Journal
NEUROSCIENCE
Volume 294, Issue -, Pages 166-171Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2015.03.022
Keywords
acetylcholine; LTP; LTD; synaptic transmission; alpha-bungarotoxin
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Funding
- Ministry of Education, Universities and Research Project Research on the Molecular Mechanisms Involved in Ageing
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The primary visual cortex (V1) is the first step in visual information processing and its function may be modulated by acetylcholine through nicotinic receptors (nAChRs). Since our previous work demonstrated that visual acuity and cortical spatial resolution limit were significantly reduced in alpha 7 knock-out (KO) mice in the absence of retinal alterations, we decided to characterize the contribution of homomeric alpha 7 nicotinic receptors (alpha 7nAChRs) to visual information processing at the cortical level. We evaluated long-term forms of synaptic plasticity in occipital slices containing V1 from alpha 7 KO mice and in wild-type (WT) slices perfused with nAChRs selective blocking agents. In alpha 7 KO mice slices, electrophysiological recordings demonstrated the absence of long-term potentiation (LTP) and long-term depression (LTD) in layer II/III after the stimulation of different intracortical pathways (layer IV or II/III). Furthermore, the acute and selective blockade of a7nAChRs in slices from WT mice with either alpha-bungarotoxin or methyllycaconitine did not alter the expression of LTP and LTD. Conversely, the perfusion with the unspecific nAChRs antagonist mecamylamine impaired LTP and LTD. Our results suggest the presence of impaired synaptic plasticity in the V1 of alpha 7 KO mice and indicate a different contribution of nAChRs to visual cortex function. (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.
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