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dc.contributor.authorGuerrero Rubio, María Alejandra-
dc.contributor.authorHernández García, Samanta-
dc.contributor.authorGarcía Carmona, Francisco-
dc.contributor.authorGandía Herrero, Fernando-
dc.date.accessioned2025-05-29T11:38:10Z-
dc.date.available2025-05-29T11:38:10Z-
dc.date.issued2021-03-12-
dc.identifier.citationAntioxidants 2021, 10, 438.es
dc.identifier.issnElectronic: 2076-3921-
dc.identifier.urihttp://hdl.handle.net/10201/155360-
dc.description© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This manuscript version is made available under the CC-BY 4.0 license http://creativecommons.org/licenses/by/4.0/. This document is the Published version of a Published Work that appeared in final form in Antioxidants. To access the final edited and published work see https://doi.org/10.3390/antiox10030438es
dc.description.abstractFlavonoids are potential nutraceutical compounds present in diary food. They are considered health-promoting compounds and promising drugs for different diseases, such as neurological and inflammatory diseases, diabetes and cancer. Therefore, toxicological and mechanistic studies should be done to assert the biological effects and identify the molecular targets of these compounds. In this work we describe the effects of six structurally-related flavonoids—baicalein, chrysin, scutellarein, 6-hydroxyflavone, 6,7-dihydroxyflavone and 7,8-dihydroxyflavone—on Caenorhabditis elegans’lifespan and stress resistance. The results showed that chrysin, 6-hydroxyflavone and baicalein prolonged C. elegans’ lifespan by up to 8.5%, 11.8% and 18.6%, respectively. The lifespan extensions caused by these flavonoids are dependent on different signaling pathways. The results suggested that chrysin’s effects are dependent on the insulin signaling pathway via DAF-16/FOXO. Baicalein and 6-hydroxyflavone’s effects are dependent on the SKN-1/Nfr2 pathway. In addition, microarray analysis showed that baicalein downregulates important age-related genes, such as mTOR and PARP.es
dc.formatapplication/pdfes
dc.format.extent17es
dc.languageenges
dc.publisherMDPIes
dc.relationThis work was supported by the Spanish Ministry of Science and Innovation, project AGL2017-86526-P (MCI/AEI/FEDER, UE) and by the “Programa de Ayudas a Grupos de Excelen-cia de la Región de Murcia, Fundación Séneca, Agencia de Ciencia y Tecnología de la Región de Murcia” (Project 19893/GERM/15). M.A. G.-R. held a contract financed by MICINN (Spain). S. H.-G. holds a contract financed by Fundación Séneca (Spain).es
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectCaenorhabditis eleganses
dc.subjectDAF-16/FOXOes
dc.subjectFlavonoidses
dc.subjectmTORes
dc.subjectPARPses
dc.subjectSKN-1/Nrf2es
dc.subject.otherCDU::5 - Ciencias puras y naturales::57 - Biología::577 - Bioquímica. Biología molecular. Biofísicaes
dc.titleFlavonoids’ effects on Caenorhabditis elegans’ longevity, fat accumulation, stress resistance and gene modulation involve mTOR, SKN-1 and DAF-16es
dc.typeinfo:eu-repo/semantics/articlees
dc.relation.publisherversionhttps://www.mdpi.com/2076-3921/10/3/438-
dc.identifier.doihttps://doi.org/10.3390/antiox10030438-
dc.contributor.departmentDepartamento de Bioquímica y Biología Molecular "A"es
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