Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Möller, Moritz, Möser, Christine V., Weiß, Ulrike, Niederberger, Ellen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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
_version_ 1784732745609510912
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
work_keys_str_mv AT mollermoritz theroleofalphasynucleininmousemodelsofacuteinflammatoryandneuropathicpain
AT moserchristinev theroleofalphasynucleininmousemodelsofacuteinflammatoryandneuropathicpain
AT weißulrike theroleofalphasynucleininmousemodelsofacuteinflammatoryandneuropathicpain
AT niederbergerellen theroleofalphasynucleininmousemodelsofacuteinflammatoryandneuropathicpain
AT mollermoritz roleofalphasynucleininmousemodelsofacuteinflammatoryandneuropathicpain
AT moserchristinev roleofalphasynucleininmousemodelsofacuteinflammatoryandneuropathicpain
AT weißulrike roleofalphasynucleininmousemodelsofacuteinflammatoryandneuropathicpain
AT niederbergerellen roleofalphasynucleininmousemodelsofacuteinflammatoryandneuropathicpain