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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Series: | International Journal of Alzheimer's Disease |
Online Access: | http://dx.doi.org/10.4061/2011/345614 |
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doaj-6698ea370b46425d9effb18003c6cde72020-11-25T00:37:51ZengHindawi LimitedInternational Journal of Alzheimer's Disease2090-02522011-01-01201110.4061/2011/345614345614Disturbed Copper Bioavailability in Alzheimer's DiseaseDaniela Kaden0Ashley I. Bush1Ruth Danzeisen2Thomas A. Bayer3Gerd Multhaup4Institute of Chemistry and Biochemistry, Freie Universität Berlin, Thielallee 63, 14195 Berlin, GermanyThe Mental Health Research Institute, The University of Melbourne, 155 Oak Street, Parkville, VIC 3052, AustraliaInternational Copper Association, 260 Madison Avenue, Floor 16, New York, 10016 NY, USADivision of Molecular Psychiatry, Georg-August-University Göttingen, University Medicine Göttingen, 37075 Göttingen, GermanyInstitute of Chemistry and Biochemistry, Freie Universität Berlin, Thielallee 63, 14195 Berlin, GermanyRecent 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.http://dx.doi.org/10.4061/2011/345614 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Daniela Kaden Ashley I. Bush Ruth Danzeisen Thomas A. Bayer Gerd Multhaup |
spellingShingle |
Daniela Kaden Ashley I. Bush Ruth Danzeisen Thomas A. Bayer Gerd Multhaup Disturbed Copper Bioavailability in Alzheimer's Disease International Journal of Alzheimer's Disease |
author_facet |
Daniela Kaden Ashley I. Bush Ruth Danzeisen Thomas A. Bayer Gerd Multhaup |
author_sort |
Daniela Kaden |
title |
Disturbed Copper Bioavailability in Alzheimer's Disease |
title_short |
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_sort |
disturbed copper bioavailability in alzheimer's disease |
publisher |
Hindawi Limited |
series |
International Journal of Alzheimer's Disease |
issn |
2090-0252 |
publishDate |
2011-01-01 |
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. |
url |
http://dx.doi.org/10.4061/2011/345614 |
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