Phenolic Antioxidants and the Protection of Low Density Lipoprotein from Peroxynitrite-Mediated Oxidations at Physiologic CO2
Dietary phenolic antioxidants have been shown to prevent LDL modifications mediated by several physiologic oxidants including peroxynitrite. However, more recent data demonstrated that CO2 affected the fate of peroxynitrite in biological fluids and significantly reduced peroxynitrite scavenging by p...
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Veröffentlicht in: | Journal of agricultural and food chemistry 2004-05, Vol.52 (10), p.2866-2874 |
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description | Dietary phenolic antioxidants have been shown to prevent LDL modifications mediated by several physiologic oxidants including peroxynitrite. However, more recent data demonstrated that CO2 affected the fate of peroxynitrite in biological fluids and significantly reduced peroxynitrite scavenging by polyphenols, raising doubts concerning their antioxidant activity. We found that the oxidation of LDL lipids mediated by peroxynitrite decreased in the presence of bicarbonate, while Trp oxidation and 3-nitroTyr formation increased, suggesting a redirection of peroxynitrite reactivity toward the protein moiety. We therefore evaluated the protective activity of some phenolic antioxidants (quercetin, oleuropein, resveratrol, (+)-catechin, (−)-epicatechin, tyrosol, α- and γ-tocopherol, ascorbate) on peroxynitrite-mediated oxidation of LDL aromatic residues. Some of these phenols protected LDL Trp from oxidation better than ascorbate or α-tocopherol, although protection at 100 μM did not exceed 30−40%. However, the same phenolic antioxidants were more active in inhibiting 3-nitroTyr formation and those with a catechin structure provided significant protection (IC50% 40−50 μM). Red wine, a polyphenol-rich beverage, showed a protective effect comparable to that of the most active phenolic antioxidants. Direct EPR studies showed that bicarbonate significantly increased the peroxynitrite-dependent formation of O-semiquinone radicals in red wine, supporting the hypothesis that polyphenols are efficient scavengers of radicals formed by peroxynitrite/CO2. Ascorbate was a poor inhibitor of peroxynitrite/CO2-induced LDL tyrosine nitration, but the simultaneous addition to the most active polyphenols halved their IC50%. In conclusion, although cooperation with other antioxidants can further decrease the IC50% of polyphenolics, as demonstrated for ascorbate, their antioxidant activity appears to occur at concentrations at least 1 order of magnitude higher than their bioavailability. Keywords: Lipoprotein; 3-nitrotyrosine; tryptophan oxidation; peroxynitrite; phenolic antioxidants; bicarbonate |
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However, more recent data demonstrated that CO2 affected the fate of peroxynitrite in biological fluids and significantly reduced peroxynitrite scavenging by polyphenols, raising doubts concerning their antioxidant activity. We found that the oxidation of LDL lipids mediated by peroxynitrite decreased in the presence of bicarbonate, while Trp oxidation and 3-nitroTyr formation increased, suggesting a redirection of peroxynitrite reactivity toward the protein moiety. We therefore evaluated the protective activity of some phenolic antioxidants (quercetin, oleuropein, resveratrol, (+)-catechin, (−)-epicatechin, tyrosol, α- and γ-tocopherol, ascorbate) on peroxynitrite-mediated oxidation of LDL aromatic residues. Some of these phenols protected LDL Trp from oxidation better than ascorbate or α-tocopherol, although protection at 100 μM did not exceed 30−40%. However, the same phenolic antioxidants were more active in inhibiting 3-nitroTyr formation and those with a catechin structure provided significant protection (IC50% 40−50 μM). Red wine, a polyphenol-rich beverage, showed a protective effect comparable to that of the most active phenolic antioxidants. Direct EPR