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Potential Involvement of Oxidative Stress, Apoptosis and Proinflammation in Ipconazole-Induced Cytotoxicity in Human Endothelial-like Cells

dc.contributor.authorRuiz Yance, Iris
dc.contributor.authorSiguas, Junior
dc.contributor.authorBardales, Brandy
dc.contributor.authorRobles Castañeda, Ingrid
dc.contributor.authorCordova, Karen
dc.contributor.authorYpushima, Alina
dc.contributor.authorEstela Villar, Esteban
dc.contributor.authorQuintana Criollo, Carlos
dc.contributor.authorEstacio, Darwin
dc.contributor.authorRodríguez, José Luis
dc.date.accessioned2024-05-14T16:54:47Z
dc.date.available2024-05-14T16:54:47Z
dc.date.issued2023-10-05
dc.description2022 Descuento MDPI
dc.description.abstractTriazole fungicides are widely used in the world, mainly in agriculture, but their abuse and possible toxic effects are being reported in some in vivo and in vitro studies that have demonstrated their danger to human health. This in vitro study evaluated the cytotoxicity, oxidative stress and proinflammation of EA.hy926 endothelial cells in response to ipconazole exposure. Using the MTT assay, ipconazole was found to produce a dose-dependent reduction (*** p < 0.001; concentrations of 20, 50 and 100 µM) of cell viability in EA.hy926 with an IC50 of 29 µM. Also, ipconazole induced a significant increase in ROS generation (** p < 0.01), caspase 3/7 (** p < 0.01), cell death (BAX, APAF1, BNIP3, CASP3 and AKT1) and proinflammatory (NLRP3, CASP1, IL1β, NFκB, IL6 and TNFα) biomarkers, as well as a reduction in antioxidant (NRF2 and GPx) biomarkers. These results demonstrated that oxidative stress, proinflammatory activity and cell death could be responsible for the cytotoxic effect produced by the fungicide ipconazole, such that this triazole compound should be considered as a possible risk factor in the development of alterations in cellular homeostasis.
dc.description.departmentDepto. de Farmacología y Toxicología
dc.description.facultyFac. de Farmacia
dc.description.fundingtypeDescuento UCM
dc.description.refereedTRUE
dc.description.sponsorshipUniversidad Intercultural de la Amazonia VPI
dc.description.statuspub
dc.identifier.citationRuiz-Yance, I., Siguas, J., Bardales, B., Robles-Castañeda, I., Cordova, K., Ypushima, A., Estela-Villar, E., Quintana-Criollo, C., Estacio, D., & Rodríguez, J. L. (2023). Potential Involvement of Oxidative Stress, Apoptosis and Proinflammation in Ipconazole-Induced Cytotoxicity in Human Endothelial-like Cells. Toxics, 11(10), 839. https://doi.org/10.3390/toxics11100839
dc.identifier.doi10.3390/toxics11100839
dc.identifier.essn2305-6304
dc.identifier.officialurlhttps://doi.org/10.3390/toxics11100839
dc.identifier.pmid37888690
dc.identifier.relatedurlhttps://www.mdpi.com/journal/toxics
dc.identifier.urihttps://hdl.handle.net/20.500.14352/104025
dc.issue.number839
dc.journal.titleToxics
dc.language.isoeng
dc.page.final14
dc.page.initial1
dc.publisherMDPI
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.cdu615
dc.subject.keywordCytotoxicity
dc.subject.keywordEA.hy926
dc.subject.keywordIpconazole fungicide
dc.subject.keywordOxidative stress
dc.subject.keywordProinflammation
dc.subject.ucmFarmacología (Farmacia)
dc.subject.unesco3209 Farmacología
dc.titlePotential Involvement of Oxidative Stress, Apoptosis and Proinflammation in Ipconazole-Induced Cytotoxicity in Human Endothelial-like Cells
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number11(10)
dspace.entity.typePublication

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