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Relative antioxidant activities of quercetin and its structurally related substances and their effects on NF-κB/CRE/AP-1 signaling in murine macrophages
Reactive oxygen species (ROS) and reactive nitrogen species (RNS) produced by the oxidative burst in activated macrophages and neutrophils cause oxidative stressimplicated diseases. Quercetin is flavonoid that occurs naturally in plants and is widely used as a nutritional supplement due to its antio...
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Published in: | Molecules and cells 2013-05, Vol.35 (5), p.410-420 |
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creator | Kim, B.H., Seoul National University College of Medicine, Seoul, Republic of Korea Choi, J.S., Gyeongdo Provincial College, Yecheon, Republic of Korea Yi, E.H., Seoul National University College of Medicine, Seoul, Republic of Korea Lee, J.K., Seoul National University College of Medicine, Seoul, Republic of Korea Won, C.H., Seoul National University College of Medicine, Seoul, Republic of Korea Ye, S.K., Seoul National University College of Medicine, Seoul, Republic of Korea Kim, M.H., Seoul National University College of Medicine, Seoul, Republic of Korea |
description | Reactive oxygen species (ROS) and reactive nitrogen species (RNS) produced by the oxidative burst in activated macrophages and neutrophils cause oxidative stressimplicated diseases. Quercetin is flavonoid that occurs naturally in plants and is widely used as a nutritional supplement due to its antioxidant and anti-inflammatory properties. In this study, we investigated antioxidant activities and mechanisms of action in zymosan-induced macrophages of quercetin and quercetin-related flavonoids such as quercitrin, isoquercitrin, quercetin 3-O-β-(2″-galloyl)-rhamnopyranoside (QGR) and quercetin 3-O-β-(2″-galloyl)-glucopyranoside (QGG) as well as gallic acid, a building moiety of QGR and QGG. QGR and QGG exhibited stronger antioxidant activities compared with quercetin, whereas quercitrin, isoquercitrin and gallic acid exhibited weak-tono antioxidant activities, assessed by 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging, superoxide production, superoxide scavenging, nitric oxide (NO) production, peroxynitrite (ONOO−) scavenging and myeloperoxidase (MPO) activity. Regarding mechanisms, the quercetincontaining flavonoids QGR and QGG differentially targeted compared with quercetin in the NF-κB signaling pathway that inhibited the DNA binding activity of the NF-κB complex without affecting the degradation and phosphorylation of IκBα and NF-κB phosphorylation. In addition, QGR and QGG inhibited CRE and activator protein (AP-1) transcriptional activity and JNK phosphorylation by inhibiting the cAMP/protein kinase A (PKA) and protein kinase C (PKC) signaling in a different manner than quercetin. Our results showed that although QGR and QGG exhibited stronger antioxidant activities than querce-tin in macrophages, their mechanisms of action in terms of the NF-κB, PKA and PKC signaling pathways were different. |
doi_str_mv | 10.1007/s10059-013-0031-z |
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Quercetin is flavonoid that occurs naturally in plants and is widely used as a nutritional supplement due to its antioxidant and anti-inflammatory properties. In this study, we investigated antioxidant activities and mechanisms of action in zymosan-induced macrophages of quercetin and quercetin-related flavonoids such as quercitrin, isoquercitrin, quercetin 3-O-β-(2″-galloyl)-rhamnopyranoside (QGR) and quercetin 3-O-β-(2″-galloyl)-glucopyranoside (QGG) as well as gallic acid, a building moiety of QGR and QGG. QGR and QGG exhibited stronger antioxidant activities compared with quercetin, whereas quercitrin, isoquercitrin and gallic acid exhibited weak-tono antioxidant activities, assessed by 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging, superoxide production, superoxide scavenging, nitric oxide (NO) production, peroxynitrite (ONOO−) scavenging and myeloperoxidase (MPO) activity. Regarding mechanisms, the quercetincontaining flavonoids QGR and QGG differentially targeted compared with quercetin in the NF-κB signaling pathway that inhibited the DNA binding activity of the NF-κB complex without affecting the degradation and phosphorylation of IκBα and NF-κB phosphorylation. In addition, QGR and QGG inhibited CRE and activator protein (AP-1) transcriptional activity and JNK phosphorylation by inhibiting the cAMP/protein kinase A (PKA) and protein kinase C (PKC) signaling in a different manner than quercetin. Our results showed that although QGR and QGG exhibited stronger antioxidant activities than querce-tin in macrophages, their mechanisms of action in terms of the NF-κB, PKA and PKC signaling pathways were different.</description><identifier>ISSN: 1016-8478</identifier><identifier>EISSN: 0219-1032</identifier><identifier>DOI: 10.1007/s10059-013-0031-z</identifier><identifier>PMID: 23649461</identifier><language>eng</language><publisher>Springer: Korean Society for Molecular and Cellular Biology</publisher><subject>ANTIOXIDANTES ; ANTIOXIDANTS ; ANTIOXYDANT ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Biotechnology ; Cell Biology ; Life Sciences ; QUERCETIN ; QUERCETINA ; QUERCETINE ; Research Article ; structurally related compounds,ROS/RNS</subject><ispartof>Molecules and cells, 2013-05, Vol.35 (5), p.410-420</ispartof><rights>The Korean Society for Molecular and Cellular Biology and Springer Netherlands 2013</rights><rights>The Korean Society for Molecular and Cellular Biology. All rights reserved. