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Alteration in angiogenic and anti-angiogenic forms of vascular endothelial growth factor-A in skeletal muscle of patients with intermittent claudication following exercise training
The aims of this study were twofold: (1) to identify whether peripheral artery disease (PAD) patients had increased muscle concentration of angiogenic VEGF-A, anti-angiogenic VEGF165b or VEGF receptor 1 (VEGF-R1) when compared with control subjects, and (2) to evaluate whether exercise training in P...
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Published in: | Vascular medicine (London, England) England), 2012-04, Vol.17 (2), p.94-100 |
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description | The aims of this study were twofold: (1) to identify whether peripheral artery disease (PAD) patients had increased muscle concentration of angiogenic VEGF-A, anti-angiogenic VEGF165b or VEGF receptor 1 (VEGF-R1) when compared with control subjects, and (2) to evaluate whether exercise training in PAD patients was associated with changes in muscle concentration of VEGF-A, VEGF165b or VEGF-R1. At baseline, 22 PAD and 30 control subjects underwent gastrocnemius muscle biopsy. Twelve PAD patients were treated with supervised exercise training (SET) and underwent muscle biopsy after 3 weeks and 12 weeks of training and had sufficient tissue to measure VEGF-A, VEGF165b and VEGF-R1 concentrations in skeletal muscle lysates by ELISA. Muscle concentrations of VEGF-A and VEGF165b were similar in PAD patients versus controls at baseline. At both time points after the start of SET, VEGF-A levels decreased and there was a trend towards increased VEGF165b concentrations. At baseline, VEGF-R1 concentrations were lower in PAD patients when compared with controls but did not change after SET. Skeletal muscle concentrations of VEGF-A are not different in PAD patients when compared with controls at baseline. SET is associated with a significant reduction in VEGF-A levels and a trend towards increased VEGF165b levels. These somewhat unexpected findings suggest that further investigation into the mechanism of vascular responses to exercise training in PAD patients is warranted. |
doi_str_mv | 10.1177/1358863X11436334 |
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At baseline, 22 PAD and 30 control subjects underwent gastrocnemius muscle biopsy. Twelve PAD patients were treated with supervised exercise training (SET) and underwent muscle biopsy after 3 weeks and 12 weeks of training and had sufficient tissue to measure VEGF-A, VEGF165b and VEGF-R1 concentrations in skeletal muscle lysates by ELISA. Muscle concentrations of VEGF-A and VEGF165b were similar in PAD patients versus controls at baseline. At both time points after the start of SET, VEGF-A levels decreased and there was a trend towards increased VEGF165b concentrations. At baseline, VEGF-R1 concentrations were lower in PAD patients when compared with controls but did not change after SET. Skeletal muscle concentrations of VEGF-A are not different in PAD patients when compared with controls at baseline. SET is associated with a significant reduction in VEGF-A levels and a trend towards increased VEGF165b levels. These somewhat unexpected findings suggest that further investigation into the mechanism of vascular responses to exercise training in PAD patients is warranted.</description><identifier>ISSN: 1358-863X</identifier><identifier>EISSN: 1477-0377</identifier><identifier>DOI: 10.1177/1358863X11436334</identifier><identifier>PMID: 22402934</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Aged ; Analysis of Variance ; Biological and medical sciences ; Biopsy ; Blood and lymphatic vessels ; Capillaries - physiopathology ; Cardiology. Vascular system ; Cardiovascular system ; Colorado ; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous ; Enzyme-Linked Immunosorbent Assay ; Exercise Therapy ; Exercise Tolerance ; Female ; Humans ; Intermittent Claudication - etiology ; Intermittent Claudication - metabolism ; Intermittent Claudication - physiopathology ; Intermittent Claudication - therapy ; Male ; Medical sciences ; Middle Aged ; Muscle, Skeletal - blood supply ; Muscle, Skeletal - metabolism ; Neovascularization, Physiologic ; North Carolina ; Peripheral Arterial Disease - complications ; Peripheral Arterial Disease - metabolism ; Peripheral Arterial Disease - physiopathology ; Peripheral Arterial Disease - therapy ; Pharmacology. Drug treatments ; Recovery of Function ; Time Factors ; Treatment Outcome ; Vascular Endothelial Growth Factor A - metabolism ; Vascular Endothelial Growth Factor Receptor-1 - metabolism ; Vasodilator agents. Cerebral vasodilators</subject><ispartof>Vascular medicine (London, England), 2012-04, Vol.17 (2), p.94-100</ispartof><rights>The Author(s) 2012</rights><rights>2015 INIST-CNRS</rights><rights>SAGE Publications © Apr 2012</rights><rights>The