Title
Chronic deficit in the expression of voltage-gated potassium channel Kv3.4 subunit in the hippocampus of pilocarpine-treated epileptic rats
Date Issued
12 January 2011
Access level
open access
Resource Type
journal article
Author(s)
Pacheco Otalora L.F.
Skinner F.
Oliveira M.S.
Farrell B.
Arshadmansab M.F.
Pandari T.
Garcia I.
Robles L.
Rosas G.
Mello C.F.
Ermolinsky B.S.
Garrido-Sanabria E.R.
Abstract
Voltage gated K+ channels (Kv) are a highly diverse group of channels critical in determining neuronal excitability. Deficits of Kv channel subunit expression and function have been implicated in the pathogenesis of epilepsy. In this study, we investigate whether the expression of the specific subunit Kv3.4 is affected during epileptogenesis following pilocarpine-induced status epilepticus. For this purpose, we used immunohistochemistry, Western blotting assays and comparative analysis of gene expression using TaqMan-based probes and delta-delta cycle threshold (ΔΔCT) method of quantitative real-time polymerase chain reaction (qPCR) technique in samples obtained from age-matched control and epileptic rats. A marked down-regulation of Kv3.4 immunoreactivity was detected in the stratum lucidum and hilus of dentate gyrus in areas corresponding to the mossy fiber system of chronically epileptic rats. Correspondingly, a 20% reduction of Kv3.4 protein levels was detected in the hippocampus of chronic epileptic rats. Real-time quantitative PCR analysis of gene expression revealed that a significant 33% reduction of transcripts for Kv3.4 (gene Kcnc4) occurred after 1 month of pilocarpine-induced status epilepticus and persisted during the chronic phase of the model. These data indicate a reduced expression of Kv3.4 channels at protein and transcript levels in the epileptic hippocampus. Down-regulation of Kv3.4 in mossy fibers may contribute to enhanced presynaptic excitability leading to recurrent seizures in the pilocarpine model of temporal lobe epilepsy. © 2010 Elsevier B.V. All rights reserved.
Start page
308
End page
316
Volume
1368
Language
English
OCDE Knowledge area
Neurociencias Bioquímica, Biología molecular
Scopus EID
2-s2.0-78651063694
PubMed ID
Source
Brain Research
ISSN of the container
00068993
Sponsor(s)
This work was supported by grants to E.R.G.S from National Institute of Health as follows: NS063950-03 , 3SC1NS063950-03S1 (ARRA), P20MD001091 , P20MD000161 , MBRS-RISE grant # 1R25GM06592501A1 . F.S, L.R. and I.G were supported by MBRS-RISE. M.F.A and F.S were support by research scholarship by LSAMP and M.S.O was supported by the PDEE grant # 3229-08-4 from CAPES, Brazil. Phase IV project founded by the National Science Foundation grant number HRD-0703584.
Sources of information: Directorio de Producción Científica Scopus