Red Wine Polyphenolic Compounds Inhibit Vascular Endothelial Growth Factor Expression in Vascular Smooth Muscle Cells by Preventing the Activation of the p38 Mitogen-Activated Protein Kinase Pathway
OBJECTIVE—Moderate consumption of red wine has a beneficial effect on the cardiovascular system. This study examines whether red wine polyphenolic compounds (RWPCs) affect vascular endothelial growth factor (VEGF) expression, a major angiogenic and proatherosclerotic factor in vascular smooth muscle...
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Veröffentlicht in: | Arteriosclerosis, thrombosis, and vascular biology thrombosis, and vascular biology, 2003-06, Vol.23 (6), p.1001-1007 |
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creator | Oak, Min-Ho Chataigneau, Marta Keravis, Thérèse Chataigneau, Thierry Beretz, Alain Andriantsitohaina, Ramaroson Stoclet, Jean-Claude Chang, Soon-Jae Schini-Kerth, Valérie B |
description | OBJECTIVE—Moderate consumption of red wine has a beneficial effect on the cardiovascular system. This study examines whether red wine polyphenolic compounds (RWPCs) affect vascular endothelial growth factor (VEGF) expression, a major angiogenic and proatherosclerotic factor in vascular smooth muscle cells (VSMCs).
METHODS AND RESULTS—VEGF mRNA expression was assessed by Northern blot analysis and the release of VEGF by immunoassay in cultured VSMCs. Short-term and long-term exposure of VSMCs to RWPCs inhibited VEGF mRNA expression and release of VEGF in response to platelet-derived growth factor AB (PDGFAB), transforming growth factor-β1, or thrombin. The PDGFAB-induced expression of VEGF was markedly reduced by SB203580 (inhibitor of p38 mitogen-activated protein kinase [MAPK]), antioxidants, and diphenylene iodonium (inhibitor of flavin-dependent enzymes), slightly reduced by PD98059 (inhibitor of MEK), and not significantly affected by wortmannin (inhibitor of PI-3-kinase) and L-JNKI (inhibitor of JNK). Short-term and long-term treatment of VSMCs with RWPCs markedly reduced PDGFAB-induced production of reactive oxygen species and phosphorylation of p38 MAPK.
CONCLUSIONS—These data indicate that RWPCs strongly inhibit growth factor–induced VEGF expression in VSMCs by preventing the redox-sensitive activation of the p38 MAPK pathway. The potential antiangiogenic and antiatherosclerotic properties of RWPCs are likely to contribute to cardiovascular protection by preventing the development of atherosclerotic lesions. |
doi_str_mv | 10.1161/01.ATV.0000070101.70534.38 |
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METHODS AND RESULTS—VEGF mRNA expression was assessed by Northern blot analysis and the release of VEGF by immunoassay in cultured VSMCs. Short-term and long-term exposure of VSMCs to RWPCs inhibited VEGF mRNA expression and release of VEGF in response to platelet-derived growth factor AB (PDGFAB), transforming growth factor-β1, or thrombin. The PDGFAB-induced expression of VEGF was markedly reduced by SB203580 (inhibitor of p38 mitogen-activated protein kinase [MAPK]), antioxidants, and diphenylene iodonium (inhibitor of flavin-dependent enzymes), slightly reduced by PD98059 (inhibitor of MEK), and not significantly affected by wortmannin (inhibitor of PI-3-kinase) and L-JNKI (inhibitor of JNK). Short-term and long-term treatment of VSMCs with RWPCs markedly reduced PDGFAB-induced production of reactive oxygen species and phosphorylation of p38 MAPK.
