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Synthesis, Neuroprotection, and Antioxidant Activity of 1,1′-Biphenylnitrones as α-Phenyl-N-tert-butylnitrone Analogues in In Vitro Ischemia Models

dc.contributor.authorChamorro, Beatriz
dc.contributor.authorGarcía-Vieira, David
dc.contributor.authorDiez-Iriepa, Daniel
dc.contributor.authorGaragarza, Estíbaliz
dc.contributor.authorChioua, Mourad
dc.contributor.authorHadjipavlou-Litina, Dimitra
dc.contributor.authorLópez-Muñoz, Francisco
dc.contributor.authorMarco-Contelles, José
dc.contributor.authorOset Gasque, María Jesús
dc.date.accessioned2023-06-17T08:25:58Z
dc.date.available2023-06-17T08:25:58Z
dc.date.issued2021-02-20
dc.description.abstractHerein, we report the neuroprotective and antioxidant activity of 1,1′-biphenyl nitrones (BPNs) 1–5 as α-phenyl-N-tert-butylnitrone analogues prepared from commercially available [1,1′-biphenyl]-4-carbaldehyde and [1,1′-biphenyl]-4,4′-dicarbaldehyde. The neuroprotection of BPNs1-5 has been measured against oligomycin A/rotenone and in an oxygen–glucose deprivation in vitro ischemia model in human neuroblastoma SH-SY5Y cells. Our results indicate that BPNs 1–5 have better neuroprotective and antioxidant properties than α-phenyl-N-tert-butylnitrone (PBN), and they are quite similar to N-acetyl-L-cysteine (NAC), which is a well-known antioxidant agent. Among the nitrones studied, homo-bis-nitrone BPHBN5, bearing two N-tert-Bu radicals at the nitrone motif, has the best neuroprotective capacity (EC50 = 13.16 ± 1.65 and 25.5 ± 3.93 μM, against the reduction in metabolic activity induced by respiratory chain blockers and oxygen–glucose deprivation in an in vitro ischemia model, respectively) as well as anti-necrotic, anti-apoptotic, and antioxidant activities (EC50 = 11.2 ± 3.94 μM), which were measured by its capacity to reduce superoxide production in human neuroblastoma SH-SY5Y cell cultures, followed by mononitrone BPMN3, with one N-Bn radical, and BPMN2, with only one N-tert-Bu substituent. The antioxidant activity of BPNs1-5 has also been analyzed for their capacity to scavenge hydroxyl free radicals (82% at 100 μM), lipoxygenase inhibition, and the inhibition of lipid peroxidation (68% at 100 μM). Results showed that although the number of nitrone groups improves the neuroprotection profile of these BPNs, the final effect is also dependent on the substitutent that is being incorporated. Thus, BPNs bearing N-tert-Bu and N-Bn groups show better neuroprotective and antioxidant properties than those substituted with Me. All these results led us to propose homo-bis-nitrone BPHBN5 as the most balanced and interesting nitrone based on its neuroprotective capacity in different neuronal models of oxidative stress and in vitro ischemia as well as its antioxidant activity.
dc.description.departmentSección Deptal. de Bioquímica y Biología Molecular (Farmacia)
dc.description.facultyFac. de Farmacia
dc.description.refereedTRUE
dc.description.sponsorshipSpanish Ministry of Economy and Competitiveness (SAF2015-65586-R): Grant to JMC
dc.description.sponsorshipCamilo José Cela University (UCJC-2019-03): Grant to JMC
dc.description.sponsorshipMinistry of Economy and Competitiveness: BC thanks the Spanish Ministry of Economy and Competitiveness for a contract supported by grant SAF2015-65586-R during 2019
dc.description.sponsorshipCamilo José Cela University: BC thanks UCJC for a pre-doctoral grant starting 01/01/2020
dc.description.sponsorshipUniversity of Alcalá: DDI thanks for pre-doctoral FPU grant
dc.description.sponsorshipSpanish Ministry of Science, Innovation and Universities: DDI thanks for pre-doctoral FPU grant
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/71887
dc.identifier.doi10.3390/molecules26041127
dc.identifier.issn1420-3049
dc.identifier.officialurlhttps://doi.org/10.3390/molecules26041127
dc.identifier.relatedurlhttps://www.mdpi.com/journal/molecules
dc.identifier.urihttps://hdl.handle.net/20.500.14352/7094
dc.issue.number4
dc.journal.titleMolecules
dc.language.isoeng
dc.page.initial1127
dc.publisherMDPI
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.cdu577.1
dc.subject.keywordAntioxidants
dc.subject.keyword1
dc.subject.keyword1′-biphenyl nitrones
dc.subject.keywordFree radical scavengers
dc.subject.keywordNeuroprotection
dc.subject.keywordOligomycin A/rotenone
dc.subject.keywordOxygen-glucose-deprivation
dc.subject.keywordα-phenyl-N-tert-butylnitrone
dc.subject.keywordSynthesis
dc.subject.ucmBioquímica (Farmacia)
dc.titleSynthesis, Neuroprotection, and Antioxidant Activity of 1,1′-Biphenylnitrones as α-Phenyl-N-tert-butylnitrone Analogues in In Vitro Ischemia Models
dc.typejournal article
dc.volume.number26
dspace.entity.typePublication
relation.isAuthorOfPublicationf1ce6be1-ac9e-453d-bfe3-12dfbfc2b2f3
relation.isAuthorOfPublication.latestForDiscoveryf1ce6be1-ac9e-453d-bfe3-12dfbfc2b2f3

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