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The Journal of Neuroscience, December 1, 2001, 21(23):9083-9091
Agonist Trapping by GABAA Receptor Channels
Matt T.
Bianchi1 and
Robert L.
Macdonald2, 3, 4
1 Neuroscience Graduate Program, University of
Michigan, Ann Arbor, Michigan 48104-1687, and Departments of
2 Neurology, 3 Molecular Physiology and
Biophysics, and 4 Pharmacology, Vanderbilt University,
Nashville, Tennessee 37212
GABAergic IPSCs have a relatively slow decay (deactivation)
that appears to result from GABAA receptor channel openings
that occur well beyond the predicted duration of free GABA at central synapses. Open and desensitized states have been suggested to prevent
dissociation of agonist from the receptor, thus prolonging deactivation. However, simultaneous assessment of GABA binding and
channel gating has not been possible. We developed a functional assay
for occupancy of the GABA binding site or sites to test the GABA
"trapping" hypothesis. Deactivation currents were compared in the
absence and presence of bicuculline, a competitive antagonist that also
allosterically inhibits GABAA receptors. This provided a
model-independent, functional test of the hypothesis that GABA is
trapped on the receptor during gating: bicuculline could only inhibit
the channel if it was open but unbound by GABA. Although bicuculline
inhibited spontaneous and neurosteroid-activated GABAA receptor currents, it failed to alter the deactivation time course of
GABA-activated GABAA receptor currents. Protection of
deactivation current from bicuculline block indicated that GABA
remained bound to the receptors while the channel was open, thus
suggesting that all open states, as well as all closed and desensitized
states from which channel opening can occur, must be GABA liganded
states. Trapping may be specific to agonists, because the positive
allosteric modulator diazepam unbound from GABAA receptors
independent of GABA binding and channel activity.
Key words:
GABAA receptor; deactivation; inverse
agonist; GABA binding; concentration jump; diazepam
Copyright © 2001 Society for Neuroscience 0270-6474/01/21239083-09$05.00/0
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