Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement

Interleukin-1 (IL-1), a proinflammatory cytokine synthesized and released by activated microglia, can cause dopaminergic neurodegeneration leading to Parkinson’s disease (PD). However, it is uncertain whether IL-1 can act directly, or by exacerbating the harmful actions of other brain insults. To as...

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Fecha de publicación:
2016
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/25968
Acceso en línea:
https://doi.org/10.1007/s12035-016-9988-x
https://repository.urosario.edu.co/handle/10336/25968
Palabra clave:
Open-field
Rotarod
Substantia nigra
Dopaminergic neuron
Microglia
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spelling 05b7114b-9683-4e4d-808a-e01b1fea1ade-1f6bd17e4-135c-470c-a747-c71b381c7396-111578f6c-5473-4b94-ac73-98a5827d7501-188afe9d0-1ceb-41ae-b4c6-5260ad657e45-1fdb28c50-703a-471c-b605-ffa64b2fbbdb-112e232aa-3b20-414c-8bac-ca86d1c2e77e-12020-08-06T16:20:20Z2020-08-06T16:20:20Z2016-06-29Interleukin-1 (IL-1), a proinflammatory cytokine synthesized and released by activated microglia, can cause dopaminergic neurodegeneration leading to Parkinson’s disease (PD). However, it is uncertain whether IL-1 can act directly, or by exacerbating the harmful actions of other brain insults. To ascertain the role of the IL-1 pathway on dopaminergic neurodegeneration and motor skills during aging, we compared mice with impaired [caspase-1 knockout (casp1?/ ? )] or overactivated IL-1 activity [IL-1 receptor antagonist knockout (IL-1ra?/? )] to wild-type (wt) mice at young and middle age. Their motor skills were evaluated by the openfield and rotarod tests, and quantification of their dopamine neurons and activated microglia within the substantia nigra were performed by immunohistochemistry. IL-1ra?/? mice showed an age-related decline in motor skills, a reduced number of dopamine neurons, and an increase in activated microglia when compared to wt or casp1?/? mice. Casp1?/? mice had similar changes in motor skills and dopamine neurons, but fewer activated microglia cells than wt mice. Our results suggest that the overactivated IL-1 pathway occurring in IL-1ra?/? mice in the absence of inflammatory interventions (e.g., intracerebral injections performed in animal models of PD) increased activated microglia, decreased the number of dopaminergic neurons, and reduced their motor skills. Decreased IL-1 activity in casp1?/? mice did not yield clear protective effects when compared with wt mice. In summary, in the absence of overt brain insults, chronic activation of the IL-1 pathway may promote pathological aspects of PD per se, but its impairment does not appear to yield advantages over wt mice.application/pdfhttps://doi.org/10.1007/s12035-016-9988-xISSN: 0893-7648EISSN: 1559-1182https://repository.urosario.edu.co/handle/10336/25968engSpringer Nature44954486Molecular NeurobiologyVol. 54Molecular Neurobiology, ISSN: 0893-7648;EISSN: 1559-1182, Vol.54 (2017); pp.4486–4495https://link.springer.com/content/pdf/10.1007/s12035-016-9988-x.pdfAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2Molecular Neurobiologyinstname:Universidad del Rosarioreponame:Repositorio Institucional EdocUROpen-fieldRotarodSubstantia nigraDopaminergic neuronMicrogliaRole of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary MovementPapel de la vía IL-1 en la neurodegeneración dopaminérgica y la disminución del movimiento voluntarioarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Andrea StojakovicGilberto Paz FilhoxMauricio Arcos-BurgosJulio LicinioMaLi WongClaudio A. MastronardiORIGINALStojakovic2017_Article_RoleOfTheIL-1PathwayInDopamine.pdfapplication/pdf1118619https://repository.urosario.edu.co/bitstreams/aa0c24cc-8ad7-4d57-a30e-04c75f95cc82/downloadc47cd4ad4403d3f52e5a61dad15532daMD51TEXTStojakovic2017_Article_RoleOfTheIL-1PathwayInDopamine.pdf.txtStojakovic2017_Article_RoleOfTheIL-1PathwayInDopamine.pdf.txtExtracted texttext/plain43619https://repository.urosario.edu.co/bitstreams/f314396d-f542-4a57-9f2a-f84219b63859/download04bc4a5ce6e1ee10f5efd21e3abc68daMD52THUMBNAILStojakovic2017_Article_RoleOfTheIL-1PathwayInDopamine.pdf.jpgStojakovic2017_Article_RoleOfTheIL-1PathwayInDopamine.pdf.jpgGenerated Thumbnailimage/jpeg4143https://repository.urosario.edu.co/bitstreams/db66cbe6-8049-4d4c-ac13-ba0dd769aba7/download2adc62883c763b52b22ab59531254db2MD5310336/25968oai:repository.urosario.edu.co:10336/259682021-06-03 00:50:22.581https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement
