Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/140855
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dc.contributor.authorLiberto, Valentina Di-
dc.contributor.authorMudò, Giuseppa-
dc.contributor.authorGarozzo, Roberta-
dc.contributor.authorFrinchi, Monica-
dc.contributor.authorFernández Dueñas, Víctor-
dc.contributor.authorIorio, Patrizia Di-
dc.contributor.authorCiccarelli, Renata-
dc.contributor.authorCaciagli, Francesco-
dc.contributor.authorCondorelli, Daniele F.-
dc.contributor.authorCiruela Alférez, Francisco-
dc.contributor.authorBelluardo, Natale-
dc.date.accessioned2019-09-26T15:15:35Z-
dc.date.available2019-09-26T15:15:35Z-
dc.date.issued2016-06-19-
dc.identifier.issn1663-9812-
dc.identifier.urihttp://hdl.handle.net/2445/140855-
dc.description.abstractGuanine-based purines (GBPs) have been recently proposed to be not only metabolic agents but also extracellular signaling molecules that regulate important functions in the central nervous system. In such way, GBPs-mediated neuroprotection, behavioral responses and neuronal plasticity have been broadly described in the literature. However, while a number of these functions (i.e., GBPs neurothophic effects) have been well-established, the molecular mechanisms behind these GBPs-dependent effects are still unknown. Furthermore, no plasma membrane receptors for GBPs have been described so far, thus GBPs are still considered orphan neuromodulators. Interestingly, an intricate and controversial functional interplay between GBPs effects and adenosine receptors activity has been recently described, thus triggering the hypothesis that GBPs mechanism of action might somehow involve adenosine receptors. Here, we review recent data describing the GBPs role in the brain. We focus on the involvement of GBPs regulating neuronal plasticity, and on the new hypothesis based on putative GBPs receptors. Overall, we expect to shed some light on the GBPs world since although these molecules might represent excellent candidates for certain neurological diseases management, the lack of putative GBPs receptors precludes any high throughput screening intent for the search of effective GBPs-based drugs.-
dc.format.extent15 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherFrontiers Media-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3389/fphar.2016.00158-
dc.relation.ispartofFrontiers in Pharmacology, 2016, vol. 7, p. 158-
dc.relation.urihttps://doi.org/10.3389/fphar.2016.00158-
dc.rightscc-by (c) Liberto, Valentina Di et al., 2016-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es-
dc.sourceArticles publicats en revistes (Patologia i Terapèutica Experimental)-
dc.subject.classificationPurines-
dc.subject.classificationTrifosfat de guanosina-
dc.subject.classificationAdenosina-
dc.subject.otherPurines-
dc.subject.otherGuanosine triphosphatase-
dc.subject.otherAdenosine-
dc.titleThe guanine-based purinergic system: the tale of an orphan neuromodulation-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec666906-
dc.date.updated2019-09-26T15:15:35Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid27378923-
Appears in Collections:Articles publicats en revistes (Patologia i Terapèutica Experimental)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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