Channelpedia

PubMed 22249839


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: Cav2.1



Title: Neuronal P/Q-type calcium channel dysfunction in inherited disorders of the CNS.

Authors: Sanjeev Rajakulendran, Diego Kaski, Michael G Hanna

Journal, date & volume: , 2012 Jan 17 , ,

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/22249839


Abstract
The past two decades have witnessed the emergence of a new and expanding field of neurological diseases--the genetic ion channelopathies. These disorders arise from mutations in genes that encode ion channel subunits, and manifest as paroxysmal attacks involving the brain or spinal cord, and/or muscle. The voltage-gated P/Q-type calcium channel (P/Q channel) is highly expressed in the cerebellum, hippocampus and cortex of the mammalian brain. The P/Q channel has a fundamental role in mediating fast synaptic transmission at central and peripheral nerve terminals. Autosomal dominant mutations in the CACNA1A gene, which encodes voltage-gated P/Q-type calcium channel subunit α(1) (the principal pore-forming subunit of the P/Q channel) are associated with episodic and progressive forms of cerebellar ataxia, familial hemiplegic migraine, vertigo and epilepsy. This Review considers, from both a clinical and genetic perspective, the various neurological phenotypes arising from inherited P/Q channel dysfunction, with a focus on recent advances in the understanding of the pathogenetic mechanisms underlying these disorders.