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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Main Authors: Daniela Kaden, Ashley I. Bush, Ruth Danzeisen, Thomas A. Bayer, Gerd Multhaup
Format: Article
Language:English
Published: Hindawi Limited 2011-01-01
Series:International Journal of Alzheimer's Disease
Online Access:http://dx.doi.org/10.4061/2011/345614
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spelling 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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AT ruthdanzeisen disturbedcopperbioavailabilityinalzheimersdisease
AT thomasabayer disturbedcopperbioavailabilityinalzheimersdisease
AT gerdmulthaup disturbedcopperbioavailabilityinalzheimersdisease
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