CONCLUSIONS—These data indicate that RWPCs strongly inhibit growth factor–induced VEGF expression in VSMCs by preventing the redox-sensitive activation of the p38 MAPK pathway. The potential antiangiogenic and antiatherosclerotic properties of RWPCs are likely to contribute to cardiovascular protection by preventing the development of atherosclerotic lesions.</description><identifier>ISSN: 1079-5642</identifier><identifier>EISSN: 1524-4636</identifier><identifier>DOI: 10.1161/01.ATV.0000070101.70534.38</identifier><identifier>PMID: 12676803</identifier><identifier>CODEN: ATVBFA</identifier><language>eng</language><publisher>Philadelphia, PA: American Heart Association, Inc</publisher><subject>Androstadienes - pharmacology ; Animals ; Antioxidants - pharmacology ; Atherosclerosis (general aspects, experimental research) ; Biological and medical sciences ; Blood and lymphatic vessels ; Cardiology. Vascular system ; Cells, Cultured - drug effects ; Cells, Cultured - metabolism ; Enzyme Inhibitors - pharmacology ; Flavonoids - pharmacology ; Humans ; Imidazoles - pharmacology ; Life Sciences ; MAP Kinase Signaling System - drug effects ; Medical sciences ; Mitogen-Activated Protein Kinases - antagonists & inhibitors ; Mitogen-Activated Protein Kinases - metabolism ; Muscle, Smooth, Vascular - cytology ; Muscle, Smooth, Vascular - drug effects ; Muscle, Smooth, Vascular - metabolism ; Onium Compounds - pharmacology ; p38 Mitogen-Activated Protein Kinases ; Pharmaceutical sciences ; Phenols - pharmacology ; Phosphorylation - drug effects ; Platelet-Derived Growth Factor - pharmacology ; Polyphenols ; Protein Processing, Post-Translational - drug effects ; Pyridines - pharmacology ; Rats ; Reactive Oxygen Species - metabolism ; RNA, Messenger - biosynthesis ; RNA, Messenger - genetics ; Thrombin - pharmacology ; Transforming Growth Factor beta - pharmacology ; Transforming Growth Factor beta1 ; Vascular Endothelial Growth Factor A - biosynthesis ; Vascular Endothelial Growth Factor A - genetics ; Wine</subject><ispartof>Arteriosclerosis, thrombosis, and vascular biology, 2003-06, Vol.23 (6), p.1001-1007</ispartof><rights>2003 American Heart Association, Inc.</rights><rights>2003 INIST-CNRS</rights><rights>Copyright American Heart Association, Inc. Jun 1 2003</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6033-64c69d3b54d2ae14eac43ac21424de1a69f110b4014d603ca193bcaa5e8ee1ff3</citedby><cites>FETCH-LOGICAL-c6033-64c69d3b54d2ae14eac43ac21424de1a69f110b4014d603ca193bcaa5e8ee1ff3</cites><orcidid>0000-0002-4770-3585 ; 0000-0002-1479-1697</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14882060$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12676803$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03202443$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Oak, Min-Ho</creatorcontrib><creatorcontrib>Chataigneau, Marta</creatorcontrib><creatorcontrib>Keravis, Thérèse</creatorcontrib><creatorcontrib>Chataigneau, Thierry</creatorcontrib><creatorcontrib>Beretz, Alain</creatorcontrib><creatorcontrib>Andriantsitohaina, Ramaroson</creatorcontrib><creatorcontrib>Stoclet, Jean-Claude</creatorcontrib><creatorcontrib>Chang, Soon-Jae</creatorcontrib><creatorcontrib>Schini-Kerth, Valérie B</creatorcontrib><title>Red Wine Polyphenolic Compounds Inhibit Vascular Endothelial Growth Factor Expression in Vascular Smooth Muscle Cells by Preventing the Activation of the p38 Mitogen-Activated Protein Kinase Pathway</title><title>Arteriosclerosis, thrombosis, and vascular biology</title><addtitle>Arterioscler Thromb Vasc Biol</addtitle><description>OBJECTIVE—Moderate consumption of red wine has a beneficial effect on the cardiovascular system. This study examines whether red wine polyphenolic compounds (RWPCs) affect vascular endothelial growth factor (VEGF) expression, a major angiogenic and proatherosclerotic factor in vascular smooth muscle cells (VSMCs).
