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
Hauptverfasser: Oak, Min-Ho, Chataigneau, Marta, Keravis, Thérèse, Chataigneau, Thierry, Beretz, Alain, Andriantsitohaina, Ramaroson, Stoclet, Jean-Claude, Chang, Soon-Jae, Schini-Kerth, Valérie B
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container_issue 6
container_start_page 1001
container_title Arteriosclerosis, thrombosis, and vascular biology
container_volume 23
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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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><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 &amp; 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&amp;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 &amp; 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 &amp; 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 &amp; 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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ispartof Arteriosclerosis, thrombosis, and vascular biology, 2003-06, Vol.23 (6), p.1001-1007
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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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