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   <subfield code="a">Whole sheep ovary cryopreservation: evaluation of a slow freezing protocol with dimethylsulphoxide</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Milan Milenkovic, Ann Wallin, Manda Ghahremani, Mats Brännström]</subfield>
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   <subfield code="a">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.</subfield>
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