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Biology of Reproduction, Vol 21, 319-324, Copyright © 1979 by Society for the Study of Reproduction
1 U. S. Department of Agriculture,
Science and Education Administration,
Animal Science Institute,
Beltsville, Maryland 20705 In 3 experiments boar sperm were treated with butylated hydroxytoluene (BHT) and
subsequently cold shocked at 0°C for 10 min. The effects of cold shock on acrosome morphology,
sperm motility and fertilizing capacity were assessed. In experiment 1 the concentrations of BHT
tested were 0, 0.1, 0.5, 1 and 2 mM. The percentages of acrosomes with a normal apical ridge
(NAR) and of motile sperm after cold shock were higher for sperm treated with 0.5, 1 or 2 mM
BHT than for unrtreated sperm (P<0.01 for each comparison). In experiment 2 the cold shock
protection provided by 2 mM BHT was compared with that of the Beltsville F5 (BF5) extender
containing egg yolk lipoprotein and the Beltsville F3 (BF3) extender containing casein. The percentage of NAR acrosomes after cold shock was significantly higher for sperm treated with BHT
than for sperm extended in BF5 or BF3. When sperm were treated with BHT and then extended
with BF5 or BF3, the percentage of NAR acrosomes after cold shock was significantly lower than
if sperm were treated only with BHT. In experiment 3 sperm that were treated with 2 mM BHT
retained their fertilizing capacity during cold shock while unprotected control sperm lost their
fertilizing capacity during cold shock. These experiments provided conclusive evidence that BHT
protects the morphological and functional integrity of the sperm membranes against cold shock
damage to the extent that boar sperm were capable of fertilizing ova.
Note:
ACKNOWLEDGMENTS
I wish to thank Ms. L. L. Schulman for skilled
technical assistance and Ms. K. L. Pursel for typing the
manuscript.
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