Nitro-linoleic acid inhibits vascular smooth muscle cell proliferation via the Keap1/Nrf2 signaling pathway
1 Department of Internal Medicine, Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, Michigan; 2 Cardiovascular Research Institute, Morehouse School of Medicine, Atlanta; 3 Atherogenics Inc., Alpharetta, Georgia; and 4 Department of Pharmacology, University of Pittsburgh Schoo...
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creator | Villacorta, Luis Zhang, Jifeng Garcia-Barrio, Minerva T Chen, Xi-lin Freeman, Bruce A Chen, Yuqing E Cui, Taixing |
description | 1 Department of Internal Medicine, Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, Michigan; 2 Cardiovascular Research Institute, Morehouse School of Medicine, Atlanta; 3 Atherogenics Inc., Alpharetta, Georgia; and 4 Department of Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
Submitted 2 March 2007
; accepted in final form 27 April 2007
Nitroalkenes, the nitration products of unsaturated fatty acids formed via NO-dependent oxidative reactions, have been demonstrated to exert strong biological actions in endothelial cells and monocytes/macrophages; however, little is known about their effects on vascular smooth muscle cells (VSMCs). The present study examined the role of nitro-linoleic acid (LNO 2 ) in the regulation of VSMC proliferation. We observed that LNO 2 inhibited VSMC proliferation in a dose-dependent manner. In addition, LNO 2 induced growth arrest of VSMCs in the G 1 /S phase of the cell cycle with an upregulation of the cyclin-dependent kinase inhibitor p27 kip1 . Furthermore, LNO 2 triggered nuclear factor-erythroid 2-related factor 2 (Nrf2) nuclear translocation and activation of the antioxidant-responsive element-driven transcriptional activity via impairing Kelch-like ECH-associating protein 1 (Keap1)-mediated negative control of Nrf2 activity in VSMCs. LNO 2 upregulated the expression of Nrf2 protein levels, but not mRNA levels, in VSMCs. A forced activation of Nrf2 led to an upregulation of p27 kip1 and growth inhibition of VSMCs. In contrast, knock down of Nrf2 using an Nrf2 siRNA approach reversed the LNO 2 -induced upregulation of p27 kip1 and inhibition of cellular proliferation in VSMCs. These studies provide the first evidence that nitroalkene LNO 2 inhibits VSMC proliferation through activation of the Keap1/Nrf2 signaling pathway, suggesting an important role of nitroalkenes in vascular biology.
nitroalkenes; nuclear factor-erythroid 2-related factor 2; Kelch-like ECH-associating protein 1
Address for reprint requests and other correspondence: T. Cui, 1150 W. Medical Ctr. Dr., MSRB III 7200, Ann Arbor, MI 48109 (e-mail: tcui{at}umich.edu ) |
doi_str_mv | 10.1152/ajpheart.00261.2007 |
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Submitted 2 March 2007
; accepted in final form 27 April 2007
Nitroalkenes, the nitration products of unsaturated fatty acids formed via NO-dependent oxidative reactions, have been demonstrated to exert strong biological actions in endothelial cells and monocytes/macrophages; however, little is known about their effects on vascular smooth muscle cells (VSMCs). The present study examined the role of nitro-linoleic acid (LNO 2 ) in the regulation of VSMC proliferation. We observed that LNO 2 inhibited VSMC proliferation in a dose-dependent manner. In addition, LNO 2 induced growth arrest of VSMCs in the G 1 /S phase of the cell cycle with an upregulation of the cyclin-dependent kinase inhibitor p27 kip1 . Furthermore, LNO 2 triggered nuclear factor-erythroid 2-related factor 2 (Nrf2) nuclear translocation and activation of the antioxidant-responsive element-driven transcriptional activity via impairing Kelch-like ECH-associating protein 1 (Keap1)-mediated negative control of Nrf2 activity in VSMCs. LNO 2 upregulated the expression of Nrf2 protein levels, but not mRNA levels, in VSMCs. A forced activation of Nrf2 led to an upregulation of p27 kip1 and growth inhibition of VSMCs. In contrast, knock down of Nrf2 using an Nrf2 siRNA approach reversed the LNO 2 -induced upregulation of p27 kip1 and inhibition of cellular proliferation in VSMCs. These studies provide the first evidence that nitroalkene LNO 2 inhibits VSMC proliferation through activation of the Keap1/Nrf2 signaling pathway, suggesting an important role of nitroalkenes in vascular biology.
