Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2169611 | Cryobiology | 2006 | 6 Pages |
Abstract
The water transport response during freezing of sperm cells of Morone chrysops (white bass, WB) was obtained using a shape-independent differential scanning calorimeter (DSC) technique. Sperm cell suspensions were frozen at a cooling rate of 20 °C/min in two different media: (1) without cryoprotective agents (CPAs), or (2) with 5% (v/v) dimethyl sulfoxide (Me2SO). For calculations, the sperm cell was modeled as a cylinder of length 24.8 μm and diameter of 0.305 μm, while the osmotically inactive cell volume (Vb) was assumed to be 0.6 Vo, where Vo was the isotonic or the initial cell volume. By fitting a model of water transport to the experimentally determined water transport data, the best fit membrane permeability parameters (reference membrane permeability to water, Lpg or Lpg[cpa] and the activation energy, ELp or ELp[cpa]) were determined, and ranged from Lpg = 0.51-1.7 Ã 10â15 m3/Ns (0.003-0.01 μm/min-atm), and ELp = 83.6-131.3 kJ/mol (20.0-31.4 kcal/mol). The parameters obtained in this study suggest that the optimal rate of cooling for M. chrysops sperm cells is â¼22 °C/min, a value that compares closely with experimentally determined optimal rates of cooling (â¼16 °C/min).
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Authors
R.V. Devireddy, W.T. Campbell, J.T. Buchanan, T.R. Tiersch,