Publication:
Isomeric O-methyl cannabidiolquinones with dual BACH1/NRF2 activity.

dc.contributor.authorCasares, Laura
dc.contributor.authorUnciti-Broceta, Juan Diego
dc.contributor.authorPrados, Maria Eugenia
dc.contributor.authorCaprioglio, Diego
dc.contributor.authorMattoteia, Daiana
dc.contributor.authorHiggins, Maureen
dc.contributor.authorApendino, Giovanni
dc.contributor.authorDinkova-Kostova, Albena T
dc.contributor.authorMuñoz, Eduardo
dc.contributor.authorde la Vega, Laureano
dc.contributor.funderCancer Research UK
dc.contributor.funderMinistry of the Economy and Competition (MINECO)
dc.contributor.funderFEDER funds
dc.date.accessioned2023-02-09T09:39:33Z
dc.date.available2023-02-09T09:39:33Z
dc.date.issued2020-08-22
dc.description.abstractOxidative stress and inflammation in the brain are two key hallmarks of neurodegenerative diseases (NDs) such as Alzheimer's, Parkinson's, Huntington's and multiple sclerosis. The axis NRF2-BACH1 has anti-inflammatory and anti-oxidant properties that could be exploited pharmacologically to obtain neuroprotective effects. Activation of NRF2 or inhibition of BACH1 are, individually, promising therapeutic approaches for NDs. Compounds with dual activity as NRF2 activators and BACH1 inhibitors, could therefore potentially provide a more robust antioxidant and anti-inflammatory effects, with an overall better neuroprotective outcome. The phytocannabinoid cannabidiol (CBD) inhibits BACH1 but lacks significant NRF2 activating properties. Based on this scaffold, we have developed a novel CBD derivative that is highly effective at both inhibiting BACH1 and activating NRF2. This new CBD derivative provides neuroprotection in cell models of relevance to Huntington's disease, setting the basis for further developments in vivo.
dc.identifier.citationCasares L, Unciti-Broceta JD, Prados ME, Caprioglio D, Mattoteia D, Higgins M, et al. Isomeric O-methyl cannabidiolquinones with dual BACH1/NRF2 activity. Redox Biol. 2020 Oct;37:101689
dc.identifier.doi10.1016/j.redox.2020.101689
dc.identifier.essn2213-2317
dc.identifier.pmcPMC7476313
dc.identifier.pmid32863231
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476313/pdf
dc.identifier.unpaywallURLhttps://doi.org/10.1016/j.redox.2020.101689
dc.identifier.urihttp://hdl.handle.net/10668/16178
dc.journal.titleRedox biology
dc.journal.titleabbreviationRedox Biol
dc.language.isoen
dc.organizationHospital Universitario Reina Sofía
dc.organizationInstituto Maimónides de Investigación Biomédica de Córdoba-IMIBIC
dc.page.number101689
dc.provenanceRealizada la curación de contenido 13/08/2024
dc.publisherElsevier
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.relation.projectIDC52419/A22869
dc.relation.projectIDC20953/A18644
dc.relation.projectIDRTC-2017-6109-1
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S2213231720308946?via%3Dihub
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCannabidiol derivative/ NRF2/ BACH1/ HMOX1/ neurodegenerative diseases
dc.subjectMice
dc.subjectNF-E2-related factor 2
dc.subjectNeurodegenerative diseases
dc.subjectOxidative stress
dc.subject.decsAnimales
dc.subject.decsAntioxidantes
dc.subject.decsFactores de transcripción con cremalleras de leucina de carácter básico
dc.subject.decsLínea celular
dc.subject.decsModelos animales de enfermedad
dc.subject.meshAnimals
dc.subject.meshAntioxidants
dc.subject.meshBasic-Leucine Zipper Transcription Factors
dc.subject.meshCell Line
dc.subject.meshDisease Models, Animal
dc.titleIsomeric O-methyl cannabidiolquinones with dual BACH1/NRF2 activity.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number37
dspace.entity.typePublication

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