In Vivo Evaluation of the Chronic Oral Toxicity of the Marine Toxin Palytoxin

<i>Palytoxin</i> (PLTX) is one of the most poisonous substances known to date and considered as an emergent toxin in Europe. Palytoxin binds to the Na<sup>+</sup>-K<sup>+</sup> ATPase, converting the enzyme in a permeant cation channel. This toxin is known for cau...

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Main Authors: Andrea Boente-Juncal, Sandra Raposo-García, Carmen Vale, M. Carmen Louzao, Paz Otero, Luis M. Botana
Format: Article
Language:English
Published: MDPI AG 2020-07-01
Series:Toxins
Subjects:
Online Access:https://www.mdpi.com/2072-6651/12/8/489
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author Andrea Boente-Juncal
Sandra Raposo-García
Carmen Vale
M. Carmen Louzao
Paz Otero
Luis M. Botana
author_facet Andrea Boente-Juncal
Sandra Raposo-García
Carmen Vale
M. Carmen Louzao
Paz Otero
Luis M. Botana
author_sort Andrea Boente-Juncal
collection DOAJ
description <i>Palytoxin</i> (PLTX) is one of the most poisonous substances known to date and considered as an emergent toxin in Europe. Palytoxin binds to the Na<sup>+</sup>-K<sup>+</sup> ATPase, converting the enzyme in a permeant cation channel. This toxin is known for causing human fatal intoxications associated with the consumption of contaminated fish and crustaceans such as crabs, groupers, mackerel, and parrotfish. Human intoxications by PLTX after consumption of contaminated fishery products are a serious health issue and can be fatal. Different reports have previously explored the acute oral toxicity of PLTX in mice. Although the presence of palytoxin in marine products is currently not regulated in Europe, the European Food Safety Authority expressed its opinion on PLTX and demanded assessment for chronic toxicity studies of this potent marine toxin. In this study, the chronic toxicity of palytoxin was evaluated after oral administration to mice by gavage during a 28-day period. After chronic exposure of mice to the toxin, a lethal dose 50 (LD<sub>50</sub>) of 0.44 µg/kg of PLTX and a No-Observed-Adverse-Effect Level (NOAEL) of 0.03 µg/kg for repeated daily oral administration of PLTX were determined. These results indicate a much higher chronic toxicity of PLTX and a lower NOAEL than that previously described in shorter treatment periods, pointing out the need to further reevaluate the levels of this compound in marine products.
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spelling doaj.art-7c522d7552154e6c8fbbf261a5a7d1e12023-11-20T08:33:34ZengMDPI AGToxins2072-66512020-07-0112848910.3390/toxins12080489In Vivo Evaluation of the Chronic Oral Toxicity of the Marine Toxin PalytoxinAndrea Boente-Juncal0Sandra Raposo-García1Carmen Vale2M. Carmen Louzao3Paz Otero4Luis M. Botana5Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica, Facultade de Veterinaria, Universidade de Santiago de Compostela, Campus Universitario s/n, 27002 Lugo, SpainDepartamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica, Facultade de Veterinaria, Universidade de Santiago de Compostela, Campus Universitario s/n, 27002 Lugo, SpainDepartamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica, Facultade de Veterinaria, Universidade de Santiago de Compostela, Campus Universitario s/n, 27002 Lugo, SpainDepartamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica, Facultade de Veterinaria, Universidade de Santiago de Compostela, Campus Universitario s/n, 27002 Lugo, SpainDepartamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica, Facultade de Veterinaria, Universidade de Santiago de Compostela, Campus Universitario s/n, 27002 Lugo, SpainDepartamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica, Facultade de Veterinaria, Universidade de Santiago de Compostela, Campus Universitario s/n, 27002 Lugo, Spain<i>Palytoxin</i> (PLTX) is one of the most poisonous substances known to date and considered as an emergent toxin in Europe. Palytoxin binds to the Na<sup>+</sup>-K<sup>+</sup> ATPase, converting the enzyme in a permeant cation channel. This toxin is known for causing human fatal intoxications associated with the consumption of contaminated fish and crustaceans such as crabs, groupers, mackerel, and parrotfish. Human intoxications by PLTX after consumption of contaminated fishery products are a serious health issue and can be fatal. Different reports have previously explored the acute oral toxicity of PLTX in mice. Although the presence of palytoxin in marine products is currently not regulated in Europe, the European Food Safety Authority expressed its opinion on PLTX and demanded assessment for chronic toxicity studies of this potent marine toxin. In this study, the chronic toxicity of palytoxin was evaluated after oral administration to mice by gavage during a 28-day period. After chronic exposure of mice to the toxin, a lethal dose 50 (LD<sub>50</sub>) of 0.44 µg/kg of PLTX and a No-Observed-Adverse-Effect Level (NOAEL) of 0.03 µg/kg for repeated daily oral administration of PLTX were determined. These results indicate a much higher chronic toxicity of PLTX and a lower NOAEL than that previously described in shorter treatment periods, pointing out the need to further reevaluate the levels of this compound in marine products.https://www.mdpi.com/2072-6651/12/8/489palytoxinmarine toxinsin vivo toxicityEFSArisk assessmentsodium-potassium ATPase
spellingShingle Andrea Boente-Juncal
Sandra Raposo-García
Carmen Vale
M. Carmen Louzao
Paz Otero
Luis M. Botana
In Vivo Evaluation of the Chronic Oral Toxicity of the Marine Toxin Palytoxin
Toxins
palytoxin
marine toxins
in vivo toxicity
EFSA
risk assessment
sodium-potassium ATPase
title In Vivo Evaluation of the Chronic Oral Toxicity of the Marine Toxin Palytoxin
title_full In Vivo Evaluation of the Chronic Oral Toxicity of the Marine Toxin Palytoxin
title_fullStr In Vivo Evaluation of the Chronic Oral Toxicity of the Marine Toxin Palytoxin
title_full_unstemmed In Vivo Evaluation of the Chronic Oral Toxicity of the Marine Toxin Palytoxin
title_short In Vivo Evaluation of the Chronic Oral Toxicity of the Marine Toxin Palytoxin
title_sort in vivo evaluation of the chronic oral toxicity of the marine toxin palytoxin
topic palytoxin
marine toxins
in vivo toxicity
EFSA
risk assessment
sodium-potassium ATPase
url https://www.mdpi.com/2072-6651/12/8/489
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