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The Journal of Neuroscience, June 8, 2005, 25(23):5511-5520; doi:10.1523/JNEUROSCI.0900-05.2005

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Neurobiology of Disease
Status Epilepticus Increases the Intracellular Accumulation of GABAA Receptors

Howard P. Goodkin,1,2 Jwu-Lai Yeh,3 and Jaideep Kapur1

Departments of 1Neurology and 2Pediatrics, University of Virginia Health Sciences Center, Charlottesville, Virginia 22908, and 3Department and Graduate Institute of Pharmacology, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan

Status epilepticus is a neurological emergency that results in mortality and neurological morbidity. It has been postulated that the reduction of inhibitory transmission during status epilepticus results from a rapid modification of GABAA receptors. However, the mechanism(s) that contributes to this modification has not been elucidated. We report, using an in vitro model of status epilepticus combined with electrophysiological and cellular imaging techniques, that prolonged epileptiform bursting results in a reduction of GABA-mediated synaptic inhibition. Furthermore, we found that constitutive internalization of GABAA receptors is rapid and accelerated by the increased neuronal activity associated with seizures. Inhibition of neuronal activity reduced the rate of internalization. These findings suggest that the rate of GABAA receptor internalization is regulated by neuronal activity and its acceleration contributes to the reduction of inhibitory transmission observed during prolonged seizures.

Key words: GABAA receptor; endocytosis; status epilepticus; neuronal activity; plasticity; synapse


Received March 7, 2005; revised April 18, 2005; accepted April 26, 2005.




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