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Kynurenines and Neurofilament Light Chain in Multiple Sclerosis
Multiple sclerosis is an autoimmune, demyelinating, and neurodegenerative disease of the central nervous system. In recent years, it has been proven that the kynurenine system plays a significant role in the development of several nervous system disorders, including multiple sclerosis. Kynurenine pa...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185147/ https://www.ncbi.nlm.nih.gov/pubmed/34113231 http://dx.doi.org/10.3389/fnins.2021.658202 |
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author | Pukoli, Dániel Polyák, Helga Rajda, Cecilia Vécsei, László |
author_facet | Pukoli, Dániel Polyák, Helga Rajda, Cecilia Vécsei, László |
author_sort | Pukoli, Dániel |
collection | PubMed |
description | Multiple sclerosis is an autoimmune, demyelinating, and neurodegenerative disease of the central nervous system. In recent years, it has been proven that the kynurenine system plays a significant role in the development of several nervous system disorders, including multiple sclerosis. Kynurenine pathway metabolites have both neurotoxic and neuroprotective effects. Moreover, the enzymes of the kynurenine pathway play an important role in immunomodulation processes, among others, as well as interacting with neuronal energy balance and various redox reactions. Dysregulation of many of the enzymatic steps in kynurenine pathway and upregulated levels of these metabolites locally in the central nervous system, contribute to the progression of multiple sclerosis pathology. This process can initiate a pathogenic cascade, including microglia activation, glutamate excitotoxicity, chronic oxidative stress or accumulated mitochondrial damage in the axons, that finally disrupt the homeostasis of neurons, leads to destabilization of neuronal cell cytoskeleton, contributes to neuro-axonal damage and neurodegeneration. Neurofilaments are good biomarkers of the neuro-axonal damage and their level reliably indicates the severity of multiple sclerosis and the treatment response. There is increasing evidence that connections exist between the molecules generated in the kynurenine metabolic pathway and the change in neurofilament concentrations. Thus the alterations in the kynurenine pathway may be an important biomarker of the course of multiple sclerosis. In our present review, we report the possible relationship and connection between neurofilaments and the kynurenine system in multiple sclerosis based on the available evidences. |
format | Online Article Text |
id | pubmed-8185147 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81851472021-06-09 Kynurenines and Neurofilament Light Chain in Multiple Sclerosis Pukoli, Dániel Polyák, Helga Rajda, Cecilia Vécsei, László Front Neurosci Neuroscience Multiple sclerosis is an autoimmune, demyelinating, and neurodegenerative disease of the central nervous system. In recent years, it has been proven that the kynurenine system plays a significant role in the development of several nervous system disorders, including multiple sclerosis. Kynurenine pathway metabolites have both neurotoxic and neuroprotective effects. Moreover, the enzymes of the kynurenine pathway play an important role in immunomodulation processes, among others, as well as interacting with neuronal energy balance and various redox reactions. Dysregulation of many of the enzymatic steps in kynurenine pathway and upregulated levels of these metabolites locally in the central nervous system, contribute to the progression of multiple sclerosis pathology. This process can initiate a pathogenic cascade, including microglia activation, glutamate excitotoxicity, chronic oxidative stress or accumulated mitochondrial damage in the axons, that finally disrupt the homeostasis of neurons, leads to destabilization of neuronal cell cytoskeleton, contributes to neuro-axonal damage and neurodegeneration. Neurofilaments are good biomarkers of the neuro-axonal damage and their level reliably indicates the severity of multiple sclerosis and the treatment response. There is increasing evidence that connections exist between the molecules generated in the kynurenine metabolic pathway and the change in neurofilament concentrations. Thus the alterations in the kynurenine pathway may be an important biomarker of the course of multiple sclerosis. In our present review, we report the possible relationship and connection between neurofilaments and the kynurenine system in multiple sclerosis based on the available evidences. Frontiers Media S.A. 2021-05-25 /pmc/articles/PMC8185147/ /pubmed/34113231 http://dx.doi.org/10.3389/fnins.2021.658202 Text en Copyright © 2021 Pukoli, Polyák, Rajda and Vécsei. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Pukoli, Dániel Polyák, Helga Rajda, Cecilia Vécsei, László Kynurenines and Neurofilament Light Chain in Multiple Sclerosis |
title | Kynurenines and Neurofilament Light Chain in Multiple Sclerosis |
title_full | Kynurenines and Neurofilament Light Chain in Multiple Sclerosis |
title_fullStr | Kynurenines and Neurofilament Light Chain in Multiple Sclerosis |
title_full_unstemmed | Kynurenines and Neurofilament Light Chain in Multiple Sclerosis |
title_short | Kynurenines and Neurofilament Light Chain in Multiple Sclerosis |
title_sort | kynurenines and neurofilament light chain in multiple sclerosis |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185147/ https://www.ncbi.nlm.nih.gov/pubmed/34113231 http://dx.doi.org/10.3389/fnins.2021.658202 |
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