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 |
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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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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.</description><identifier>ISSN: 1613-4125</identifier><identifier>EISSN: 1613-4133</identifier><identifier>DOI: 10.1002/mnfr.201000064</identifier><identifier>PMID: 20540150</identifier><language>eng</language><publisher>Weinheim: Wiley‐VCH Verlag</publisher><subject>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</subject><ispartof>Molecular nutrition & food research, 2010-11, Vol.54 (11), p.1556-1567</ispartof><rights>Copyright © 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4044-6ccc089b9d97c38ddf1eb53d74f9fb4e81600baa90cb9568f4e11ca6f808981d3</citedby><cites>FETCH-LOGICAL-c4044-6ccc089b9d97c38ddf1eb53d74f9fb4e81600baa90cb9568f4e11ca6f808981d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmnfr.201000064$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmnfr.201000064$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23428679$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20540150$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mally, Angela</creatorcontrib><creatorcontrib>Graff, Carmen</creatorcontrib><creatorcontrib>Schmal, Olga</creatorcontrib><creatorcontrib>Moro, Sabrina</creatorcontrib><creatorcontrib>Hamberger, Carolin</creatorcontrib><creatorcontrib>Schauer, Ute M</creatorcontrib><creatorcontrib>Brück, Jens</creatorcontrib><creatorcontrib>Özden, Sibel</creatorcontrib><creatorcontrib>Sieber, Max</creatorcontrib><creatorcontrib>Steger, Ulrich</creatorcontrib><creatorcontrib>Schrenk, Dieter</creatorcontrib><creatorcontrib>Hard, Gordon C</creatorcontrib><creatorcontrib>Chipman, James Kevin</creatorcontrib><creatorcontrib>Dekant, Wolfgang</creatorcontrib><title>Functional and proliferative effects of repeated low‐dose oral administration of furan in rat liver</title><title>Molecular nutrition & food research</title><addtitle>Mol. Nutr. Food Res</addtitle><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.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Bile Acids and Salts - analysis</subject><subject>Bile Acids and Salts - blood</subject><subject>Biological and medical sciences</subject><subject>Carcinogenicity</subject><subject>Carcinogenicity Tests</subject><subject>Carcinogens, Environmental - metabolism</subject><subject>Carcinogens, Environmental - toxicity</subject><subject>Cell Proliferation</subject><subject>DNA Damage</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Furan</subject><subject>Furans - administration & dosage</subject><subject>Furans - toxicity</subject><subject>liver</subject><subject>Liver - physiopathology</subject><subject>Male</subject><subject>Metabolomics</subject><subject>Organ Size</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><issn>1613-4125</issn><issn>1613-4133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtu1DAUhq0K1Bvddkm9YZnhOHYce4kqpgWVQaIUlpbjC3KbiUd2htIdj8Az8iQ4SpmyY-Uj6_t-H_8InRJYEID69XrwaVFDmQE420OHhBNaMULps91cNwfoKOdbAEpqRvfRQQ0NA9LAIXLL7WDGEAfdYz1YvEmxD94lPYbvDjvvnRkzjh4nt3F6dBb38f73z182Zodjmiy7DkPI46TEYUL9NukBhwGXK9yXnPQCPfe6z-7k8TxGN8u3n88vq6uPF-_O31xVhgFjFTfGgJCdtLI1VFjriesaalvmpe-YE4QDdFpLMJ1suPDMEWI096JYglh6jBZzrkkx5-S82qSw1ulBEVBTX2rqS-36KsLLWdhsu7WzO_xvQQV49QjobHTvy89MyE8cZbXgrSycnLn70LuH_zyrPqyWn_5doprd0qL7sXN1ulO8pW2jvq4uVC3e11xcf1Grwp_NvNdR6W-p7HNzXeIoEAkSWk7_AP11nx8</recordid><startdate>201011</startdate><enddate>201011</enddate><creator>Mally, Angela</creator><creator>Graff, Carmen</creator><creator>Schmal, Olga</creator><creator>Moro, Sabrina</creator><creator>Hamberger, Carolin</creator><creator>Schauer, Ute M</creator><creator>Brück, Jens</creator><creator>Özden, Sibel</creator><creator>Sieber, Max</creator><creator>Steger, Ulrich</creator><creator>Schrenk, Dieter</creator><creator>Hard, Gordon C</creator><creator>Chipman, James Kevin</creator><creator>Dekant, Wolfgang</creator><general>Wiley‐VCH Verlag</general><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201011</creationdate><title>Functional and proliferative effects of repeated low‐dose oral administration of furan in rat liver</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4044-6ccc089b9d97c38ddf1eb53d74f9fb4e81600baa90cb9568f4e11ca6f808981d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Bile Acids and Salts - analysis</topic><topic>Bile Acids and Salts - blood</topic><topic>Biological and medical sciences</topic><topic>Carcinogenicity</topic><topic>Carcinogenicity Tests</topic><topic>Carcinogens, Environmental - metabolism</topic><topic>Carcinogens, Environmental - toxicity</topic><topic>Cell Proliferation</topic><topic>DNA Damage</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Furan</topic><topic>Furans - administration & dosage</topic><topic>Furans - toxicity</topic><topic>liver</topic><topic>Liver - physiopathology</topic><topic>Male</topic><topic>Metabolomics</topic><topic>Organ Size</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mally, Angela</creatorcontrib><creatorcontrib>Graff, Carmen</creatorcontrib><creatorcontrib>Schmal, Olga</creatorcontrib><creatorcontrib>Moro, Sabrina</creatorcontrib><creatorcontrib>Hamberger, Carolin</creatorcontrib><creatorcontrib>Schauer, Ute M</creatorcontrib><creatorcontrib>Brück, Jens</creatorcontrib><creatorcontrib>Özden, Sibel</creatorcontrib><creatorcontrib>Sieber, Max</creatorcontrib><creatorcontrib>Steger, Ulrich</creatorcontrib><creatorcontrib>Schrenk, Dieter</creatorcontrib><creatorcontrib>Hard, Gordon C</creatorcontrib><creatorcontrib>Chipman, James Kevin</creatorcontrib><creatorcontrib>Dekant, Wolfgang</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Molecular nutrition & food research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mally, Angela</au><au>Graff, Carmen</au><au>Schmal, Olga</au><au>Moro, Sabrina</au><au>Hamberger, Carolin</au><au>Schauer, Ute M</au><au>Brück, Jens</au><au>Özden, Sibel</au><au>Sieber, Max</au><au>Steger, Ulrich</au><au>Schrenk, Dieter</au><au>Hard, Gordon C</au><au>Chipman, James Kevin</au><au>Dekant, Wolfgang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional and proliferative effects of repeated low‐dose oral administration of furan in rat liver</atitle><jtitle>Molecular nutrition & food research</jtitle><addtitle>Mol. Nutr. Food Res</addtitle><date>2010-11</date><risdate>2010</risdate><volume>54</volume><issue>11</issue><spage>1556</spage><epage>1567</epage><pages>1556-1567</pages><issn>1613-4125</issn><eissn>1613-4133</eissn><abstract>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.</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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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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