Previous data showed that a Na+-transmembrane flux was accompanied with acr
osome reaction of sperm. However, the electrophysiological recording and ch
aracterization of Na+ current in human sperm membrane have not been yet rep
orted. In the present investigation, membrane proteins extracted from human
sperms were reassembled into liposome bilayer, and then the liposomes were
fused by dehydration-rehydration into giant liposomes with the diameter of
more than 10 mum. By patch clamping the giant liposomes two kinds of singl
e channel currents were recorded in a NaCl solution system. Both of them we
re Na+-carried, TTX-sensitive and strongly rectifying, but with different u
nit conductance and open probability. Moreover, bursting activity and chann
el-substates as well as two open time constants were observed in the larger
channel.