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PMID: 7472485 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Basal forebrain cholinergic lesions disrupt increments but not decrements in conditioned stimulus processing.

Chiba AA, Bucci DJ, Holland PC, Gallagher M

Abstract

Magnocellular neurons in the basal forebrain provide the major cholinergic innervation of cortex. Recent research suggests that this cholinergic system plays an important role in the regulation of attentional processes. The present study examined the ability of rats with selective immunotoxic lesions of these neurons (made with 192 IgG-saporin) to modulate attention within an associative learning framework. Each rat was exposed to conditioned stimuli (CS) that were either consistent or inconsistent predictors of subsequent cues. Intact control rats showed increased CS associability when that cue was an inconsistent predictor of a subsequent cue, whereas lesioned rats were impaired in increasing attention to the CS when its established relation to another cue was modified. In a separate experiment designed to test latent inhibition, it was shown that removal of the corticopetal cholinergic neurons spared a decrement in associability that occurs when rats are extensively preexposed to a CS prior to conditioning. These data indicate that the cholinergic innervation of cortex is critical for incrementing, but not for decrementing attentional processing. The specific behavioral tests used to assess the role of the basal forebrain cholinergic system in the present study were previously used to identify a role for the amygdala central nucleus in attention (Holland and Gallagher, 1993b). Those studies, together with the results in this report, indicate that regulation of attentional processes during associative learning may be mediated by projections from the amygdala to the basal forebrain cholinergic system.

MeSH Terms
Animals Antibodies, Monoclonal/pharmacology Association Learning/physiology Attention/physiology Behavior, Animal/physiology Cholinergic Agents/pharmacology Conditioning, Classical/physiology Cues Immunotoxins/pharmacology Male N-Glycosyl Hydrolases Neural Inhibition Parasympathetic Nervous System/drug effects,physiology Prosencephalon/drug effects,physiology Rats Rats, Inbred Strains Ribosome Inactivating Proteins, Type 1 Saporins
Chemicals
192 IgG-saporin Antibodies, Monoclonal Cholinergic Agents Immunotoxins Ribosome Inactivating Proteins, Type 1 N-Glycosyl Hydrolases Saporins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Chiba A A
Department of Psychology, University of North Carolina at Chapel Hill 27599, USA.
Bucci D J
Holland P C
Gallagher M
Article Info
Journal
The Journal of neuroscience : the official journal of the Society for Neuroscience
Abbr.
J Neurosci
ISSN
0270-6474
Published
1995-11-00
Pages
7315-22
Language
English
Region
United States
NLM ID
8102140
PMCID
PMC6578087
Subset
IM
Grants
NIMH NIH HHS · F32-MH1099 · United States
NIMH NIH HHS · KO5-MH01149 · United States
NIA NIH HHS · P0-AG09973 · United States
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