Literature DB >> 20842419

Whole sheep ovary cryopreservation: evaluation of a slow freezing protocol with dimethylsulphoxide.

Milan Milenkovic1, Ann Wallin, Manda Ghahremani, Mats Brännström.   

Abstract

PURPOSE: To evaluate a slow freezing method for whole ovary cryopreservation by evaluating effects of added cryoprotectant.
METHODS: Sheep ovaries were isolated during surgery, flushed with either Ringer-Acetate or dimethylsulphoxide and cryopreserved by slow freezing. After rapid thawing, viability was assessed by ovarian in vitro perfusion, cell culture, histology and fluorescent live-dead assay.
RESULTS: Production of cyclic AMP and progesterone was slightly higher in the dimethylsulphoxide group. Cultured ovarian cells from dimethylsulphoxide-preserved ovaries secreted larger amounts of progesterone than cells from Ringer-Acetate preserved. Light microscopy of ovarian biopsies obtained after perfusion, revealed well-preserved tissue in the dimethysulphoxide group but not in the Ringer-Acetate group. The density of small follicles and ovarian cell viability were higher in dimethysulphoxide ovaries compared to Ringer-Acetate ovaries.
CONCLUSIONS: Equilibrium with its protective effect can be achieved by slow freezing protocol, with an additional protective effect by the presence of dimethylsulphoxide.

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Year:  2010        PMID: 20842419      PMCID: PMC3045486          DOI: 10.1007/s10815-010-9477-5

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  51 in total

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Review 2.  Oocyte cryopreservation: is it time to remove its experimental label?

Authors:  Nicole Noyes; Jeffrey Boldt; Zsolt Peter Nagy
Journal:  J Assist Reprod Genet       Date:  2010-02-06       Impact factor: 3.412

3.  Viability and function of the cryopreserved whole ovary: in vitro studies in the sheep.

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4.  Ovarian tissue viability following whole ovine ovary cryopreservation: assessing the effects of sphingosine-1-phosphate inclusion.

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10.  Optimal perfusion of an intact ovary as a prerequisite for successful ovarian cryopreservation.

Authors:  R Gerritse; C C M Beerendonk; M S L Tijink; A Heetkamp; J A M Kremer; D D M Braat; J R Westphal
Journal:  Hum Reprod       Date:  2007-12-02       Impact factor: 6.918

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  3 in total

1.  The human postmenopausal ovary as a tool for evaluation of cryopreservation protocols towards whole ovary cryopreservation.

Authors:  Milan Milenkovic; Manda Gharemani; Anette Bergh; Ann Wallin; Johan Mölne; Elvedin Fazlagic; Eirik Eliassen; Jarl Kahn; Mats Brännström
Journal:  J Assist Reprod Genet       Date:  2011-02-25       Impact factor: 3.412

2.  Cryopreservation and re-culture of a 2.3 litre biomass for use in a bioartificial liver device.

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3.  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
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