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Aquaporin-4 and epilepsy.

Abstract
Recent studies have implicated glial cells in modulation of synaptic transmission, so it is plausible that glial cells may have a functional role in the hyperexcitability characteristic of epilepsy. Indeed, alterations in distinct astrocyte membrane channels, receptors, and transporters have all been associated with the epileptic state. This review focuses on the potential roles of the glial water channel aquaporin-4 (AQP4) in modulation of brain excitability and in epilepsy. We will review studies of mice lacking AQP4 (Aqp4(-/-) mice) or α-syntrophin (an AQP4 anchoring protein) and discuss the available human studies demonstrating alterations of AQP4 in human epilepsy tissue specimens. We will conclude with new studies of AQP4 regulation and discuss the potential role of AQP4 in the development of epilepsy (epileptogenesis). While many questions remain unanswered, the available data indicate that AQP4 and its molecular partners may represent important new therapeutic targets.
AuthorsDevin K Binder, Erlend A Nagelhus, Ole Petter Ottersen
JournalGlia (Glia) Vol. 60 Issue 8 Pg. 1203-14 (Aug 2012) ISSN: 1098-1136 [Electronic] United States
PMID22378467 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
CopyrightCopyright © 2012 Wiley Periodicals, Inc.
Chemical References
  • Aquaporin 4
Topics
  • Animals
  • Aquaporin 4 (genetics, metabolism)
  • Disease Models, Animal
  • Epilepsy (metabolism, pathology)
  • Humans
  • Mice
  • Mice, Transgenic
  • Neuroglia (metabolism)

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