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Comparative effectiveness of preventive treatment with dimethyl fumarate-loaded solid lipid nanoparticles and oral dimethyl fumarate in a mouse model of multiple sclerosis

dc.contributor.authorSilva, Gisela Bevilacqua Rolfsen Ferreira da [UNESP]
dc.contributor.authorNeves, Sofia Pereira das
dc.contributor.authorOliveira, Susana Cristina Roque
dc.contributor.authorMarques, Fernanda
dc.contributor.authorOliveira, Anselmo Gomes de [UNESP]
dc.contributor.authorLeite, Fábio de Lima
dc.contributor.authorCerqueira, João José
dc.contributor.institutionUniversity of Minho
dc.contributor.institutionBraga/Guimarães
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2023-03-01T20:28:06Z
dc.date.available2023-03-01T20:28:06Z
dc.date.issued2022-10-01
dc.description.abstractBackground: Orally administered dimethyl fumarate (DMF) presents gastrointestinal adverse effects, such as pain and diarrhea, in addition to flushing and lymphopenia. Objective: Solid lipid nanoparticles (SLNs) with DMF were developed for subcutaneous administration. Methods: DMF-incorporated SLNs and free DMF were tested in mice induced with experimental autoimmune encephalomyelitis (EAE). Results: Preventive treatment of free or incorporated DMF were able to reduce the EAE clinical scores, increase the weight of the animals, reduce the lesion area (demyelination and infiltration), reduce microglial fluorescence intensity and reduce the number of microglial cells and astrocytes, when compared to untreated EAE animals. Groups that received DMF had reduced numbers of T cells, B cells and natural killer (NK) cells in the blood, when compared to the non-induced group. Conclusions: DMF incorporated in SLNs was as effective as free DMF in reducing the clinical scores of the animals, but with reduced administrations when given subcutaneously. In addition, SLN-DMF preventive treatment partially prevented a reduction in the percentages of T and B cells, in the blood, when compared to preventive treatment with free DMF (oral), which suggests reduction of lymphopenia.en
dc.description.affiliationLife and Health Sciences Research Institute (ICVS) School of Medicine University of Minho Campus de Gualtar
dc.description.affiliationICVS/3B's - PT Government Associate Laboratory Braga/Guimarães
dc.description.affiliationNanoneurobiophysics Research Group Department of Physics Chemistry and Mathematics Federal University of São Carlos (UFSCAR), São Paulo
dc.description.affiliationSão Paulo State University (UNESP) Department of Drugs and Medicines, São Paulo
dc.description.affiliationUnespSão Paulo State University (UNESP) Department of Drugs and Medicines, São Paulo
dc.identifierhttp://dx.doi.org/10.1016/j.jaut.2022.102893
dc.identifier.citationJournal of Autoimmunity, v. 132.
dc.identifier.doi10.1016/j.jaut.2022.102893
dc.identifier.issn1095-9157
dc.identifier.issn0896-8411
dc.identifier.scopus2-s2.0-85136273225
dc.identifier.urihttp://hdl.handle.net/11449/240680
dc.language.isoeng
dc.relation.ispartofJournal of Autoimmunity
dc.sourceScopus
dc.subjectDimethyl fumarate
dc.subjectExperimental autoimmune encephalomyelitis
dc.subjectMultiple sclerosis
dc.subjectSolid lipid nanoparticles
dc.subjectSubcutaneous route
dc.titleComparative effectiveness of preventive treatment with dimethyl fumarate-loaded solid lipid nanoparticles and oral dimethyl fumarate in a mouse model of multiple sclerosisen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0002-0791-6447 0000-0002-0791-6447 0000-0002-0791-6447 0000-0002-0791-6447[1]

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