nitroalkenes; nuclear factor-erythroid 2-related factor 2; Kelch-like ECH-associating protein 1
Address for reprint requests and other correspondence: T. Cui, 1150 W. Medical Ctr. Dr., MSRB III 7200, Ann Arbor, MI 48109 (e-mail: tcui{at}umich.edu )</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00261.2007</identifier><identifier>PMID: 17468336</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Cell Proliferation - drug effects ; Cells, Cultured ; Cellular biology ; Cyclin-Dependent Kinase Inhibitor p27 - metabolism ; Dose-Response Relationship, Drug ; Fatty acids ; Inhibitor drugs ; Intracellular Signaling Peptides and Proteins ; Kelch-Like ECH-Associated Protein 1 ; Kinases ; Linoleic Acids - administration & dosage ; Male ; Muscle, Smooth, Vascular - cytology ; Muscle, Smooth, Vascular - drug effects ; Muscle, Smooth, Vascular - physiology ; Myocytes, Smooth Muscle - cytology ; Myocytes, Smooth Muscle - drug effects ; Myocytes, Smooth Muscle - physiology ; NF-E2-Related Factor 2 - metabolism ; Nitric oxide ; Nitro Compounds - administration & dosage ; Proteins - metabolism ; Rats ; Rats, Sprague-Dawley ; Signal Transduction - drug effects ; Signal Transduction - physiology ; Studies</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2007-07, Vol.293 (1), p.H770-H776</ispartof><rights>Copyright American Physiological Society Jul 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c586t-83d86714b7f2530f46dc29f467bd8d036b9fb2c8f09e78316478fb93d8fa6b043</citedby><cites>FETCH-LOGICAL-c586t-83d86714b7f2530f46dc29f467bd8d036b9fb2c8f09e78316478fb93d8fa6b043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17468336$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Villacorta, Luis</creatorcontrib><creatorcontrib>Zhang, Jifeng</creatorcontrib><creatorcontrib>Garcia-Barrio, Minerva T</creatorcontrib><creatorcontrib>Chen, Xi-lin</creatorcontrib><creatorcontrib>Freeman, Bruce A</creatorcontrib><creatorcontrib>Chen, Yuqing E</creatorcontrib><creatorcontrib>Cui, Taixing</creatorcontrib><title>Nitro-linoleic acid inhibits vascular smooth muscle cell proliferation via the Keap1/Nrf2 signaling pathway</title><title>American journal of physiology. Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>1 Department of Internal Medicine, Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, Michigan; 2 Cardiovascular Research Institute, Morehouse School of Medicine, Atlanta; 3 Atherogenics Inc., Alpharetta, Georgia; and 4 Department of Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
Submitted 2 March 2007
; accepted in final form 27 April 2007
Nitroalkenes, the nitration products of unsaturated fatty acids formed via NO-dependent oxidative reactions, have been demonstrated to exert strong biological actions in endothelial cells and monocytes/macrophages; however, little is known about their effects on vascular smooth muscle cells (VSMCs). The present study examined the role of nitro-linoleic acid (LNO 2 ) in the regulation of VSMC proliferation. We observed that LNO 2 inhibited VSMC proliferation in a dose-dependent manner. In addition, LNO 2 induced growth arrest of VSMCs in the G 1 /S phase of the cell cycle with an upregulation of the cyclin-dependent kinase inhibitor p27 kip1 . Furthermore, LNO 2 triggered nuclear factor-erythroid 2-related factor 2 (Nrf2) nuclear translocation and activation of the antioxidant-responsive element-driven transcriptional activity via impairing Kelch-like ECH-associating protein 1 (Keap1)-mediated negative control of Nrf2 activity in VSMCs. LNO 2 upregulated the expression of Nrf2 protein levels, but not mRNA levels, in VSMCs. A forced activation of Nrf2 led to an upregulation of p27 kip1 and growth inhibition of VSMCs. In contrast, knock down of Nrf2 using an Nrf2 siRNA approach reversed the LNO 2 -induced upregulation of p27 kip1 and inhibition of cellular proliferation in VSMCs. These studies provide the first evidence that nitroalkene LNO 2 inhibits VSMC proliferation through activation of the Keap1/Nrf2 signaling pathway, suggesting an important role of nitroalkenes in vascular biology.
