In vitro models for neuropathic pain phenotypic screening in brain therapeutics

dc.contributor.affiliationUniversidade de Santiago de Compostela. Centro de Investigación en Medicina Molecular e Enfermidades Crónicases_ES
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéuticaes_ES
dc.contributor.authorMartínez Rodríguez, Antón Leandro
dc.contributor.authorBrea Floriani, José Manuel
dc.contributor.authorLópez, D.
dc.contributor.authorCosme Boullosa, Neila
dc.contributor.authorBarro Fernández, Mateo
dc.contributor.authorMonroy, X.
dc.contributor.authorBurgueño, J.
dc.contributor.authorMerlos, M.
dc.contributor.authorLoza García, María Isabel
dc.date.accessioned2024-05-20T15:42:02Z
dc.date.available2024-05-20T15:42:02Z
dc.date.issued2024
dc.description.abstractThe discovery of brain therapeutics faces a significant challenge due to the low translatability of preclinical results into clinical success. To address this gap, several efforts have been made to obtain more translatable neuronal models for phenotypic screening. These models allow the selection of active compounds without predetermined knowledge of drug targets. In this review, we present an overview of various existing models within the field, examining their strengths and limitations, particularly in the context of neuropathic pain research. We illustrate the usefulness of these models through a comparative review in three crucial areas: i) the development of novel phenotypic screening strategies specifically for neuropathic pain, ii) the validation of the models for both primary and secondary screening assays, and iii) the use of the models in target deconvolution processeses_ES
dc.description.peerreviewedSIes_ES
dc.description.sponsorshipThe authors disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: The research for this work was supported by the Agencia Estatal de Investigación (PID2020-119428RB-I00) and Xunta de Galicia (ED431C 2022/20) and European Regional Development Fund (ERDF). NC was in receipt of a predoctoral grant (ED481A 2021) from Xunta de Galicia and MB was in receipt of a predoctoral grant (ED481A-2020) from Xunta de Galiciaes_ES
dc.identifier.citationPharmacological Research, Volume 202, 2024, 107111es_ES
dc.identifier.doi10.1016/j.phrs.2024.107111
dc.identifier.issn1043-6618
dc.identifier.urihttp://hdl.handle.net/10347/33869
dc.journal.titlePharmacological Research
dc.language.isoenges_ES
dc.page.initial107111
dc.publisherElsevieres_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.phrs.2024.107111es_ES
dc.rightsAtribución 4.0 Internacional
dc.rights© 2024 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)es_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectPhenotypic screeninges_ES
dc.subjectImmortalized cell lineses_ES
dc.subjectIn vitro modelses_ES
dc.subjectNeuropathic paines_ES
dc.subjectIn vitro pharmacologyes_ES
dc.subjectEarly drug discoveryes_ES
dc.titleIn vitro models for neuropathic pain phenotypic screening in brain therapeuticses_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dc.volume.number202
dspace.entity.typePublication
relation.isAuthorOfPublicationefe7f464-2f77-4a92-915f-fda4128451fa
relation.isAuthorOfPublication67b19be7-64a8-45c8-a6e4-ed48a4410ef8
relation.isAuthorOfPublication7765cb9b-b630-44dc-9477-dd266a62bb3c
relation.isAuthorOfPublication.latestForDiscoveryefe7f464-2f77-4a92-915f-fda4128451fa

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