We have characterized ionic changes triggered by progesterone in human
spermatozoa. This steroid, which is a fast-acting stimulator of the a
crosome reaction, triggered a rapid increase in the cytoplasmic Ca2+ c
oncentration ([Ca2+]i) which was entirely due to influx across the pla
sma membrane, as it was obliterated by chelation of extracellular Ca2. Ca2+ fluxes were insensitive to verapamil and pertussis toxin, thus
suggesting that they did not occur via voltage-gated channels and did
not involve a pertussis toxin-sensitive G protein, and were potentiate
d in Na+-free, choline-containing or methylglucamine-containing medium
. Progesterone also caused a depolarization of the plasma membrane in
Na+-containing as well as in choline- or methyl-glucamine-containing s
aline; depolarization was larger in the absence of extracellular Ca2+,
suggesting that Na+ and Ca2+ fluxes occurred through the same channel
. Progesterone was able to trigger the acrosome reaction in the three
media investigated (Na+, choline and methylglucamine), provided that e
xtracellular Ca2+ was also present. We conclude that progesterone acti
vates a membrane ion channel that is permeable to monovalent cations a
s well as to Ca2+.