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   <subfield code="a">The human postmenopausal ovary as a tool for evaluation of cryopreservation protocols towards whole ovary cryopreservation</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Milan Milenkovic, Manda Gharemani, Anette Bergh, Ann Wallin, Johan Mölne, Elvedin Fazlagic, Eirik Eliassen, Jarl Kahn, Mats Brännström]</subfield>
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   <subfield code="a">Purpose: Cryopreservation of a complete ovary may be a future method for fertility preservation in cancer patients. Difficulties exist in cryopreservation of the relatively large ovarian tissue mass. This study evaluates whether a human postmenopausal ovary can be used, as a complement to animal models, in studies of this research field. Methods: Postmenopausal human ovaries (n = 10) were isolated and flushed through ovarian arteries with either the cryoprotectant dimethylsulphoxide or Ringer-Acetate, followed by slow freezing. After thawing, production of androgens during in vitro perfusion and morphology (light/electron microscopy) were assessed. Results: The dimethylsulphoxide-cryopreserved ovaries showed larger secretion of androgens during perfusion than Ringer Acetate-cryopreserved ovaries. Light microscopy showed well preserved morphology in both groups. Electron microscopy revealed normal appearance of stroma and vessels in the dimethylsulphoxide group. Conclusions: The study demonstrates the potential to use the postmenopausal human ovary for further studies aiming at optimizing cryopreservation protocols, with special reference to ovarian vascularity and stroma.</subfield>
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   <subfield code="a">Springer Science+Business Media, LLC, 2011</subfield>
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   <subfield code="a">Androgens</subfield>
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   <subfield code="a">Cryopreservation</subfield>
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   <subfield code="u">Department of Obstetrics and Gynecology, Sahlgrenska Academy, University of Gothenburg, SE-41345, Gothenburg, Sweden</subfield>
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   <subfield code="u">Division of Obstetrics and Gynecology, Telemark Hospital, 3710, Skien, Norway</subfield>
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