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dc.contributor.authorPino, Javier del-
dc.contributor.authorMarco-Contelles, José-
dc.contributor.authorLópez-Muñoz, Francisco-
dc.contributor.authorRomero Jódar, Alejandro-
dc.contributor.authorRamos, Eva-
dc.date.accessioned2019-02-13T12:22:26Z-
dc.date.available2019-02-13T12:22:26Z-
dc.date.issued2018-
dc.identifierdoi: 10.1021/acschemneuro.8b00203-
dc.identifierissn: 1948-7193-
dc.identifiere-issn: 1948-7193-
dc.identifier.citationACS Chemical Neuroscience 9: 2880- 2885 (2018)-
dc.identifier.urihttp://hdl.handle.net/10261/175993-
dc.description.abstractThere is clear evidence that neuroinflammation plays a crucial role in the pathogenesis of Alzheimer's disease. Consequently, modulating the inflammatory environment in brain has become a powerful and attractive strategy to deal with Alzheimer's disease physiopathology. In spite of the neuroprotective capacity shown by ASS234, a multitarget propargylamine targeted for Alzheimer's disease, its regulation of inflammation in the brain still remains unexplored. Therefore, we aimed to characterize possible anti-inflammatory effects of ASS234, counteracting induced inflammatory effects in RAW 264.7 cells and evaluating seven neuroinflammation related genes expression profiling (IL-6, IL-10, IL1β, NF-κB, TNF-α, TNFR1, and TGF-β), after ASS234 (5 μM) treatment in SH-SY5Y cells. The analysis of the obtained fold changes lead us to conclude that ASS234 may play an important role facing the neuroinflammatory environment in Alzheimer's disease pathology.-
dc.description.sponsorshipJ.M.-C. is indebted to MINECO for Grants SAF2012-33304 and SAF2015-65586-R. The authors thank Camilo José Cela University [Project 2015-21 (HISCHEMAO)] for its continued support.-
dc.publisherAmerican Chemical Society-
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/SAF2012-33304-
dc.relationinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/SAF2015-65586-R-
dc.rightsclosedAccess-
dc.titleNeuroinflammation Signaling Modulated by ASS234, a Multitarget Small Molecule for Alzheimer's Disease Therapy-
dc.typeartículo-
dc.identifier.doi10.1021/acschemneuro.8b00203-
dc.relation.publisherversionhttp://dx.doi.org/10.1021/acschemneuro.8b00203-
dc.date.updated2019-02-13T12:22:26Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.contributor.funderMinisterio de Economía, Industria y Competitividad (España)-
dc.contributor.funderUniversidad Camilo José Cela-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100010198es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100008742es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeartículo-
item.grantfulltextnone-
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