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Characterization of Fe, Cu and Zn in organs of PDAPP transgenic mice by XRF spectrometry
Author(s) -
Zhang Z. Y.,
Liu N. Q.,
Li F. L.,
Zhang J.,
Zhu H.,
Qin C.,
Zou Z. Y.,
Tang X. W.
Publication year - 2006
Publication title -
x‐ray spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.447
H-Index - 45
eISSN - 1097-4539
pISSN - 0049-8246
DOI - 10.1002/xrs.898
Subject(s) - genetically modified mouse , transgene , neurodegeneration , zinc , homeostasis , chemistry , disease , metabolism , gene , biology , microbiology and biotechnology , medicine , biochemistry , organic chemistry
A large body of evidence indicates that abnormalities in the levels of iron, copper and zinc and their metabolism are associated with neurodegenerative diseases. However, it is difficult to decide whether any observed changes of trace elements reflect the primary disease process or are secondary to a primary process or mechanism. In the present study, Fe, Cu and Zn in organs of transgenic mice which express the familial Alzheimer's disease (AD) gene and normal mice of the same species and ages were determined by X‐ray fluorescence (XRF) spectrometry. The results show that Fe concentrations in a variety of organs and tissues were significantly increased whereas Zn concentrations decreased in the transgenic mice as compared with the ‘normals’. The levels of Cu in transgenic mice were also altered. Data obtained in the present study suggest that expression of the familial AD gene in mice results in altered homeostasis of Fe, Cu and Zn in organs of the animals, which may in turn accelerate the process of neurodegeneration. Copyright © 2006 John Wiley & Sons, Ltd.