Non-linear cortico-cortical interactions modulated by cholinergic afferences from the rat basal forebrain

Citation
Aep. Villa et al., Non-linear cortico-cortical interactions modulated by cholinergic afferences from the rat basal forebrain, BIOSYSTEMS, 58(1-3), 2000, pp. 219-228
Citations number
43
Categorie Soggetti
Experimental Biology
Journal title
BIOSYSTEMS
ISSN journal
03032647 → ACNP
Volume
58
Issue
1-3
Year of publication
2000
Pages
219 - 228
Database
ISI
SICI code
0303-2647(200010/12)58:1-3<219:NCIMBC>2.0.ZU;2-W
Abstract
In the adult rat most of basal forebrain cholinergic neurons (BFCN) express the low-affinity p75 nerve growth factor receptor (NGFr). The immunotoxin 192 IgG-saporin (SAP) provokes a selective loss of NGFr-positive BFCN, some what similar to the loss of integrity of BFCN associated with human senile dementia of Alzheimer's type, whereas NGF exerts a trophic action on BFCN. Cortico-cortical interactions are modulated by cholinergic projections of B FCN and it is proposed that alterations of these projections by SAP and by NGF produce opposite effects. This hypothesis was tested by recording multi ple local field potentials (LFPs) in the rat temporal cortex and applying b ispectral analysis to measure phase-coupled frequencies, somewhat analogous to frequencies of resonance. Choline acetyltransferase (ChAT) activity was measured in the septal area in order to assess the effects of the treatmen ts. NGF-treatment increased ChAT activity by 45% and frequencies of non-lin ear coupling were shifted towards frequencies higher than 70 Hz, thus sugge sting the presence of increased functional interactions in the short range. By contrast, SAP provoked a decrease of nearly 40% in ChAT activity and an increase of phase-coupling in the low frequencies (< 50 Hz), being interpr eted as a decreased functional cortico-cortical interaction. Bispectral ana lysis revealed features of the effect of BFCN on cortical activity that cou ld not be observed by other means and offers as a valuable tool of study th at could be extended to the EEG of Alzheimer's patients. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.