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Volume 17, Number 10,
Issue of May 15, 1997
pp. 3467-3475
Copyright ©1997 Society for Neuroscience
Silent GABAA Synapses during Flurazepam Withdrawal
Are Region-Specific in the Hippocampal Formation
Received Dec. 3, 1996; revised Jan. 16, 1997; accepted March 3, 1997.
Pierrick Poisbeau,
Stephen R. Williams, and
Istvan Mody
Reed Neurological Research Center, University of California at Los
Angeles School of Medicine, Department of Neurology, Los Angeles,
California 90095-1769
Whole-cell patch-clamp recordings were made from CA1 pyramidal and
dentate gyrus granule cells (GCs) in hippocampal slices to assess the
effects of withdrawal from chronic flurazepam (FRZ) treatment on the
function of synaptic GABAA receptors. In slices from
control rats, acute perfusion of FRZ (30 µM) increased
the monoexponential decay time constant of miniature IPSCs (mIPSCs) in
CA1 and GCs (from 3.4 ± 0.6 to 7.6 ± 2.1 msec and from
4.2 ± 0.6 to 7.1 ± 1.8 msec, respectively) but did not
change their mean conductance, 10-90% rise time, or frequency of
occurrence. Withdrawal (2-5 d) from chronic in vivo FRZ
treatment (40-110 mg/kg per day, per os) resulted in a dramatic loss
of mIPSCs in CA1 neurons. On day 5 of withdrawal, no mIPSCs could be
recorded in 40% of CA1 pyramidal cells. In the remaining 60% of the
neurons, mIPSCs had a reduced mean conductance (from 0.78 ± 0.12 nS in vehicle-treated controls to 0.31 ± 0.05 nS) and a
diminished frequency of occurrence (from 20.7 ± 7.9 to 4.1 ± 0.6 Hz). We have estimated that >80% of GABAA synapses
on CA1 pyramidal cells had become silent, whereas at still-active
synapses the number of functional GABAA receptor channels
decreased by 60%. This reduction rapidly reverted to control levels on
day 6 of withdrawal. FRZ withdrawal did not alter mIPSC properties in
GCs. Our results are consistent with the hypothesis that chronic
benzodiazepine treatment leads to a reduced number of functional
synaptic GABAA receptors in a region-specific manner that
may stem from differences in the subunit composition of synaptic
GABAA receptors.
Key words:
withdrawal;
inhibitory synapses;
drug dependence;
benzodiazepines;
GABAA;
IPSCs;
hippocampus
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