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Prog Neurobiol. 2011 Oct;95(2):104-32. doi: 10.1016/j.pneurobio.2011.07.003. Epub 2011 Jul 23.

GABAergic synchronization in the limbic system and its role in the generation of epileptiform activity.

Author information

1
Montreal Neurological Institute and Departments of Neurology & Neurosurgery, and of Physiology, McGill University, Montreal H3A 2B4 Quebec, Canada. massimo.avoli@mcgill.ca

Abstract

GABA is the main inhibitory neurotransmitter in the adult forebrain, where it activates ionotropic type A and metabotropic type B receptors. Early studies have shown that GABA(A) receptor-mediated inhibition controls neuronal excitability and thus the occurrence of seizures. However, more complex, and at times unexpected, mechanisms of GABAergic signaling have been identified during epileptiform discharges over the last few years. Here, we will review experimental data that point at the paradoxical role played by GABA(A) receptor-mediated mechanisms in synchronizing neuronal networks, and in particular those of limbic structures such as the hippocampus, the entorhinal and perirhinal cortices, or the amygdala. After having summarized the fundamental characteristics of GABA(A) receptor-mediated mechanisms, we will analyze their role in the generation of network oscillations and their contribution to epileptiform synchronization. Whether and how GABA(A) receptors influence the interaction between limbic networks leading to ictogenesis will be also reviewed. Finally, we will consider the role of altered inhibition in the human epileptic brain along with the ability of GABA(A) receptor-mediated conductances to generate synchronous depolarizing events that may lead to ictogenesis in human epileptic disorders as well.

PMID:
21802488
PMCID:
PMC4878907
DOI:
10.1016/j.pneurobio.2011.07.003
[Indexed for MEDLINE]
Free PMC Article

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