Literature DB >> 17625348

Effects of isolation method and pre-treatment with ethylene glycol or raffinose before vitrification on in vitro viability of mouse preantral follicles.

Masashi Nagano1, Eufrocina P Atabay, Edwin C Atabay, Mitsugu Hishinuma, Seiji Katagiri, Yoshiyuki Takahashi.   

Abstract

Effects of isolation and vitrification protocols on follicular survival after warming were examined. Mouse preantral follicles enzymatically or mechanically isolated from ovaries of 12-day-old mice were exposed either to 2 M ethylene glycol (EG) for 2 or 5 min, or to ascending concentrations (0.15 then 0.3 M) of raffinose for 2 or 5 min each (2-2 and 5-5 min). They were then exposed to a vitrification solution (VS) composed of 6 M EG and 0.3 M raffinose for 0.5, 1, or 2 min before vitrification. Mechanically isolated follicles showed higher survival than enzymatically isolated follicles, regardless of periods of exposure to EG or raffinose and subsequent exposure to VS. After 10 days of culture, follicular growth and maturational ability of oocytes derived from vitrified follicles exposed to 2 M EG for 5 min and to VS for 1 min were higher than those from follicles exposed to raffinose solutions for 2-2 min and to VS for 1 min. Histological evaluation revealed that exposure of preantral follicles to raffinose solutions caused cytoplasmic vacuolation in granulosa cells which could be due to cellular shrinkage during dehydration; whereas, exposure to 2 M EG induced morphological alterations in follicles only to a lesser extent.

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Year:  2007        PMID: 17625348     DOI: 10.2220/biomedres.28.153

Source DB:  PubMed          Journal:  Biomed Res        ISSN: 0388-6107            Impact factor:   1.203


  7 in total

1.  Ultrastructural and Morphalogical Changes of Mouse Ovarian Tissues Following Direct Cover Vitrification with Different Cryoprotectants.

Authors:  Maryam Ghavami; Daryoush Mohammadnejad; Rahim Beheshti; Jafar Solmani-Rad; Ali Abedelahi
Journal:  J Reprod Infertil       Date:  2015 Jul-Sep

2.  Preservation of mouse ovarian tissue follicle morphology and ultra-structure after vitrifying in biotechnological protocols.

Authors:  Hamid Tayefi Nasrabadi; Maryam Gavami; Abolfazl Akbarzadeh; Rahim Beheshti; Daryosh Mohammadnejad; Ali Abedelahi
Journal:  J Ovarian Res       Date:  2015-03-06       Impact factor: 4.234

Review 3.  Fertility preservation among the cancer patients by ovarian tissue cryopreservation, transplantation, and follicular development.

Authors:  Ali Abedelahi; Mostafa Rezaei-Tavirani; Daryosh Mohammadnejad
Journal:  Iran J Cancer Prev       Date:  2013

4.  Comparison of the enzymatic efficiency of Liberase TM and tumor dissociation enzyme: effect on the viability of cells digested from fresh and cryopreserved human ovarian cortex.

Authors:  Viola Maria Schmidt; Vladimir Isachenko; Gunter Rappl; Gohar Rahimi; Bettina Hanstein; Bernd Morgenstern; Peter Mallmann; Evgenia Isachenko
Journal:  Reprod Biol Endocrinol       Date:  2018-06-02       Impact factor: 5.211

5.  Comparison of the Oocyte Quality Derived from Two-Dimensional Follicle Culture Methods and Developmental Competence of In Vitro Grown and Matured Oocytes.

Authors:  Jaewang Lee; Eun Jung Kim; Hyun Sun Kong; Hye Won Youm; Seul Ki Kim; Jung Ryeol Lee; Chang Suk Suh; Seok Hyun Kim
Journal:  Biomed Res Int       Date:  2018-04-04       Impact factor: 3.411

6.  Innovative multi-protectoral approach increases survival rate after vitrification of ovarian tissue and isolated follicles with improved results in comparison with conventional method.

Authors:  Dmitry Nikiforov; Valentina Russo; Delia Nardinocchi; Nicola Bernabò; Mauro Mattioli; Barbara Barboni
Journal:  J Ovarian Res       Date:  2018-08-07       Impact factor: 4.234

7.  Cryopreservation of Induced Pluripotent Stem Cell-Derived Dopaminergic Neurospheres for Clinical Application.

Authors:  Satoe Hiramatsu; Asuka Morizane; Tetsuhiro Kikuchi; Daisuke Doi; Kenji Yoshida; Jun Takahashi
Journal:  J Parkinsons Dis       Date:  2022       Impact factor: 5.520

  7 in total

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