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PMID: 7898665 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Behavioural, histochemical and biochemical consequences of selective immunolesions in discrete regions of the basal forebrain cholinergic system.

Neuroscience ·Vol. 63 ·No. 1 ·1994-11-00 ·Pages 95-122

Torres EM, Perry TA, Blockland A, Wilkinson LS, Wiley RG, Lappi DA, Dunnet SB

Abstract

The effectiveness of a recently developed immunotoxin, 192 IgG-saporin, was evaluated for making selective lesions of subgroups of basal forebrain cholinergic neurons. Following a pilot series of injections into the nucleus basalis magnocellularis to establish the effective dose for intraparenchymal lesions, separate groups of rats received injections of the immunotoxin into the septum, into the diagonal band of Broca or into the nucleus basalis magnocellularis. The lesions produced extensive and effective loss of cholinergic neurons in the discrete areas of the basal forebrain, as identified by loss of cells staining for acetylcholinesterase and p75NGFr, with a parallel loss of acetylcholinesterase staining and choline acetyltransferase activity in the target areas associated with each injection site in the dorsolateral neocortex, cingulate cortex and hippocampus. The selectivity of the lesion for cholinergic neurons was supported by the lack of gliosis and sparing of small to medium-sized cells at the site of injection of the toxin, including the glutamate decarboxylase immunoreactive cells that contribute to the septohippocampal projection. In spite of the extensive disturbance in the cholinergic innervation of the neocortex and hippocampus, immunotoxin lesions produced no detectable deficit in the Morris water maze task in any of the lesion sites within the basal forebrain. By contrast small but significant deficits were seen on tests of nocturnal activity (septal and nucleus basalis magnocellularis lesions), open field activity (septal and diagonal band lesions), passive avoidance (nucleus basalis magnocellularis lesions) and delayed non-matching to position (septal lesions). The results indicate that the 192 IgG-saporin provides a powerful tool for making effective lesions of the basal forebrain cholinergic neurons, and that the behavioural sequelae of such lesions warrant further detailed investigation.

MeSH Terms
Acetylcholinesterase/metabolism Animals Avoidance Learning/physiology Behavior, Animal/physiology Female Glutamate Decarboxylase/metabolism Hippocampus/enzymology,metabolism Histocytochemistry Immunoglobulin G/toxicity Immunotoxins/toxicity Motor Activity/physiology N-Glycosyl Hydrolases Parasympathetic Nervous System/metabolism,physiology Parvalbumins/immunology,metabolism Plant Proteins/toxicity Prosencephalon/metabolism,physiology Rats Rats, Sprague-Dawley Receptors, Nerve Growth Factor/immunology,metabolism Ribosome Inactivating Proteins, Type 1 Saporins
Chemicals
Immunoglobulin G Immunotoxins Parvalbumins Plant Proteins Receptors, Nerve Growth Factor Ribosome Inactivating Proteins, Type 1 Acetylcholinesterase N-Glycosyl Hydrolases Saporins Glutamate Decarboxylase
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Torres E M
MRC Cambridge Centre for Brain Repair, University of Cambridge, U.K.
Perry T A
Blockland A
Wilkinson L S
Wiley R G
Lappi D A
Dunnet S B
Article Info
Journal
Neuroscience
Abbr.
Neuroscience
ISSN
0306-4522
Published
1994-11-00
Pages
95-122
Language
English
Region
United States
NLM ID
7605074
Subset
IM
Grants
NIDDK NIH HHS · DK-18811 · United States
Wellcome Trust · United Kingdom
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