Voltage-gated ionic currents were recorded from cultured trout astrocy
tes with the whole-cell variation of the patch-clamp technique. In a s
ubpopulation of astrocytes depolarizations above -40 mV activated a fa
st transient inward current that was identified as a sodium current by
ion substitution experiments, its current reversal potential, and its
TTX-sensitivity. Regarding threshold of activation, peak current volt
age, and amplitude this current closely resembled those previously des
cribed for mammalian astrocytes. Voltage-dependence of inactivation an
d kinetics, however, markedly differed from the ''glial-like'' sodium
current occurring in mammalian hippocampal or optic nerve astrocytes,
since the sodium current of trout astrocytes exhibited a faster time c
ourse of activation and decay and a more depolarized steady-state inac
tivation curve with midpoints close to -60 mV. During a period of 2 we
eks in culture the biophysical properties of the sodium current did no
t change significantly, albeit a continuous decrease in current densit
y was observed. At depolarizing voltage steps positive to -40 mV, addi
tionally voltage-gated potassium outward currents were evoked, which c
ould be separated into a steady-state current with delayed rectifier p
roperties and an inactivating component resembling the A-type current.
Moreover, in a subpopulation of astrocytes an inward potassium curren
t was elicited at hyperpolarizing potentials, which exhibited biophysi
cal features consistent with the potassium inward rectifier of mammali
an astrocytes. (C) 1994 Wiley-Liss, Inc.