Occurrence of lipophilic marine toxins in shellfish from Galicia (NW of Spain) and synergies among them

Lipophilic marine toxins pose a serious threat for consumers and an enormous economic problem for shellfish producers. Synergistic interaction among toxins may play an important role in the toxicity of shellfish and consequently in human intoxications. In order to study the toxic profile of molluscs...

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Published inMarine drugs Vol. 13; no. 4; pp. 1666 - 1687
Main Authors Rodríguez, Laura P, González, Virginia, Martínez, Aníbal, Paz, Beatriz, Lago, Jorge, Cordeiro, Victoria, Blanco, Lucía, Vieites, Juan Manuel, Cabado, Ana G
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 25.03.2015
MDPI
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Summary:Lipophilic marine toxins pose a serious threat for consumers and an enormous economic problem for shellfish producers. Synergistic interaction among toxins may play an important role in the toxicity of shellfish and consequently in human intoxications. In order to study the toxic profile of molluscs, sampled during toxic episodes occurring in different locations in Galicia in 2014, shellfish were analyzed by liquid chromatography tandem mass spectrometry (LC-MS/MS), the official method for the detection of lipophilic toxins. The performance of this procedure was demonstrated to be fit for purpose and was validated in house following European guidelines. The vast majority of toxins present in shellfish belonged to the okadaic acid (OA) group and some samples from a particular area contained yessotoxin (YTX). Since these toxins occur very often with other lipophilic toxins, we evaluated the potential interactions among them. A human neuroblastoma cell line was used to study the possible synergies of OA with other lipophilic toxins. Results show that combination of OA with dinophysistoxin 2 (DTX2) or YTX enhances the toxicity triggered by OA, decreasing cell viability and cell proliferation, depending on the toxin concentration and incubation time. The effects of other lipophilic toxins as 13-desmethyl Spirolide C were also evaluated in vitro.
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ISSN:1660-3397
1660-3397
DOI:10.3390/md13041666