Comparative mutagenic effects of structurally similar flavonoids quercetin and taxifolin on tester strains Salmonella typhimurium TA102 and Escherichia coli WP-2 uvrA
Quercetin (QT) and Taxifolin (TF) are structurally similar plant polyphenols. Both have been reported to have therapeutic potential as anti-cancer drugs and antioxidants. Mutagenic effects of QT and TF were evaluated using Salmonella typhimurium TA102 and Escherichia coli WP-2 uvrA tester strains. E...
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Veröffentlicht in: | Environmental and molecular mutagenesis 2009-07, Vol.50 (6), p.451-459 |
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description | Quercetin (QT) and Taxifolin (TF) are structurally similar plant polyphenols. Both have been reported to have therapeutic potential as anti-cancer drugs and antioxidants. Mutagenic effects of QT and TF were evaluated using Salmonella typhimurium TA102 and Escherichia coli WP-2 uvrA tester strains. Either in the presence or absence of S9 mix, QT was mutagenic to TA102 and WP2 uvrA. However, the mutagenicity of QT was significantly enhanced in the presence of S9 mix. Likewise, in the presence of Iron (Fe2+) and NADPH generating system (NGS) and absence of S9 mix, QT induced significantly high mutations in both TA102 and WP-2 uvrA. Mutagenicity of QT decreased in both strains in the presence of Iron (Fe2+) or NGS alone. TF was not mutagenic in the presence or absence of S9 mix in both TA102 and WP-2 uvrA 2, regardless of the presence of iron or NGS. Incorporation of antioxidants (ascorbate, superoxide dismutase (SOD), catalase (CAT)) and/or iron chelators (desferroxamine (DF) and ethylenediamine-tetraacetate (EDTA)) in the test systems markedly decreased QT-induced mutations in both tester strains. These results suggest that QT but not TF, could induce mutations in the presence or absence of rat liver S9 or Iron (Fe2+) and NGS in both tester strains by redox cycling and Fenton reactions to produce oxygen free radicals. Our results indicate that a minor structural variation between the two plant polyphenols could elicit a marked difference in their genotoxicities. These results provide a basis for further study into the potential use of QT in combination with iron supplements. Environ. Mol. Mutagen. 2009. |
doi_str_mv | 10.1002/em.20487 |
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Both have been reported to have therapeutic potential as anti-cancer drugs and antioxidants. Mutagenic effects of QT and TF were evaluated using Salmonella typhimurium TA102 and Escherichia coli WP-2 uvrA tester strains. Either in the presence or absence of S9 mix, QT was mutagenic to TA102 and WP2 uvrA. However, the mutagenicity of QT was significantly enhanced in the presence of S9 mix. Likewise, in the presence of Iron (Fe2+) and NADPH generating system (NGS) and absence of S9 mix, QT induced significantly high mutations in both TA102 and WP-2 uvrA. Mutagenicity of QT decreased in both strains in the presence of Iron (Fe2+) or NGS alone. TF was not mutagenic in the presence or absence of S9 mix in both TA102 and WP-2 uvrA 2, regardless of the presence of iron or NGS. Incorporation of antioxidants (ascorbate, superoxide dismutase (SOD), catalase (CAT)) and/or iron chelators (desferroxamine (DF) and ethylenediamine-tetraacetate (EDTA)) in the test systems markedly decreased QT-induced mutations in both tester strains. These results suggest that QT but not TF, could induce mutations in the presence or absence of rat liver S9 or Iron (Fe2+) and NGS in both tester strains by redox cycling and Fenton reactions to produce oxygen free radicals. Our results indicate that a minor structural variation between the two plant polyphenols could elicit a marked difference in their genotoxicities. These results provide a basis for further study into the potential use of QT in combination with iron supplements. Environ. Mol. Mutagen. 2009.