METHODS AND RESULTS—VEGF mRNA expression was assessed by Northern blot analysis and the release of VEGF by immunoassay in cultured VSMCs. Short-term and long-term exposure of VSMCs to RWPCs inhibited VEGF mRNA expression and release of VEGF in response to platelet-derived growth factor AB (PDGFAB), transforming growth factor-β1, or thrombin. The PDGFAB-induced expression of VEGF was markedly reduced by SB203580 (inhibitor of p38 mitogen-activated protein kinase [MAPK]), antioxidants, and diphenylene iodonium (inhibitor of flavin-dependent enzymes), slightly reduced by PD98059 (inhibitor of MEK), and not significantly affected by wortmannin (inhibitor of PI-3-kinase) and L-JNKI (inhibitor of JNK). Short-term and long-term treatment of VSMCs with RWPCs markedly reduced PDGFAB-induced production of reactive oxygen species and phosphorylation of p38 MAPK.
CONCLUSIONS—These data indicate that RWPCs strongly inhibit growth factor–induced VEGF expression in VSMCs by preventing the redox-sensitive activation of the p38 MAPK pathway. The potential antiangiogenic and antiatherosclerotic properties of RWPCs are likely to contribute to cardiovascular protection by preventing the development of atherosclerotic lesions.</description><subject>Androstadienes - pharmacology</subject><subject>Animals</subject><subject>Antioxidants - pharmacology</subject><subject>Atherosclerosis (general aspects, experimental research)</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Cardiology. Vascular system</subject><subject>Cells, Cultured - drug effects</subject><subject>Cells, Cultured - metabolism</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Flavonoids - pharmacology</subject><subject>Humans</subject><subject>Imidazoles - pharmacology</subject><subject>Life Sciences</subject><subject>MAP Kinase Signaling System - drug effects</subject><subject>Medical sciences</subject><subject>Mitogen-Activated Protein Kinases - antagonists & inhibitors</subject><subject>Mitogen-Activated Protein Kinases - metabolism</subject><subject>Muscle, Smooth, Vascular - cytology</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Muscle, Smooth, Vascular - metabolism</subject><subject>Onium Compounds - pharmacology</subject><subject>p38 Mitogen-Activated Protein Kinases</subject><subject>Pharmaceutical sciences</subject><subject>Phenols - pharmacology</subject><subject>Phosphorylation - drug effects</subject><subject>Platelet-Derived Growth Factor - pharmacology</subject><subject>Polyphenols</subject><subject>Protein Processing, Post-Translational - drug effects</subject><subject>Pyridines - pharmacology</subject><subject>Rats</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>RNA, Messenger - biosynthesis</subject><subject>RNA, Messenger - genetics</subject><subject>Thrombin - pharmacology</subject><subject>Transforming Growth Factor beta - pharmacology</subject><subject>Transforming Growth Factor beta1</subject><subject>Vascular Endothelial Growth Factor A - biosynthesis</subject><subject>Vascular Endothelial Growth Factor A - genetics</subject><subject>Wine</subject><issn>1079-5642</issn><issn>1524-4636</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkttuEzEQhlcIREvgFZBVCSQuNvi0zoa7KOpJpCKCUi4tr3e26-LYwfY25AV5LpwmIhKWLJ--f2Zs_0VxRvCYEEE-YjKe3d6N8a5NMMnLCa4YH7P6WXFKKspLLph4nud4Mi0rwelJ8SrGh4xzSvHL4oRQMRE1ZqfFn6_Qoh_GAVp6u1334Lw1Gs39au0H10Z07XrTmITuVNSDVQGdu9anHqxRFl0Gv0k9ulA6-Xzyex0gRuMdMu4o-LbyWYBuhqgtoDlYG1GzRcsAj-CScfcoh0MzncyjSjux75521qxGNyb5e3Dl4TTXugw-QQ7_2TgVc9Uq9Ru1fV286JSN8OYwjorvF-e386ty8eXyej5blFpgxkrBtZi2rKl4SxUQDkpzpjQlnPIWiBLTjhDccEx4mwVakSlrtFIV1ACk69io-LCP2ysr18GsVNhKr4y8mi3kbg8ziinn7JFk9v2eXQf_a4CY5MpEna-vHPghygljjFNBM3j2H_jgh-DyPSTNP1YLTOsMfdpDOvgYA3T_0hMsd7aQmMhsC3m0hXyyhWQ78dtDhqFZQXuUHnyQgXcHIP-asl1QTpt45HhdU5xfZFTwPbfxNkGIP-2wgSB7UDb1u9ScCVyVFGOWcYzL3AljfwE3MdJh</recordid><startdate>200306</startdate><enddate>200306</enddate><creator>Oak, Min-Ho</creator><creator>Chataigneau, Marta</creator><creator>Keravis, Thérèse</creator><creator>Chataigneau, Thierry</creator><creator>Beretz, Alain</creator><creator>Andriantsitohaina, Ramaroson</creator><creator>Stoclet, Jean-Claude</creator><creator>Chang, Soon-Jae</creator><creator>Schini-Kerth, Valérie B</creator><general>American Heart Association, Inc</general><general>Lippincott</general><general>American Heart Association</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>K9.