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-b154bbb0c1c63e7e5b1127e014e1f4871f31d8dacca8f8154ec826a068ebe7743</citedby><cites>FETCH-LOGICAL-c464t-b154bbb0c1c63e7e5b1127e014e1f4871f31d8dacca8f8154ec826a068ebe7743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887868/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3887868/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids></links><search><creatorcontrib>Kim, B.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><creatorcontrib>Choi, J.S., Gyeongdo Provincial College, Yecheon, Republic of Korea</creatorcontrib><creatorcontrib>Yi, E.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><creatorcontrib>Lee, J.K., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><creatorcontrib>Won, C.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><creatorcontrib>Ye, S.K., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><creatorcontrib>Kim, M.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><title>Relative antioxidant activities of quercetin and its structurally related substances and their effects on NF-κB/CRE/AP-1 signaling in murine macrophages</title><title>Molecules and cells</title><addtitle>Mol Cells</addtitle><description>Reactive oxygen species (ROS) and reactive nitrogen species (RNS) produced by the oxidative burst in activated macrophages and neutrophils cause oxidative stressimplicated diseases. Quercetin is flavonoid that occurs naturally in plants and is widely used as a nutritional supplement due to its antioxidant and anti-inflammatory properties. In this study, we investigated antioxidant activities and mechanisms of action in zymosan-induced macrophages of quercetin and quercetin-related flavonoids such as quercitrin, isoquercitrin, quercetin 3-O-β-(2″-galloyl)-rhamnopyranoside (QGR) and quercetin 3-O-β-(2″-galloyl)-glucopyranoside (QGG) as well as gallic acid, a building moiety of QGR and QGG. QGR and QGG exhibited stronger antioxidant activities compared with quercetin, whereas quercitrin, isoquercitrin and gallic acid exhibited weak-tono antioxidant activities, assessed by 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging, superoxide production, superoxide scavenging, nitric oxide (NO) production, peroxynitrite (ONOO−) scavenging and myeloperoxidase (MPO) activity. Regarding mechanisms, the quercetincontaining flavonoids QGR and QGG differentially targeted compared with quercetin in the NF-κB signaling pathway that inhibited the DNA binding activity of the NF-κB complex without affecting the degradation and phosphorylation of IκBα and NF-κB phosphorylation. In addition, QGR and QGG inhibited CRE and activator protein (AP-1) transcriptional activity and JNK phosphorylation by inhibiting the cAMP/protein kinase A (PKA) and protein kinase C (PKC) signaling in a different manner than quercetin. Our results showed that although QGR and QGG exhibited stronger antioxidant activities than querce-tin in macrophages, their mechanisms of action in terms of the NF-κB, PKA and PKC signaling pathways were different.</description><subject>ANTIOXIDANTES</subject><subject>ANTIOXIDANTS</subject><subject>ANTIOXYDANT</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Cell Biology</subject><subject>Life Sciences</subject><subject>QUERCETIN</subject><subject>QUERCETINA</subject><subject>QUERCETINE</subject><subject>Research Article</subject><subject>structurally related compounds,ROS/RNS</subject><issn>1016-8478</issn><issn>0219-1032</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kUGOFCEUhonROO3oAVyYcAFsXlFV0BuTsTOjxomajq4JRT2qmVRTLVCTmbmJV_EQnkk6ZUzcuOEl8H9fgJ-Ql8BfA-dyncrabBgHwTgXwB4ekRWvYMOAi-oxWQGHlqlaqjPyLKUbzkG2lXpKzirR1pu6hRX5scPRZH-L1ITspzvfl0mNLVs-e0x0cvT7jNFi9qFkeupzoinH2eY5mnG8p_FkwJ6muUvZBFugUy7v0UeKzqEtxBTopyv26-fb9XZ3ub74woAmPwQz-jDQYj7M0QekB2PjdNybAdNz8sSZMeGLP_OcfLu6_Lp9z64_v_uwvbhmtm7rzDpo6q7ruAXbCpTYdACVRA41gquVBCegV72x1iinShitqlrDW4UdSlmLc_Jm8R7n7oC9xZDLu_Qx-oOJ93oyXv97EvxeD9OtFkpJ1aoigEVQrp5SRPeXBa5PPemlJ1160qee9ENhqoVJJRsGjPpmmmP5jvRf6NUCOTNpM0Sf9MddxaHhpVneiN_aEKK4</recordid><startdate>20130501</startdate><enddate>20130501</enddate><creator>Kim, B.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creator><creator>Choi, J.S., Gyeongdo Provincial College, Yecheon, Republic of Korea</creator><creator>Yi, E.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creator><creator>Lee, J.K., Seoul National University College of Medicine, Seoul, Republic of Korea</creator><creator>Won, C.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creator><creator>Ye, S.K., Seoul National University College of Medicine, Seoul, Republic of Korea</creator><creator>Kim, M.