Show simple item record

dc.contributor.authorBernal Chico, Ana ORCID
dc.contributor.authorTepavcevic, Vanja
dc.contributor.authorManterola Juaristi, Andrea
dc.contributor.authorUtrilla, Carmen
dc.contributor.authorMatute Almau, Carlos José
dc.contributor.authorMato Santos, Susana ORCID
dc.date.accessioned2023-02-09T17:18:29Z
dc.date.available2023-02-09T17:18:29Z
dc.date.issued2023-01
dc.identifier.citationGLIA 71(1) : 103-126 (2023)es_ES
dc.identifier.issn0894-1491
dc.identifier.issn1098-1136
dc.identifier.urihttp://hdl.handle.net/10810/59745
dc.description.abstractThe discovery of cannabinoid receptors as the primary molecular targets of psychotropic cannabinoid Delta(9)-tetrahydrocannabinol (Delta(9)-THC) in late 1980s paved the way for investigations on the effects of cannabis-based therapeutics in brain pathology. Ever since, a wealth of results obtained from studies on human tissue samples and animal models have highlighted a promising therapeutic potential of cannabinoids and endocannabinoids in a variety of neurological disorders. However, clinical success has been limited and major questions concerning endocannabinoid signaling need to be satisfactorily addressed, particularly with regard to their role as modulators of glial cells in neurodegenerative diseases. Indeed, recent studies have brought into the limelight diverse, often unexpected functions of astrocytes, oligodendrocytes, and microglia in brain injury and disease, thus providing scientific basis for targeting glial cells to treat brain disorders. This Review summarizes the current knowledge on the molecular and cellular hallmarks of endocannabinoid signaling in glial cells and its clinical relevance in neurodegenerative and chronic inflammatory disorders.es_ES
dc.description.sponsorshipCIBERNED, Grant/Award Number: CB06/05/0076; ARSEP Foundation; European Regional Development Fund (FEDER) and Instituto de Salud Carlos III (ISCIII), Grant/Award Number: PI18/00513; Basque Government, Grant/Award Numbers: PIBA19-0059, IT1203-19; Spanish Ministry of Science and Innovation, Grant/Award Number: SAF2016-75292-Res_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/SAF2016-75292-Res_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectCB1es_ES
dc.subjectCB2es_ES
dc.subjectendocannabinoidses_ES
dc.subjectglial cellses_ES
dc.subjectneurodegenerative diseaseses_ES
dc.titleEndocannabinoid signaling in brain diseases: Emerging relevance of glial cellses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2022 The Authors. GLIA published by Wiley Periodicals LLC. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.es_ES
dc.rights.holderAtribución-NoComercial-SinDerivadas 3.0 España*
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/10.1002/glia.24172es_ES
dc.identifier.doi10.1002/glia.24172
dc.departamentoesNeurocienciases_ES
dc.departamentoeuNeurozientziakes_ES


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record

© 2022 The Authors. GLIA published by Wiley Periodicals LLC.
This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
Except where otherwise noted, this item's license is described as © 2022 The Authors. GLIA published by Wiley Periodicals LLC. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.