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Effect of ouabain on calcium signaling in rodent brain: A systematic review of in vitro studies

The Na(+)/K(+)-ATPase is an integral membrane ion pump, essential to maintaining osmotic balance in cells in the presence of cardiotonic steroids; more specifically, ouabain can be an endogenous modulator of the Na(+)/K(+)-ATPase. Here, we conducted a systematic review of the in vitro effects of car...

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Detalles Bibliográficos
Autores principales: Leite, Jacqueline Alves, Pôças, Elisa, Maia, Gisele Silva, Barbosa, Leandro, Quintas, Luis Eduardo M., Kawamoto, Elisa Mitiko, da Silva, Maria Luiza Correia, Scavone, Cristoforo, de Carvalho, Luciana E. Drumond
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9465813/
https://www.ncbi.nlm.nih.gov/pubmed/36105192
http://dx.doi.org/10.3389/fphar.2022.916312
Descripción
Sumario:The Na(+)/K(+)-ATPase is an integral membrane ion pump, essential to maintaining osmotic balance in cells in the presence of cardiotonic steroids; more specifically, ouabain can be an endogenous modulator of the Na(+)/K(+)-ATPase. Here, we conducted a systematic review of the in vitro effects of cardiotonic steroids on Ca(2+) in the brain of rats and mice. Methods: The review was carried out using the PubMed, Virtual Health Library, and EMBASE databases (between 12 June 2020 and 30 June 2020) and followed the guidelines described in the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA). Results: in total, 829 references were identified in the electronic databases; however, only 20 articles were considered, on the basis of the inclusion criteria. The studies demonstrated the effects of ouabain on Ca(2+) signaling in synaptosomes, brain slices, and cultures of rat and mouse cells. In addition to the well-known cytotoxic effects of high doses of ouabain, resulting from indirect stimulation of the reverse mode of the Na(+)/Ca(2+) exchanger and increased intracellular Ca(2+), other effects have been reported. Ouabain-mediated Ca(2+) signaling was able to act increasing cholinergic, noradrenergic and glutamatergic neurotransmission. Furthermore, ouabain significantly increased intracellular signaling molecules such as InsPs, IP3 and cAMP. Moreover treatment with low doses of ouabain stimulated myelin basic protein synthesis. Ouabain-induced intracellular Ca(2+) increase may promote the activation of important cell signaling pathways involved in cellular homeostasis and function. Thus, the study of the application of ouabain in low doses being promising for application in neurological diseases. Systematic Review Registration: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42020204498, identifier CRD42020204498.