Research Article
Impaired and spared cholinergic functions in the hippocampus after lesions of the medial septum/vertical limb of the diagonal band with 192 IgG-saporin
Article first published online: 12 JAN 2004
DOI: 10.1002/hipo.10160
Copyright © 2004 Wiley-Liss, Inc.
Additional Information
How to Cite
Chang, Q. and Gold, P. E. (2004), Impaired and spared cholinergic functions in the hippocampus after lesions of the medial septum/vertical limb of the diagonal band with 192 IgG-saporin. Hippocampus, 14: 170–179. doi: 10.1002/hipo.10160
Publication History
- Issue published online: 9 MAR 2004
- Article first published online: 12 JAN 2004
- Manuscript Accepted: 13 MAR 2003
Funded by
- U.S. Public Health Service/NIA. Grant Number: AG 07648
- National Institute of Neurological Diseases and Stroke (NINDS). Grant Number: NS 32914
- USDA. Grant Number: 00-35200-9839
- Alzheimer's Association
- Abstract
- References
- Cited By
Keywords:
- physostigmine;
- acetylcholine;
- septohippocampal;
- memory;
- spatial working memory
Abstract
To lesion the cholinergic input to the hippocampus, rats received injections of 192 IgG-saporin into the medial septum/vertical limb of the diagonal band (MS/VDB). The lesions produced near-total loss of choline acetyltransferase (ChAT)-positive neurons in the MS/VDB. The loss was accompanied, however, by only partial decreases (to 40% of control levels) in acetylcholine (ACh) release in the hippocampus. Moreover, ACh release in the hippocampus increased when lesioned and control rats were tested on a spontaneous alternation task, indicating that there was significant residual cholinergic function in the hippocampus. The lesions were sufficient to impair spontaneous alternation scores. However, this impairment could be reversed by either systemic or intrahippocampal injections of the indirect cholinergic agonist, physostigmine, providing additional evidence of residual and effective cholinergic functions in the hippocampus of lesioned rats. Moreover, systemic injections of physostigmine at doses that produced mild tremors in control rats led to more severe tremors in the lesioned rats, suggesting upregulation of cholinergic mechanisms after saporin lesions, likely in brain areas other than the hippocampus. Thus, these findings provide evidence for decreases in cholinergic input to the hippocampus accompanied by deficits on a spontaneous alternation tasks. The findings also provide evidence for considerable residual cholinergic input to the hippocampus after saporin lesions of the MS/VDB. Together, the results suggest that 192 IgG-saporin lesions of the MS/VDB, using methods often employed, do not fully remove septohippocampal cholinergic input to the hippocampus but are nonetheless sufficient to produce impairments on a task impaired by hippocampal lesions. © 2004 Wiley-Liss, Inc.

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