PubMed 21640179
Referenced in: none
Automatically associated channels: Cav3.1 , Cav3.2 , Cav3.3 , Kir2.3
Title: Anti-epileptic drugs delay age-related loss of spiral ganglion neurons via T-type calcium channel.
Authors: Debin Lei, Xia Gao, Philip Perez, Kevin K Ohlemiller, Chien-Chang Chen, Kevin P Campbell, Aizhen Yang Hood, Jianxin Bao
Journal, date & volume: Hear. Res., 2011 Aug , 278, 106-12
PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/21640179
Abstract
Loss of spiral ganglion neurons is a major cause of age-related hearing loss (presbycusis). Despite being the third most prevalent condition afflicting elderly persons, there are no known medications to prevent presbycusis. Because calcium signaling has long been implicated in age-related neuronal death, we investigated T-type calcium channels. This family is comprised of three members (Ca(v)3.1, Ca(v)3.2, and Ca(v)3.3), based on their respective main pore-forming alpha subunits: α1G, α1H, and α1I. In the present study, we report a significant delay of age-related loss of cochlear function and preservation of spiral ganglion neurons in α1H null and heterozygous mice, clearly demonstrating an important role for Ca(v)3.2 in age-related neuronal loss. Furthermore, we show that anticonvulsant drugs from a family of T-type calcium channel blockers can significantly preserve spiral ganglion neurons during aging. To our knowledge, this is the first report of drugs capable of diminishing age-related loss of spiral ganglion neurons.