A post-mortem comparison of the cortical cholinergic system in Alzheimer's disease and Pick's disease

Assessment of neurochemical markers in the frontal cortex indicates that choline acetyltransferase is significantly decreased in Alzheimer's and Gerstmann Straussler dementias but not in Pick's dementia. It therefore appears that the cholinergic innervation of the cortex from the basal for...

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Published inJournal of the neurological sciences Vol. 62; no. 1; pp. 211 - 217
Main Authors Wood, P.L., Etienne, P., Lal, S., Nair, N.P.V., Finlayson, M.H., Gauthier, S., Palo, J., Haltia, M., Paetau, A., Bird, E.D.
Format Journal Article
LanguageEnglish
Published Shannon Elsevier B.V 01.12.1983
Elsevier Science
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Abstract Assessment of neurochemical markers in the frontal cortex indicates that choline acetyltransferase is significantly decreased in Alzheimer's and Gerstmann Straussler dementias but not in Pick's dementia. It therefore appears that the cholinergic innervation of the cortex from the basal forebrain is intact in Pick's disease. Cortical somatostatin was decreased only in Alzheimer's disease (AD), indicating that loss of somatostatin is not a constant feature in different forms of dementia. Muscarinic binding sites were unaltered in Pick's disease and Gerstmann-Straussler syndrome but were decreased in a subpopulation of AD patients. These data suggest that in some cases of AD a significant loss of cholinoceptive neurones in the cortex is evident.
AbstractList Assessment of neurochemical markers in the frontal cortex indicates that choline acetyltransferase is significantly decreased in Alzheimer's and Gerstmann-Straussler dementias but not in Pick's dementia. It therefore appears that the cholinergic innervation of the cortex from the basal forebrain is intact in Pick's disease. Cortical somatostatin was decreased only in Alzheimer's disease (AD), indicating that loss of somatostatin is not a constant feature in different forms of dementia. Muscarinic binding sites were unaltered in Pick's disease and Gerstmann-Straussler syndrome but were decreased in a subpopulation of AD patients. These data suggest that in some cases of AD a significant loss of cholinoceptive neurones in the cortex is evident.
Author Lal, S.
Wood, P.L.
Haltia, M.
Paetau, A.
Etienne, P.
Nair, N.P.V.
Finlayson, M.H.
Gauthier, S.
Palo, J.
Bird, E.D.
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  surname: Finlayson
  fullname: Finlayson, M.H.
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  organization: Department of Neurology, University of Helsinki, Helsinki Finland
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  surname: Haltia
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  surname: Bird
  fullname: Bird, E.D.
  organization: McLean Hospital, Brain Tissue Resource Centre, Belmont, MA U.S.A
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Issue 1
Keywords Pick's disease
Choline acetyltransferase
Somatostatin
Muscarinic receptors
Alzheimer's disease
Gerstmann-Straussler syndrome
Human
Cerebral cortex
Nervous system diseases
Alzheimer disease
Autopsy
Pick disease
Degenerative disease
Muscarinic receptor
Neuropeptide
Language English
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Snippet Assessment of neurochemical markers in the frontal cortex indicates that choline acetyltransferase is significantly decreased in Alzheimer's and Gerstmann...
Assessment of neurochemical markers in the frontal cortex indicates that choline acetyltransferase is significantly decreased in Alzheimer's and...
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StartPage 211
SubjectTerms Adult
Aged
Alzheimer Disease - metabolism
Alzheimer Disease - pathology
Alzheimer's disease
Biological and medical sciences
Cerebral Cortex - metabolism
Cerebral Cortex - pathology
Choline acetyltransferase
Choline O-Acetyltransferase - metabolism
Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
Dementia - metabolism
Dementia - pathology
Female
Gerstmann-Straussler syndrome
Humans
Male
Medical sciences
Middle Aged
Muscarinic receptors
Neurology
Oxotremorine - metabolism
Pick's disease
Quinuclidinyl Benzilate - metabolism
Receptors, Muscarinic - metabolism
Somatostatin
Somatostatin - metabolism
Title A post-mortem comparison of the cortical cholinergic system in Alzheimer's disease and Pick's disease
URI https://dx.doi.org/10.1016/0022-510X(83)90200-9
https://www.ncbi.nlm.nih.gov/pubmed/6142096
https://search.proquest.com/docview/80867648
Volume 62
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