کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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3939075 | 1253548 | 2008 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Comparison of spindle and chromosome configuration in in vitro- and in vivo-matured mouse oocytes after vitrification Comparison of spindle and chromosome configuration in in vitro- and in vivo-matured mouse oocytes after vitrification](/preview/png/3939075.png)
ObjectiveTo compare the cytogenetic changes in in vitro- and in vivo-matured oocytes after vitrification.DesignIn vitro experiments using murine model.SettingAnimal model study in university laboratory.Animal(s)CD-1 mice.Intervention(s)In vitro maturation and vitrification of oocytes.Main Outcome Measure(s)Post-warming survival, analysis of spindle and chromosome configurations, aneuploidy screening of parthenogenetically activated oocytes, extent of DNA fragmentation, and early embryonic development after IVF.Result(s)Eighty percent of germinal vesicle-stage oocytes matured after in vitro maturation and were cryopreserved by vitrification (n = 354). There was no significant difference in the post-warming survival of in vitro- and in vivo-matured oocytes (94.1% vs. 91.8%, respectively). The majority of in vitro- and in vivo-matured oocytes maintained normal meiotic spindle morphology and chromosome alignment (88.2% vs. 86.9%, respectively) after vitrification and the incidence of aneuploidy was not increased (11.5% vs. 9.3%). However, in vitro-matured oocytes showed a higher rate of DNA fragmentation after vitrification compared to in vivo-matured oocytes. After vitrification, the cleavage and blastocyst formation rates of in vitro-matured oocytes were significantly lower than those of in vivo-matured oocytes (37.0% vs. 60.0% and 5.4% vs. 18.9%, respectively).Conclusion(s)Vitrification of in vitro-matured mouse oocytes results in high survival rates, normal meiotic spindle and chromosome alignment, and no increased incidence of aneuploidy. A possible cause of the reduced developmental competence of in vitro-matured and vitrified oocytes may be due to DNA fragmentation.
Journal: Fertility and Sterility - Volume 90, Issue 4, Supplement, October 2008, Pages 1424–1432