Influence of the antioxidant quercetin in vivo on the level of nitric oxide determined by electron paramagnetic resonance in rat brain during global ischemia and reperfusion
We characterized the changes in nitric oxide (NO) levels in the brain during global forebrain ischemia and reperfusion and tested the ability of the natural flavonoid, quercetin, and a synthetic flavonoid, FB277, to increase the amount of available NO by elimination of the superoxide radicals produc...
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description | We characterized the changes in nitric oxide (NO) levels in the brain during global forebrain ischemia and reperfusion and tested the ability of the natural flavonoid, quercetin, and a synthetic flavonoid, FB277, to increase the amount of available NO by elimination of the superoxide radicals produced during reperfusion. In Sprague–Dawley rats, we used a four-vessel occlusion model of forebrain ischemia (15 min) and reperfusion (30 min). Brain NO was measured on samples of cerebral cortex and cerebellum
ex vivo by electron paramagnetic resonance (EPR) spectroscopy. The spin trap used was diethyldithiocarbamate sodium salt (DETC) associated with ferrous citrate. The complex Fe(DETC)
2NO was detected at 77 K as a triplet signal at
g = 2.035. Groups of animals were treated with quercetin or FB277 (3-morpholinomethyl-3′,4′,5,7-tetramethoxyflavone) or polyethylene glycol-conjugated superoxide dismutase (PEG-SOD). In control (intact anesthetized animals), the signal was about 3 times greater in the cortex than in the cerebellum. During ischemia, the signal rose to 110% in cortex (NS) and 283% in cerebellum (
P < 0.05). In reperfusion, it fell again to 91% of control in cerebellum (NS) and 35% in cortex (
P < 0.05). Treatment by quercetin (5 mg/kg i.v.) of intact and ischemia-reperfusion groups did not significantly change the signal amplitude in the cerebellum, but did double it in the cortex (to 76% of control) for the ischemia-reperfusion group (
P < 0.05). In contrast, FB277 (3.75 mg/kg i.v.) did not increase the signal in the cortex during ischemia-reperfusion, but did do so in the cerebellum (to 152% of control,
P < 0.05). The results obtained for PEG-SOD (10,000 U/kg i.v.) were similar to those for FB277. In separate
in vitro measurements, we found that quercetin but not FB277 efficiently scavenged superoxide. We hypothesize that quercetin but not FB277 scavenged superoxide anions released in the cortex during reperfusion, thus diminishing the amount of NO removed by the formation of peroxynitrite. The lack of effect of PEG-SOD may be related to the need for chronic treatment to obtain protection. |
doi_str_mv | 10.1016/S0006-2952(98)00296-2 |
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ex vivo by electron paramagnetic resonance (EPR) spectroscopy. The spin trap used was diethyldithiocarbamate sodium salt (DETC) associated with ferrous citrate. The complex Fe(DETC)
2NO was detected at 77 K as a triplet signal at
g = 2.035. Groups of animals were treated with quercetin or FB277 (3-morpholinomethyl-3′,4′,5,7-tetramethoxyflavone) or polyethylene glycol-conjugated superoxide dismutase (PEG-SOD). In control (intact anesthetized animals), the signal was about 3 times greater in the cortex than in the cerebellum. During ischemia, the signal rose to 110% in cortex (NS) and 283% in cerebellum (
P < 0.05). In reperfusion, it fell again to 91% of control in cerebellum (NS) and 35% in cortex (
P < 0.05). Treatment by quercetin (5 mg/kg i.v.) of intact and ischemia-reperfusion groups did not significantly change the signal amplitude in the cerebellum, but did double it in the cortex (to 76% of control) for the ischemia-reperfusion group (
P < 0.05). In contrast, FB277 (3.75 mg/kg i.v.) did not increase the signal in the cortex during ischemia-reperfusion, but did do so in the cerebellum (to 152% of control,
P < 0.05). The results obtained for PEG-SOD (10,000 U/kg i.v.) were similar to those for FB277. In separate
