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Disturbed Copper Bioavailability in Alzheimer's Disease

Recent data from in vitro, animal, and human studies have shed new light on the positive roles of copper in many aspects of AD. Copper promotes the non-amyloidogenic processing of APP and thereby lowers the Aβ production in cell culture systems, and it increases lifetime and decreases soluble amyloi...

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Autores principales: Kaden, Daniela, Bush, Ashley I., Danzeisen, Ruth, Bayer, Thomas A., Multhaup, Gerd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227474/
https://www.ncbi.nlm.nih.gov/pubmed/22145082
http://dx.doi.org/10.4061/2011/345614
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author Kaden, Daniela
Bush, Ashley I.
Danzeisen, Ruth
Bayer, Thomas A.
Multhaup, Gerd
author_facet Kaden, Daniela
Bush, Ashley I.
Danzeisen, Ruth
Bayer, Thomas A.
Multhaup, Gerd
author_sort Kaden, Daniela
collection PubMed
description Recent data from in vitro, animal, and human studies have shed new light on the positive roles of copper in many aspects of AD. Copper promotes the non-amyloidogenic processing of APP and thereby lowers the Aβ production in cell culture systems, and it increases lifetime and decreases soluble amyloid production in APP transgenic mice. In a clinical trial with Alzheimer patients, the decline of Aβ levels in CSF, which is a diagnostic marker, is diminished in the verum group (8 mg copper/day), indicating a beneficial effect of the copper treatment. These observations are in line with the benefit of treatment with compounds aimed at normalizing metal levels in the brain, such as PBT2. The data reviewed here demonstrate that there is an apparent disturbance in metal homeostasis in AD. More research is urgently needed to understand how this disturbance can be addressed therapeutically.
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spelling pubmed-32274742011-12-05 Disturbed Copper Bioavailability in Alzheimer's Disease Kaden, Daniela Bush, Ashley I. Danzeisen, Ruth Bayer, Thomas A. Multhaup, Gerd Int J Alzheimers Dis Review Article Recent data from in vitro, animal, and human studies have shed new light on the positive roles of copper in many aspects of AD. Copper promotes the non-amyloidogenic processing of APP and thereby lowers the Aβ production in cell culture systems, and it increases lifetime and decreases soluble amyloid production in APP transgenic mice. In a clinical trial with Alzheimer patients, the decline of Aβ levels in CSF, which is a diagnostic marker, is diminished in the verum group (8 mg copper/day), indicating a beneficial effect of the copper treatment. These observations are in line with the benefit of treatment with compounds aimed at normalizing metal levels in the brain, such as PBT2. The data reviewed here demonstrate that there is an apparent disturbance in metal homeostasis in AD. More research is urgently needed to understand how this disturbance can be addressed therapeutically. SAGE-Hindawi Access to Research 2011 2011-11-15 /pmc/articles/PMC3227474/ /pubmed/22145082 http://dx.doi.org/10.4061/2011/345614 Text en Copyright © 2011 Daniela Kaden et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Kaden, Daniela
Bush, Ashley I.
Danzeisen, Ruth
Bayer, Thomas A.
Multhaup, Gerd
Disturbed Copper Bioavailability in Alzheimer's Disease
title Disturbed Copper Bioavailability in Alzheimer's Disease
title_full Disturbed Copper Bioavailability in Alzheimer's Disease
title_fullStr Disturbed Copper Bioavailability in Alzheimer's Disease
title_full_unstemmed Disturbed Copper Bioavailability in Alzheimer's Disease
title_short Disturbed Copper Bioavailability in Alzheimer's Disease
title_sort disturbed copper bioavailability in alzheimer's disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3227474/
https://www.ncbi.nlm.nih.gov/pubmed/22145082
http://dx.doi.org/10.4061/2011/345614
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