Literature DB >> 28277744

A modified vitrification method reduces spindle and chromosome abnormalities.

Minghui Liu1, Wenhui Zhou1, Dapeng Chu1, Lei Fu1, Wei Sha1, Shan Liu1, Yuan Li1.   

Abstract

Development of an effective system for oocyte-cryopreservation is of clinical relevance in reproductive medicine. However, oocyte-preservation is not as effective as embryo preservation. In this study, we used a 37°C pre-equilibrium temperature as part of a modified vitrification method for human oocyte cryopreservation. The effect of the new method on spindle configuration, chromosomal arrangement, and mitochondrial distribution was investigated in in vitro-matured human oocytes. A total of 101 in vitro-matured oocytes were randomly assigned for vitrification at pre-equilibrium temperature of 37°C (37°C Group, n=50) or at room temperature (RT Group, 22-24°C, n=51). The time needed for vitrification in the 37°C group was significantly shorter than that in the RT group. Defective spindles were found in 45.5% and 69.0% oocytes in the 37°C group and RT group, respectively (p < 0.05). Abnormal chromosomes were found in 47.7% and 71.4% oocytes, respectively (p < 0.05). There were no significant differences with respect to oocyte survival rate and mitochondrial distribution pattern between the two groups. These results indicate that vitrification at a pre-equilibrium temperature of 37°C may reduce the incidence of defective spindle configuration and chromosomal abnormalities in in-vitro-matured human oocytes. ABBREVIATIONS: ICSI: intracytoplasmic sperm injection; FSH: follicle-stimulating hormone; MII: metaphase II; EG: ethylene glycol; PROH: 1,2-propanediol.

Entities:  

Keywords:  Human oocyte; pre-equilibrium temperature; vitrification

Mesh:

Year:  2017        PMID: 28277744     DOI: 10.1080/19396368.2017.1285370

Source DB:  PubMed          Journal:  Syst Biol Reprod Med        ISSN: 1939-6368            Impact factor:   3.061


  3 in total

1.  Melatonin improves the first cleavage of parthenogenetic embryos from vitrified-warmed mouse oocytes potentially by promoting cell cycle progression.

Authors:  Bo Pan; Izhar Hyder Qazi; Shichao Guo; Jingyu Yang; Jianpeng Qin; Tianyi Lv; Shengqin Zang; Yan Zhang; Changjun Zeng; Qingyong Meng; Hongbing Han; Guangbin Zhou
Journal:  J Anim Sci Biotechnol       Date:  2021-07-16

2.  Vitrification of Mouse MII Oocyte Decreases the Mitochondrial DNA Copy Number, TFAM Gene Expression and Mitochondrial Enzyme Activity.

Authors:  Mahboobeh Amoushahi; Mojdeh Salehnia; Seyed Javad Mowla
Journal:  J Reprod Infertil       Date:  2017 Oct-Dec

3.  The Error-Prone Kinetochore-Microtubule Attachments During Meiosis I in Vitrified Oocytes.

Authors:  Lei Gao; Yunpeng Hou; Shenming Zeng; Junyou Li; Shien Zhu; Xiangwei Fu
Journal:  Front Cell Dev Biol       Date:  2020-07-09
  3 in total

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