in vitro measurements, we found that quercetin but not FB277 efficiently scavenged superoxide. We hypothesize that quercetin but not FB277 scavenged superoxide anions released in the cortex during reperfusion, thus diminishing the amount of NO removed by the formation of peroxynitrite. The lack of effect of PEG-SOD may be related to the need for chronic treatment to obtain protection.</description><identifier>ISSN: 0006-2952</identifier><identifier>EISSN: 1873-2968</identifier><identifier>DOI: 10.1016/S0006-2952(98)00296-2</identifier><identifier>PMID: 9890569</identifier><identifier>CODEN: BCPCA6</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; antioxidants ; Antioxidants - pharmacology ; Biological and medical sciences ; Brain - drug effects ; Brain - metabolism ; Brain Ischemia - drug therapy ; Brain Ischemia - metabolism ; electron paramagnetic resonance ; Electron Spin Resonance Spectroscopy ; flavonoids ; Flavonoids - pharmacology ; Free Radical Scavengers - pharmacology ; General and cellular metabolism. Vitamins ; global brain ischemia and reperfusion ; Male ; Medical sciences ; Molecular Structure ; Morpholines - pharmacology ; Nitric Oxide - metabolism ; nitric oxide measurement ; Pharmacology. Drug treatments ; Polyethylene Glycols - pharmacology ; Prosencephalon - blood supply ; Quercetin - pharmacology ; Rats ; Rats, Sprague-Dawley ; Reperfusion Injury - drug therapy ; Reperfusion Injury - metabolism ; Superoxide Dismutase - pharmacology ; superoxide scavenging ; Superoxides - metabolism</subject><ispartof>Biochemical pharmacology, 1999-01, Vol.57 (2), p.199-208</ispartof><rights>1999 Elsevier Science Inc.</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-5ca475c2ac1c13500eec7173902418b8692ff27b6c81b152b3a405cda0e8214d3</citedby><cites>FETCH-LOGICAL-c507t-5ca475c2ac1c13500eec7173902418b8692ff27b6c81b152b3a405cda0e8214d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0006-2952(98)00296-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3552,27931,27932,46002</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1670020$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9890569$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shutenko, Zhanna</creatorcontrib><creatorcontrib>Henry, Yann</creatorcontrib><creatorcontrib>Pinard, Elisabeth</creatorcontrib><creatorcontrib>Seylaz, Jacques</creatorcontrib><creatorcontrib>Potier, Pierre</creatorcontrib><creatorcontrib>Berthet, Fabienne</creatorcontrib><creatorcontrib>Girard, Pierre</creatorcontrib><creatorcontrib>Sercombe, Richard</creatorcontrib><title>Influence of the antioxidant quercetin in vivo on the level of nitric oxide determined by electron paramagnetic resonance in rat brain during global ischemia and reperfusion</title><title>Biochemical pharmacology</title><addtitle>Biochem Pharmacol</addtitle><description>We characterized the changes in nitric oxide (NO) levels in the brain during global forebrain ischemia and reperfusion and tested the ability of the natural flavonoid, quercetin, and a synthetic flavonoid, FB277, to increase the amount of available NO by elimination of the superoxide radicals produced during reperfusion. In Sprague–Dawley rats, we used a four-vessel occlusion model of forebrain ischemia (15 min) and reperfusion (30 min). Brain NO was measured on samples of cerebral cortex and cerebellum
ex vivo by electron paramagnetic resonance (EPR) spectroscopy. The spin trap used was diethyldithiocarbamate sodium salt (DETC) associated with ferrous citrate. The complex Fe(DETC)
2NO was detected at 77 K as a triplet signal at
g = 2.035. Groups of animals were treated with quercetin or FB277 (3-morpholinomethyl-3′,4′,5,7-tetramethoxyflavone) or polyethylene glycol-conjugated superoxide dismutase (PEG-SOD). In control (intact anesthetized animals), the signal was about 3 times greater in the cortex than in the cerebellum. During ischemia, the signal rose to 110% in cortex (NS) and 283% in cerebellum (
P < 0.05). In reperfusion, it fell again to 91% of control in cerebellum (NS) and 35% in cortex (
P < 0.05). Treatment by quercetin (5 mg/kg i.v.) of intact and ischemia-reperfusion groups did not significantly change the signal amplitude in the cerebellum, but did double it in the cortex (to 76% of control) for the ischemia-reperfusion group (
P < 0.05). In contrast, FB277 (3.75 mg/kg i.v.) did not increase the signal in the cortex during ischemia-reperfusion, but did do so in the cerebellum (to 152% of control,
P < 0.05). The results obtained for PEG-SOD (10,000 U/kg i.v.) were similar to those for FB277. In separate
