The purpose of this study was to examine cation channel activity in the api
cal membrane of the outer medullary collecting duct of the inner stripe (OM
CDi) using the patch-clamp technique. In freshly isolated and lumen-opened
rabbit OMCDi, we have observed a single channel conductance of 23.3 +/- 0.6
pS (n = 17) in cell-attached (c/a) patches with high KCl in the bath and i
n the pipette at room temperature. Channel open probability varied among pa
tches from 0.06 +/- 0.01 at -60 mV (n = 5) to 0.31 +/- 0.04 at 60 mV (n = 6
) and consistently increased upon membrane depolarization. In inside-out (i
/o) patches with symmetrical KCl solutions, the channel conductance (22.8 /- 0.8 pS; n = 10) was similar as in the c/a configuration. Substitution of
the majority of Cl- with gluconate from KCl solution in the pipette and ba
th did not significantly alter reversal potential (E-rev) or the channel co
nductance (19.7 +/- 1.1 pS in asymmetrical potassium gluconate, n. = 4; 21.
4 +/- 0.5 pS in symmetrical potassium gluconate, n = 3). Experiments with 1
0-fold lower KCl concentration in bath solution in i/o patches shifted E-re
v to near the E-rev of K+. The estimated permeability of K+ vs. Cl- was ove
r 10, and the conductance was 13.4 +/- 0.1 pS (n = 3). The channel did not
discriminate between K+ and Na+, as evidenced by a lack of a shift in the E
-rev with different K+ and Na+ concentration solutions in i/o patches (n =
3). The current studies demonstrate the presence of cation channels in the
apical membrane of native OMCDi cells that could participate in K+ secretio
n or Na+ absorption.