DSP Toxin Distribution across Organs in Mice after Acute Oral Administration

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéuticagl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Fisioloxíagl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Química Analítica, Nutrición e Bromatoloxíagl
dc.contributor.authorLouzao Ojeda, María del Carmen
dc.contributor.authorAbal Camaño, Paula
dc.contributor.authorCostas Sánchez, Celia
dc.contributor.authorSuzuki, Toshiyuki
dc.contributor.authorWatanabe, Ryuichi
dc.contributor.authorVilariño del Río, Natalia
dc.contributor.authorBotana López, Ana María
dc.contributor.authorBotana López, Luis Miguel
dc.contributor.authorRodríguez Vieytes, Mercedes
dc.date.accessioned2021-01-14T10:34:28Z
dc.date.available2021-01-14T10:34:28Z
dc.date.issued2021
dc.description.abstractOkadaic acid (OA) and its main structural analogs dinophysistoxin-1 (DTX1) and dinophysistoxin-2 (DTX2) are marine lipophilic phycotoxins distributed worldwide that can be accumulated by edible shellfish and can cause diarrheic shellfish poisoning (DSP). In order to study their toxicokinetics, mice were treated with different doses of OA, DTX1, or DTX2 and signs of toxicity were recorded up to 24 h. Toxin distribution in the main organs from the gastrointestinal tract was assessed by liquid chromatography-mass spectrometry (LC/MS/MS) analysis. Our results indicate a dose-dependency in gastrointestinal absorption of these toxins. Twenty-four hours post-administration, the highest concentration of toxin was detected in the stomach and, in descending order, in the large intestine, small intestine, and liver. There was also a different toxicokinetic pathway between OA, DTX1, and DTX2. When the same toxin doses are compared, more OA than DTX1 is detected in the small intestine. OA and DTX1 showed similar concentrations in the stomach, liver, and large intestine tissues, but the amount of DTX2 is much lower in all these organs, providing information on DSP toxicokinetics for human safety assessmentgl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThe research leading to these results received funding from the following FEDER cofunded grants: Ministerio de Ciencia e Innovación AGL2016-78728-R (AEI/FEDER, UE), IISCIII/PI19/001248; Conselleria de Cultura, Educacion e Ordenación Universitaria, Xunta de Galicia, 2017 GRC GI-1682 (ED431C 2017/01); and European Union Interreg AlertoxNet EAPA-317-2016, Interreg Agritox EAPA-998-2018, and H2020 778069-EMERTOX. Celia Costas is supported by a fellowship from the Ministerio de Ciencia, Innovación y Universidades grant FPU18/05681gl
dc.identifier.citationLouzao, M.C.; Abal, P.; Costas, C.; Suzuki, T.; Watanabe, R.; Vilariño, N.; Botana, A.M.; R. Vieytes, M.; Botana, L.M. DSP Toxin Distribution across Organs in Mice after Acute Oral Administration. Mar. Drugs 2021, 19, 23gl
dc.identifier.doi10.3390/md19010023
dc.identifier.essn1660-3397
dc.identifier.urihttp://hdl.handle.net/10347/24180
dc.language.isoenggl
dc.publisherMDPIgl
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/778069
dc.relation.projectIDinfo:eu-repo/grantAgreement/MINECO/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/AGL2016-78728-R/ES
dc.relation.publisherversionhttps://doi.org/10.3390/md19010023gl
dc.rights© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)gl
dc.rightsAtribución 4.0 Internacional
dc.rights.accessRightsopen accessgl
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectDinophysistoxin-1gl
dc.subjectDinophysistoxin-2gl
dc.subjectLC/MS/MSgl
dc.subjectOkadaic acidgl
dc.subjectToxicokineticgl
dc.titleDSP Toxin Distribution across Organs in Mice after Acute Oral Administrationgl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscoveryf4b4507e-435b-4890-8d9f-bbe7bb5d9adb

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