VOLUME-SENSITIVE CHLORIDE CHANNELS BLOCKED BY NEUROPROTECTIVE DRUGS IN HUMAN GLIAL-CELLS (U-138MG)

Authors
Citation
Ar. Bausch et G. Roy, VOLUME-SENSITIVE CHLORIDE CHANNELS BLOCKED BY NEUROPROTECTIVE DRUGS IN HUMAN GLIAL-CELLS (U-138MG), Glia, 18(1), 1996, pp. 73-77
Citations number
27
Categorie Soggetti
Neurosciences
Journal title
GliaACNP
ISSN journal
08941491
Volume
18
Issue
1
Year of publication
1996
Pages
73 - 77
Database
ISI
SICI code
0894-1491(1996)18:1<73:VCCBBN>2.0.ZU;2-6
Abstract
Glial cell swelling in hypotonic media activates an anionic channel th at was found previously to be permeable to amino acids. It is possible that the same channel is also activated when glial cells swell in pat hologic conditions, like ischemia or hypoxia, and it could be partly r esponsible for the release of glutamate appearing in such conditions. Many drugs have been developed to block glutamate release during ische mia. Six of these drugs were tested on human glial cells (U-138MG) in vitro to determine if they could block the swelling-activated anionic channels. Three of them, phenytoin, lidocaine, and flunarizine, had no effect. The other three could block the anionic channels: riluzole, n izofenone, and BW1003C87. Such blocking was reversible and the half in hibition concentration (ICE,) of each of these drugs was within that o bserved for their inhibition of glutamate release by various authors. An important advantage of these three drugs is their capacity to inhib it glutamate release after the beginning of ischemia. It is concluded that the volume-sensitive anionic channel could be partly responsible for glutamate release during a cerebral ischemia. (C) 1996 Wiley-Liss, Inc.