4.7 Article

In vivo subchronic effects of ciguatoxin-related compounds, reevaluation of their toxicity

Journal

ARCHIVES OF TOXICOLOGY
Volume 96, Issue 9, Pages 2621-2638

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00204-022-03315-0

Keywords

Maitotoxin 1; Ciguatoxin; Gambierone; Maitotoxin 3 (MTX3) or 44-methylgambierone; Ciguatera fish poisoning; In vivo; Acute toxicity; Subchronic toxicity

Categories

Funding

  1. CRUE-CSIC agreement
  2. Springer Nature

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Ciguatoxins are marine compounds produced by dinoflagellates that can cause food poisoning. This study investigated the effects of ciguatoxin-related compounds on mice and highlighted the need to reevaluate their in vivo activity. It also emphasized the importance of using standardized procedures and certified reference materials to determine the levels of these environmental contaminants in food.
Ciguatoxins are marine compounds that share a ladder-shaped polyether structure produced by dinoflagellates of the genus Gambierdiscus and Fukuyoa, and include maitotoxins (MTX1 and MTX3), ciguatoxins (CTX3C) and analogues (gambierone), components of one of the most frequent human foodborne illness diseases known as ciguatera fish poisoning. This disease was previously found primarily in tropical and subtropical areas but nowadays, the dinoflagellates producers of ciguatoxins had spread to European coasts. One decade ago, the European Food Safety Authority has raised the need to complete the toxicological available data for the ciguatoxin group of compounds. Thus, in this work, the in vivo effects of ciguatoxin-related compounds have been investigated using internationally adopted guidelines for the testing of chemicals. Intraperitoneal acute toxicity was tested for maitotoxin 1 at doses between 200 and 3200 ng/kg and the acute oral toxicity of Pacific Ciguatoxin CTX3C at 330 and 1050 ng/kg and maitotoxin 1 at 800 ng/kg were also evaluated showing not effects on mice survival after a 96 h observation period. Therefore, for the following experiments the oral subchronic doses were between 172 and 1760 ng/kg for gambierone, 10 and 102 ng/kg for Pacific Ciguatoxin CTX3C, 550 and 1760 ng/kg for maitotoxin 3 and 800, 2560 and 5000 ng/kg for maitotoxin 1. The results presented here raise the need to reevaluate the in vivo activity of these agents. Although the intraperitoneal lethal dose of maitotoxin 1 is assumed to be 50 ng/kg, without chemical purity identifications and description of the bioassay procedures, in this work, an intraperitoneal lethal dose of 1107 ng/kg was obtained. Therefore, the data presented here highlight the need to use a common procedure and certified reference material to clearly establish the levels of these environmental contaminants in food.

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