Record Display for the EPA National Library Catalog


Main Title Spatial Learning Deficits Are Not Solely Due to Cholinergic Deficits Following Medial Septal Lesions with Colchicine.
Author Barone, S. ; Nanry, K. P. ; Mundy, W. R. ; McGinty, J. F. ; Tilson, H. A. ;
CORP Author National Inst. of Environmental Health Sciences, Research Triangle Park, NC. Lab. of Molecular and Integrative Neuroscience. ;East Carolina Univ. School of Medicine, Greenville, NC.;Health Effects Research Lab., Research Triangle Park, NC. Neurotoxicology Div.
Publisher c1991
Year Published 1991
Report Number EPA/600/J-92/251;
Stock Number PB92-206317
Additional Subjects Cholinergic receptors ; Colchicine ; Hippocampus ; Learning disorders ; Rats ; Choline acetyltransferase ; Neurochemistry ; Histology ; Immunohistochemistry ; Reprints ;
Library Call Number Additional Info Location Last
NTIS  PB92-206317 Some EPA libraries have a fiche copy filed under the call number shown. 07/26/2022
Collation 12p
Colchicine was infused bilaterally into the cerebrolateral ventricles (3.75 micrograms/side) or directly into the medial septum (5 micrograms) of adult, male Fischer-344 rats (n=48), and effects on behavior and cholinergic markers were determined. Rats receiving intracerebroventricular (ICV) administration of colchicine were hyperaggressive during the first week after administration and were hyperactive when tested during 60-min sessions at weekly intervals during the first 3 weeks after colchicine treatment. ICV colchicine also interfered with the acquisition of a spatial task in the water maze. Rats receiving colchicine directly into the medial septum were also aggressive and hyperactive, but were not impaired in the acquisition of the water-maze task. It was subsequently found that direct administration and ICV administration of colchicine both decreased the number of choline acetyltransferase (ChAT) immunoreactive cells in the medial septum by at least 50% of vehicle-treated rats and decreased ChAT enzyme activity in both the right and the left hippocampus to about 50% of control levels. The results of these experiments do not support the generally accepted hypothesis that spatial learning deficits seen in animals with medial septum lesions are solely due to a lesion-associated cholinergic deficit in the hippocampus.