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Melatonin-sulforaphane hybrid ITH12674 attenuates glial response in vivo by blocking LPS binding to MD2 and receptor oligomerization

dc.contributor.authorMichalska Dziama, Patrycja
dc.contributor.authorBuendia, Izaskun
dc.contributor.authorDuarte, Pablo
dc.contributor.authorFernandez-Mendivil, Cristina
dc.contributor.authorNegredo, Pilar
dc.contributor.authorCuadrado, Antonio
dc.contributor.authorLopez, Manuela
dc.contributor.authorLeon, Rafael
dc.date.accessioned2024-02-09T11:31:04Z
dc.date.available2024-02-09T11:31:04Z
dc.date.issued2019
dc.description.abstractNeuroinflammation is increasingly associated to the onset and progression of neurodegenerative diseases. Furthermore, several lines of evidence have demonstrated the capacity of aberrant protein aggregates to activate the immune response, accelerating the advance of the disease. Compound ITH12674 is a melatonin-sulforaphane hybrid designed to exert a dual drug-prodrug mechanism of action that combines potent NRF2 induction and free radical scavenger activity. ITH12674 also showed neuroprotective properties in oxidative stress related models, that were dependant on its NRF2 inducing properties. Given the high impact of neuroinflammation in the pathogenesis of neurodegeneration, we foresaw to study the anti inflammatory properties of ITH12674. ITH12674 reduced inflammatory markers in glial cell cultures and hippocampal tissue after LPS administration. The anti-inflammatory effect was related to inhibition of TLR4 receptors due to a direct interaction with the TLR4/MD2 complex at the hydrophobic cavity of MD2. ITH12674 is endowed with anti-inflammatory properties, that are complementary to the NRF2 inducing activity and neuroprotective properties. Thus, ITH12674 could be of potential interest for the treatment of diseases with chronic neuroinflammation
dc.description.departmentDepto. de Química en Ciencias Farmacéuticas
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipInstituto de Salud Carlos III
dc.description.sponsorshipFederación Española de Enfermedades Raras
dc.description.sponsorshipMinisterio de Ciencia, Innovación y Universidades (España)
dc.description.sponsorshipFundación La Caixa
dc.description.sponsorshipComunidad de Madrid
dc.description.sponsorshipMinisterio de Educación, Cultura y Deporte (España)
dc.description.sponsorshipFundación Teófilo Hernando
dc.description.statuspub
dc.identifier.citationMichalska, Patrycja, et al. «Melatonin-Sulforaphane Hybrid ITH12674 Attenuates Glial Response in Vivo by Blocking LPS Binding to MD2 and Receptor Oligomerization». Pharmacological Research, vol. 152, febrero de 2020, p. 104597. https://doi.org/10.1016/j.phrs.2019.104597.
dc.identifier.doi10.1016/j.phrs.2019.104597
dc.identifier.officialurlhttps://doi.org/10.1016/j.phrs.2019.104597
dc.identifier.urihttps://hdl.handle.net/20.500.14352/100863
dc.issue.number152
dc.journal.titlePharmacological Research
dc.language.isoeng
dc.publisherElsevier
dc.relation.projectIDinfo:eu-repo/grantAgreement/CP16/00014
dc.relation.projectIDinfo:eu-repo/grantAgreement/PI17/01700
dc.relation.projectIDinfo:eu-repo/grantAgreement/CI17-00048
dc.relation.projectIDinfo:eu-repo/grantAgreement/B2017/BMD-3827
dc.relation.projectIDinfo:eu-repo/grantAgreement/RTI2018-095793-B-I00
dc.relation.projectIDinfo:eu-repo/grantAgreement/13/0373716/03977
dc.relation.projectIDinfo:eu-repo/grantAgreement/15/03269
dc.relation.projectIDinfo:eu-repo/grantAgreement/FJCI-2016/28282
dc.rights.accessRightsrestricted access
dc.subject.keywordITH12674
dc.subject.keywordNeuroinflammation
dc.subject.keywordNeurodegenerative diseases
dc.subject.keywordAntiinflammatory properties
dc.subject.keywordMD2 antagonist
dc.subject.keywordTLR4 inhibitor
dc.subject.keywordNRF2
dc.subject.keywordNuclear factor (erythroid-derived 2)-like 2
dc.subject.keywordMulti-target
dc.subject.ucmCiencias Biomédicas
dc.subject.unesco32 Ciencias Médicas
dc.titleMelatonin-sulforaphane hybrid ITH12674 attenuates glial response in vivo by blocking LPS binding to MD2 and receptor oligomerization
dc.typejournal article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublication298927e3-bd5b-46ad-bdbe-b818ade8cfb1
relation.isAuthorOfPublication.latestForDiscovery298927e3-bd5b-46ad-bdbe-b818ade8cfb1

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