Objective: To evaluate whether human spermatozoa preserved in electrolyte-f
ree (EF) solution at 4 degreesC possess normal penetrating capacity.
Study design: The acrosomal status of human spermatozoa cool preserved in E
F solution was evaluated before preservation and before and after reinitiat
ion by using chlortetracycline staining. The zona-free hamster egg sperm pe
netration test was performed using spermatozoa cool preserved in EF solutio
n.
Results: The percentages of capacitated and acrosome-reacted spermatozoa co
ol preserved in EF solution before reinitiation were similar to those of fr
esh spermatozoa, but they significantly increased after reinitiation. The p
enetration rate and fertility index of spermatozoa cool preserved in EF sol
ution were comparable to those of fresh spermatozoa (48.3% vs. 50.8% and 1.
37 +/-0.15 vs. 1.29 +/-0.10, respectively).
Conclusion: Human spermatozoa cool preserved in EF solution for one week ca
n possess as much penetrating capacity as fresh spermatozoa.