Rapid eye movement sleep deprivation induces changes in the high-affinity binding of [H-3]-ouabain to the rat cortical membranes

dc.contributor.authorBignotto, Magda
dc.contributor.authorAndrade, UJA de
dc.contributor.authorCarvalho, JGB de
dc.contributor.authorVenditti, Marco Antonio Campana [UNIFESP]
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.date.accessioned2016-01-24T12:41:02Z
dc.date.available2016-01-24T12:41:02Z
dc.date.issued2006-03-27
dc.description.abstractRapid eye movement sleep (REMS) suppresses seizures. On the other hand, REMS deprivation (REMSD) increases brain susceptibility to seizures. Sodium-postassium/ATPase is involved in the control of brain excitability. Ouabain, a cardiotonic glycoside, binds to a regulatory extracellular allosteric site in the sodium-potassium/ATPase inhibiting/stimulating its activity depending on its concentration. Endogenous ouabain-like substances exist in the brain; therefore, changes in the ouabain binding site may be involved in the increased brain excitability induced by REMSD. Adult, Wistar male rats were deprived of REMS for 96 hours by the flower-pot method (REMSD). A stress control group was kept in the same environment on a larger platform (LP). A third group of rats was kept in the same room in their home-cages (CONTROL). After REMSD all rats were sacrificed by decapitation and their cerebral cortex dissected. High-affinity [H-3]-ouabain binding was carried out in cortical crude membrane preparation using 8 concentrations of [H-3]-ouabain (1-24 nM). the results show a statistically significant increase of KID in the REMSD rats compared to both CONTROL and LP groups. There were no statistically significant differences in th B-max among the experimental groups. There was also no change either in cortical activity of K+ stimulated p-nitrophenylphosphatase, the dephosphorylation reaction of phosphorylated sodium-potassium/ATPase or in Mg2+-stimulated p-nitrophenylphosphatase. An increase in the KD of [H-3]-ouabain binding to the sodium-potassium/ATPase in REMSD rats indicates a lower affinity to the endogenous inhibitors/stimulators of the enzyme. Therefore, this decreased affinity of the endogenous ouabain-like substances may be involved in the increased excitability induced by REMSD. (c) 2005 Elsevier Ireland Ltd. All rights reserved.en
dc.description.affiliationUniversidade Federal de São Paulo, Escola Paulista Med, Dept Psicobiol, BR-04023 São Paulo, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Escola Paulista Med, Dept Psicobiol, BR-04023 São Paulo, Brazil
dc.description.sourceWeb of Science
dc.format.extent143-147
dc.identifierhttp://dx.doi.org/10.1016/j.neulet.2005.11.027
dc.identifier.citationNeuroscience Letters. Clare: Elsevier B.V., v. 396, n. 2, p. 143-147, 2006.
dc.identifier.doi10.1016/j.neulet.2005.11.027
dc.identifier.issn0304-3940
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/28795
dc.identifier.wosWOS:000235861900013
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofNeuroscience Letters
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.rights.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.subjectREM sleep deprivationen
dc.subjectcerebral cortexen
dc.subject[H-3]-ouabainen
dc.subjectNa+-K(+)ATPaseen
dc.subjectbrain excitabilityen
dc.titleRapid eye movement sleep deprivation induces changes in the high-affinity binding of [H-3]-ouabain to the rat cortical membranesen
dc.typeinfo:eu-repo/semantics/article
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