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Metal Ions in Neuroscience
Metal ions are believed to participate in many neurodegenerative conditions. In excitotoxic cell death there is convincing evidence for the participation of Ca(2+) and Zn(2+) ions although the exact molecular mechanisms by which these metals exert their effects are unclear. Only in one instance has...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
1997
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365058/ https://www.ncbi.nlm.nih.gov/pubmed/18475782 http://dx.doi.org/10.1155/MBD.1997.125 |
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author | Ragan, C. Ian |
author_facet | Ragan, C. Ian |
author_sort | Ragan, C. Ian |
collection | PubMed |
description | Metal ions are believed to participate in many neurodegenerative conditions. In excitotoxic cell death there is convincing evidence for the participation of Ca(2+) and Zn(2+) ions although the exact molecular mechanisms by which these metals exert their effects are unclear. Only in one instance has the metal binding site of metalloenzymes been exploited for therapeutic purposes and this is the use of Li(+) in the treatment of bipolar affective disorder. Again the exact molecular target is not clear but is likely to involve a Mg(2+)-dependent enzyme of an intracellular signalling pathway. In Parkinson's disease, the selective loss of dopaminergic neurones in the substantia nigra may be caused by radical-mediated damage and there is good evidence to suggest that Fe(2+) or (3+) is important in promoting formation of radical species. The evidence that free radicals are important in mediating other neurodegenerative conditions is less strong but still substantial enough to suggest that removal of reactive oxygen species or preventing their formation may be a valid approach to therapy. |
format | Text |
id | pubmed-2365058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-23650582008-05-12 Metal Ions in Neuroscience Ragan, C. Ian Met Based Drugs Research Article Metal ions are believed to participate in many neurodegenerative conditions. In excitotoxic cell death there is convincing evidence for the participation of Ca(2+) and Zn(2+) ions although the exact molecular mechanisms by which these metals exert their effects are unclear. Only in one instance has the metal binding site of metalloenzymes been exploited for therapeutic purposes and this is the use of Li(+) in the treatment of bipolar affective disorder. Again the exact molecular target is not clear but is likely to involve a Mg(2+)-dependent enzyme of an intracellular signalling pathway. In Parkinson's disease, the selective loss of dopaminergic neurones in the substantia nigra may be caused by radical-mediated damage and there is good evidence to suggest that Fe(2+) or (3+) is important in promoting formation of radical species. The evidence that free radicals are important in mediating other neurodegenerative conditions is less strong but still substantial enough to suggest that removal of reactive oxygen species or preventing their formation may be a valid approach to therapy. Hindawi Publishing Corporation 1997 /pmc/articles/PMC2365058/ /pubmed/18475782 http://dx.doi.org/10.1155/MBD.1997.125 Text en Copyright © 1997 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ 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 | Research Article Ragan, C. Ian Metal Ions in Neuroscience |
title | Metal Ions in Neuroscience |
title_full | Metal Ions in Neuroscience |
title_fullStr | Metal Ions in Neuroscience |
title_full_unstemmed | Metal Ions in Neuroscience |
title_short | Metal Ions in Neuroscience |
title_sort | metal ions in neuroscience |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2365058/ https://www.ncbi.nlm.nih.gov/pubmed/18475782 http://dx.doi.org/10.1155/MBD.1997.125 |
work_keys_str_mv | AT ragancian metalionsinneuroscience |