Synthesis, Neuroprotection, and Antioxidant Activity of 1,1′-Biphenylnitrones as α-Phenyl-N-tert-butylnitrone Analogues in In Vitro Ischemia Models
dc.contributor.author | Chamorro, Beatriz | |
dc.contributor.author | García-Vieira, David | |
dc.contributor.author | Diez-Iriepa, Daniel | |
dc.contributor.author | Garagarza, Estíbaliz | |
dc.contributor.author | Chioua, Mourad | |
dc.contributor.author | Hadjipavlou-Litina, Dimitra | |
dc.contributor.author | López-Muñoz, Francisco | |
dc.contributor.author | Marco-Contelles, José | |
dc.contributor.author | Oset Gasque, María Jesús | |
dc.date.accessioned | 2023-06-17T08:25:58Z | |
dc.date.available | 2023-06-17T08:25:58Z | |
dc.date.issued | 2021-02-20 | |
dc.description.abstract | Herein, 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.department | Sección Deptal. de Bioquímica y Biología Molecular (Farmacia) | |
dc.description.faculty | Fac. de Farmacia | |
dc.description.refereed | TRUE | |
dc.description.sponsorship | Spanish Ministry of Economy and Competitiveness (SAF2015-65586-R): Grant to JMC | |
dc.description.sponsorship | Camilo José Cela University (UCJC-2019-03): Grant to JMC | |
dc.description.sponsorship | Ministry 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.sponsorship | Camilo José Cela University: BC thanks UCJC for a pre-doctoral grant starting 01/01/2020 | |
dc.description.sponsorship | University of Alcalá: DDI thanks for pre-doctoral FPU grant | |
dc.description.sponsorship | Spanish Ministry of Science, Innovation and Universities: DDI thanks for pre-doctoral FPU grant | |
dc.description.status | pub | |
dc.eprint.id | https://eprints.ucm.es/id/eprint/71887 | |
dc.identifier.doi | 10.3390/molecules26041127 | |
dc.identifier.issn | 1420-3049 | |
dc.identifier.officialurl | https://doi.org/10.3390/molecules26041127 | |
dc.identifier.relatedurl | https://www.mdpi.com/journal/molecules | |
dc.identifier.uri | https://hdl.handle.net/20.500.14352/7094 | |
dc.issue.number | 4 | |
dc.journal.title | Molecules | |
dc.language.iso | eng | |
dc.page.initial | 1127 | |
dc.publisher | MDPI | |
dc.rights | Atribución 3.0 España | |
dc.rights.accessRights | open access | |
dc.rights.uri | https://creativecommons.org/licenses/by/3.0/es/ | |
dc.subject.cdu | 577.1 | |
dc.subject.keyword | Antioxidants | |
dc.subject.keyword | 1 | |
dc.subject.keyword | 1′-biphenyl nitrones | |
dc.subject.keyword | Free radical scavengers | |
dc.subject.keyword | Neuroprotection | |
dc.subject.keyword | Oligomycin A/rotenone | |
dc.subject.keyword | Oxygen-glucose-deprivation | |
dc.subject.keyword | α-phenyl-N-tert-butylnitrone | |
dc.subject.keyword | Synthesis | |
dc.subject.ucm | Bioquímica (Farmacia) | |
dc.title | Synthesis, Neuroprotection, and Antioxidant Activity of 1,1′-Biphenylnitrones as α-Phenyl-N-tert-butylnitrone Analogues in In Vitro Ischemia Models | |
dc.type | journal article | |
dc.volume.number | 26 | |
dspace.entity.type | Publication | |
relation.isAuthorOfPublication | f1ce6be1-ac9e-453d-bfe3-12dfbfc2b2f3 | |
relation.isAuthorOfPublication.latestForDiscovery | f1ce6be1-ac9e-453d-bfe3-12dfbfc2b2f3 |
Download
Original bundle
1 - 1 of 1