nitroalkenes; nuclear factor-erythroid 2-related factor 2; Kelch-like ECH-associating protein 1
Address for reprint requests and other correspondence: T. Cui, 1150 W. Medical Ctr. Dr., MSRB III 7200, Ann Arbor, MI 48109 (e-mail: tcui{at}umich.edu )</description><subject>Animals</subject><subject>Cell Proliferation - drug effects</subject><subject>Cells, Cultured</subject><subject>Cellular biology</subject><subject>Cyclin-Dependent Kinase Inhibitor p27 - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Fatty acids</subject><subject>Inhibitor drugs</subject><subject>Intracellular Signaling Peptides and Proteins</subject><subject>Kelch-Like ECH-Associated Protein 1</subject><subject>Kinases</subject><subject>Linoleic Acids - administration & dosage</subject><subject>Male</subject><subject>Muscle, Smooth, Vascular - cytology</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Muscle, Smooth, Vascular - physiology</subject><subject>Myocytes, Smooth Muscle - cytology</subject><subject>Myocytes, Smooth Muscle - drug effects</subject><subject>Myocytes, Smooth Muscle - physiology</subject><subject>NF-E2-Related Factor 2 - metabolism</subject><subject>Nitric oxide</subject><subject>Nitro Compounds - administration & dosage</subject><subject>Proteins - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Signal Transduction - drug effects</subject><subject>Signal Transduction - physiology</subject><subject>Studies</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1u1DAUhSMEokPhCZCQxYJdpv5JbIcFEqooRVRlU9aW49iJBycOtjNl3h4PM0wBidVd3PMd3XNPUbxEcI1QjS_kZh60DGkNIaZojSFkj4pV3uAS1aR5XKwgoaSkiNRnxbMYNxDCmlHytDhDrKKcELoqvt3aFHzp7OSdtgpIZTtgp8G2NkWwlVEtTgYQR-_TAMYlKqeB0s6BOXhnjQ4yWT-BrZUgDRp81nJGF7fBYBBtP8ls3INZpuFe7p4XT4x0Ub84zvPi69WHu8vr8ubLx0-X729KVXOaSk46ThmqWmZwTaCpaKdwkwdrO97lTG1jWqy4gY1mnCBaMW7aJlNG0hZW5Lx4d_Cdl3bUndJTCtKJOdhRhp3w0oq_N5MdRO-3AiMGeUOywZujQfDfFx2TGG3ch5aT9ksUDObvVXWTha__EW78EnLqKDBuKMeE70XkIFLBxxi0OV2CoNg3KX43KX41KfZNZurVnyEemGN1WfD2IBhsP9zboMU87KL1zvc7cbU4d6d_pJM1bohA4poxKObOZHj9f_h0zgNEfgLXq8Qa</recordid><startdate>20070701</startdate><enddate>20070701</enddate><creator>Villacorta, Luis</creator><creator>Zhang, Jifeng</creator><creator>Garcia-Barrio, Minerva T</creator><creator>Chen, Xi-lin</creator><creator>Freeman, Bruce A</creator><creator>Chen, Yuqing E</creator><creator>Cui, Taixing</creator><general>American Physiological Society</general><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>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20070701</creationdate><title>Nitro-linoleic acid inhibits vascular smooth muscle cell proliferation via the Keap1/Nrf2 signaling pathway</title><author>Villacorta, Luis ; Zhang, Jifeng ; Garcia-Barrio, Minerva T ; Chen, Xi-lin ; Freeman, Bruce A ; Chen, Yuqing E ; Cui, Taixing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c586t-83d86714b7f2530f46dc29f467bd8d036b9fb2c8f09e78316478fb93d8fa6b043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Cell Proliferation - drug effects</topic><topic>Cells, Cultured</topic><topic>Cellular biology</topic><topic>Cyclin-Dependent Kinase Inhibitor p27 - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Fatty acids</topic><topic>Inhibitor drugs</topic><topic>Intracellular Signaling Peptides and Proteins</topic><topic>Kelch-Like ECH-Associated Protein 1</topic><topic>Kinases</topic><topic>Linoleic Acids - administration & dosage</topic><topic>Male</topic><topic>Muscle, Smooth, Vascular - cytology</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Muscle, Smooth, Vascular - physiology</topic><topic>Myocytes, Smooth Muscle - cytology</topic><topic>Myocytes, Smooth Muscle - drug effects</topic><topic>Myocytes, Smooth Muscle - physiology</topic><topic>NF-E2-Related Factor 2 - metabolism</topic><topic>Nitric oxide</topic><topic>Nitro Compounds - administration & dosage</topic><topic>Proteins - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Signal Transduction - drug effects</topic><topic>Signal Transduction - physiology</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Villacorta, Luis</creatorcontrib><creatorcontrib>Zhang, Jifeng</creatorcontrib><creatorcontrib>Garcia-Barrio, Minerva