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Neuroprotection and immunomodulation by dimethyl fumarate and a heterologous fibrin biopolymer after ventral root avulsion and reimplantation

dc.contributor.authorKempe, Paula R.G.
dc.contributor.authorChiarotto, Gabriela Bortolança
dc.contributor.authorBarraviera, Benedito [UNESP]
dc.contributor.authorFerreira, Rui Seabra [UNESP]
dc.contributor.authorde Oliveira, Alexandre L.R.
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2020-12-12T02:15:10Z
dc.date.available2020-12-12T02:15:10Z
dc.date.issued2020-01-01
dc.description.abstractBackground: Ventral root avulsion (VRA) is an experimental approach in which there is an abrupt separation of the motor roots from the surface of the spinal cord. As a result, most of the axotomized motoneurons degenerate by the second week after injury, and the significant loss of synapses and increased glial reaction triggers a chronic inflammatory state. Pharmacological treatment associated with root reimplantation is thought to overcome the degenerative effects of VRA. Therefore, treatment with dimethyl fumarate (DMF), a drug with neuroprotective and immunomodulatory effects, in combination with a heterologous fibrin sealant/biopolymer (FS), a biological glue, may improve the regenerative response. Methods: Adult female Lewis rats were subjected to VRA of L4-L6 roots followed by reimplantation and daily treatment with DMF for four weeks. Survival times were evaluated 1, 4 or 12 weeks after surgery. Neuronal survival assessed by Nissl staining, glial reactivity (anti-GFAP for astrocytes and anti-Iba-1 for microglia) and synapse preservation (anti-VGLUT1 for glutamatergic inputs and anti-GAD65 for GABAergic inputs) evaluated by immunofluorescence, gene expression (pro- and anti-inflammatory molecules) and motor function recovery were measured. Results: Treatment with DMF at a dose of 15 mg/kg was found to be neuroprotective and immunomodulatory because it preserved motoneurons and synapses and decreased astrogliosis and microglial reactions, as well as downregulated the expression of pro-inflammatory gene transcripts. Conclusion: The pharmacological benefit was further enhanced when associated with root reimplantation with FS, in which animals recovered at least 50% of motor function, showing the efficacy of employing multiple regenerative approaches following spinal cord root injury.en
dc.description.affiliationLaboratory of Nerve Regeneration University of Campinas (UNICAMP)
dc.description.affiliationCenter for the Study of Venoms and Venomous Animals (CEVAP) São Paulo State University (UNESP)
dc.description.affiliationUnespCenter for the Study of Venoms and Venomous Animals (CEVAP) São Paulo State University (UNESP)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipIdFAPESP: 2016/25478-9
dc.description.sponsorshipIdFAPESP: 2018/05006-0
dc.description.sponsorshipIdFAPESP: 2018/25845-7
dc.description.sponsorshipIdCNPq: 303085/2017-7
dc.description.sponsorshipIdCNPq: 303224/20185
dc.identifierhttp://dx.doi.org/10.1590/1678-9199-JVATITD-2019-0093
dc.identifier.citationJournal of Venomous Animals and Toxins Including Tropical Diseases, v. 26.
dc.identifier.doi10.1590/1678-9199-JVATITD-2019-0093
dc.identifier.fileS1678-91992020000100313.pdf
dc.identifier.issn1678-9199
dc.identifier.issn1678-9180
dc.identifier.scieloS1678-91992020000100313
dc.identifier.scopus2-s2.0-85087927581
dc.identifier.urihttp://hdl.handle.net/11449/200754
dc.language.isoeng
dc.relation.ispartofJournal of Venomous Animals and Toxins Including Tropical Diseases
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectDimethyl-fumarate
dc.subjectFibrin sealant
dc.subjectImmunomodulation
dc.subjectNeuroprotection
dc.subjectVentral root avulsion
dc.titleNeuroprotection and immunomodulation by dimethyl fumarate and a heterologous fibrin biopolymer after ventral root avulsion and reimplantationen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.lattes6840524602748457[3]
unesp.author.orcid0000-0002-9855-5594[3]

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