Functional and proliferative effects of repeated low‐dose oral administration of furan in rat liver

Scope: Furan, a food contaminant formed during heat processing, induces hepatocellular tumors in rodents and high incidences of cholangiocarcinomas in rats even at the lowest dose (2 mg/kg b.w.) administered. Initial estimates suggested that human intake of furan may be as high as 3.5 μg/kg b.w./day...

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Veröffentlicht in:Molecular nutrition & food research 2010-11, Vol.54 (11), p.1556-1567
Hauptverfasser: Mally, Angela, Graff, Carmen, Schmal, Olga, Moro, Sabrina, Hamberger, Carolin, Schauer, Ute M, Brück, Jens, Özden, Sibel, Sieber, Max, Steger, Ulrich, Schrenk, Dieter, Hard, Gordon C, Chipman, James Kevin, Dekant, Wolfgang
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container_end_page 1567
container_issue 11
container_start_page 1556
container_title Molecular nutrition & food research
container_volume 54
creator Mally, Angela
Graff, Carmen
Schmal, Olga
Moro, Sabrina
Hamberger, Carolin
Schauer, Ute M
Brück, Jens
Özden, Sibel
Sieber, Max
Steger, Ulrich
Schrenk, Dieter
Hard, Gordon C
Chipman, James Kevin
Dekant, Wolfgang
description Scope: Furan, a food contaminant formed during heat processing, induces hepatocellular tumors in rodents and high incidences of cholangiocarcinomas in rats even at the lowest dose (2 mg/kg b.w.) administered. Initial estimates suggested that human intake of furan may be as high as 3.5 μg/kg b.w./day, indicating a relatively narrow margin of exposure. The aim of this study was to establish dose-response data for cytotoxicity, regenerative cell proliferation and secondary oxidative DNA damage in livers of male F344 rats treated with furan at doses ≤2 mg/kg b.w. for 28 days. Methods and results: No significant signs of hepatotoxicity other than a mild, dose‐dependent increase in serum cholesterol and unconjugated bile acids, and no evidence of oxidative DNA damage were seen. Histopathological alterations and proliferative changes were restricted to subcapsular areas of the left and caudate liver lobes. Conclusion: Although statistically significant effects were only seen at the 2 mg/kg b.w. dose during the course of our study, a ∼two and ∼threefold increase in 5‐bromo‐2′‐deoxyuridine labeling index was observed at 0.1 and 0.5 mg/kg b.w., respectively, suggesting that chronic exposure to doses even below 2 mg/kg b.w. may cause proliferative changes in rat liver and highlighting the need to assess furan carcinogenicity at lower doses.
doi_str_mv 10.1002/mnfr.201000064
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Methods and results: No significant signs of hepatotoxicity other than a mild, dose‐dependent increase in serum cholesterol and unconjugated bile acids, and no evidence of oxidative DNA damage were seen. Histopathological alterations and proliferative changes were restricted to subcapsular areas of the left and caudate liver lobes. Conclusion: Although statistically significant effects were only seen at the 2 mg/kg b.w. dose during the course of our study, a ∼two and ∼threefold increase in 5‐bromo‐2′‐deoxyuridine labeling index was observed at 0.1 and 0.5 mg/kg b.w., respectively, suggesting that chronic exposure to doses even below 2 mg/kg b.w. may cause proliferative changes in rat liver and highlighting the need to assess furan carcinogenicity at lower doses.</abstract><cop>Weinheim</cop><pub>Wiley‐VCH Verlag</pub><pmid>20540150</pmid><doi>10.1002/mnfr.201000064</doi><tpages>12</tpages></addata></record>
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source MEDLINE; Wiley Online Library All Journals
subjects Administration, Oral
Animals
Apoptosis
Bile Acids and Salts - analysis
Bile Acids and Salts - blood
Biological and medical sciences
Carcinogenicity
Carcinogenicity Tests
Carcinogens, Environmental - metabolism
Carcinogens, Environmental - toxicity
Cell Proliferation
DNA Damage
Food industries
Fundamental and applied biological sciences. Psychology
Furan
Furans - administration & dosage
Furans - toxicity
liver
Liver - physiopathology
Male
Metabolomics
Organ Size
Rats
Rats, Inbred F344
title Functional and proliferative effects of repeated low‐dose oral administration of furan in rat liver
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