A channel was identified in cell-attached recordings in rat hippocampal neu
rones maintained in culture. This channel, which was highly active at the r
esting membrane potential, was present in most (73 %) parches studied. The
channel was characterized by long duration openings and a high open probabi
lity (P-o, mean value 0.73 at -70 mV) at negative patch potentials with mil
d voltage dependence over the range -40 to -120 mV. It showed inward rectif
ication. There were up to five active channels in cell-attached recordings
in experiments where the cells were bathed in sodium-containing Locke solut
ion. The single channel conductances in cell-attached recordings with 140 o
r 40 mM K+ in the patch pipette were 26 and 12 pS, respectively. The channe
l was therefore selective for K+ over Na+. The channel was not permeable to
Rb+ ions. The single channel conductance was 24 pS in excised inside-out p
atches bathed in symmetrical K+ (140mM) solutions. Examination of the chann
el kinetics revealed that both the open and closed time distributions could
be fitted by the sum of three exponentials, there being no pronounced volt
age sensitivity between -60 and -120 mV. The 26 pS K+ channel was insensiti
ve to extracellular TEA, apamin, 4-AP and dequalinium. Neither was it sensi
tive to intracellular Ca2+. Extracellular Ba2+ was effective in reversibly
blocking the channel, the IC50 being 2.0 mM. There was no obvious effect of
bath application of the K+ channel opener, lemakalim, or a cAMP analogue.
This channel appears to contribute a significant proportion (at least 30 %)
of the resting conductance in these neurones.