Cargando…
A Sub-Acute Dosing Study of Saxitoxin and Tetrodotoxin Mixtures in Mice Suggests That the Current Paralytic Shellfish Toxin Regulatory Limit Is Fit for Purpose
Paralytic shellfish poisoning is a worldwide problem induced by shellfish contaminated with paralytic shellfish toxins. To protect human health, a regulatory limit for these toxins in shellfish flesh has been adopted by many countries. In a recent study, mice were dosed with saxitoxin and tetrodotox...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467072/ https://www.ncbi.nlm.nih.gov/pubmed/37505706 http://dx.doi.org/10.3390/toxins15070437 |
_version_ | 1785099032675221504 |
---|---|
author | Finch, Sarah C. Webb, Nicola G. Boundy, Michael J. Harwood, D. Tim Munday, John S. Sprosen, Jan M. Somchit, Chanatda Broadhurst, Ric B. |
author_facet | Finch, Sarah C. Webb, Nicola G. Boundy, Michael J. Harwood, D. Tim Munday, John S. Sprosen, Jan M. Somchit, Chanatda Broadhurst, Ric B. |
author_sort | Finch, Sarah C. |
collection | PubMed |
description | Paralytic shellfish poisoning is a worldwide problem induced by shellfish contaminated with paralytic shellfish toxins. To protect human health, a regulatory limit for these toxins in shellfish flesh has been adopted by many countries. In a recent study, mice were dosed with saxitoxin and tetrodotoxin mixtures daily for 28 days showing toxicity at low concentrations, which appeared to be at odds with other work. To further investigate this reported toxicity, we dosed groups of mice with saxitoxin and tetrodotoxin mixtures daily for 21 days. In contrast to the previous study, no effects on mouse bodyweight, food consumption, heart rate, blood pressure, grip strength, blood chemistry or hematology were observed. Furthermore, no histological findings were associated with dosing in this trial. The dose rates in this study were 2.6, 3.8 and 4.9 times greater, respectively, than the highest dose of the previous study. As rapid mortality in three out of five mice was observed in the previous study, the deaths are likely to be due to the methodology used rather than the shellfish toxins. To convert animal data to that used in a human risk assessment, a 100-fold safety factor is required. After applying this safety factor, the dose rates used in the current study were 3.5, 5.0 and 6.5 times greater, respectively, than the acute reference dose for each toxin type set by the European Union. Furthermore, it has previously been proposed that tetrodotoxin be included in the paralytic shellfish poisoning suite of toxins. If this were done, the highest dose rate used in this study would be 13 times the acute reference dose. This study suggests that the previous 28-day trial was flawed and that the current paralytic shellfish toxin regulatory limit is fit for purpose. An additional study, feeding mice a diet laced with the test compounds at higher concentrations than those of the current experiment, would be required to comment on whether the current paralytic shellfish toxin regulatory limit should be modified. |
format | Online Article Text |
id | pubmed-10467072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104670722023-08-31 A Sub-Acute Dosing Study of Saxitoxin and Tetrodotoxin Mixtures in Mice Suggests That the Current Paralytic Shellfish Toxin Regulatory Limit Is Fit for Purpose Finch, Sarah C. Webb, Nicola G. Boundy, Michael J. Harwood, D. Tim Munday, John S. Sprosen, Jan M. Somchit, Chanatda Broadhurst, Ric B. Toxins (Basel) Article Paralytic shellfish poisoning is a worldwide problem induced by shellfish contaminated with paralytic shellfish toxins. To protect human health, a regulatory limit for these toxins in shellfish flesh has been adopted by many countries. In a recent study, mice were dosed with saxitoxin and tetrodotoxin mixtures daily for 28 days showing toxicity at low concentrations, which appeared to be at odds with other work. To further investigate this reported toxicity, we dosed groups of mice with saxitoxin and tetrodotoxin mixtures daily for 21 days. In contrast to the previous study, no effects on mouse bodyweight, food consumption, heart rate, blood pressure, grip strength, blood chemistry or hematology were observed. Furthermore, no histological findings were associated with dosing in this trial. The dose rates in this study were 2.6, 3.8 and 4.9 times greater, respectively, than the highest dose of the previous study. As rapid mortality in three out of five mice was observed in the previous study, the deaths are likely to be due to the methodology used rather than the shellfish toxins. To convert animal data to that used in a human risk assessment, a 100-fold safety factor is required. After applying this safety factor, the dose rates used in the current study were 3.5, 5.0 and 6.5 times greater, respectively, than the acute reference dose for each toxin type set by the European Union. Furthermore, it has previously been proposed that tetrodotoxin be included in the paralytic shellfish poisoning suite of toxins. If this were done, the highest dose rate used in this study would be 13 times the acute reference dose. This study suggests that the previous 28-day trial was flawed and that the current paralytic shellfish toxin regulatory limit is fit for purpose. An additional study, feeding mice a diet laced with the test compounds at higher concentrations than those of the current experiment, would be required to comment on whether the current paralytic shellfish toxin regulatory limit should be modified. MDPI 2023-07-03 /pmc/articles/PMC10467072/ /pubmed/37505706 http://dx.doi.org/10.3390/toxins15070437 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Finch, Sarah C. Webb, Nicola G. Boundy, Michael J. Harwood, D. Tim Munday, John S. Sprosen, Jan M. Somchit, Chanatda Broadhurst, Ric B. A Sub-Acute Dosing Study of Saxitoxin and Tetrodotoxin Mixtures in Mice Suggests That the Current Paralytic Shellfish Toxin Regulatory Limit Is Fit for Purpose |
title | A Sub-Acute Dosing Study of Saxitoxin and Tetrodotoxin Mixtures in Mice Suggests That the Current Paralytic Shellfish Toxin Regulatory Limit Is Fit for Purpose |
title_full | A Sub-Acute Dosing Study of Saxitoxin and Tetrodotoxin Mixtures in Mice Suggests That the Current Paralytic Shellfish Toxin Regulatory Limit Is Fit for Purpose |
title_fullStr | A Sub-Acute Dosing Study of Saxitoxin and Tetrodotoxin Mixtures in Mice Suggests That the Current Paralytic Shellfish Toxin Regulatory Limit Is Fit for Purpose |
title_full_unstemmed | A Sub-Acute Dosing Study of Saxitoxin and Tetrodotoxin Mixtures in Mice Suggests That the Current Paralytic Shellfish Toxin Regulatory Limit Is Fit for Purpose |
title_short | A Sub-Acute Dosing Study of Saxitoxin and Tetrodotoxin Mixtures in Mice Suggests That the Current Paralytic Shellfish Toxin Regulatory Limit Is Fit for Purpose |
title_sort | sub-acute dosing study of saxitoxin and tetrodotoxin mixtures in mice suggests that the current paralytic shellfish toxin regulatory limit is fit for purpose |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10467072/ https://www.ncbi.nlm.nih.gov/pubmed/37505706 http://dx.doi.org/10.3390/toxins15070437 |
work_keys_str_mv | AT finchsarahc asubacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT webbnicolag asubacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT boundymichaelj asubacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT harwooddtim asubacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT mundayjohns asubacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT sprosenjanm asubacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT somchitchanatda asubacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT broadhurstricb asubacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT finchsarahc subacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT webbnicolag subacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT boundymichaelj subacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT harwooddtim subacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT mundayjohns subacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT sprosenjanm subacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT somchitchanatda subacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose AT broadhurstricb subacutedosingstudyofsaxitoxinandtetrodotoxinmixturesinmicesuggeststhatthecurrentparalyticshellfishtoxinregulatorylimitisfitforpurpose |