</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-4770-3585</orcidid><orcidid>https://orcid.org/0000-0002-1479-1697</orcidid></search><sort><creationdate>200306</creationdate><title>Red Wine Polyphenolic Compounds Inhibit Vascular Endothelial Growth Factor Expression in Vascular Smooth Muscle Cells by Preventing the Activation of the p38 Mitogen-Activated Protein Kinase Pathway</title><author>Oak, Min-Ho ; Chataigneau, Marta ; Keravis, Thérèse ; Chataigneau, Thierry ; Beretz, Alain ; Andriantsitohaina, Ramaroson ; Stoclet, Jean-Claude ; Chang, Soon-Jae ; Schini-Kerth, Valérie B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6033-64c69d3b54d2ae14eac43ac21424de1a69f110b4014d603ca193bcaa5e8ee1ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Androstadienes - pharmacology</topic><topic>Animals</topic><topic>Antioxidants - pharmacology</topic><topic>Atherosclerosis (general aspects, experimental research)</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Cardiology. Vascular system</topic><topic>Cells, Cultured - drug effects</topic><topic>Cells, Cultured - metabolism</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Flavonoids - pharmacology</topic><topic>Humans</topic><topic>Imidazoles - pharmacology</topic><topic>Life Sciences</topic><topic>MAP Kinase Signaling System - drug effects</topic><topic>Medical sciences</topic><topic>Mitogen-Activated Protein Kinases - antagonists & inhibitors</topic><topic>Mitogen-Activated Protein Kinases - metabolism</topic><topic>Muscle, Smooth, Vascular - cytology</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Onium Compounds - pharmacology</topic><topic>p38 Mitogen-Activated Protein Kinases</topic><topic>Pharmaceutical sciences</topic><topic>Phenols - pharmacology</topic><topic>Phosphorylation - drug effects</topic><topic>Platelet-Derived Growth Factor - pharmacology</topic><topic>Polyphenols</topic><topic>Protein Processing, Post-Translational - drug effects</topic><topic>Pyridines - pharmacology</topic><topic>Rats</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>RNA, Messenger - biosynthesis</topic><topic>RNA, Messenger - genetics</topic><topic>Thrombin - pharmacology</topic><topic>Transforming Growth Factor beta - pharmacology</topic><topic>Transforming Growth Factor beta1</topic><topic>Vascular Endothelial Growth Factor A - biosynthesis</topic><topic>Vascular Endothelial Growth Factor A - genetics</topic><topic>Wine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oak, Min-Ho</creatorcontrib><creatorcontrib>Chataigneau, Marta</creatorcontrib><creatorcontrib>Keravis, Thérèse</creatorcontrib><creatorcontrib>Chataigneau, Thierry</creatorcontrib><creatorcontrib>Beretz, Alain</creatorcontrib><creatorcontrib>Andriantsitohaina, Ramaroson</creatorcontrib><creatorcontrib>Stoclet, Jean-Claude</creatorcontrib><creatorcontrib>Chang, Soon-Jae</creatorcontrib><creatorcontrib>Schini-Kerth, Valérie B</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>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Arteriosclerosis, thrombosis, and vascular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oak, Min-Ho</au><au>Chataigneau, Marta</au><au>Keravis, Thérèse</au><au>Chataigneau, Thierry</au><au>Beretz, Alain</au><au>Andriantsitohaina, Ramaroson</au><au>Stoclet, Jean-Claude</au><au>Chang, Soon-Jae</au><au>Schini-Kerth, Valérie B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Red Wine Polyphenolic Compounds Inhibit Vascular Endothelial Growth Factor Expression in Vascular Smooth Muscle Cells by Preventing the Activation of the p38 Mitogen-Activated Protein Kinase Pathway</atitle><jtitle>Arteriosclerosis, thrombosis, and vascular biology</jtitle><addtitle>Arterioscler Thromb Vasc Biol</addtitle><date>2003-06</date><risdate>2003</risdate><volume>23</volume><issue>6</issue><spage>1001</spage><epage>1007</epage><pages>1001-1007</pages><issn>1079-5642</issn><eissn>1524-4636</eissn><coden>ATVBFA</coden><abstract>OBJECTIVE—Moderate consumption of red wine has a beneficial effect on the cardiovascular system. This study examines whether red wine polyphenolic compounds (RWPCs) affect vascular endothelial growth factor (VEGF) expression, a major angiogenic and proatherosclerotic factor in vascular smooth muscle cells (VSMCs).