in vitro measurements, we found that quercetin but not FB277 efficiently scavenged superoxide. We hypothesize that quercetin but not FB277 scavenged superoxide anions released in the cortex during reperfusion, thus diminishing the amount of NO removed by the formation of peroxynitrite. The lack of effect of PEG-SOD may be related to the need for chronic treatment to obtain protection.</description><subject>Animals</subject><subject>antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Brain - drug effects</subject><subject>Brain - metabolism</subject><subject>Brain Ischemia - drug therapy</subject><subject>Brain Ischemia - metabolism</subject><subject>electron paramagnetic resonance</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>flavonoids</subject><subject>Flavonoids - pharmacology</subject><subject>Free Radical Scavengers - pharmacology</subject><subject>General and cellular metabolism. Vitamins</subject><subject>global brain ischemia and reperfusion</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Molecular Structure</subject><subject>Morpholines - pharmacology</subject><subject>Nitric Oxide - metabolism</subject><subject>nitric oxide measurement</subject><subject>Pharmacology. Drug treatments</subject><subject>Polyethylene Glycols - pharmacology</subject><subject>Prosencephalon - blood supply</subject><subject>Quercetin - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Reperfusion Injury - drug therapy</subject><subject>Reperfusion Injury - metabolism</subject><subject>Superoxide Dismutase - pharmacology</subject><subject>superoxide scavenging</subject><subject>Superoxides - metabolism</subject><issn>0006-2952</issn><issn>1873-2968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU2LFDEQbURZx9WfsJCDiB5Gk3QnnZxEFj8WFjyo55BOqmcj6WRMugf3R_kfrZ4Z1qMQqFTy3qvivaa5YvQto0y--0YplVuuBX-t1RtKucbuUbNhqm_xWarHzeYB8rR5VuvPtVWSXTQXWmkqpN40f27SGBdIDkgeyXwHxKY55N_BYyW_FigO5pAInkM4ZJLTERThAHFlpDCX4MhKAOJhhjKFBJ4M9wQiuLkgYW-LnewuoZAjBWpOdp2HksXOZCgWb34pIe3ILubBRhKqu4MpWFzGI2MPZVxqyOl582S0scKLc71sfnz6-P36y_b26-eb6w-3WydoP2-Fs10vHLeOOdYKSgFcz_pWU94xNSip-TjyfpBOsYEJPrS2o8J5S0Fx1vn2snl10t2XjB7U2Uy4EsRoE-SlGqmF6CXtEChOQFdyrQVGsy9hsuXeMGrWmMwxJrNmYLQyx5gMR97VecAyTOAfWOdc8P_l-d9WZ-NY0LFQ_4nLHpUowt6fYIBmHAIUU11Yw_ShoPnG5_CfRf4CofCyWQ</recordid><startdate>19990115</startdate><enddate>19990115</enddate><creator>Shutenko, Zhanna</creator><creator>Henry, Yann</creator><creator>Pinard, Elisabeth</creator><creator>Seylaz, Jacques</creator><creator>Potier, Pierre</creator><creator>Berthet, Fabienne</creator><creator>Girard, Pierre</creator><creator>Sercombe, Richard</creator><general>Elsevier Inc</general><general>Elsevier Science</general><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>19990115</creationdate><title>Influence of the antioxidant quercetin in vivo on the level of nitric oxide determined by electron paramagnetic resonance in rat brain during global ischemia and reperfusion</title><author>Shutenko, Zhanna ; Henry, Yann ; Pinard, Elisabeth ; Seylaz, Jacques ; Potier, Pierre ; Berthet, Fabienne ; Girard, Pierre ; Sercombe, Richard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-5ca475c2ac1c13500eec7173902418b8692ff27b6c81b152b3a405cda0e8214d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>antioxidants</topic><topic>Antioxidants - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Brain - drug effects</topic><topic>Brain - metabolism</topic><topic>Brain Ischemia - drug therapy</topic><topic>Brain Ischemia - metabolism</topic><topic>electron paramagnetic resonance</topic><topic>Electron Spin Resonance Spectroscopy</topic><topic>flavonoids</topic><topic>Flavonoids - pharmacology</topic><topic>Free Radical Scavengers - pharmacology</topic><topic>General and cellular metabolism. Vitamins</topic><topic>global brain ischemia and reperfusion</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Molecular Structure</topic><topic>Morpholines - pharmacology</topic><topic>Nitric Oxide - metabolism</topic><topic>nitric oxide measurement</topic><topic>Pharmacology. Drug treatments</topic><topic>Polyethylene Glycols - pharmacology</topic><topic>Prosencephalon - blood supply</topic><topic>Quercetin - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Reperfusion Injury - drug therapy</topic><topic>Reperfusion Injury - metabolism</topic><topic>Superoxide Dismutase - pharmacology</topic><topic>superoxide