Evaluation of serum and liver toxicokinetics for furan and liver DNA adduct formation in male Fischer 344 rats. (December 2015)

• Record Type: Journal Article
• Authors: Churchwell, M.I.; Scheri, R.C.; Von Tungeln, L.S.; Gamboa da Costa, G.; Beland, F.A.; Doerge, D.R.
• Is Part Of: Food and chemical toxicology. Volume 86(2015)
• Page Start: 1
• Page End: 8
• Publication Date: 2015-12
• Subjects: Furan -- Hepatotoxicity -- Hepatocarcinogen -- Mass spectrometry -- Pharmacokinetics; Toxicology -- Periodicals; Food poisoning -- Periodicals; Food Poisoning -- Periodicals; Toxicology -- Periodicals; Toxicologie -- Périodiques; Intoxications alimentaires -- Périodiques; Food poisoning; Toxicology; Periodicals; Electronic journals; 615.9
• DOI: 10.1016/j.fct.2015.08.029
• Languages: English
• ISSNs: 0278-6915

Abstract

Abstract: Furan is a food processing contaminant found in many common cooked foods that induces liver toxicity and liver cancer in animal models treated with sufficient doses. The metabolism of furan occurs primarily in the liver where CYP 2E1 produces a highly reactive bis -electrophile, cis -2-butene-1, 4-dial (BDA). BDA reacts with nucleophilic groups in amino acids and DNA in vitro to form covalent adducts. Evidence for BDA-nucleoside adduct formation in vivo is limited but important for assessing the carcinogenic hazard of dietary furan. This study used controlled dosing with furan in Fischer 344 rats to measure serum and liver toxicokinetics and the possible formation of BDA-nucleoside adducts in vivo. After gavage exposure, furan concentrations in the liver were consistently higher than those in whole blood (∼6-fold), which is consistent with portal vein delivery of a lipophilic compound into the liver. Formation of BDA-2′-deoxycytidine in furan-treated rat liver DNA was not observed using LC/MS/MS after single doses as high as 9.2 mg/kg bw or repeated dosing for up to 360 days above a consistent background level (1-2 adducts per 10 8 nucleotides). This absence of BDA-nucleoside adduct formation is consistent with the general lack of evidence for genotoxicity of furan in vivo. Highlights: After gavage, furan is rapidly eliminated from blood (t1/2 1.3 h) and liver (t1/2 0.62 h). Liver concentrations of furan are ∼6-fold greater than blood concentrations. Single and repeated furan dosing of F344 rats does not produce BDA-dC DNA adducts.