Abstract

The aim of this study was to evaluate mitochondrial alteration and ATP content of germinal vesicle (GV) oocytes isolated from fresh and vitrified ovaries. After superovulation, the ovaries from adult mice were collected and divided into control and vitrified groups. GV oocytes were isolated mechanically from each group. Half were cultured for 24 hours and their maturation was assessed. Metaphase II oocytes were collected and submitted to in vitro fertilization and their fertilization rates and development to the blastocyst stage were evaluated. In the remaining GV oocytes, ATP levels were quantified, and mitochondrial distribution, mitochondrial membrane potential, and intracellular free calcium were detected with rhodamine 123, JC-1 and Flou-4 AM staining, using laser-scanning confocal microscopy. Maturation and fertilization rates of GV oocytes and the developmental rates of subsequent embryos were significantly lower in vitrified samples (P < 0.05). The ATP content and Ca2+ levels differed significantly in fresh and vitrified GV oocytes (P < 0.05). Most mitochondria were seen as large and homogenous aggregates (66.6%) in fresh GV oocytes compared to vitrified oocytes (50%). No significant differences in mitochondrial membrane potential were found between the groups. The lower maturation and fertilization rates of GV oocytes from vitrified ovaries may be due to changes in their mitochondrial function and distribution.

Highlights

  • Vitrification is a method for cryopreservation of oocytes, embryos, and ovarian tissue

  • The metaphase II (MII) stage was reached by 86.9% ± 4.51 of germinal vesicle (GV) oocytes in the control group and 50.20%±6.97 in the vitrified group

  • Data on the developmental rates of immature (GV) oocytes collected from vitrified ovarian tissue is limited, this study has focused on this subject

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Summary

Introduction

Vitrification is a method for cryopreservation of oocytes, embryos, and ovarian tissue. Cryopreservation causes alterations in the physical and chemical properties of oocytes and embryos, including loss of cell membrane and cytoskeletal integrity, mitochondrial depolarization, and increased production of reactive oxygen species [9,10,11,12,13,14,15]. These alterations are associated with osmotic forces created during dehydration, cooling, rehydration, and warming and may affect mainly cytoplasmic activities such as mitochondrial function, metabolism, and intracellular signaling pathways

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