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
Hauptverfasser: Ferroni, Flavia, Maccaglia, Alessandro, Pietraforte, Donatella, Turco, Laura, Minetti, Maurizio
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container_end_page 2874
container_issue 10
container_start_page 2866
container_title Journal of agricultural and food chemistry
container_volume 52
creator Ferroni, Flavia
Maccaglia, Alessandro
Pietraforte, Donatella
Turco, Laura
Minetti, Maurizio
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
doi_str_mv 10.1021/jf034270n
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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. 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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&amp;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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ispartof Journal of agricultural and food chemistry, 2004-05, Vol.52 (10), p.2866-2874
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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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