Bioavailability profiling shows differences in OA, DTX1 and DTX2 toxins that justify their toxicity

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Fisioloxía
dc.contributor.authorRodríguez Santos, Luis
dc.contributor.authorCostas, Celia
dc.contributor.authorLouzao Ojeda, María del Carmen
dc.contributor.authorCagide, Eva
dc.contributor.authorÁlvarez, Mercedes
dc.contributor.authorRodríguez Cañás, Inés
dc.contributor.authorRaposo García, Sandra
dc.contributor.authorVale González, María del Carmen
dc.contributor.authorRodríguez Vieytes, Mercedes
dc.contributor.authorLolo, Manuel
dc.contributor.authorBotana López, Luis Miguel
dc.date.accessioned2025-02-21T13:32:22Z
dc.date.available2025-02-21T13:32:22Z
dc.date.issued2024-09-28
dc.description.abstractThe marine toxins of the Okadaic acid (OA) group are natural compounds produced by dinoflagellates that enters the food chain by accumulating in seafood. They are responsible for Diarrhetic Shellfish Poisoning (DSP) events in humans over the world and therefore are also jointly named as Diarrhetic Shellfish Toxins (DSTs). The main objective of this study was to evaluate symptoms, toxicity, absorption, distribution, and elimination of OA, Dinophysistoxin-1 (DTX1), and Dinophysistoxin-2 (DTX2) at the sublethal dose of 90 μg toxin/kg bw administered through voluntary feeding to mice. The toxin comparison highlighted that OA and DTX1 induced more severe and specific symptoms such as diarrhea. After oral ingestion toxins were distributed through the entire organism being detected in liver, kidney, stomach, small and large intestine. Predominant excretion of the toxins was observed in feces, with OA exhibiting fast elimination, while DTX2 was showing prolonged excretion. The passage and accumulation of toxins in gastrointestinal organs instigated macroscopic damage in the stomach, small and large intestine that could persist up to 120 h. These findings highlight the importance of pharmacokinetic of sublethal doses of DSTs administered by voluntary feeding in their toxicity and their implication for public health.
dc.description.peerreviewedSI
dc.description.sponsorshipThe research leading to these results has received funding from the following grants. From Conselleria de Cultura, Educacion e Ordenación Universitaria, Xunta de Galicia, GRC (ED431C 2021/01). From Ministerio de Ciencia e Innovación, Grant CPP2021-008447 funded by MCIN/AEI/10.13039/501100011033 and by The European Union NextGenerationEU/PRT, PID 2020-11262RB-C21. From Interreg EAPA-0032/2022 – BEAP-MAR (cofunded by the EU), from European Union HORIZON-MSCA-2022-DN-01-MSCA Doctoral Networks 2022 101119901-BIOTOXDoc, and HORIZON-CL6-2023-CIRCBIO-01 COMBO - 101135438.
dc.identifier.citationReferences Rodríguez-Santos, L., Costas, C., Louzao, M. C., Cagide, E., Alvarez, M., Rodríguez-Cañás, I., Raposo-García, S., Vale, C., Vieytes, M. R., Lolo, M., & Botana, L. M. (2024). Bioavailability profiling shows differences in OA, DTX1 and DTX2 toxins that justify their toxicity. Chemosphere, 36610.1016/j.chemosphere.2024.143419
dc.identifier.doi10.1016/j.chemosphere.2024.143419
dc.identifier.essn1879-1298
dc.identifier.issn0045-6535
dc.identifier.urihttps://hdl.handle.net/10347/39844
dc.journal.titleChemosphere
dc.language.isoeng
dc.publisherElsevier
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/CPP2021-008447/ES/Evaluación de los efectos de las toxinas diarreicas de mariscos (DSP) tras una ingesta continuada y sus implicaciones neurológicas (CRONIC-DSP)/
dc.relation.publisherversionhttps://doi.org/10.1016/j.chemosphere.2024.143419
dc.rights© 2024 The Authors. Published by Elsevier Ltd
dc.rightsAttribution-NonCommercial 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectDiarrhetic shellfish poisoning
dc.subjectOkadaic acid
dc.subjectPharmacokinetic
dc.subjectVoluntary feeding
dc.titleBioavailability profiling shows differences in OA, DTX1 and DTX2 toxins that justify their toxicity
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number366
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscovery5e4bdb6e-ef45-44b1-adc1-4835dfd1f1ce

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