Suprazero cooling conditions significantly influence subzero permeability parameters of mammalian ovarian tissue

• Published in: Molecular reproduction and development Vol. 73; no. 3; pp. 330 - 341
• Main Authors: Devireddy, R.V., Li, G., Leibo, S.P.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01-03-2006; Wiley-Liss
• Subjects: Animals; Biological and medical sciences; Biological Transport - physiology; Calorimetry - methods; Cells, Cultured; cryopreservation; Cryopreservation - methods; Culture Media - chemistry; differential scanning calorimetry; Dimethyl Sulfoxide - chemistry; Female; Fundamental and applied biological sciences. Psychology; Glycerol - chemistry; Horses; Krogh model; Mammalian female genital system; membrane permeability; Morphology. Physiology; optimal rate of freezing storage; Ovary - cytology; Ovary - physiology; Permeability; Temperature; Tissue Culture Techniques; Vertebrates: reproduction; Water - metabolism; Differential scanning calorimetry; Cooling; Krogh model; membrane permeability; In vitro; cryopreservation; Water permeability; Ovary; Tissue; Vertebrata; optimal rate of freezing storage; Mammalia; Female genital system; Horse; Perissodactyla; Cryoprotective agent; Ungulata
• ISSN: 1040-452X; 1098-2795
• DOI: 10.1002/mrd.20418

To model the cryobiological responses of cells and tissues, permeability characteristics are often measured at suprazero temperatures and the measured values are used to predict the responses at subzero temperatures. The purpose of the present study was to determine whether the rate of cooling from +25 to +4°C influenced the measured water transport response of ovarian tissue at subzero temperatures in the presence or absence of cryoprotective agents (CPAs). Sections of freshly collected equine ovarian tissue were first cooled either at 40°C/min or at 0.5°C/min from 25 to 4°C, and then cooled to subzero temperatures. A shape‐independent differential scanning calorimeter (DSC) technique was used to measure the volumetric shrinkage during freezing of equine ovarian tissue sections. After ice was induced to form in the extracellular fluid within the specimen, the sample was frozen from the phase change temperature to −50°C at 5°C/min. Replicate samples were frozen in isotonic medium alone or in medium containing 0.85 M glycerol or 0.85 M dimethylsulfoxide. The water transport response of ovarian tissue samples cooled at 40°C/min from 25 to 4°C was significantly different (confidence level >95%) from that of tissue samples cooled at 0.5°C/min, whether in the presence or absence of CPAs. We fitted a model of water transport to the experimentally‐derived volumetric shrinkage data and determined the best‐fit membrane permeability parameters (Lpg and ELp) of equine ovarian tissue during freezing. Subzero water transport parameters of ovarian tissue samples cooled at 0.5°C/min from 25 to 4°C ranged from: Lpg = 0.06 to 0.73 µm/min·atm and ELp = 6.1 to 20.5 kcal/mol. The corresponding parameters of samples cooled at 40°C/min from 25 to 4°C ranged from: Lpg = 0.04 to 0.61 µm/min·atm and ELp = 8.2 to 54.2 kcal/mol. Calculations made of the theoretical response of tissue at subzero temperatures suggest that the optimal cooling rates to cryopreserve ovarian tissue are significantly dependent upon suprazero cooling conditions. Mol. Reprod. Dev. © 2005 Wiley‐Liss, Inc.