scavenging</topic><topic>Superoxides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shutenko, Zhanna</creatorcontrib><creatorcontrib>Henry, Yann</creatorcontrib><creatorcontrib>Pinard, Elisabeth</creatorcontrib><creatorcontrib>Seylaz, Jacques</creatorcontrib><creatorcontrib>Potier, Pierre</creatorcontrib><creatorcontrib>Berthet, Fabienne</creatorcontrib><creatorcontrib>Girard, Pierre</creatorcontrib><creatorcontrib>Sercombe, Richard</creatorcontrib><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>Biochemical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shutenko, Zhanna</au><au>Henry, Yann</au><au>Pinard, Elisabeth</au><au>Seylaz, Jacques</au><au>Potier, Pierre</au><au>Berthet, Fabienne</au><au>Girard, Pierre</au><au>Sercombe, Richard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of the antioxidant quercetin in vivo on the level of nitric oxide determined by electron paramagnetic resonance in rat brain during global ischemia and reperfusion</atitle><jtitle>Biochemical pharmacology</jtitle><addtitle>Biochem Pharmacol</addtitle><date>1999-01-15</date><risdate>1999</risdate><volume>57</volume><issue>2</issue><spage>199</spage><epage>208</epage><pages>199-208</pages><issn>0006-2952</issn><eissn>1873-2968</eissn><coden>BCPCA6</coden><abstract>We characterized the changes in nitric oxide (NO) levels in the brain during global forebrain ischemia and reperfusion and tested the ability of the natural flavonoid, quercetin, and a synthetic flavonoid, FB277, to increase the amount of available NO by elimination of the superoxide radicals produced during reperfusion. In Sprague–Dawley rats, we used a four-vessel occlusion model of forebrain ischemia (15 min) and reperfusion (30 min). Brain NO was measured on samples of cerebral cortex and cerebellum
ex vivo by electron paramagnetic resonance (EPR) spectroscopy. The spin trap used was diethyldithiocarbamate sodium salt (DETC) associated with ferrous citrate. The complex Fe(DETC)
2NO was detected at 77 K as a triplet signal at
g = 2.035. Groups of animals were treated with quercetin or FB277 (3-morpholinomethyl-3′,4′,5,7-tetramethoxyflavone) or polyethylene glycol-conjugated superoxide dismutase (PEG-SOD). In control (intact anesthetized animals), the signal was about 3 times greater in the cortex than in the cerebellum. During ischemia, the signal rose to 110% in cortex (NS) and 283% in cerebellum (
P < 0.05). In reperfusion, it fell again to 91% of control in cerebellum (NS) and 35% in cortex (
P < 0.05). Treatment by quercetin (5 mg/kg i.v.) of intact and ischemia-reperfusion groups did not significantly change the signal amplitude in the cerebellum, but did double it in the cortex (to 76% of control) for the ischemia-reperfusion group (
P < 0.05). In contrast, FB277 (3.75 mg/kg i.v.) did not increase the signal in the cortex during ischemia-reperfusion, but did do so in the cerebellum (to 152% of control,
P < 0.05). The results obtained for PEG-SOD (10,000 U/kg i.v.) were similar to those for FB277. In separate
in vitro measurements, we found that quercetin but not FB277 efficiently scavenged superoxide. We hypothesize that quercetin but not FB277 scavenged superoxide anions released in the cortex during reperfusion, thus diminishing the amount of NO removed by the formation of peroxynitrite. The lack of effect of PEG-SOD may be related to the need for chronic treatment to obtain protection.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>9890569</pmid><doi>10.1016/S0006-2952(98)00296-2</doi><tpages>10</tpages></addata></record> |
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subjects | Animals antioxidants Antioxidants - pharmacology Biological and medical sciences Brain - drug effects Brain - metabolism Brain Ischemia - drug therapy Brain Ischemia - metabolism electron paramagnetic resonance Electron Spin Resonance Spectroscopy flavonoids Flavonoids - pharmacology Free Radical Scavengers - pharmacology General and cellular metabolism. Vitamins global brain ischemia and reperfusion Male Medical sciences Molecular Structure Morpholines - pharmacology Nitric Oxide - metabolism nitric oxide measurement Pharmacology. Drug treatments Polyethylene Glycols - pharmacology Prosencephalon - blood supply Quercetin - pharmacology Rats Rats, Sprague-Dawley Reperfusion Injury - drug therapy Reperfusion Injury - metabolism Superoxide Dismutase - pharmacology superoxide scavenging Superoxides - metabolism |
title | Influence of the antioxidant quercetin in vivo on the level of nitric oxide determined by electron paramagnetic resonance in rat brain during global ischemia and reperfusion |
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