Synergistic Effect of Brevetoxin BTX-3 and Ciguatoxin CTX3C in Human Voltage-Gated Nav1.6 Sodium Channels

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéuticaes_ES
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Fisioloxíaes_ES
dc.contributor.authorRaposo García, Sandra
dc.contributor.authorCostas Sánchez, Celia
dc.contributor.authorLouzao Ojeda, María del Carmen
dc.contributor.authorRodríguez Vieytes, Mercedes
dc.contributor.authorVale González, María del Carmen
dc.contributor.authorBotana López, Luis Miguel
dc.date.accessioned2024-05-22T14:39:59Z
dc.date.available2024-05-22T14:39:59Z
dc.date.issued2023
dc.description.abstractEmerging marine biotoxins such as ciguatoxins and brevetoxins have been widely and independently studied as food pollutants. Their maximum levels in food components were set without considering their possible synergistic effects as consequence of their coexistence in seafood and their action at the same cellular target. The absolute lack of data and regulations of the possible combined effects that both marine biotoxins may have raised the need to analyze their direct in vitro effects using electrophysiology techniques. The results presented in this study indicate that ciguatoxins and brevetoxins had a synergistic effect on human Nav1.6 voltage-gated sodium channels by hyperpolarizing their activation and inactivation states. The results presented here indicate that brevetoxin 3 (BTX-3) acts as partial agonist of human sodium channels, while ciguatoxin 3C (CTX3C) was a full agonist, explaining the differences in the effect of each toxin in the channel. Therefore, this work sets the cellular basis to further apply this type of studies to other food toxicants that may act synergistically and thus implement the corresponding regulatory limits considering their coexistence and the risks to human and animal health derived from ites_ES
dc.description.peerreviewedSIes_ES
dc.description.sponsorshipThe research leading to these results has received funding from the following grants. From Campus Terra (USC), BreveRiesgo (2022-PU011) CLIMIGAL (2022- PU016). From Conselleria de Cultura, Educacion e Ordenación Universitaria, Xunta de Galicia, GRC (ED431C 2021/01). From European Union, Interreg EAPA-0032/2022─BEAP-MAR, HORIZON-MSCA-2022-DN-01-MSCA Doctoral Networks 2022 101119901-BIOTOXDoc, and HORIZON-CL6-2023-CIRCBIO-01 COMBO-101135438es_ES
dc.identifier.citationChem. Res. Toxicol. 2023, 36, 1990−2000es_ES
dc.identifier.doi10.1021/acs.chemrestox.3c00267
dc.identifier.essn1520-5010
dc.identifier.issn0893-228X
dc.identifier.urihttp://hdl.handle.net/10347/33886
dc.issue.number12
dc.journal.titleChemical Research in Toxicology
dc.language.isoenges_ES
dc.page.final2000
dc.page.initial1990
dc.publisherAmerican Chemical Society (ACS)es_ES
dc.relation.publisherversionhttps://doi.org/10.1021/acs.chemrestox.3c00267es_ES
dc.rightsAtribución 4.0 Internacional
dc.rights© 2023 American Chemical Society. This publication is licensed under CC-BY 4.0es_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectAgonistses_ES
dc.subjectGeneticses_ES
dc.subjectSodiumes_ES
dc.subjectToxicological synergyes_ES
dc.subjectToxinses_ES
dc.titleSynergistic Effect of Brevetoxin BTX-3 and Ciguatoxin CTX3C in Human Voltage-Gated Nav1.6 Sodium Channelses_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dc.volume.number36
dspace.entity.typePublication
relation.isAuthorOfPublication5e4bdb6e-ef45-44b1-adc1-4835dfd1f1ce
relation.isAuthorOfPublication91f88e2e-ed1a-43f4-a16c-8d8d5c998e40
relation.isAuthorOfPublicationb75e4b1c-c91a-43e8-a99f-908cb6e08346
relation.isAuthorOfPublication9a18ed42-77b6-4760-8303-ff4070a87ca6
relation.isAuthorOfPublication.latestForDiscoveryb75e4b1c-c91a-43e8-a99f-908cb6e08346

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