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Inflammation and the pathophysiology of Alzheimer's disease

There is increasing evidence that a chronic inflammatory response in the brain in Alzheimer's disease (AD) ultimately leads to neuronal injury and cognitive decline. Microglia, the primary immune effector cells of the brain, are thought to be key to this process. This paper discusses the eviden...

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Autor principal: Greer, M. Murphy Jr.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Les Laboratoires Servier 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181600/
https://www.ncbi.nlm.nih.gov/pubmed/22034457
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author Greer, M. Murphy Jr.
author_facet Greer, M. Murphy Jr.
author_sort Greer, M. Murphy Jr.
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description There is increasing evidence that a chronic inflammatory response in the brain in Alzheimer's disease (AD) ultimately leads to neuronal injury and cognitive decline. Microglia, the primary immune effector cells of the brain, are thought to be key to this process. This paper discusses the evidence for inflammation in AD, and describes the mechanism whereby microglia generate neurotoxic cytokines, reactive oxygen species, and nitric oxide. Evidence that the cytokine macrophage colony-stimulating factor (M-CSF) is an important cofactor in microglial activation in AD is presented. Ongoing work using organotypic hippocampal expiant cultures to model the inflammatory process in the AD brain is also discussed. Potential avenues for therapeutic intervention are outlined.
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spelling pubmed-31816002011-10-27 Inflammation and the pathophysiology of Alzheimer's disease Greer, M. Murphy Jr. Dialogues Clin Neurosci Basic Research There is increasing evidence that a chronic inflammatory response in the brain in Alzheimer's disease (AD) ultimately leads to neuronal injury and cognitive decline. Microglia, the primary immune effector cells of the brain, are thought to be key to this process. This paper discusses the evidence for inflammation in AD, and describes the mechanism whereby microglia generate neurotoxic cytokines, reactive oxygen species, and nitric oxide. Evidence that the cytokine macrophage colony-stimulating factor (M-CSF) is an important cofactor in microglial activation in AD is presented. Ongoing work using organotypic hippocampal expiant cultures to model the inflammatory process in the AD brain is also discussed. Potential avenues for therapeutic intervention are outlined. Les Laboratoires Servier 2000-09 /pmc/articles/PMC3181600/ /pubmed/22034457 Text en Copyright: © 2000 LLS http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Basic Research
Greer, M. Murphy Jr.
Inflammation and the pathophysiology of Alzheimer's disease
title Inflammation and the pathophysiology of Alzheimer's disease
title_full Inflammation and the pathophysiology of Alzheimer's disease
title_fullStr Inflammation and the pathophysiology of Alzheimer's disease
title_full_unstemmed Inflammation and the pathophysiology of Alzheimer's disease
title_short Inflammation and the pathophysiology of Alzheimer's disease
title_sort inflammation and the pathophysiology of alzheimer's disease
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3181600/
https://www.ncbi.nlm.nih.gov/pubmed/22034457
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