studies showed that bicarbonate significantly increased the peroxynitrite-dependent formation of O-semiquinone radicals in red wine, supporting the hypothesis that polyphenols are efficient scavengers of radicals formed by peroxynitrite/CO2. Ascorbate was a poor inhibitor of peroxynitrite/CO2-induced LDL tyrosine nitration, but the simultaneous addition to the most active polyphenols halved their IC50%. In conclusion, although cooperation with other antioxidants can further decrease the IC50% of polyphenolics, as demonstrated for ascorbate, their antioxidant activity appears to occur at concentrations at least 1 order of magnitude higher than their bioavailability. Keywords: Lipoprotein; 3-nitrotyrosine; tryptophan oxidation; peroxynitrite; phenolic antioxidants; bicarbonate</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf034270n</identifier><identifier>PMID: 15137827</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>alpha-tocopherol ; antioxidant activity ; antioxidants ; Antioxidants - pharmacology ; ascorbic acid ; bicarbonates ; Bicarbonates - pharmacology ; Biological and medical sciences ; carbon dioxide ; Carbon Dioxide - chemistry ; Feeding. Feeding behavior ; free radical scavengers ; free radicals ; Fundamental and applied biological sciences. Psychology ; Lipid Peroxidation - drug effects ; Lipoproteins, LDL - chemistry ; low density lipoprotein ; oxidants ; oxidation ; peroxynitrite ; Peroxynitrous Acid - chemistry ; phenolic compounds ; Phenols - pharmacology ; polyphenols ; red wines ; tryptophan ; tyrosine ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Wine - analysis</subject><ispartof>Journal of agricultural and food chemistry, 2004-05, Vol.52 (10), p.2866-2874</ispartof><rights>Copyright © 2004 American Chemical Society</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jf034270n$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jf034270n$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15738203$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15137827$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ferroni, Flavia</creatorcontrib><creatorcontrib>Maccaglia, Alessandro</creatorcontrib><creatorcontrib>Pietraforte, Donatella</creatorcontrib><creatorcontrib>Turco, Laura</creatorcontrib><creatorcontrib>Minetti, Maurizio</creatorcontrib><title>Phenolic Antioxidants and the Protection of Low Density Lipoprotein from Peroxynitrite-Mediated Oxidations at Physiologic CO2</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>Dietary phenolic antioxidants have been shown to prevent LDL modifications mediated by several physiologic oxidants including peroxynitrite. However, more recent data demonstrated that CO2 affected the fate of peroxynitrite in biological fluids and significantly reduced peroxynitrite scavenging by polyphenols, raising doubts concerning their antioxidant activity. We found that the oxidation of LDL lipids mediated by peroxynitrite decreased in the presence of bicarbonate, while Trp oxidation and 3-nitroTyr formation increased, suggesting a redirection of peroxynitrite reactivity toward the protein moiety. We therefore evaluated the protective activity of some phenolic antioxidants (quercetin, oleuropein, resveratrol, (+)-catechin, (−)-epicatechin, tyrosol, α- and γ-tocopherol, ascorbate) on peroxynitrite-mediated oxidation of LDL aromatic residues. Some of these phenols protected LDL Trp from oxidation better than ascorbate or α-tocopherol, although protection at 100 μM did not exceed 30−40%. However, the same phenolic antioxidants were more active in inhibiting 3-nitroTyr formation and those with a catechin structure provided significant protection (IC50% 40−50 μM). Red wine, a polyphenol-rich beverage, showed a protective effect comparable to that of the most active phenolic antioxidants. Direct EPR studies showed that bicarbonate significantly increased the peroxynitrite-dependent formation of O-semiquinone radicals in red wine, supporting the hypothesis that