</description><identifier>ISSN: 0893-6692</identifier><identifier>EISSN: 1098-2280</identifier><identifier>DOI: 10.1002/em.20487</identifier><identifier>PMID: 19326464</identifier><identifier>CODEN: EMMUEG</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Antioxidants - pharmacology ; Ascorbic Acid - pharmacology ; Biological and medical sciences ; Catalase - metabolism ; Deferoxamine - pharmacology ; Edetic Acid - pharmacology ; Escherichia coli ; Escherichia coli - drug effects ; Escherichia coli - enzymology ; flavonoids ; free radicals ; Fundamental and applied biological sciences. Psychology ; Genetics of eukaryotes. Biological and molecular evolution ; Iron - pharmacology ; Iron Chelating Agents - pharmacology ; iron chelators ; Liver Extracts ; Medical sciences ; Microbial Sensitivity Tests ; Mutagenesis - drug effects ; mutagenicity ; Mutagenicity Tests ; Mutation - genetics ; NADP - pharmacology ; Quercetin - analogs & derivatives ; Quercetin - chemistry ; Quercetin - toxicity ; Rats ; Salmonella typhimurium ; Salmonella typhimurium - drug effects ; Salmonella typhimurium - enzymology ; Superoxide Dismutase - metabolism ; Toxicology</subject><ispartof>Environmental and molecular mutagenesis, 2009-07, Vol.50 (6), p.451-459</ispartof><rights>Copyright © 2009 Wiley‐Liss, Inc.</rights><rights>2009 INIST-CNRS</rights><rights>Copyright 2009 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5097-ae0ba5de851100106cab898522df16aeeb409202eb2ee9a288118242019546a23</citedby><cites>FETCH-LOGICAL-c5097-ae0ba5de851100106cab898522df16aeeb409202eb2ee9a288118242019546a23</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%2Fem.20487$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fem.20487$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21684267$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19326464$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Makena, Patrudu S</creatorcontrib><creatorcontrib>Pierce, Samuel C</creatorcontrib><creatorcontrib>Chung, King-Thom</creatorcontrib><creatorcontrib>Sinclair, Scott E</creatorcontrib><title>Comparative mutagenic effects of structurally similar flavonoids quercetin and taxifolin on tester strains Salmonella typhimurium TA102 and Escherichia coli WP-2 uvrA</title><title>Environmental and molecular mutagenesis</title><addtitle>Environ. Mol. Mutagen</addtitle><description>Quercetin (QT) and Taxifolin (TF) are structurally similar plant polyphenols. Both have been reported to have therapeutic potential as anti-cancer drugs and antioxidants. Mutagenic effects of QT and TF were evaluated using Salmonella typhimurium TA102 and Escherichia coli WP-2 uvrA tester strains. Either in the presence or absence of S9 mix, QT was mutagenic to TA102 and WP2 uvrA. However, the mutagenicity of QT was significantly enhanced in the presence of S9 mix. Likewise, in the presence of Iron (Fe2+) and NADPH generating system (NGS) and absence of S9 mix, QT induced significantly high mutations in both TA102 and WP-2 uvrA. Mutagenicity of QT decreased in both strains in the presence of Iron (Fe2+) or NGS alone. TF was not mutagenic in the presence or absence of S9 mix in both TA102 and WP-2 uvrA 2, regardless of the presence of iron or NGS. Incorporation of antioxidants (ascorbate, superoxide dismutase (SOD), catalase (CAT)) and/or iron chelators (desferroxamine (DF) and ethylenediamine-tetraacetate (EDTA)) in the test systems markedly decreased QT-induced mutations in both tester strains. These results suggest that QT but not TF, could induce mutations in the presence or absence of rat liver S9 or Iron (Fe2+) and NGS in both tester strains by redox cycling and Fenton reactions to produce oxygen free radicals. Our results indicate that a minor structural variation between the two plant polyphenols could elicit a marked difference in their genotoxicities. These results provide a basis for further study into the potential use of QT in combination with iron supplements. Environ. Mol. Mutagen. 