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dc.contributor.authorNúñez Molina, Ángel-
dc.contributor.authorBuño, Washinton-
dc.date.accessioned2013-02-20T16:14:39Z-
dc.date.available2013-02-20T16:14:39Z-
dc.date.issued1992-
dc.identifierdoi: 10.1016/0014-4886(92)90061-T-
dc.identifierissn: 0014-4886-
dc.identifier.citationExperimental Neurology 115: 266- 270 (1992)-
dc.identifier.urihttp://hdl.handle.net/10261/67093-
dc.description.abstractThe effects of intracellular diffusion of the lidocaine derivative anesthetic QX-314 and of Cs+, which block Na+ and K+ conductances, respectively, were investigated in vivo in rat CA1 and CA3 pyramidal neurons to demonstrate slow Ca2+-related events. QX-314 loading prevented fast Na+ spikes, but slower presumably Ca2+ spikes remained. A slower and a faster duration type of QX-314-resistant spikes were observed. The former had high thresholds, while the latter was activated at moderate depolarized levels. The slower and the faster QX-314-resistant spikes fired at frequencies up to 8/s and 35/s and were 35-60 and 5-10 ms in duration, respectively. With Cs+ loading, pyramidal neurons depolarized and slow, presumably Ca2+, and fast Na+ spikes widened. Fast spikes usually showed a prominent shoulder and a slower repolarization. No differences were observed between drug effects in CA1 and CA3 neurons. In terms of their possible participation in θ rhythm genesis the slow QX-314-resistant events display the correct frequency and duration and can oscillate regeneratively.-
dc.language.isoeng-
dc.publisherAcademic Press-
dc.rightsclosedAccess-
dc.titleIntracellular effects of QX-314 and Cs+ in hippocampal pyramidal neurons in vivo-
dc.typeartículo-
dc.identifier.doi10.1016/0014-4886(92)90061-T-
dc.date.updated2013-02-20T16:14:39Z-
dc.description.versionPeer Reviewed-
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