified groups. Cleavage and blastocyst development were significantly lower in vitrified groups than in control. Caffeine supplementation during the last 6 h of IVM did not significantly improve the cleavage and blastocyst rates in vitrified group. In conclusion, caffeine treatment during in vitro maturation has no positive impact on the quality and development of vitrified/warmed ovine GV-oocytes after IVM/IVF and embryo culture. Keywords: Caffeine, GV, MPF/MAPK, Oocytes, Ovine, Vitrificationhttp://www.sciencedirect.com/science/article/pii/S2314459917301539
collection DOAJ
language English
format Article
sources DOAJ
author Adel R. Moawad
Inchul Choi
Jie Zhu
Abou Bakr A. EL-Wishy
Dasari Amarnath
Wenchao Chen
Keith H.S. Campbell
spellingShingle Adel R. Moawad
Inchul Choi
Jie Zhu
Abou Bakr A. EL-Wishy
Dasari Amarnath
Wenchao Chen
Keith H.S. Campbell
Caffeine and oocyte vitrification: Sheep as an animal model
International Journal of Veterinary Science and Medicine
author_facet Adel R. Moawad
Inchul Choi
Jie Zhu
Abou Bakr A. EL-Wishy
Dasari Amarnath
Wenchao Chen
Keith H.S. Campbell
author_sort Adel R. Moawad
title Caffeine and oocyte vitrification: Sheep as an animal model
title_short Caffeine and oocyte vitrification: Sheep as an animal model
title_full Caffeine and oocyte vitrification: Sheep as an animal model
title_fullStr Caffeine and oocyte vitrification: Sheep as an animal model
title_full_unstemmed Caffeine and oocyte vitrification: Sheep as an animal model
title_sort caffeine and oocyte vitrification: sheep as an animal model
publisher Taylor & Francis Group
series International Journal of Veterinary Science and Medicine
issn 2314-4599
publishDate 2018-01-01
description Oocyte cryopreservation is valuable way of preserving the female germ line. Vitrification of immature ovine oocytes decreased the levels of both maturation promoting factor (MPF) and mitogen-activated protein kinase (MAPK) in metaphase II (MII) oocytes after IVM. Our aims were 1) to evaluate the effects of vitrification of ovine GV-oocytes on spindle assembly, MPF/MAP kinases activities, and preimplantation development following IVM and IVF, 2) to elucidate the impact of caffeine supplementation during IVM on the quality and development of vitrified/warmed ovine GV-oocytes. Cumulus-oocyte complexes (COCs) from mature ewes were divided into vitrified, toxicity and control groups. Oocytes from each group were matured in vitro for 18 h in caffeine free IVM medium and denuded oocytes were incubated in maturation medium supplemented with 10 mM (+) or without (−) caffeine for another 6 h. At 24 h.p.m., oocytes were evaluated for spindle configuration, MPF/MAP kinases activities or fertilized and cultured in vitro for 7 days. Caffeine supplementation did not significantly affect the percentages of oocytes with normal spindle assembly in all the groups. Caffeine supplementation during IVM did not increase the activities of both kinases in vitrified groups. Cleavage and blastocyst development were significantly lower in vitrified groups than in control. Caffeine supplementation during the last 6 h of IVM did not significantly improve the cleavage and blastocyst rates in vitrified group. In conclusion, caffeine treatment during in vitro maturation has no positive impact on the quality and development of vitrified/warmed ovine GV-oocytes after IVM/IVF and embryo culture. Keywords: Caffeine, GV, MPF/MAPK, Oocytes, Ovine, Vitrification
url http://www.sciencedirect.com/science/article/pii/S2314459917301539
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