2009.</description><subject>Animals</subject><subject>Antioxidants - pharmacology</subject><subject>Ascorbic Acid - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Catalase - metabolism</subject><subject>Deferoxamine - pharmacology</subject><subject>Edetic Acid - pharmacology</subject><subject>Escherichia coli</subject><subject>Escherichia coli - drug effects</subject><subject>Escherichia coli - enzymology</subject><subject>flavonoids</subject><subject>free radicals</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetics of eukaryotes. Biological and molecular evolution</subject><subject>Iron - pharmacology</subject><subject>Iron Chelating Agents - pharmacology</subject><subject>iron chelators</subject><subject>Liver Extracts</subject><subject>Medical sciences</subject><subject>Microbial Sensitivity Tests</subject><subject>Mutagenesis - drug effects</subject><subject>mutagenicity</subject><subject>Mutagenicity Tests</subject><subject>Mutation - genetics</subject><subject>NADP - pharmacology</subject><subject>Quercetin - analogs & derivatives</subject><subject>Quercetin - chemistry</subject><subject>Quercetin - toxicity</subject><subject>Rats</subject><subject>Salmonella typhimurium</subject><subject>Salmonella typhimurium - drug effects</subject><subject>Salmonella typhimurium - enzymology</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Toxicology</subject><issn>0893-6692</issn><issn>1098-2280</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kctuEzEUhkcIRENB4gnAGwSbKbbH49jLKKQFKdzUliytE-dMYxiPgz0TmhfiOXGaUFasLEvf-c7lL4rnjJ4xSvlb9GecCjV-UIwY1arkXNGHxYgqXZVSan5SPEnpO6WMCc0fFydMV1wKKUbF72nwG4jQuy0SP_Rwg52zBJsGbZ9IaEjq42D7IULb7khy3rUQSdPCNnTBrRL5OWC02LuOQLciPdy6JrT5FzrSY-ox7g3gukQuofWhw7YF0u82a-eH6AZPriaM8rviWbJrjM6uHRCbJWTxpeRk2MbJ0-JRA23CZ8f3tLg-n11N35fzzxcfppN5aWuqxyUgXUK9QlWzfBdGpYWl0qrmfNUwCYhLQTWnHJccUQNXijHFBadM10ICr06L1wfvJoa8WOqNd8nuR-4wDMmMhRgzWVORyTcH0saQUsTGbKLzEHeGUbMPxaA3d6Fk9MVROiw9rv6BxxQy8OoIQLLQNhE669I9x5lUgsu9qDxwv1yLu_82NLOPfxsfeZdzuL3nIf4w2TauzeLThVlU376eazk37zL_8sA3EAzcxDzD9WU-TkXzziIftPoDdlW8ig</recordid><startdate>200907</startdate><enddate>200907</enddate><creator>Makena, Patrudu S</creator><creator>Pierce, Samuel C</creator><creator>Chung, King-Thom</creator><creator>Sinclair, Scott E</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</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><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>200907</creationdate><title>Comparative mutagenic effects of structurally similar flavonoids quercetin and taxifolin on tester strains Salmonella typhimurium TA102 and Escherichia coli WP-2 uvrA</title><author>Makena, Patrudu S ; Pierce, Samuel C ; Chung, King-Thom ; Sinclair, Scott E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5097-ae0ba5de851100106cab898522df16aeeb409202eb2ee9a288118242019546a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Antioxidants - pharmacology</topic><topic>Ascorbic Acid - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Catalase - metabolism</topic><topic>Deferoxamine - pharmacology</topic><topic>Edetic Acid - pharmacology</topic><topic>Escherichia coli</topic><topic>Escherichia coli - drug effects</topic><topic>Escherichia coli - enzymology</topic><topic>flavonoids</topic><topic>free radicals</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics of eukaryotes. Biological and molecular evolution</topic><topic>Iron - pharmacology</topic><topic>Iron Chelating Agents - pharmacology</topic><topic>iron chelators</topic><topic>Liver Extracts</topic><topic>Medical sciences</topic><topic>Microbial Sensitivity Tests</topic><topic>Mutagenesis - drug effects</topic><topic>mutagenicity</topic><topic>Mutagenicity Tests</topic><topic>Mutation - genetics</topic><topic>NADP - pharmacology</topic><topic>Quercetin - analogs & derivatives</topic><topic>Quercetin - chemistry</topic><topic>Quercetin - toxicity</topic><topic>Rats</topic><topic>Salmonella typhimurium</topic><topic>Salmonella