Author(s) 2012 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-8ca18869d70046f87f40cd8c91825153c444b007e0fb929e9f7bc1568f4fffb63</citedby><cites>FETCH-LOGICAL-c524t-8ca18869d70046f87f40cd8c91825153c444b007e0fb929e9f7bc1568f4fffb63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25835685$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22402934$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jones, W Schuyler</creatorcontrib><creatorcontrib>Duscha, Brian D</creatorcontrib><creatorcontrib>Robbins, Jennifer L</creatorcontrib><creatorcontrib>Duggan, Natasha N</creatorcontrib><creatorcontrib>Regensteiner, Judith G</creatorcontrib><creatorcontrib>Kraus, William E</creatorcontrib><creatorcontrib>Hiatt, William R</creatorcontrib><creatorcontrib>Dokun, Ayotunde O</creatorcontrib><creatorcontrib>Annex, Brian H</creatorcontrib><title>Alteration in angiogenic and anti-angiogenic forms of vascular endothelial growth factor-A in skeletal muscle of patients with intermittent claudication following exercise training</title><title>Vascular medicine (London, England)</title><addtitle>Vasc Med</addtitle><description>The aims of this study were twofold: (1) to identify whether peripheral artery disease (PAD) patients had increased muscle concentration of angiogenic VEGF-A, anti-angiogenic VEGF165b or VEGF receptor 1 (VEGF-R1) when compared with control subjects, and (2) to evaluate whether exercise training in PAD patients was associated with changes in muscle concentration of VEGF-A, VEGF165b or VEGF-R1. At baseline, 22 PAD and 30 control subjects underwent gastrocnemius muscle biopsy. Twelve PAD patients were treated with supervised exercise training (SET) and underwent muscle biopsy after 3 weeks and 12 weeks of training and had sufficient tissue to measure VEGF-A, VEGF165b and VEGF-R1 concentrations in skeletal muscle lysates by ELISA. Muscle concentrations of VEGF-A and VEGF165b were similar in PAD patients versus controls at baseline. At both time points after the start of SET, VEGF-A levels decreased and there was a trend towards increased VEGF165b concentrations. At baseline, VEGF-R1 concentrations were lower in PAD patients when compared with controls but did not change after SET. Skeletal muscle concentrations of VEGF-A are not different in PAD patients when compared with controls at baseline. SET is associated with a significant reduction in VEGF-A levels and a trend towards increased VEGF165b levels. These somewhat unexpected findings suggest that further investigation into the mechanism of vascular responses to exercise training in PAD patients is warranted.</description><subject>Aged</subject><subject>Analysis of Variance</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>Blood and lymphatic vessels</subject><subject>Capillaries - physiopathology</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular system</subject><subject>Colorado</subject><subject>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Exercise Therapy</subject><subject>Exercise Tolerance</subject><subject>Female</subject><subject>Humans</subject><subject>Intermittent Claudication - etiology</subject><subject>Intermittent Claudication - metabolism</subject><subject>Intermittent Claudication - physiopathology</subject><subject>Intermittent Claudication - therapy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Muscle, Skeletal - blood supply</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Neovascularization, Physiologic</subject><subject>North Carolina</subject><subject>Peripheral Arterial Disease - complications</subject><subject>Peripheral Arterial Disease - metabolism</subject><subject>Peripheral Arterial Disease - physiopathology</subject><subject>Peripheral Arterial Disease - therapy</subject><subject>Pharmacology. Drug treatments</subject><subject>Recovery of Function</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>Vascular Endothelial Growth Factor A - metabolism</subject><subject>Vascular Endothelial Growth Factor Receptor-1 - metabolism</subject><subject>Vasodilator agents. Cerebral vasodilators</subject><issn>1358-863X</issn><issn>1477-0377</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqNkk2LFDEQhhtR3HX17kmCIHhpTTrpTnIRhsUvWPCi4C1k0klP1nQyJukd_V_-QGuYcXddEDyEhKqn3qpUVdM8JfgVIZy_JrQXYqBfCWF0oJTda04J47zFlPP78AZ3u_efNI9KucQY80GSh81J1zHcScpOm1-rUG3W1aeIfEQ6Tj5NNnoDzxFO9e0tm0t5Lig5dKWLWYLOyMYx1Y0NXgc05bSrG-S0qSm3q71e-WaDreCbl2KC3YduIZmNtaCdB9hHSD_7WsGETNDL6M2hGpdCSDsfJ2R_2Gx8sahm7SNYHjcPnA7FPjneZ82Xd28_n39oLz69_3i-umhN37HaCqMJtEeOHGM2OMEdw2YURhLR9aSnhjG2hp5Y7Nayk1Y6vjakH4Rjzrn1QM-aNwfd7bKe7WigxqyD2mY_6_xTJe3V357oN2pKV4oOWLKOgMDLo0BO3xdbqpp9MTYEHW1aiiJCcipwL_4DhenB0LpBAPr8DnqZlhyhE0pKCgsgCAYIHyCTUynZuuuyCVb75VF3lwdCnt3-7nXAn20B4MURgPHr4LKOMJcbrhcUutcD1x64oid7U9w_E_8GXP3eYQ</recordid><startdate>20120401</startdate><enddate>20120401</enddate><creator>Jones, W Schuyler</creator><creator>Duscha, Brian D</creator><creator>Robbins, Jennifer