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Volume 17, Number 19,
Issue of October 1, 1997
pp. 7532-7540
Copyright ©1997 Society for Neuroscience
Rapid Seizure-Induced Reduction of Benzodiazepine and
Zn2+ Sensitivity of Hippocampal Dentate Granule Cell
GABAA Receptors
Received March 7, 1997; revised June 24, 1997; accepted July 21, 1997.
Jaideep Kapur1 and
Robert L. Macdonald1, 2
Departments of 1 Neurology and
2 Physiology, University of Michigan Medical Center, Ann
Arbor, Michigan 48104-1687
Fast synaptic inhibition in the forebrain is mediated primarily by
GABA acting on GABAA receptors (GABARs). GABARs are
regulated by numerous positive (barbiturates, benzodiazepines, and
neurosteroids) and negative (picrotoxin, bicuculline, and
Zn2+) allosteric modulators. The sensitivity of
GABARs to GABA and to allosteric modulators changes gradually during
normal development, during development of chronic epilepsy, and after
prolonged exposure to GABAR agonists. Here we report the development of
rapid functional plasticity of GABARs occurring over 45 min of
continuous seizures (status epilepticus) in rats. Seizures induced in
rats by administration of lithium followed by pilocarpine were readily
terminated by the benzodiazepine diazepam when administered early
during the seizures (after 10 min of seizures). However, during status
epilepticus, there was a substantial reduction of diazepam potency for
termination of the seizures. To determine whether the loss of
sensitivity of the animals to diazepam was caused by an alteration of
GABAR functional properties, we obtained whole-cell GABAR currents from hippocampal dentate granule cells isolated acutely from control rats
and from rats undergoing status epilepticus. GABAR properties were
characterized by determining GABA sensitivity and the sensitivity of
GABARs to regulation by benzodiazepines, barbiturates, and Zn2+. When compared with those from naive controls,
GABAR currents from rats undergoing status epilepticus were less
sensitive to diazepam and Zn2+ but retained their
sensitivity to GABA and pentobarbital. We conclude that the prolonged
seizures of status epilepticus rapidly altered the functional
properties of hippocampal dentate granule cell GABARs.
Key words:
status epilepticus;
seizures;
GABA;
diazepam;
benzodiazepines;
zinc;
GABAA receptors;
pentobarbital;
barbiturates;
dentate gyrus;
granule cells;
hippocampus
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