typhimurium - drug effects</topic><topic>Salmonella typhimurium - enzymology</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Makena, Patrudu S</creatorcontrib><creatorcontrib>Pierce, Samuel C</creatorcontrib><creatorcontrib>Chung, King-Thom</creatorcontrib><creatorcontrib>Sinclair, Scott E</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><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Environmental and molecular mutagenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Makena, Patrudu S</au><au>Pierce, Samuel C</au><au>Chung, King-Thom</au><au>Sinclair, Scott E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative mutagenic effects of structurally similar flavonoids quercetin and taxifolin on tester strains Salmonella typhimurium TA102 and Escherichia coli WP-2 uvrA</atitle><jtitle>Environmental and molecular mutagenesis</jtitle><addtitle>Environ. Mol. Mutagen</addtitle><date>2009-07</date><risdate>2009</risdate><volume>50</volume><issue>6</issue><spage>451</spage><epage>459</epage><pages>451-459</pages><issn>0893-6692</issn><eissn>1098-2280</eissn><coden>EMMUEG</coden><abstract>Quercetin (QT) and Taxifolin (TF) are structurally similar plant polyphenols. Both have been reported to have therapeutic potential as anti-cancer drugs and antioxidants. Mutagenic effects of QT and TF were evaluated using Salmonella typhimurium TA102 and Escherichia coli WP-2 uvrA tester strains. Either in the presence or absence of S9 mix, QT was mutagenic to TA102 and WP2 uvrA. However, the mutagenicity of QT was significantly enhanced in the presence of S9 mix. Likewise, in the presence of Iron (Fe2+) and NADPH generating system (NGS) and absence of S9 mix, QT induced significantly high mutations in both TA102 and WP-2 uvrA. Mutagenicity of QT decreased in both strains in the presence of Iron (Fe2+) or NGS alone. TF was not mutagenic in the presence or absence of S9 mix in both TA102 and WP-2 uvrA 2, regardless of the presence of iron or NGS. Incorporation of antioxidants (ascorbate, superoxide dismutase (SOD), catalase (CAT)) and/or iron chelators (desferroxamine (DF) and ethylenediamine-tetraacetate (EDTA)) in the test systems markedly decreased QT-induced mutations in both tester strains. These results suggest that QT but not TF, could induce mutations in the presence or absence of rat liver S9 or Iron (Fe2+) and NGS in both tester strains by redox cycling and Fenton reactions to produce oxygen free radicals. Our results indicate that a minor structural variation between the two plant polyphenols could elicit a marked difference in their genotoxicities. These results provide a basis for further study into the potential use of QT in combination with iron supplements. Environ. Mol. Mutagen. 2009.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19326464</pmid><doi>10.1002/em.20487</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Antioxidants - pharmacology Ascorbic Acid - pharmacology Biological and medical sciences Catalase - metabolism Deferoxamine - pharmacology Edetic Acid - pharmacology Escherichia coli Escherichia coli - drug effects Escherichia coli - enzymology flavonoids free radicals Fundamental and applied biological sciences. Psychology Genetics of eukaryotes. Biological and molecular evolution Iron - pharmacology Iron Chelating Agents - pharmacology iron chelators Liver Extracts Medical sciences Microbial Sensitivity Tests Mutagenesis - drug effects mutagenicity Mutagenicity Tests Mutation - genetics NADP - pharmacology Quercetin - analogs & derivatives Quercetin - chemistry Quercetin - toxicity Rats Salmonella typhimurium Salmonella typhimurium - drug effects Salmonella typhimurium - enzymology Superoxide Dismutase - metabolism Toxicology |
title | Comparative mutagenic effects of structurally similar flavonoids quercetin and taxifolin on tester strains Salmonella typhimurium TA102 and Escherichia coli WP-2 uvrA |
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