dc.title.TranslatedTitle.spa.fl_str_mv Papel de la vía IL-1 en la neurodegeneración dopaminérgica y la disminución del movimiento voluntario
title Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement
spellingShingle Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement
Open-field
Rotarod
Substantia nigra
Dopaminergic neuron
Microglia
title_short Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement
title_full Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement
title_fullStr Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement
title_full_unstemmed Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement
title_sort Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement
dc.subject.keyword.spa.fl_str_mv Open-field
Rotarod
Substantia nigra
Dopaminergic neuron
Microglia
topic Open-field
Rotarod
Substantia nigra
Dopaminergic neuron
Microglia
description Interleukin-1 (IL-1), a proinflammatory cytokine synthesized and released by activated microglia, can cause dopaminergic neurodegeneration leading to Parkinson’s disease (PD). However, it is uncertain whether IL-1 can act directly, or by exacerbating the harmful actions of other brain insults. To ascertain the role of the IL-1 pathway on dopaminergic neurodegeneration and motor skills during aging, we compared mice with impaired [caspase-1 knockout (casp1?/ ? )] or overactivated IL-1 activity [IL-1 receptor antagonist knockout (IL-1ra?/? )] to wild-type (wt) mice at young and middle age. Their motor skills were evaluated by the openfield and rotarod tests, and quantification of their dopamine neurons and activated microglia within the substantia nigra were performed by immunohistochemistry. IL-1ra?/? mice showed an age-related decline in motor skills, a reduced number of dopamine neurons, and an increase in activated microglia when compared to wt or casp1?/? mice. Casp1?/? mice had similar changes in motor skills and dopamine neurons, but fewer activated microglia cells than wt mice. Our results suggest that the overactivated IL-1 pathway occurring in IL-1ra?/? mice in the absence of inflammatory interventions (e.g., intracerebral injections performed in animal models of PD) increased activated microglia, decreased the number of dopaminergic neurons, and reduced their motor skills. Decreased IL-1 activity in casp1?/? mice did not yield clear protective effects when compared with wt mice. In summary, in the absence of overt brain insults, chronic activation of the IL-1 pathway may promote pathological aspects of PD per se, but its impairment does not appear to yield advantages over wt mice.
publishDate 2016
dc.date.created.spa.fl_str_mv 2016-06-29
dc.date.accessioned.none.fl_str_mv 2020-08-06T16:20:20Z
dc.date.available.none.fl_str_mv 2020-08-06T16:20:20Z
dc.type.eng.fl_str_mv article
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dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1007/s12035-016-9988-x
dc.identifier.issn.none.fl_str_mv ISSN: 0893-7648
EISSN: 1559-1182
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/25968
url https://doi.org/10.1007/s12035-016-9988-x
https://repository.urosario.edu.co/handle/10336/25968
identifier_str_mv ISSN: 0893-7648
EISSN: 1559-1182
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 4495
dc.relation.citationStartPage.none.fl_str_mv 4486
dc.relation.citationTitle.none.fl_str_mv Molecular Neurobiology
dc.relation.citationVolume.none.fl_str_mv Vol. 54
dc.relation.ispartof.spa.fl_str_mv Molecular Neurobiology, ISSN: 0893-7648;EISSN: 1559-1182, Vol.54 (2017); pp.4486–4495
dc.relation.uri.spa.fl_str_mv https://link.springer.com/content/pdf/10.1007/s12035-016-9988-x.pdf
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dc.source.spa.fl_str_mv Molecular Neurobiology
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