Fig. 1. Na+, K+-pump currents in cortical neurons and its ATP
dependence. Identification of the membrane current associated with activities
of the Na+, K+-ATPase. (A) Whole-cell recordings of the
Na+, K+-pump current, Ipump, in
cultured cortical neurons. At the holding potential of 60 mV, an inward
current was triggered by an acute application of the Na+,
K+-pump inhibitor ouabain (1 mM) or strophanthidin (500 µM),
corresponding to the block of a tonic activity of the Na+,
K+-pump. The effect of strophanthidin was reversible, an outward
current appeared owing to reactivation of the Na+,
K+-ATPase. (B) The membrane current associated with the
Na+, K+-pump was highly dependent on the presence of
intracellular Na+ ([Na+]i) and extracellular
K+ ([K+]o). When Na+ was removed
from the pipette internal solution or K+ was removed from the
extracellular solution, little membrane current was observed upon application
of 500 µM strophanthidin. (C) The I-V relationship of Na+,
K+-pump current obtained by subtracting I-V curves constructed by
membrane current responses to various voltage steps from the 100 mV
holding potential in the presence and absence of 1 mM ouabain. The reversal
potential of the pump current estimated from the I-V curve is about 133
mV. The relationship showed an outward rectification at depolarized potentials
and a decrease of the current at very positive potentials, both are consistent
with previous reports of the pump current
(De Weer et al., 1988).
Voltage pulses were applied every 4 seconds with increments of 20 mV starting
at 100 mV. n=10. (D) The ATP-dependence of
Ipump was revealed by comparison of the currents recorded
with microelectrodes containing either 5 mM ATP or ATP-free internal solution.
In the presence of ATP, there was no time-dependent decline of
Ipump; without ATP in the internal solution,
Ipump was greatly diminished 10 minutes after establishing
the whole-cell configuration. n=10 and 8 for ATP and ATP-free groups,
respectively. *P<0.05 compared with the current at 1-2
minutes.