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Repeated intracerebroventricular infusion of nicotine prevents kainate-induced neurotoxicity by activating the α7 nicotinic acetylcholine receptor

Authors
Shin E.-J.Chae J.S.Jung M.-E.Bing G.Ko K.H.Kim W.-K.Wie M.B.Cheon M.-A.Nah S.-Y.Kim H.-C.
Issue Date
2007
Keywords
α7 nicotinic acetylcholine receptor; AP-1 DNA binding activity; Hippocampus; Kainic acid; Neuroprotection; Nicotine
Citation
Epilepsy Research, v.73, no.3, pp 292 - 298
Pages
7
Indexed
SCOPUS
Journal Title
Epilepsy Research
Volume
73
Number
3
Start Page
292
End Page
298
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/18392
DOI
10.1016/j.eplepsyres.2006.11.004
ISSN
0920-1211
1872-6844
Abstract
We examined whether (-)-nicotine infusion can affect kainic acid (KA)-induced neurotoxicity in rats. Although treatment with a single nicotine infusion (0.5 or 1.0 μg/side, i.c.v.) failed to attenuate KA-induced neurotoxicity, repeated nicotine infusions (1.0 μg/side/day for 10 days) attenuated the seizures, the severe loss of cells in hippocampal regions CA1 and CA3, the increase in activator protein (AP)-1 DNA binding activity, and mortality after KA administration. α-Bungarotoxin and mecamylamine blocked the neuroprotective effects of nicotine. These results suggest that repeated nicotine treatment provides α7 nicotinic acetylcholine receptor-mediated neuroprotection against KA toxicity. © 2006 Elsevier B.V. All rights reserved.
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