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PMID: 4071042 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Plasticity of hippocampal circuitry in Alzheimer's disease.

Science (New York, N.Y.) ·Vol. 230 ·No. 4730 ·1985-12-06 ·Pages 1179-81

Geddes JW, Monaghan DT, Cotman CW, Lott IT, Kim RC, Chui HC

Abstract

Two markers of neuronal plasticity were used to compare the response of the human central nervous system to neuronal loss resulting from Alzheimer's disease with the response of rats to a similar neuronal loss induced by lesions. In rats that had received lesions of the entorhinal cortex, axon sprouting of commissural and associational fibers into the denervated molecular layer of the dentate gyrus was paralleled by a spread in the distribution of tritiated kainic acid-binding sites. A similar expansion of kainic acid receptor distribution was observed in hippocampal samples obtained postmortem from patients with Alzheimer's disease. An enhancement of acetylcholinesterase activity in the dentate gyrus molecular layer, indicative of septal afferent sprouting, was also observed in those patients with a minimal loss of cholinergic neurons. These results are evidence that the central nervous system is capable of a plastic response in Alzheimer's disease. Adaptive growth responses occur along with the degenerative events.

MeSH Terms
Acetylcholinesterase/metabolism Alzheimer Disease/pathology Animals Hippocampus/enzymology,pathology Humans Kainic Acid/metabolism Male Neuronal Plasticity Neurons/pathology Rats Rats, Inbred Strains
Chemicals
Acetylcholinesterase Kainic Acid
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Geddes J W
Monaghan D T
Cotman C W
Lott I T
Kim R C
Chui H C
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1985-12-06
Pages
1179-81
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIA NIH HHS · AG00538 · United States
NIMH NIH HHS · MH 19691 · United States
NIA NIH HHS · P50AG5142 · United States
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