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The Role of AlphαSynuclein in Mouse Models of Acute, Inflammatory and Neuropathic Pain
(1) AlphαSynuclein (αSyn) is a synaptic protein which is expressed in the nervous system and has been linked to neurodegenerative diseases, in particular Parkinson’s disease (PD). Symptoms of PD are mainly due to overexpression and aggregation of αSyn and include pain. However, the interconnection o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221919/ https://www.ncbi.nlm.nih.gov/pubmed/35741096 http://dx.doi.org/10.3390/cells11121967 |
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author | Möller, Moritz Möser, Christine V. Weiß, Ulrike Niederberger, Ellen |
author_facet | Möller, Moritz Möser, Christine V. Weiß, Ulrike Niederberger, Ellen |
author_sort | Möller, Moritz |
collection | PubMed |
description | (1) AlphαSynuclein (αSyn) is a synaptic protein which is expressed in the nervous system and has been linked to neurodegenerative diseases, in particular Parkinson’s disease (PD). Symptoms of PD are mainly due to overexpression and aggregation of αSyn and include pain. However, the interconnection of αSyn and pain has not been clarified so far. (2) We investigated the potential effects of a αSyn knock-out on the nociceptive behaviour in mouse models of acute, inflammatory and neuropathic pain. Furthermore, we assessed the impact of αSyn deletion on pain-related cellular and molecular mechanisms in the spinal cord in these models. (3) Our results showed a reduction of acute cold nociception in αSyn knock-out mice while responses to acute heat and mechanical noxious stimulation were similar in wild type and knock-out mice. Inflammatory nociception was not affected by αSyn knock-out which is also mirrored by unaltered inflammatory gene expression. In contrast, in the SNI model of neuropathic pain, αSyn knock-out mice showed decreased mechanical allodynia as compared to wild type mice. This effect was associated with reduced proinflammatory mechanisms and suppressed activation of MAP kinase signalling in the spinal cord while endogenous antinociceptive mechanisms are not inhibited. (4) Our data indicate that αSyn plays a role in neuropathy and its inhibition might be useful to ameliorate pain symptoms after nerve injury. |
format | Online Article Text |
id | pubmed-9221919 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-92219192022-06-24 The Role of AlphαSynuclein in Mouse Models of Acute, Inflammatory and Neuropathic Pain Möller, Moritz Möser, Christine V. Weiß, Ulrike Niederberger, Ellen Cells Article (1) AlphαSynuclein (αSyn) is a synaptic protein which is expressed in the nervous system and has been linked to neurodegenerative diseases, in particular Parkinson’s disease (PD). Symptoms of PD are mainly due to overexpression and aggregation of αSyn and include pain. However, the interconnection of αSyn and pain has not been clarified so far. (2) We investigated the potential effects of a αSyn knock-out on the nociceptive behaviour in mouse models of acute, inflammatory and neuropathic pain. Furthermore, we assessed the impact of αSyn deletion on pain-related cellular and molecular mechanisms in the spinal cord in these models. (3) Our results showed a reduction of acute cold nociception in αSyn knock-out mice while responses to acute heat and mechanical noxious stimulation were similar in wild type and knock-out mice. Inflammatory nociception was not affected by αSyn knock-out which is also mirrored by unaltered inflammatory gene expression. In contrast, in the SNI model of neuropathic pain, αSyn knock-out mice showed decreased mechanical allodynia as compared to wild type mice. This effect was associated with reduced proinflammatory mechanisms and suppressed activation of MAP kinase signalling in the spinal cord while endogenous antinociceptive mechanisms are not inhibited. (4) Our data indicate that αSyn plays a role in neuropathy and its inhibition might be useful to ameliorate pain symptoms after nerve injury. MDPI 2022-06-19 /pmc/articles/PMC9221919/ /pubmed/35741096 http://dx.doi.org/10.3390/cells11121967 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Möller, Moritz Möser, Christine V. Weiß, Ulrike Niederberger, Ellen The Role of AlphαSynuclein in Mouse Models of Acute, Inflammatory and Neuropathic Pain |
title | The Role of AlphαSynuclein in Mouse Models of Acute, Inflammatory and Neuropathic Pain |
title_full | The Role of AlphαSynuclein in Mouse Models of Acute, Inflammatory and Neuropathic Pain |
title_fullStr | The Role of AlphαSynuclein in Mouse Models of Acute, Inflammatory and Neuropathic Pain |
title_full_unstemmed | The Role of AlphαSynuclein in Mouse Models of Acute, Inflammatory and Neuropathic Pain |
title_short | The Role of AlphαSynuclein in Mouse Models of Acute, Inflammatory and Neuropathic Pain |
title_sort | role of alphαsynuclein in mouse models of acute, inflammatory and neuropathic pain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9221919/ https://www.ncbi.nlm.nih.gov/pubmed/35741096 http://dx.doi.org/10.3390/cells11121967 |
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