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The Journal of Neurophysiology Vol. 82 No. 1 July 1999, pp. 248-254
Copyright ©1999 by the American Physiological Society
Department of Physiology, University of Saskatchewan, Saskatoon, Saskatchewan, S7N 5E5 Canada
Bekar, Lane K. and
Wolfgang Walz.
Evidence for Chloride Ions as Intracellular Messenger Substances
in Astrocytes. J. Neurophysiol. 82: 248-254, 1999.
Cultured rat hippocampal astrocytes were used to
investigate the mechanism underlying the suppression of
Ba2+-sensitive K+ currents by GABAA
receptor activation. Muscimol application had two effects on whole cell
currents: opening of the well-known Cl
channel of the
GABAA receptor and a secondary longer-lasting blockade of
outward K+ currents displaying both peak and plateau
phases. This blockade was independent of both Na+ (inside
and outside) and ATP in the pipette. It also seemed to be independent
of muscimol binding to the receptor because picrotoxin application
showed no effect on the K+ conductance. The effect is
blocked when anion efflux is prevented by replacing Cl
with gluconate (both inside and out) and is enhanced with more permeant
anions such as Br
and I
. Moreover, the
effect is reproduced in the absence of muscimol by promoting
Cl
efflux via lowering of extracellular Cl
levels. These results, along with the requirement for Cl
efflux in muscimol experiments, show a strong dependency of the secondary blockade on Cl
efflux through the
Cl
channel of the GABAA receptor. We
therefore conclude that changes in the intracellular Cl
concentration alter the outward K+ conductances of
astrocytes. Such a Cl
-mediated modulation of an
astrocytic K+ conductance will have important consequences
for the progression of spreading depression through brain tissue and
for astrocytic swelling in pathological situations.
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