METHODS AND RESULTS—VEGF mRNA expression was assessed by Northern blot analysis and the release of VEGF by immunoassay in cultured VSMCs. Short-term and long-term exposure of VSMCs to RWPCs inhibited VEGF mRNA expression and release of VEGF in response to platelet-derived growth factor AB (PDGFAB), transforming growth factor-β1, or thrombin. The PDGFAB-induced expression of VEGF was markedly reduced by SB203580 (inhibitor of p38 mitogen-activated protein kinase [MAPK]), antioxidants, and diphenylene iodonium (inhibitor of flavin-dependent enzymes), slightly reduced by PD98059 (inhibitor of MEK), and not significantly affected by wortmannin (inhibitor of PI-3-kinase) and L-JNKI (inhibitor of JNK). Short-term and long-term treatment of VSMCs with RWPCs markedly reduced PDGFAB-induced production of reactive oxygen species and phosphorylation of p38 MAPK.
CONCLUSIONS—These data indicate that RWPCs strongly inhibit growth factor–induced VEGF expression in VSMCs by preventing the redox-sensitive activation of the p38 MAPK pathway. The potential antiangiogenic and antiatherosclerotic properties of RWPCs are likely to contribute to cardiovascular protection by preventing the development of atherosclerotic lesions.</abstract><cop>Philadelphia, PA</cop><cop>Hagerstown, MD</cop><pub>American Heart Association, Inc</pub><pmid>12676803</pmid><doi>10.1161/01.ATV.0000070101.70534.38</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-4770-3585</orcidid><orcidid>https://orcid.org/0000-0002-1479-1697</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Androstadienes - pharmacology Animals Antioxidants - pharmacology Atherosclerosis (general aspects, experimental research) Biological and medical sciences Blood and lymphatic vessels Cardiology. Vascular system Cells, Cultured - drug effects Cells, Cultured - metabolism Enzyme Inhibitors - pharmacology Flavonoids - pharmacology Humans Imidazoles - pharmacology Life Sciences MAP Kinase Signaling System - drug effects Medical sciences Mitogen-Activated Protein Kinases - antagonists & inhibitors Mitogen-Activated Protein Kinases - metabolism Muscle, Smooth, Vascular - cytology Muscle, Smooth, Vascular - drug effects Muscle, Smooth, Vascular - metabolism Onium Compounds - pharmacology p38 Mitogen-Activated Protein Kinases Pharmaceutical sciences Phenols - pharmacology Phosphorylation - drug effects Platelet-Derived Growth Factor - pharmacology Polyphenols Protein Processing, Post-Translational - drug effects Pyridines - pharmacology Rats Reactive Oxygen Species - metabolism RNA, Messenger - biosynthesis RNA, Messenger - genetics Thrombin - pharmacology Transforming Growth Factor beta - pharmacology Transforming Growth Factor beta1 Vascular Endothelial Growth Factor A - biosynthesis Vascular Endothelial Growth Factor A - genetics Wine |
title | Red Wine Polyphenolic Compounds Inhibit Vascular Endothelial Growth Factor Expression in Vascular Smooth Muscle Cells by Preventing the Activation of the p38 Mitogen-Activated Protein Kinase Pathway |
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