polyphenols are efficient scavengers of radicals formed by peroxynitrite/CO2. Ascorbate was a poor inhibitor of peroxynitrite/CO2-induced LDL tyrosine nitration, but the simultaneous addition to the most active polyphenols halved their IC50%. In conclusion, although cooperation with other antioxidants can further decrease the IC50% of polyphenolics, as demonstrated for ascorbate, their antioxidant activity appears to occur at concentrations at least 1 order of magnitude higher than their bioavailability. Keywords: Lipoprotein; 3-nitrotyrosine; tryptophan oxidation; peroxynitrite; phenolic antioxidants; bicarbonate</description><subject>alpha-tocopherol</subject><subject>antioxidant activity</subject><subject>antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>ascorbic acid</subject><subject>bicarbonates</subject><subject>Bicarbonates - pharmacology</subject><subject>Biological and medical sciences</subject><subject>carbon dioxide</subject><subject>Carbon Dioxide - chemistry</subject><subject>Feeding. Feeding behavior</subject><subject>free radical scavengers</subject><subject>free radicals</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Lipoproteins, LDL - chemistry</subject><subject>low density lipoprotein</subject><subject>oxidants</subject><subject>oxidation</subject><subject>peroxynitrite</subject><subject>Peroxynitrous Acid - chemistry</subject><subject>phenolic compounds</subject><subject>Phenols - pharmacology</subject><subject>polyphenols</subject><subject>red wines</subject><subject>tryptophan</subject><subject>tyrosine</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Wine - analysis</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkk2P0zAQhi0EYsvCgT8AvsAt4LHjODmuyqfI0ki7KyQulteZbF1Su8SuaA_8d1y1LJxG8vvomfFoCHkO7A0wDm9XAxMlV8w_IDOQnBUSoH5IZiyHRS0rOCNPYlwxxmqp2GNyBhKEqrmakd_dEn0YnaUXPrmwc73xKVLje5qWSLspJLQ58DQMtA2_6Dv00aU9bd0mbA6p83SYwpp2OIXd3rs0uYTFJfbOJOzp4qA8CLI00W65jy6M4S43nC_4U_JoMGPEZ6d6Tm4-vL-efyraxcfP84u2MII3qUAEFFxAbZHDAKbuseYV4q3llenBNlUtEUpVNZWQ0A-yFJY3ElX-Lu_z4zl5ffTmiX9uMSa9dtHiOBqPYRu1ggYaDmUGX5zA7e0ae72Z3NpMe_13YRl4dQJMtGYcJuOti_9xStScicwVR87FhLv73Ew_dKWEkvq6u9LfL-dfvsqW6W-Zf3nkBxO0uZuy8-aKMxCMNSVrFPzrbGzUq7CdfN6YBqYPJ6DvT0D8AUm4npo</recordid><startdate>20040519</startdate><enddate>20040519</enddate><creator>Ferroni, Flavia</creator><creator>Maccaglia, Alessandro</creator><creator>Pietraforte, Donatella</creator><creator>Turco, Laura</creator><creator>Minetti, Maurizio</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>7X8</scope></search><sort><creationdate>20040519</creationdate><title>Phenolic Antioxidants and the Protection of Low Density Lipoprotein from Peroxynitrite-Mediated Oxidations at Physiologic CO2</title><author>Ferroni, Flavia ; Maccaglia, Alessandro ; Pietraforte, Donatella ; Turco, Laura ; Minetti, Maurizio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a329t-ee1e32318ce21f1a8de826eebc26ad1c9685e147696351df543c295e78572d963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>alpha-tocopherol</topic><topic>antioxidant activity</topic><topic>antioxidants</topic><topic>Antioxidants - pharmacology</topic><topic>ascorbic acid</topic><topic>bicarbonates</topic><topic>Bicarbonates - pharmacology</topic><topic>Biological and medical sciences</topic><topic>carbon dioxide</topic><topic>Carbon Dioxide - chemistry</topic><topic>Feeding. Feeding behavior</topic><topic>free radical scavengers</topic><topic>free radicals</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Lipoproteins, LDL - chemistry</topic><topic>low density lipoprotein</topic><topic>oxidants</topic><topic>oxidation</topic><topic>peroxynitrite</topic><topic>Peroxynitrous Acid - chemistry</topic><topic>phenolic compounds</topic><topic>Phenols - pharmacology</topic><topic>polyphenols</topic><topic>red wines</topic><topic>tryptophan</topic><topic>tyrosine</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Wine - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ferroni, Flavia</creatorcontrib><creatorcontrib>Maccaglia, Alessandro</creatorcontrib><creatorcontrib>Pietraforte, Donatella</creatorcontrib><creatorcontrib>Turco, Laura</creatorcontrib><creatorcontrib>Minetti, Maurizio</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>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ferroni, Flavia</au><au>Maccaglia, Alessandro</au><au>Pietraforte, Donatella</au><au>Turco, Laura</au><au>Minetti, Maurizio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phenolic Antioxidants and the Protection of Low Density Lipoprotein from Peroxynitrite-Mediated Oxidations at Physiologic CO2</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2004-05-19</date><risdate>2004</risdate><volume>52</volume><issue>10</issue><spage>2866</spage><epage>2874</epage><pages>2866-2874</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>Dietary phenolic antioxidants have been shown to prevent LDL modifications mediated by several physiologic oxidants including peroxynitrite. However, more recent data demonstrated that CO2 affected the fate of peroxynitrite in biological fluids and significantly reduced peroxynitrite scavenging by polyphenols, raising doubts concerning their antioxidant activity. We found that the oxidation of LDL lipids mediated by peroxynitrite decreased in the presence of bicarbonate, while Trp oxidation and 3-nitroTyr formation increased, suggesting a redirection of peroxynitrite reactivity toward the protein moiety. We therefore evaluated the protective activity of some phenolic antioxidants (quercetin, oleuropein, resveratrol, (+)-catechin, (−)-epicatechin, tyrosol, α- and γ-tocopherol, ascorbate) on peroxynitrite-mediated oxidation of LDL aromatic residues. Some of these phenols protected LDL Trp from oxidation better than ascorbate or α-tocopherol, although protection at 100 μM did not exceed 30−40%. However, the same phenolic antioxidants were more active in inhibiting 3-nitroTyr formation and those with a catechin structure provided significant protection (IC50% 40−50 μM). Red wine, a polyphenol-rich beverage, showed a protective effect comparable to that of the most active phenolic antioxidants. Direct EPR studies showed that bicarbonate significantly increased the peroxynitrite-dependent formation of O-semiquinone radicals in red wine, supporting the hypothesis that polyphenols are efficient scavengers of radicals formed by peroxynitrite/CO2. Ascorbate was a poor inhibitor of peroxynitrite/CO2-induced LDL tyrosine nitration, but the simultaneous addition to the most active polyphenols halved their IC50%. In conclusion, although cooperation with other antioxidants can further decrease the IC50% of polyphenolics, as demonstrated for ascorbate, their antioxidant activity appears to occur at concentrations at least 1 order of magnitude higher than their bioavailability. Keywords: Lipoprotein; 3-nitrotyrosine; tryptophan oxidation; peroxynitrite; phenolic antioxidants; bicarbonate</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>15137827</pmid><doi>10.1021/jf034270n</doi><tpages>9</tpages></addata></record> |
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subjects | alpha-tocopherol antioxidant activity antioxidants Antioxidants - pharmacology ascorbic acid bicarbonates Bicarbonates - pharmacology Biological and medical sciences carbon dioxide Carbon Dioxide - chemistry Feeding. Feeding behavior free radical scavengers free radicals Fundamental and applied biological sciences. Psychology Lipid Peroxidation - drug effects Lipoproteins, LDL - chemistry low density lipoprotein oxidants oxidation peroxynitrite Peroxynitrous Acid - chemistry phenolic compounds Phenols - pharmacology polyphenols red wines tryptophan tyrosine Vertebrates: anatomy and physiology, studies on body, several organs or systems Wine - analysis |
title | Phenolic Antioxidants and the Protection of Low Density Lipoprotein from Peroxynitrite-Mediated Oxidations at Physiologic CO2 |
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