This study investigated the use of human follicular fluid and pentoxif
ylline as inducers of the human sperm acrosome reaction in vitro. Moti
le sperm suspensions were prepared using a discontinuous Percoll gradi
ent, preincubated for 3 h, divided into aliquots and exposed to variou
s concentrations of non-heat-inactivated follicular fluid for 1 and 24
h and pentoxifylline for 30 min. Detection of the acrosome reaction i
nvolved the combined use of a fluorescent vital stain, H33258, and flu
orescein isothiocyanate-conjugated peanut agglutinin (FITC-PNA). A sho
rt (1 h) exposure to follicular fluid at Concentrations of 50% or more
, did not compromise sperm motility and significantly increased the pr
oportion of spermatozoa having completed the acrosome reaction. Simila
rly, a 30 min exposure to pentoxifylline also significantly increased
the proportion of spermatozoa having completed the acrosome reaction.