Advances in Clinical Toxicology (ACT)

ISSN: 2577-4328

Upcoming Article

Re-evaluation of the genotoxicity of currently used food dyes in mouse multiple organs via continuous administration by drinking using the comet assay

Abstract

Among currently used food dyes, we have reported that four azo dye and three xanthene dyes that were given to mice by single gavage at a low dose (10 or 100 mg/kg) induced DNA damage in mouse gastrointestinal tract (GI-tract). When the susception of carcinogenicity by genotoxic mechanism cannot be excluded, ADI cannot be set for food additives, pesticides, and veterinary drugs. Therefore, it is serious issues whether observed their genotoxicity in mouse GI-tract lead to their carcinogenicity. Although carcinogenicity is examined by long-term administration in feed or drinking water, in vivo genotoxicity tests have been traditionally performed by single intraperitoneal or gavage administration at MTD. Here, we examined the genotoxicity of food dyes given continuously by drinking, to re-evaluate DNA damage induced by food dyes given by gavage in mouse GI-tract. Although single gavage of food dyes at 2000 mg/kg induced DNA damage in GI-tract, their administration by continuous drinking at daily intake higher than 2000 mg/kg did not induce DNA damage in GI-tract. Based on our previous discussion that the results from continuous administration by drinking or feeding are likely to reflect carcinogenicity by genotoxic mechanisms better than the results from single gavage administration, in spite of the presence of positive responses in mouse GI-tract by single gavage of food dyes, the absence of positive response in mouse GI-tract by continuous drinking administration of food dyes could be considered to show the absence of carcinogenicity by genotoxic mechanisms.

Note: This article has been accepted for publication in the next issue.  A peer‑reviewed version will be posted soon.
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