Antioxidant Activity of Isoflavones and Their Major Metabolites Using Different in Vitro Assays
Isoflavone phytoestrogens found mainly in soybeans and clover are widely studied phytochemicals. Genistein and daidzein, the major isoflavones found in soy, have received the most attention. However, they undergo extensive metabolism in the intestine and the liver, which might affect their biologica...
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description | Isoflavone phytoestrogens found mainly in soybeans and clover are widely studied phytochemicals. Genistein and daidzein, the major isoflavones found in soy, have received the most attention. However, they undergo extensive metabolism in the intestine and the liver, which might affect their biological properties, e.g. their antioxidant capacities. Furthermore, the biological activities of other naturally occurring isoflavones, for instance, glycitein from soy or biochanin A from red clover, have not yet been studied in detail. The aim of this study was to investigate the antioxidant activities of six naturally occurring isoflavones and their corresponding oxidative and bacterial metabolites. The oxygen radical absorbance capacity assay as well as the in vitro oxidation of low density lipoproteins with the conjugated diene and the thiobarbituric acid reacting substances formation as end points were used. The oxidative metabolites of genistein and daidzein as well as equol exhibited the highest antioxidant activities in all three assays. With few exceptions, they were more effective than the positive controls quercetin and ascorbic acid. Formononetin, the 4‘-O-methyl ether of daidzein, showed the lowest antioxidant property. Because the antioxidant efficacy of isoflavones as effective antioxidants is evident at concentrations well within the range found in the plasma of subjects consuming soy products, this biological activity could be of physiological relevance. Keywords: Isoflavones; bacterial and oxidative metabolites; antioxidant activity; ORAC assay; in vitro oxidation of low-density lipoproteins |
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Genistein and daidzein, the major isoflavones found in soy, have received the most attention. However, they undergo extensive metabolism in the intestine and the liver, which might affect their biological properties, e.g. their antioxidant capacities. Furthermore, the biological activities of other naturally occurring isoflavones, for instance, glycitein from soy or biochanin A from red clover, have not yet been studied in detail. The aim of this study was to investigate the antioxidant activities of six naturally occurring isoflavones and their corresponding oxidative and bacterial metabolites. The oxygen radical absorbance capacity assay as well as the in vitro oxidation of low density lipoproteins with the conjugated diene and the thiobarbituric acid reacting substances formation as end points were used. The oxidative metabolites of genistein and daidzein as well as equol exhibited the highest antioxidant activities in all three assays. With few exceptions, they were more effective than the positive controls quercetin and ascorbic acid. Formononetin, the 4‘-O-methyl ether of daidzein, showed the lowest antioxidant property. Because the antioxidant efficacy of isoflavones as effective antioxidants is evident at concentrations well within the range found in the plasma of subjects consuming soy products, this biological activity could be of physiological relevance. Keywords: Isoflavones; bacterial and oxidative metabolites; antioxidant activity; ORAC assay; in vitro oxidation of low-density lipoproteins</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf053112o</identifier><identifier>PMID: 16608210</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>antioxidant activity ; antioxidants ; Antioxidants - pharmacology ; assays ; Bacteria - metabolism ; bacterial metabolites ; biochanin A ; Biological and medical sciences ; daidzein ; Equol ; Food industries ; formononetin ; free radical scavengers ; free radicals ; Fundamental and applied biological sciences. Psychology ; genistein ; Genistein - metabolism ; Genistein - pharmacology ; Glycine max - chemistry ; glycitein ; isoflavones ; Isoflavones - metabolism ; Isoflavones - pharmacology ; Lipid Peroxidation - drug effects ; Lipoproteins, LDL - chemistry ; low density lipoprotein ; metabolites ; oxidation ; Oxidation-Reduction ; oxidative metabolites ; oxygen ; oxygen radical absorbance capacity ; prunetin ; Thiobarbituric Acid Reactive Substances - analysis</subject><ispartof>Journal of agricultural and food chemistry, 2006-04, Vol.54 (8), p.2926-2931</ispartof><rights>Copyright © 2006 American Chemical Society</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a405t-732f809c8d61b98a0ac99b9ee82a6c1a04ce244e4b8ed0e4428ec34ad1bde4253</citedby><cites>FETCH-LOGICAL-a405t-732f809c8d61b98a0ac99b9ee82a6c1a04ce244e4b8ed0e4428ec34ad1bde4253</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jf053112o$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jf053112o$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17708994$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16608210$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rüfer, Corinna E</creatorcontrib><creatorcontrib>Kulling, Sabine E</creatorcontrib><title>Antioxidant Activity of Isoflavones and Their Major Metabolites Using Different in Vitro Assays</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>Isoflavone phytoestrogens found mainly in soybeans and clover are widely studied phytochemicals. Genistein and daidzein, the major isoflavones found in soy, have received the most attention. However, they undergo extensive metabolism in the intestine and the liver, which might affect their biological properties, e.g. their antioxidant capacities. Furthermore, the biological activities of other naturally occurring isoflavones, for instance, glycitein from soy or biochanin A from red clover, have not yet been studied in detail. The aim of this study was to investigate the antioxidant activities of six naturally occurring isoflavones and their corresponding oxidative and bacterial metabolites. The oxygen radical absorbance capacity assay as well as the in vitro oxidation of low density lipoproteins with the conjugated diene and the thiobarbituric acid reacting substances formation as end points were used. The oxidative metabolites of genistein and daidzein as well as equol exhibited the highest antioxidant activities in all three assays. With few exceptions, they were more effective than the positive controls quercetin and ascorbic acid. Formononetin, the 4‘-O-methyl ether of daidzein, showed the lowest antioxidant property. Because the antioxidant efficacy of isoflavones as effective antioxidants is evident at concentrations well within the range found in the plasma of subjects consuming soy products, this biological activity could be of physiological relevance. Keywords: Isoflavones; bacterial and oxidative metabolites; antioxidant activity; ORAC assay; in vitro oxidation of low-density lipoproteins</description><subject>antioxidant activity</subject><subject>antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>assays</subject><subject>Bacteria - metabolism</subject><subject>bacterial metabolites</subject><subject>biochanin A</subject><subject>Biological and medical sciences</subject><subject>daidzein</subject><subject>Equol</subject><subject>Food industries</subject><subject>formononetin</subject><subject>free radical scavengers</subject><subject>free radicals</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>genistein</subject><subject>Genistein - metabolism</subject><subject>Genistein - pharmacology</subject><subject>Glycine max - chemistry</subject><subject>glycitein</subject><subject>isoflavones</subject><subject>Isoflavones - metabolism</subject><subject>Isoflavones - pharmacology</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Lipoproteins, LDL - chemistry</subject><subject>low density lipoprotein</subject><subject>metabolites</subject><subject>oxidation</subject><subject>Oxidation-Reduction</subject><subject>oxidative metabolites</subject><subject>oxygen</subject><subject>oxygen radical absorbance capacity</subject><subject>prunetin</subject><subject>Thiobarbituric Acid Reactive Substances - analysis</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0Mtu1DAUBmALgehQWPACkA1ILALHjp3Yy1G5FcpFdAaxs04cu3jIxMX2VJ23xzBRu2FjL86n3z4_IY8pvKTA6KuNA9FQysIdsqCCQS0olXfJAsqwlqKlR-RBShsAkKKD--SIti1IRmFB9HLKPlz7AadcLU32Vz7vq-Cq0xTciFdhsqnCaahWP62P1SfchHLajH0YfS6zdfLTRfXaO2ejLRl-qr77HEO1TAn36SG553BM9tF8H5P12zerk_f12Zd3pyfLsxo5iFx3DXMSlJFDS3slEdAo1StrJcPWUARuLOPc8l7aASznTFrTcBxoP1jORHNMnh9yL2P4vbMp661Pxo4jTjbskm472bZMdQW-OEATQ0rROn0Z_RbjXlPQf9vUN20W-2QO3fVbO9zKub4Cns0Ak8HRRZyMT7eu60AqxYurD86nbK9v5hh_lY81ndCrr-dafFDs4w_4pj8X__TgHQaNF7Fkrs8Z0AYodEL9W2N-GU3Sm7CLU2n3Pyv8AeDUoSQ</recordid><startdate>20060419</startdate><enddate>20060419</enddate><creator>Rüfer, Corinna E</creator><creator>Kulling, Sabine E</creator><general>American Chemical Society</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>7X8</scope></search><sort><creationdate>20060419</creationdate><title>Antioxidant Activity of Isoflavones and Their Major Metabolites Using Different in Vitro