| Literature DB >> 24200923 |
N Chen1, Y Gao2, N Yan3, C Liu4, J-G Zhang1, W-M Xing5, D-M Kong6, F-G Meng7.
Abstract
Kainic acid (KA) administration is known to cause seizures and neuronal death in the hippocampus. High-frequency stimulation (HFS) of the hippocampus can be a promising method in the treatment of epilepsy while the mechanism of action is unknown yet. It remains unknown whether HFS is neuroprotective for hippocampal neurons following KA-induced seizures in macaques, although HFS has neuroprotective effects in animal models of Parkinson's disease. We therefore examined the effects of HFS on KA-induced seizures and neuronal survival in macaque's hippocampus. Seizure frequency following KA that led to seizures in macaques was strongly reduced by HFS of the hippocampus. In addition, administration of KA led to marked neuronal apoptosis in the hippocampus, accompanied by increased levels of Bax, activated caspase-3 and decreased levels of Bcl-2. HFS was found to attenuate changes in apoptosis-related proteins and robustly decreased neuronal loss following KA administration. These data indicate that hippocampal HFS can protect hippocampal neurons against KA neurotoxicity, and that HFS neuroprotection is likely to operate with inhibition of apoptosis.Entities:
Keywords: 3,3′-diaminobenzidine; DAB; DBS; EDTA; GCSs; HFS; IPG; KA; MRI; PBS; TLE; TUNEL; TdT; apoptosis; deep brain stimulation; deep brain stimulation (DBS); ethylenediaminetetraacetic acid; generalized clonic seizures; high-frequency stimulation; high-frequency stimulation (HFS); hippocampus; internal pulse generator; kainic acid; kainic acid (KA); magnetic resonance imaging; neuroprotection; phosphate-buffered saline; temporal lobe epilepsy; terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling; terminal deoxynucleotidyltransferase
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Year: 2013 PMID: 24200923 DOI: 10.1016/j.neuroscience.2013.10.059
Source DB: PubMed Journal: Neuroscience ISSN: 0306-4522 Impact factor: 3.590