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creator><general>Korean Society for Molecular and Cellular Biology</general><general>Korea Society for Molecular and Cellular Biology</general><scope>FBQ</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20130501</creationdate><title>Relative antioxidant activities of quercetin and its structurally related substances and their effects on NF-κB/CRE/AP-1 signaling in murine macrophages</title><author>Kim, B.H., Seoul National University College of Medicine, Seoul, Republic of Korea ; Choi, J.S., Gyeongdo Provincial College, Yecheon, Republic of Korea ; Yi, E.H., Seoul National University College of Medicine, Seoul, Republic of Korea ; Lee, J.K., Seoul National University College of Medicine, Seoul, Republic of Korea ; Won, C.H., Seoul National University College of Medicine, Seoul, Republic of Korea ; Ye, S.K., Seoul National University College of Medicine, Seoul, Republic of Korea ; Kim, M.H., Seoul National University College of Medicine, Seoul, Republic of Korea</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-b154bbb0c1c63e7e5b1127e014e1f4871f31d8dacca8f8154ec826a068ebe7743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>ANTIOXIDANTES</topic><topic>ANTIOXIDANTS</topic><topic>ANTIOXYDANT</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Biotechnology</topic><topic>Cell Biology</topic><topic>Life Sciences</topic><topic>QUERCETIN</topic><topic>QUERCETINA</topic><topic>QUERCETINE</topic><topic>Research Article</topic><topic>structurally related compounds,ROS/RNS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, B.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><creatorcontrib>Choi, J.S., Gyeongdo Provincial College, Yecheon, Republic of Korea</creatorcontrib><creatorcontrib>Yi, E.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><creatorcontrib>Lee, J.K., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><creatorcontrib>Won, C.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><creatorcontrib>Ye, S.K., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><creatorcontrib>Kim, M.H., Seoul National University College of Medicine, Seoul, Republic of Korea</creatorcontrib><collection>AGRIS</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecules and cells</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, B.H., Seoul National University College of Medicine, Seoul, Republic of Korea</au><au>Choi, J.S., Gyeongdo Provincial College, Yecheon, Republic of Korea</au><au>Yi, E.H., Seoul National University College of Medicine, Seoul, Republic of Korea</au><au>Lee, J.K., Seoul National University College of Medicine, Seoul, Republic of Korea</au><au>Won, C.H., Seoul National University College of Medicine, Seoul, Republic of Korea</au><au>Ye, S.K., Seoul National University College of Medicine, Seoul, Republic of Korea</au><au>Kim, M.H., Seoul National University College of Medicine, Seoul, Republic of Korea</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relative antioxidant activities of quercetin and its structurally related substances and their effects on NF-κB/CRE/AP-1 signaling in murine macrophages</atitle><jtitle>Molecules and cells</jtitle><stitle>Mol Cells</stitle><date>2013-05-01</date><risdate>2013</risdate><volume>35</volume><issue>5</issue><spage>410</spage><epage>420</epage><pages>410-420</pages><issn>1016-8478</issn><eissn>0219-1032</eissn><abstract>Reactive oxygen species (ROS) and reactive nitrogen species (RNS) produced by the oxidative burst in activated macrophages and neutrophils cause oxidative stressimplicated diseases. Quercetin is flavonoid that occurs naturally in plants and is widely used as a nutritional supplement due to its antioxidant and anti-inflammatory properties. In this study, we investigated antioxidant activities and mechanisms of action in zymosan-induced macrophages of quercetin and quercetin-related flavonoids such as quercitrin, isoquercitrin, quercetin 3-O-β-(2″-galloyl)-rhamnopyranoside (QGR) and quercetin 3-O-β-(2″-galloyl)-glucopyranoside (QGG) as well as gallic acid, a building moiety of QGR and QGG. QGR and QGG exhibited stronger antioxidant activities compared with quercetin, whereas quercitrin, isoquercitrin and gallic acid exhibited weak-tono antioxidant activities, assessed by 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging, superoxide production, superoxide scavenging, nitric oxide (NO) production, peroxynitrite (ONOO−) scavenging and myeloperoxidase (MPO) activity. Regarding mechanisms, the quercetincontaining flavonoids QGR and QGG differentially targeted compared with quercetin in the NF-κB signaling pathway that inhibited the DNA binding activity of the NF-κB complex without affecting the degradation and phosphorylation of IκBα and NF-κB phosphorylation. In addition, QGR and QGG inhibited CRE and activator protein (AP-1) transcriptional activity and JNK phosphorylation by inhibiting the cAMP/protein kinase A (PKA) and protein kinase C (PKC) signaling in a different manner than quercetin. Our results showed that although QGR and QGG exhibited stronger antioxidant activities than querce-tin in macrophages, their mechanisms of action in terms of the NF-κB, PKA and PKC signaling pathways were different.</abstract><cop>Springer</cop><pub>Korean Society for Molecular and Cellular Biology</pub><pmid>23649461</pmid><doi>10.1007/s10059-013-0031-z</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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title | Relative antioxidant activities of quercetin and its structurally related substances and their effects on NF-κB/CRE/AP-1 signaling in murine macrophages |
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