By Geoffrey Collins (auth.), David E. Pegg, Armand M. Karow Jr. (eds.)
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Extra info for The Biophysics of Organ Cryopreservation
Example text
D. J. Bickis, and P. Edwards, Some observations about the dimethyl sulfoxide permeation in tissues of dog kidney during perfusion, Cryobiology 3:373 (1967) • 85. A. J. S. Filo, Function of autotransplanted kidneys after hypothermic perfusion with dimethylsulfoxide, Cryobiology 14:23 (1977). 86. E. Pegg, Perfusion of rabbit kidneys with cryoprotective agents, Cryobiology 9:411 (1972). 87. B. M. Guttman, Kinetics of permeation and intracellular events associated with Me2 SO permeation of rabbit kidneys during perfusion at 10°C, Cryooiology 19:41 (1982).
5 molar is sufficient to come very close to vitrifying the kidney when it is cooled down below the glass-transition temperature. I am also concerned about many effects of dextrose, not only those brought up by Dr. Fonteles which occur at higher temperatures. I am worried about the Maillard reaction; about the permeation of glucose and subsequent swelling of cells; about the possibility at high tempertures that all that glucose will cause an accumulation of lactic acid and lowering of pH; but I do not think that these are terribly serious problems at 2°C.
Our ability to control vascular pores is much greater now than when we set aside our thoughts of impermeant CPAs for organs. Maybe this is the time to look at them again. ~ 1. E. Lovelock, The protective action of neutral solutes against haemolysis by freezing and thawing, Biochem. J. 56:265 (1954) • 2. M. M. , Ultrastructure-function correlative studies for cardiac cryopreservation. V. Absence of a correlation between electrolyte toxicity and cryoinjury in the slowly frozen, cryoprotected rat heart, Cryobiology 14:418 (1977) • 3.