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Acute Oral Toxicity of Pinnatoxin G in Mice

Pinnatoxin G (PnTx-G) is a marine cyclic imine toxin produced by the dinoflagellate Vulcanodinium rugosum, frequently detected in edible shellfish from Ingril Lagoon (France). As other pinnatoxins, to date, no human poisonings ascribed to consumption of PnTx-G contaminated seafood have been reported...

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Autores principales: Sosa, Silvio, Pelin, Marco, Cavion, Federica, Hervé, Fabienne, Hess, Philipp, Tubaro, Aurelia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076786/
https://www.ncbi.nlm.nih.gov/pubmed/32012834
http://dx.doi.org/10.3390/toxins12020087
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author Sosa, Silvio
Pelin, Marco
Cavion, Federica
Hervé, Fabienne
Hess, Philipp
Tubaro, Aurelia
author_facet Sosa, Silvio
Pelin, Marco
Cavion, Federica
Hervé, Fabienne
Hess, Philipp
Tubaro, Aurelia
author_sort Sosa, Silvio
collection PubMed
description Pinnatoxin G (PnTx-G) is a marine cyclic imine toxin produced by the dinoflagellate Vulcanodinium rugosum, frequently detected in edible shellfish from Ingril Lagoon (France). As other pinnatoxins, to date, no human poisonings ascribed to consumption of PnTx-G contaminated seafood have been reported, despite its potent antagonism at nicotinic acetylcholine receptors and its high and fast-acting toxicity after intraperitoneal or oral administration in mice. The hazard characterization of PnTx-G by oral exposure is limited to a single acute toxicity study recording lethality and clinical signs in non-fasted mice treated by gavage or through voluntary food ingestion, which showed differences in PnTx-G toxic potency. Thus, an acute toxicity study was carried out using 3 h-fasted CD-1 female mice, administered by gavage with PnTx-G (8–450 µg kg(−1)). At the dose of 220 µg kg(−1) and above, the toxin induced a rapid onset of clinical signs (piloerection, prostration, hypothermia, abdominal breathing, paralysis of the hind limbs, and cyanosis), leading to the death of mice within 30 min. Except for moderate mucosal degeneration in the small intestine recorded at doses of 300 µg kg(−1), the toxin did not induce significant morphological changes in the other main organs and tissues, or alterations in blood chemistry parameters. This acute oral toxicity study allowed to calculate an oral LD(50) for PnTx-G equal to 208 μg kg(−1) (95% confidence limits: 155–281 µg kg(−1)) and to estimate a provisional NOEL of 120 µg kg(−1).
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spelling pubmed-70767862020-03-20 Acute Oral Toxicity of Pinnatoxin G in Mice Sosa, Silvio Pelin, Marco Cavion, Federica Hervé, Fabienne Hess, Philipp Tubaro, Aurelia Toxins (Basel) Article Pinnatoxin G (PnTx-G) is a marine cyclic imine toxin produced by the dinoflagellate Vulcanodinium rugosum, frequently detected in edible shellfish from Ingril Lagoon (France). As other pinnatoxins, to date, no human poisonings ascribed to consumption of PnTx-G contaminated seafood have been reported, despite its potent antagonism at nicotinic acetylcholine receptors and its high and fast-acting toxicity after intraperitoneal or oral administration in mice. The hazard characterization of PnTx-G by oral exposure is limited to a single acute toxicity study recording lethality and clinical signs in non-fasted mice treated by gavage or through voluntary food ingestion, which showed differences in PnTx-G toxic potency. Thus, an acute toxicity study was carried out using 3 h-fasted CD-1 female mice, administered by gavage with PnTx-G (8–450 µg kg(−1)). At the dose of 220 µg kg(−1) and above, the toxin induced a rapid onset of clinical signs (piloerection, prostration, hypothermia, abdominal breathing, paralysis of the hind limbs, and cyanosis), leading to the death of mice within 30 min. Except for moderate mucosal degeneration in the small intestine recorded at doses of 300 µg kg(−1), the toxin did not induce significant morphological changes in the other main organs and tissues, or alterations in blood chemistry parameters. This acute oral toxicity study allowed to calculate an oral LD(50) for PnTx-G equal to 208 μg kg(−1) (95% confidence limits: 155–281 µg kg(−1)) and to estimate a provisional NOEL of 120 µg kg(−1). MDPI 2020-01-28 /pmc/articles/PMC7076786/ /pubmed/32012834 http://dx.doi.org/10.3390/toxins12020087 Text en © 2020 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/).
spellingShingle Article
Sosa, Silvio
Pelin, Marco
Cavion, Federica
Hervé, Fabienne
Hess, Philipp
Tubaro, Aurelia
Acute Oral Toxicity of Pinnatoxin G in Mice
title Acute Oral Toxicity of Pinnatoxin G in Mice
title_full Acute Oral Toxicity of Pinnatoxin G in Mice
title_fullStr Acute Oral Toxicity of Pinnatoxin G in Mice
title_full_unstemmed Acute Oral Toxicity of Pinnatoxin G in Mice
title_short Acute Oral Toxicity of Pinnatoxin G in Mice
title_sort acute oral toxicity of pinnatoxin g in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7076786/
https://www.ncbi.nlm.nih.gov/pubmed/32012834
http://dx.doi.org/10.3390/toxins12020087
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