Abstract
Summary
Ca2+ was added to a buffered medium containing various combinations of K+, fructose, CN-, ouabain, and BSA. Constant osmolarity, pH, and temperature of the incubation media were maintained. Without K+ in the medium, Ca2+ limited the duration of rapid swelling of spermatozoa by causing early onset of shrinkage to about 90% of initial cell volume. Shrinkage occurred sooner as the Ca2+ level increased, and was associated with a fuzzy microscopic appearance of the sperm cells. Addition of 2.25 to 3.0 mM K+, and to a lesser extent 1.0 mM of fructose, delayed the onset of swelling and subsequent shrinkage associated with Ca2+ alone. This delay also was observed in a variety of media which promoted good sperm motility. BSA was able to counteract the effects of Ca2+, but this was abolished by addition of CN-. Fructose overcame the CN- effect, indicating that the process is energy related. It appears likely that Ca2+ enters the cell only after energy sources are depleted, and its presence there causes structural and permeability changes in spermatozoa.
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