Assays</title><author>Rüfer, Corinna E ; Kulling, Sabine E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a405t-732f809c8d61b98a0ac99b9ee82a6c1a04ce244e4b8ed0e4428ec34ad1bde4253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>antioxidant activity</topic><topic>antioxidants</topic><topic>Antioxidants - pharmacology</topic><topic>assays</topic><topic>Bacteria - metabolism</topic><topic>bacterial metabolites</topic><topic>biochanin A</topic><topic>Biological and medical sciences</topic><topic>daidzein</topic><topic>Equol</topic><topic>Food industries</topic><topic>formononetin</topic><topic>free radical scavengers</topic><topic>free radicals</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>genistein</topic><topic>Genistein - metabolism</topic><topic>Genistein - pharmacology</topic><topic>Glycine max - chemistry</topic><topic>glycitein</topic><topic>isoflavones</topic><topic>Isoflavones - metabolism</topic><topic>Isoflavones - pharmacology</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Lipoproteins, LDL - chemistry</topic><topic>low density lipoprotein</topic><topic>metabolites</topic><topic>oxidation</topic><topic>Oxidation-Reduction</topic><topic>oxidative metabolites</topic><topic>oxygen</topic><topic>oxygen radical absorbance capacity</topic><topic>prunetin</topic><topic>Thiobarbituric Acid Reactive Substances - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rüfer, Corinna E</creatorcontrib><creatorcontrib>Kulling, Sabine 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>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rüfer, Corinna E</au><au>Kulling, Sabine E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antioxidant Activity of Isoflavones and Their Major Metabolites Using Different in Vitro Assays</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2006-04-19</date><risdate>2006</risdate><volume>54</volume><issue>8</issue><spage>2926</spage><epage>2931</epage><pages>2926-2931</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>Isoflavone phytoestrogens found mainly in soybeans and clover are widely studied phytochemicals. Genistein and daidzein, the major isoflavones found in soy, have received the most attention. However, they undergo extensive metabolism in the intestine and the liver, which might affect their biological properties, e.g. their antioxidant capacities. Furthermore, the biological activities of other naturally occurring isoflavones, for instance, glycitein from soy or biochanin A from red clover, have not yet been studied in detail. The aim of this study was to investigate the antioxidant activities of six naturally occurring isoflavones and their corresponding oxidative and bacterial metabolites. The oxygen radical absorbance capacity assay as well as the in vitro oxidation of low density lipoproteins with the conjugated diene and the thiobarbituric acid reacting substances formation as end points were used. The oxidative metabolites of genistein and daidzein as well as equol exhibited the highest antioxidant activities in all three assays. With few exceptions, they were more effective than the positive controls quercetin and ascorbic acid. Formononetin, the 4‘-O-methyl ether of daidzein, showed the lowest antioxidant property. Because the antioxidant efficacy of isoflavones as effective antioxidants is evident at concentrations well within the range found in the plasma of subjects consuming soy products, this biological activity could be of physiological relevance. Keywords: Isoflavones; bacterial and oxidative metabolites; antioxidant activity; ORAC assay; in vitro oxidation of low-density lipoproteins</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>16608210</pmid><doi>10.1021/jf053112o</doi><tpages>6</tpages></addata></record> |
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subjects | antioxidant activity antioxidants Antioxidants - pharmacology assays Bacteria - metabolism bacterial metabolites biochanin A Biological and medical sciences daidzein Equol Food industries formononetin free radical scavengers free radicals Fundamental and applied biological sciences. Psychology genistein Genistein - metabolism Genistein - pharmacology Glycine max - chemistry glycitein isoflavones Isoflavones - metabolism Isoflavones - pharmacology Lipid Peroxidation - drug effects Lipoproteins, LDL - chemistry low density lipoprotein metabolites oxidation Oxidation-Reduction oxidative metabolites oxygen oxygen radical absorbance capacity prunetin Thiobarbituric Acid Reactive Substances - analysis |
title | Antioxidant Activity of Isoflavones and Their Major Metabolites Using Different in Vitro Assays |
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