T</creatorcontrib><creatorcontrib>Chen, Xi-lin</creatorcontrib><creatorcontrib>Freeman, Bruce A</creatorcontrib><creatorcontrib>Chen, Yuqing E</creatorcontrib><creatorcontrib>Cui, Taixing</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Villacorta, Luis</au><au>Zhang, Jifeng</au><au>Garcia-Barrio, Minerva T</au><au>Chen, Xi-lin</au><au>Freeman, Bruce A</au><au>Chen, Yuqing E</au><au>Cui, Taixing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nitro-linoleic acid inhibits vascular smooth muscle cell proliferation via the Keap1/Nrf2 signaling pathway</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2007-07-01</date><risdate>2007</risdate><volume>293</volume><issue>1</issue><spage>H770</spage><epage>H776</epage><pages>H770-H776</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>1 Department of Internal Medicine, Cardiovascular Center, University of Michigan Medical Center, Ann Arbor, Michigan; 2 Cardiovascular Research Institute, Morehouse School of Medicine, Atlanta; 3 Atherogenics Inc., Alpharetta, Georgia; and 4 Department of Pharmacology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
Submitted 2 March 2007
; accepted in final form 27 April 2007
Nitroalkenes, the nitration products of unsaturated fatty acids formed via NO-dependent oxidative reactions, have been demonstrated to exert strong biological actions in endothelial cells and monocytes/macrophages; however, little is known about their effects on vascular smooth muscle cells (VSMCs). The present study examined the role of nitro-linoleic acid (LNO 2 ) in the regulation of VSMC proliferation. We observed that LNO 2 inhibited VSMC proliferation in a dose-dependent manner. In addition, LNO 2 induced growth arrest of VSMCs in the G 1 /S phase of the cell cycle with an upregulation of the cyclin-dependent kinase inhibitor p27 kip1 . Furthermore, LNO 2 triggered nuclear factor-erythroid 2-related factor 2 (Nrf2) nuclear translocation and activation of the antioxidant-responsive element-driven transcriptional activity via impairing Kelch-like ECH-associating protein 1 (Keap1)-mediated negative control of Nrf2 activity in VSMCs. LNO 2 upregulated the expression of Nrf2 protein levels, but not mRNA levels, in VSMCs. A forced activation of Nrf2 led to an upregulation of p27 kip1 and growth inhibition of VSMCs. In contrast, knock down of Nrf2 using an Nrf2 siRNA approach reversed the LNO 2 -induced upregulation of p27 kip1 and inhibition of cellular proliferation in VSMCs. These studies provide the first evidence that nitroalkene LNO 2 inhibits VSMC proliferation through activation of the Keap1/Nrf2 signaling pathway, suggesting an important role of nitroalkenes in vascular biology.
nitroalkenes; nuclear factor-erythroid 2-related factor 2; Kelch-like ECH-associating protein 1
Address for reprint requests and other correspondence: T. Cui, 1150 W. Medical Ctr. Dr., MSRB III 7200, Ann Arbor, MI 48109 (e-mail: tcui{at}umich.edu )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>17468336</pmid><doi>10.1152/ajpheart.00261.2007</doi><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; American Physiological Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Animals Cell Proliferation - drug effects Cells, Cultured Cellular biology Cyclin-Dependent Kinase Inhibitor p27 - metabolism Dose-Response Relationship, Drug Fatty acids Inhibitor drugs Intracellular Signaling Peptides and Proteins Kelch-Like ECH-Associated Protein 1 Kinases Linoleic Acids - administration & dosage Male Muscle, Smooth, Vascular - cytology Muscle, Smooth, Vascular - drug effects Muscle, Smooth, Vascular - physiology Myocytes, Smooth Muscle - cytology Myocytes, Smooth Muscle - drug effects Myocytes, Smooth Muscle - physiology NF-E2-Related Factor 2 - metabolism Nitric oxide Nitro Compounds - administration & dosage Proteins - metabolism Rats Rats, Sprague-Dawley Signal Transduction - drug effects Signal Transduction - physiology Studies |
title | Nitro-linoleic acid inhibits vascular smooth muscle cell proliferation via the Keap1/Nrf2 signaling pathway |
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