Abstract
Palytoxin (PLTX) is a marine toxin that nowadays is recognized amongst the most toxic compounds isolated from natural products. Originally, the toxin was only identified in a single tidal pool of the island of Maui (Hawaii). Currently, this compound is considered as an emergent toxin in Europe and its prevalence in continental European waters has increased during the last years. The high toxicity of palytoxin is related with the binding to the Na+-K+ ATPase, converting this ubiquitously distributed enzyme in a permeant cation channel [1-3]. Several reports have shown that this toxin is responsible for human fatal intoxications, either after inhalation of toxin-containing marine aerosols or after ingestion of marine products contaminated with PLTX, such as crabs, groupers, mackerel, and parrotfish. So far, different groups have explored the acute oral toxicity of PLTX in mice however, discrepancies in the PLTX source as well as in the monitoring time for the toxic effects yielded controversial results. Although the presence of palytoxin in marine products is not yet currently regulated in Europe, the European Food Safety Authority (EFSA) expressed its opinion on PLTX toxicity and prompted the need to obtain more data regarding the in vivo toxicity of this compound [4]. Therefore, in this study, the acute and chronic toxicity of palytoxin was evaluated after oral administration of the toxin to mice either in a single dose and in a follow-up period of 96 hours or after chronic administration during a 28-day period. After chronic exposure of mice to the toxin, a lethal dose 50 (LD50) of 0.44 µg/kg of PLTX, much lower than that observed in the acute experiments, and a No-Observed-Adverse-Effect Level (NOAEL) of 0.03 µg/kg for repeated daily oral administration of PLTX were determined. Therefore, these data indicate a much higher chronic toxicity of PLTX and a lower NOAEL than that previously described in shorter treatment periods remarking the need to further evaluate the potential teratogenic effects of this emerging marine toxin in mammals. References Artigas, P.; Gadsby, D.C. Ion occlusion/deocclusion partial reactions in individual palytoxin-modified Na+/K+ pumps. Ann N Y Acad Sci 2003, 986, 116-126. Artigas, P.; Gadsby, D.C. Na+/K+-pump ligands modulate gating of palytoxin-induced ion channels. Proc Natl Acad Sci U S A 2003, 100, 501-505. Artigas, P.; Gadsby, D.C. Large diameter of palytoxin-induced Na+/K+ pump channels and modulation of palytoxin interaction by Na+/K+ pump ligands. J Gen Physiol 2004, 123, 357-376. EFSA. Panel on contaminants in the food chain (CONTAM). Scientific Opinion on marine biotoxins in shellfish–Palytoxin group. EFSA Journal, 2009; Vol. 7, p 1393.
Highlights
ResultsPalytoxin (PLTX) is a marine toxin recognized amongst most poisonous substances known to date
Survival times and dead rate induced by single oral administration of PLTX to mice corresponding with each treatment
Oral doses of PLTX administered to mice for a 28-day period
Summary
ResultsPalytoxin (PLTX) is a marine toxin recognized amongst most poisonous substances known to date. Up-and down procedure followed under OECD guidelines for PLTX single oral administration. Dose response curve with the LD50 for PLTX after single oral administration of 599.3 μg/kg (95% Confidence intervals (CI) from 508 to 707 μg/kg R2 0.9712). Results are expressed as means ± SEM of the data obtained from three to nine animals.
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