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Pathological Alteration in the Choroid Plexus of Alzheimer’s Disease: Implication for New Therapy Approaches

Morphological alterations of choroid plexus in Alzheimer’s disease (AD) have been extensively investigated. These changes include epithelial atrophy, thickening of the basement membrane, and stroma fibrosis. As a result, synthesis, secretory, and transportation functions are significantly altered re...

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Autores principales: Krzyzanowska, Agnieszka, Carro, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342675/
https://www.ncbi.nlm.nih.gov/pubmed/22563316
http://dx.doi.org/10.3389/fphar.2012.00075
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author Krzyzanowska, Agnieszka
Carro, Eva
author_facet Krzyzanowska, Agnieszka
Carro, Eva
author_sort Krzyzanowska, Agnieszka
collection PubMed
description Morphological alterations of choroid plexus in Alzheimer’s disease (AD) have been extensively investigated. These changes include epithelial atrophy, thickening of the basement membrane, and stroma fibrosis. As a result, synthesis, secretory, and transportation functions are significantly altered resulting in decreased cerebrospinal fluid (CSF) turnover. Recent studies discuss the potential impacts of these changes, including the possibility of reduced resistance to stress insults and slow clearance of toxic compounds from CSF with specific reference to the amyloid peptide. Here, we review new evidences for AD-related changes in the choroid plexus. The data suggest that the significantly altered functions of the choroid plexus contribute to the multiparametric pathogenesis of late-onset AD.
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spelling pubmed-33426752012-05-04 Pathological Alteration in the Choroid Plexus of Alzheimer’s Disease: Implication for New Therapy Approaches Krzyzanowska, Agnieszka Carro, Eva Front Pharmacol Pharmacology Morphological alterations of choroid plexus in Alzheimer’s disease (AD) have been extensively investigated. These changes include epithelial atrophy, thickening of the basement membrane, and stroma fibrosis. As a result, synthesis, secretory, and transportation functions are significantly altered resulting in decreased cerebrospinal fluid (CSF) turnover. Recent studies discuss the potential impacts of these changes, including the possibility of reduced resistance to stress insults and slow clearance of toxic compounds from CSF with specific reference to the amyloid peptide. Here, we review new evidences for AD-related changes in the choroid plexus. The data suggest that the significantly altered functions of the choroid plexus contribute to the multiparametric pathogenesis of late-onset AD. Frontiers Research Foundation 2012-05-03 /pmc/articles/PMC3342675/ /pubmed/22563316 http://dx.doi.org/10.3389/fphar.2012.00075 Text en Copyright © 2012 Krzyzanowska and Carro. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Pharmacology
Krzyzanowska, Agnieszka
Carro, Eva
Pathological Alteration in the Choroid Plexus of Alzheimer’s Disease: Implication for New Therapy Approaches
title Pathological Alteration in the Choroid Plexus of Alzheimer’s Disease: Implication for New Therapy Approaches
title_full Pathological Alteration in the Choroid Plexus of Alzheimer’s Disease: Implication for New Therapy Approaches
title_fullStr Pathological Alteration in the Choroid Plexus of Alzheimer’s Disease: Implication for New Therapy Approaches
title_full_unstemmed Pathological Alteration in the Choroid Plexus of Alzheimer’s Disease: Implication for New Therapy Approaches
title_short Pathological Alteration in the Choroid Plexus of Alzheimer’s Disease: Implication for New Therapy Approaches
title_sort pathological alteration in the choroid plexus of alzheimer’s disease: implication for new therapy approaches
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342675/
https://www.ncbi.nlm.nih.gov/pubmed/22563316
http://dx.doi.org/10.3389/fphar.2012.00075
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