dc.creatorMarques, KB
dc.creatorSantos, LMB
dc.creatorOliveira, ALR
dc.date2006
dc.dateDEC
dc.date2014-11-18T07:00:00Z
dc.date2015-11-26T16:52:18Z
dc.date2014-11-18T07:00:00Z
dc.date2015-11-26T16:52:18Z
dc.date.accessioned2018-03-28T23:39:14Z
dc.date.available2018-03-28T23:39:14Z
dc.identifierEuropean Journal Of Neuroscience. Blackwell Publishing, v. 24, n. 11, n. 3053, n. 3062, 2006.
dc.identifier0953-816X
dc.identifierWOS:000243361700009
dc.identifier10.1111/j.1460-9568.2006.05184.x
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/74379
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/74379
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/74379
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1276244
dc.descriptionDuring the course of experimental autoimmune encephalomyelitis, a massive loss of motor and sensitive function occurs, which has been classically attributed to the demyelination process. In rats, the clinical signs disappear within 5 days following complete tetraplegia, indicating that demyelination might not be the only cause for the rapid evolution of the disease. The present work investigated the occurrence of experimental autoimmune encephalomyelitis-induced changes of the synaptic covering of spinal motoneurons during exacerbation and after remission. The terminals were typed with transmission electron microscopy as C-, F- and S-type. Immunohistochemical analysis of synaptophysin, glial fibrillary acidic protein and the microglia/macrophage marker F4/80 were also used in order to draw a correlation between the synaptic changes and the glial reaction. The ultrastructural analysis showed that, during exacerbation, there was a strong retraction of both F- and S-type terminals. In this sense, both the covering as well as the length of the remaining terminals suffered great reductions. However, the retracted terminals rapidly returned to apposition, although the mean length remained shorter. A certain level of sprouting may have occurred as, after remission, the number of F-terminals was greater than in the control group. The immunohistochemical analysis showed that the peak of synaptic loss was coincident with an increased macro- and microglial reaction. Our results suggest that the major changes occurring in the spinal cord network during the time course of the disease may contribute significantly to the origin of the clinical signs as well as help to explain their rapid recovery.
dc.description24
dc.description11
dc.description3053
dc.description3062
dc.languageen
dc.publisherBlackwell Publishing
dc.publisherOxford
dc.publisherInglaterra
dc.relationEuropean Journal Of Neuroscience
dc.relationEur. J. Neurosci.
dc.rightsfechado
dc.sourceWeb of Science
dc.subjectExperimental Autoimmune Encephalomyelitis
dc.subjectAdaptive Functional-changes
dc.subjectNervous-system
dc.subjectChromatolysed Motoneurones
dc.subjectMicroglial Cells
dc.subjectBrain
dc.subjectCord
dc.subjectCat
dc.subjectInvolvement
dc.subjectTerminals
dc.titleSpinal motoneuron synaptic plasticity during the course of an animal model of multiple sclerosis
dc.typeArtículos de revistas


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