39 THE EFFECTS OF RESVERATROL DURING IN VITRO MATURATION ON THE DEVELOPMENTAL COMPETENCE OF PORCINE OOCYTES VITRIFIED AT THE IMMATURE STAGE
Autor: | Tamas Somfai, Thanh Quang Dang-Nguyen, Kazuhiro Kikuchi, Takashi Nagai, E. C. S. Santos, Ruth Appeltant, Hiroyuki Kaneko, N. Junko |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
medicine.medical_specialty Cryoprotectant Theriogenology Reproductive technology Biology Oogenesis Andrology 03 medical and health sciences 0302 clinical medicine Endocrinology Genetics medicine Blastocyst Molecular Biology 030219 obstetrics & reproductive medicine Embryo culture Oocyte In vitro maturation 030104 developmental biology medicine.anatomical_structure Reproductive Medicine Immunology Animal Science and Zoology Developmental Biology Biotechnology |
Zdroj: | Reproduction, Fertility and Development. 29:127 |
ISSN: | 1031-3613 |
Popis: | Previously, live offspring have been produced from porcine oocytes vitrified at the immature stage (Somfai et al. 2014 PLoS One 9, e97731); however, their embryo developmental rates remain low. The aim of our current research was to test the effects of resveratrol, an antioxidant and anti-apoptotic agent on the developmental competence of immature vitrified oocytes during in vitro maturation (IVM) after warming. Follicular porcine cumulus-oocyte complexes (COC) were vitrified on Cryotop® sheets (Kitazato Corp. Shizuoka, Japan) using the cryoprotectant treatment and warming method of Somfai et al. (2015 J. Reprod. Dev. 61, 571–579). After warming, the oocytes were subjected to IVM for 46 h in a chemically defined porcine oocyte medium (POM) enriched with 10 ng mL−1 epidermal growth factor, 10 IU mL−1 eCG, and 10 IU mL−1 hCG. During the first 22 h of IVM, the medium was supplemented with 1 mM dibutyryl cAMP. The following 24 h of IVM was performed in POM without dibutyryl cAMP. Vitrified/warmed COC (vitrified group) and freshly collected COC (control group) were matured either in the absence or presence of 2 µM resveratrol (RES− and RES+, respectively) throughout the entire IVM. At the end of IVM, oocytes were denuded and their survival was evaluated. Then, those with 1 polar body (PB1+) were selected for parthenogenetic activation (Day 0). Activated oocytes were cultured for 7 days in PZM-3. Survival, nuclear maturation, cleavage, and blastocyst rates were assessed. The experiment was replicated 5 times. Results were analysed by one-way ANOVA and Tukey’s multiple comparison test. Vitrification reduced the percentage of live oocytes after IVM both in RES− and RES+ groups in a similar manner (47.9 and 51.8%, respectively) compared with control RES− and RES+ groups (99.4 and 100%, respectively; P |
Databáze: | OpenAIRE |
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