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dc.contributor.authorAasen, J A B
dc.contributor.authorEspenes, A
dc.contributor.authorMiles, C O
dc.contributor.authorSamdal, I A
dc.contributor.authorHess, P
dc.contributor.authorAune, T
dc.date.accessioned2011-07-13T15:03:17Z
dc.date.available2011-07-13T15:03:17Z
dc.date.issued2011
dc.identifier.citationJohn A.B. Aasen, Arild Espenes, Christopher O. Miles, Ingunn A. Samdal, Philipp Hess, Tore Aune, Combined oral toxicity of azaspiracid-1 and yessotoxin in female NMRI mice, Toxicon, Volume 57, Issue 6, May 2011, Pages 909-917, ISSN 0041-0101, DOI: 10.1016/j.toxicon.2011.03.014en_GB
dc.identifier.issn0041-0101
dc.identifier.urihttp://hdl.handle.net/10793/419
dc.identifier.urihttp://dx.doi.org/10.1016/j.toxicon.2011.03.014
dc.descriptionNOTICE: this is the author’s version of a work that was accepted for publication in Toixcon. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Toxicon, [Volume 57, Issue 6, May 2011] doi:10.1016/j.toxicon.2011.03.014 http://www.sciencedirect.com/science/article/pii/S0041010111001000en_GB
dc.descriptionpeer-reviewed
dc.description.abstractFor many years, the presence of yessotoxins (YTXs) in shellfish has contributed to the outcome of the traditional mouse bioassay and has on many occasions caused closure of shellfisheries. Since YTXs do not appear to cause diarrhoea in man and exert low oral toxicity in animal experiments, it has been suggested that they should be removed from regulation. Before doing so, it is important to determine whether the oral toxicity of YTXs is enhanced when present together with shellfish toxins known to cause damage to the gastrointestinal tract. Consequently, mice were given high doses of YTX, at 1 or 5 mg/kg body weight, either alone or together with azaspiracid-1 (AZA1) at 200 μg/kg. The latter has been shown to induce damage to the small intestine at this level. The combined exposure caused no clinical effects, and no pathological changes were observed in internal organs. These results correspond well with the very low levels of YTX detected in internal organs by means of LCMS/MS and ELISA after dosing. Indeed, the very low absorption of YTX when given alone remained largely unchanged when YTX was administered in combination with AZA1. Thus, the oral toxicity of YTX is not enhanced in the presence of sub-lethal levels of AZA1.en_GB
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.relation.ispartofseriesToxicon;57 (6)
dc.subjectAzaspiracid-1en_GB
dc.subjectAZA1en_GB
dc.subjectYessotoxinen_GB
dc.subjectYTXen_GB
dc.subjectMarine algal toxinsen_GB
dc.subjectAbsorptionen_GB
dc.subjectPathologyen_GB
dc.subjectSublethalen_GB
dc.subjectNMRIen_GB
dc.subjectMiceen_GB
dc.subjectLC-MS/MSen_GB
dc.subjectoral toxicityen_GB
dc.titleCombined oral toxicity of azaspiracid-1 and yessotoxin in female NMRI miceen_GB
dc.typeArticleen_GB
refterms.dateFOA2018-01-12T03:06:56Z


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