The voltage-gated Ca2+ current in cone photoreceptors operates over on
ly a small part of the physiological voltage range produced by light a
nd, consequently, appears insufficient for controlling transmitter rel
ease. We have used a whole-cell voltage clamp to measure membrane curr
ent and the capacitance change produced by exocytosis in solitary cone
and rod photoreceptors isolated from the salamander retina. In both t
ypes of photoreceptor, Ca2+ influx through voltage-gated Ca2+ channels
initiated exocytosis. In addition, Ca2+ influx through a cGMP-gated c
hannel in the inner segment and synaptic processes of cones also initi
ated exocytosis. The cGMP-gated current sustained exocytosis over the
entire physiological voltage range.