Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/4622
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dc.contributor.authorMandić, M.en_US
dc.contributor.authorMitić, K.en_US
dc.contributor.authorNedeljković, P.en_US
dc.contributor.authorPerić, M.en_US
dc.contributor.authorBožić, B.en_US
dc.contributor.authorLunić, T.en_US
dc.contributor.authorBačić, A.en_US
dc.contributor.authorRajilić-Stojanović, M.en_US
dc.contributor.authorPeković, S.en_US
dc.contributor.authorBožić-Nedeljković, B.en_US
dc.date.accessioned2022-10-13T08:11:12Z-
dc.date.available2022-10-13T08:11:12Z-
dc.date.issued2022-03-17-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/4622-
dc.description.abstractThe present study aimed to investigate the neuroprotective effects of the vitamin B complex (B1, B2, B3, B5, B6, and B12—VBC), by studying the changes in the femoral nerve, quadriceps muscle, popliteal lymph nodes and gut microbiota in the rat model of multiple sclerosis, experimental autoimmune encephalomyelitis (EAE). VBC treatment attenuated clinical signs of EAE during the disease, and reduced the duration of EAE thereby contributing to a faster recovery. In VBC-treated EAE rats, a significant decrease in nerve and muscle nuclear density was revealed during the onset period of the disease, while a marked increase was detected at the end of the disease, compared with untreated EAE rats. In the lymph nodes of VBC-treated EAE rats, a fewer number of lymphoid follicles in the cortical area and smaller epithelioid granulomas were detected. The changes in microbiota composition were examined using 16S rRNA gene sequencing and bioinformatics analysis, which revealed the potential of VBC treatment in establishing and/or maintaining gut microbiota homeostasis. Finally, the present study demonstrated that VBC treatment ameliorated the cellular changes in the affected peripheral nerve, muscles innervated by this nerve, and the gut microbiota dysbiosis which occurred during the EAE.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.relation.ispartofNutrientsen_US
dc.subjectExperimental autoimmune encephalomyelitisen_US
dc.subjectGut microbiotaen_US
dc.subjectNerveen_US
dc.subjectMuscle nuclear densityen_US
dc.subjectNeuroprotectionen_US
dc.subjectPopliteal lymph nodesen_US
dc.subjectVitamin B complexen_US
dc.titleVitamin B Complex and Experimental Autoimmune Encephalomyelitis—Attenuation of the Clinical Signs and Gut Microbiota Dysbiosisen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/nu14061273-
dc.description.rankM21en_US
dc.description.impact5,719en_US
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.orcid0000-0003-1417-8320-
crisitem.author.orcid0000-0003-0091-8797-
crisitem.author.orcid0000-0001-9910-2741-
crisitem.author.orcid0000-0002-1238-1731-
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