Brevetoxin B is a clastogen in rats, but lacks mutagenic potential in the SP-98/100 Ames test

• Published in: Toxicon (Oxford) Vol. 54; no. 6; pp. 851 - 856
• Main Authors: Leighfield, Tod A., Muha, Noah, Ramsdell, John S.
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier Ltd 01.11.2009; Elsevier
• Subjects: Animal poisons toxicology. Antivenoms; Animals; Biological and medical sciences; Brevetoxin; Chemical mutagenesis; Comet Assay; DNA adducts; DNA Fragmentation; Epoxidation; Harmful algal bloom; Karenia brevis; Liver - drug effects; Male; Marine Toxins - toxicity; Medical sciences; Metabolism; Mutagenicity Tests; Mutagens - toxicity; Oxocins - toxicity; Plant poisons toxicology; Rats; Rats, Inbred F344; Toxicology; Brevetoxin; Epoxidation; Harmful algal bloom; DNA adducts; Metabolism; Karenia brevis; Rat; Toxicity; Algae; Rodentia; Mutagen; Vertebrata; Chromosome break; Mammalia; Dinophyta; Ames test; Animal; DNA; Plant origin; Bloom; Molecular adduct
• ISSN: 0041-0101; 1879-3150; 1879-3150
• DOI: 10.1016/j.toxicon.2009.06.018

Brevetoxins are polyether toxins produced by the dinoflagellate Karenia brevis that are released into the air and are known to cause respiratory hemorrhage in manatees and irritation in humans. Brevetoxin has been previously reported to cause DNA breakage and chromosomal aberrations in in vitro cell assays. The toxin is subject to epoxidation reaction and the formation of nucleic acid adducts in cultured lung fibroblasts and in lung tissue after intratracheal administration to rats. We have exposed rats intratracheally to brevetoxin B (45 μg/kg) and analyzed liver cells for DNA fragmentation using a comet assay. Brevetoxin B (PbTx2) treated rats showed a two to three-fold increase in the amount of DNA in the comet tails, indicating that brevetoxin has in vivo clastogenic activity. We next tested brevetoxin B for mutagenic activity using the Ames 98/100 mutagenesis assay. Brevetoxin B at concentrations from 0.064 to 200 μg/mL failed to cause histidine revertants. Oxidative metabolism of brevetoxin B resulting from Aroclor 1259-induced rat liver microsomes also failed to cause histidine revertants. Finally, direct application of the brevetoxin B epoxide (PbTx6) in the Ames 98/100 assay at concentrations from 0.064 to 200 μg/mL failed to induce histidine revertants. These studies indicate that brevetoxin B retains clastogenic activity after intratracheal administration to the rat. Although brevetoxin B has been shown to form nucleic acid adducts in the lung, neither brevetoxin B nor its epoxide metabolite has mutagenic potential as assessed by the Ames 98/100 test.