1. The membrane properties of cone inner segments dissociated enzymati
cally from monkey retina were studied under voltage-clamp conditions u
sing patch pipettes in the whole-cell clamp configuration. 2. A nonina
ctivating, voltage-gated calcium current was evoked at potentials posi
tive to -60 mV and peaked between -30 and -20 mV when barium was subst
ituted for calcium. Cadmium (50 mu M) but not nickel (50 mu M) blocked
the current. 3. A large calcium-activated anion current (I-An) was ob
served when the membrane potential was set to a level between -60 and
30 mV. The reversal potential of I-An was O mV with chloride as the so
le anion and about -30 and -40 mV when methanesulfonate and D-aspartat
e, respectively, replaced intracellular chloride to set the equilibriu
m potential for chloride at -50 mV. I-An inactivated and oscillated wh
en the membrane potential was maintained at depolarized levels, contra
ry to calcium-activated anionic currents seen in photoreceptors of oth
er species. 4. A sustained-type potassium current was activated by dep
olarizations positive to -50 mV. The time course of activation and dea
ctivation were voltage dependent. This potassium current was partially
blocked by 20 mM tetraethylammonium ions. 5. A transient potassium cu
rrent was activated by depolarizations positive to -20 mV. This curren
t was blocked by 4-amino-pyridine (2 mM) and inactivated with a time c
onstant of similar to 500 ms. The amplitude in response to voltage ste
ps to 45 mV was decreased by prepulses to voltages more positive than
-30 mV. 6. Hyperpolarization negative to -65 mV activated an inward cu
rrent that was completely blocked by external cesium (10 mM). The reve
rsal potential suggested a conductance mechanism permeable to both sod
ium and potassium ions. 7. A calcium-activated potassium current, whic
h was found in salamander photoreceptors, was not detected. 8. The pre
sence of these conductances is expected to influence the membrane pote
ntial and the time course of the light response in monkey cones.