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Cerebrospinal fluid protein carbonylation identifies oxidative damage in autoimmune demyelination

Oxidative damage occurs in multiple sclerosis, but is difficult to identify antemortem and remains an unknown contributor to disease progression. Carbonylation is a quantitative measure of protein oxidation. Cerebrospinal fluid samples from multiple sclerosis patients showed elevated carbonylated pr...

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Autor principal: Irani, David N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288463/
https://www.ncbi.nlm.nih.gov/pubmed/28168214
http://dx.doi.org/10.1002/acn3.379
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author Irani, David N.
author_facet Irani, David N.
author_sort Irani, David N.
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description Oxidative damage occurs in multiple sclerosis, but is difficult to identify antemortem and remains an unknown contributor to disease progression. Carbonylation is a quantitative measure of protein oxidation. Cerebrospinal fluid samples from multiple sclerosis patients showed elevated carbonylated protein levels compared to controls. In experimental autoimmune encephalomyelitis, carbonylated protein levels in cerebrospinal fluid correlated tightly with those found in inflamed spinal cord tissues. Furthermore, concentrations in cerebrospinal fluid and spinal cord responded in parallel to an antioxidant intervention that also attenuated disease symptoms. These data suggest that carbonylated cerebrospinal fluid proteins could be a quantitative, sensitive, and disease‐relevant biomarker in multiple sclerosis.
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spelling pubmed-52884632017-02-06 Cerebrospinal fluid protein carbonylation identifies oxidative damage in autoimmune demyelination Irani, David N. Ann Clin Transl Neurol Brief Communications Oxidative damage occurs in multiple sclerosis, but is difficult to identify antemortem and remains an unknown contributor to disease progression. Carbonylation is a quantitative measure of protein oxidation. Cerebrospinal fluid samples from multiple sclerosis patients showed elevated carbonylated protein levels compared to controls. In experimental autoimmune encephalomyelitis, carbonylated protein levels in cerebrospinal fluid correlated tightly with those found in inflamed spinal cord tissues. Furthermore, concentrations in cerebrospinal fluid and spinal cord responded in parallel to an antioxidant intervention that also attenuated disease symptoms. These data suggest that carbonylated cerebrospinal fluid proteins could be a quantitative, sensitive, and disease‐relevant biomarker in multiple sclerosis. John Wiley and Sons Inc. 2016-12-20 /pmc/articles/PMC5288463/ /pubmed/28168214 http://dx.doi.org/10.1002/acn3.379 Text en © 2016 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Brief Communications
Irani, David N.
Cerebrospinal fluid protein carbonylation identifies oxidative damage in autoimmune demyelination
title Cerebrospinal fluid protein carbonylation identifies oxidative damage in autoimmune demyelination
title_full Cerebrospinal fluid protein carbonylation identifies oxidative damage in autoimmune demyelination
title_fullStr Cerebrospinal fluid protein carbonylation identifies oxidative damage in autoimmune demyelination
title_full_unstemmed Cerebrospinal fluid protein carbonylation identifies oxidative damage in autoimmune demyelination
title_short Cerebrospinal fluid protein carbonylation identifies oxidative damage in autoimmune demyelination
title_sort cerebrospinal fluid protein carbonylation identifies oxidative damage in autoimmune demyelination
topic Brief Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288463/
https://www.ncbi.nlm.nih.gov/pubmed/28168214
http://dx.doi.org/10.1002/acn3.379
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