L</creator><creator>Duggan, Natasha N</creator><creator>Regensteiner, Judith G</creator><creator>Kraus, William E</creator><creator>Hiatt, William R</creator><creator>Dokun, Ayotunde O</creator><creator>Annex, Brian H</creator><general>SAGE Publications</general><general>Arnold</general><general>Sage Publications Ltd</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7Z</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7QO</scope><scope>5PM</scope></search><sort><creationdate>20120401</creationdate><title>Alteration in angiogenic and anti-angiogenic forms of vascular endothelial growth factor-A in skeletal muscle of patients with intermittent claudication following exercise training</title><author>Jones, W Schuyler ; Duscha, Brian D ; Robbins, Jennifer L ; Duggan, Natasha N ; Regensteiner, Judith G ; Kraus, William E ; Hiatt, William R ; Dokun, Ayotunde O ; Annex, Brian H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-8ca18869d70046f87f40cd8c91825153c444b007e0fb929e9f7bc1568f4fffb63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Aged</topic><topic>Analysis of Variance</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>Blood and lymphatic vessels</topic><topic>Capillaries - physiopathology</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular system</topic><topic>Colorado</topic><topic>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Exercise Therapy</topic><topic>Exercise Tolerance</topic><topic>Female</topic><topic>Humans</topic><topic>Intermittent Claudication - etiology</topic><topic>Intermittent Claudication - metabolism</topic><topic>Intermittent Claudication - physiopathology</topic><topic>Intermittent Claudication - therapy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Muscle, Skeletal - blood supply</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Neovascularization, Physiologic</topic><topic>North Carolina</topic><topic>Peripheral Arterial Disease - complications</topic><topic>Peripheral Arterial Disease - metabolism</topic><topic>Peripheral Arterial Disease - physiopathology</topic><topic>Peripheral Arterial Disease - therapy</topic><topic>Pharmacology. Drug treatments</topic><topic>Recovery of Function</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>Vascular Endothelial Growth Factor A - metabolism</topic><topic>Vascular Endothelial Growth Factor Receptor-1 - metabolism</topic><topic>Vasodilator agents. 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At baseline, 22 PAD and 30 control subjects underwent gastrocnemius muscle biopsy. Twelve PAD patients were treated with supervised exercise training (SET) and underwent muscle biopsy after 3 weeks and 12 weeks of training and had sufficient tissue to measure VEGF-A, VEGF165b and VEGF-R1 concentrations in skeletal muscle lysates by ELISA. Muscle concentrations of VEGF-A and VEGF165b were similar in PAD patients versus controls at baseline. At both time points after the start of SET, VEGF-A levels decreased and there was a trend towards increased VEGF165b concentrations. At baseline, VEGF-R1 concentrations were lower in PAD patients when compared with controls but did not change after SET. Skeletal muscle concentrations of VEGF-A are not different in PAD patients when compared with controls at baseline. SET is associated with a significant reduction in VEGF-A levels and a trend towards increased VEGF165b levels. These somewhat unexpected findings suggest that further investigation into the mechanism of vascular responses to exercise training in PAD patients is warranted.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>22402934</pmid><doi>10.1177/1358863X11436334</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Analysis of Variance Biological and medical sciences Biopsy Blood and lymphatic vessels Capillaries - physiopathology Cardiology. Vascular system Cardiovascular system Colorado Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous Enzyme-Linked Immunosorbent Assay Exercise Therapy Exercise Tolerance Female Humans Intermittent Claudication - etiology Intermittent Claudication - metabolism Intermittent Claudication - physiopathology Intermittent Claudication - therapy Male Medical sciences Middle Aged Muscle, Skeletal - blood supply Muscle, Skeletal - metabolism Neovascularization, Physiologic North Carolina Peripheral Arterial Disease - complications Peripheral Arterial Disease - metabolism Peripheral Arterial Disease - physiopathology Peripheral Arterial Disease - therapy Pharmacology. Drug treatments Recovery of Function Time Factors Treatment Outcome Vascular Endothelial Growth Factor A - metabolism Vascular Endothelial Growth Factor Receptor-1 - metabolism Vasodilator agents. Cerebral vasodilators |
title | Alteration in angiogenic and anti-angiogenic forms of vascular endothelial growth factor-A in skeletal muscle of patients with intermittent claudication following exercise training |
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