Modulation of collateral artery growth in a porcine hindlimb ligation model using MCP-1
For an appropriate extrapolation to patients with peripheral arterial obstructive disease, we tested the efficacy of monocyte chemoattractant protein 1 (MCP-1) treatment in a porcine hindlimb ligation model. In 40 minipigs, a femoral artery ligation was performed. Control animals were examined immed...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 2003-04, Vol.53 (4), p.1422-1428 |
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container_title | American journal of physiology. Heart and circulatory physiology |
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creator | VOSKUIL, Michiel VAN ROYEN, Niels HOEFER, Imo E SEIDLER, Randolph GUTH, Brian D BODE, Christoph SCHAPER, Wolfgang PIEK, Jan J BUSCHMANN, Ivo R |
description | For an appropriate extrapolation to patients with peripheral arterial obstructive disease, we tested the efficacy of monocyte chemoattractant protein 1 (MCP-1) treatment in a porcine hindlimb ligation model. In 40 minipigs, a femoral artery ligation was performed. Control animals were examined immediately after ligation (n = 4) or after 2 wk of intra-arterial infusion of PBS (n = 11). A second group of animals was evaluated after intra-arterial infusion of 2.0 mu g/h of MCP-1 for 48 h (followed by 12 days of PBS; n = 13) or 2 wk continuously (n = 12). In the terminal experiment after 2 wk, resting flow to the leg and peripheral arterial pressures were assessed without vasodilatation. Subsequently, vascular conductance was determined by using a pump-driven extracorporal circulation during maximal vasodilatation. The results showed that resting blood flow to the hindlimb was 53% of the normal after 2 wk of infusion of PBS, compared with 81% in both MCP-1 treatment groups (P < 0.05). Collateral conductance was 645 +/- 346 ml x min-1 x mmHg-1 after 2 wk of infusion with PBS, compared with 1,070 +/- 530 and 1,158 +/- 535 ml x min-1 x mmHg-1 after 48 h and 2 wk treatment with MCP-1, respectively (P < 0.05). Modulation of the process of arteriogenesis is feasible in this large animal model via intra-arterial infusion of the Cys-Cys-chemokine MCP-1. [PUBLICATION ABSTRACT] |
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In 40 minipigs, a femoral artery ligation was performed. Control animals were examined immediately after ligation (n = 4) or after 2 wk of intra-arterial infusion of PBS (n = 11). A second group of animals was evaluated after intra-arterial infusion of 2.0 mu g/h of MCP-1 for 48 h (followed by 12 days of PBS; n = 13) or 2 wk continuously (n = 12). In the terminal experiment after 2 wk, resting flow to the leg and peripheral arterial pressures were assessed without vasodilatation. Subsequently, vascular conductance was determined by using a pump-driven extracorporal circulation during maximal vasodilatation. The results showed that resting blood flow to the hindlimb was 53% of the normal after 2 wk of infusion of PBS, compared with 81% in both MCP-1 treatment groups (P < 0.05). Collateral conductance was 645 +/- 346 ml x min-1 x mmHg-1 after 2 wk of infusion with PBS, compared with 1,070 +/- 530 and 1,158 +/- 535 ml x min-1 x mmHg-1 after 48 h and 2 wk treatment with MCP-1, respectively (P < 0.05). Modulation of the process of arteriogenesis is feasible in this large animal model via intra-arterial infusion of the Cys-Cys-chemokine MCP-1. [PUBLICATION ABSTRACT]</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>Bethesda, MD: American Physiological Society</publisher><subject>Biological and medical sciences ; Blood vessels ; Cardiovascular system ; Circulatory system ; Hogs ; Medical research ; Medical sciences ; Miscellaneous ; Pharmacology. Drug treatments</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2003-04, Vol.53 (4), p.1422-1428</ispartof><rights>2003 INIST-CNRS</rights><rights>Copyright American Physiological Society Apr 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14646341$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>VOSKUIL, Michiel</creatorcontrib><creatorcontrib>VAN ROYEN, Niels</creatorcontrib><creatorcontrib>HOEFER, Imo E</creatorcontrib><creatorcontrib>SEIDLER, Randolph</creatorcontrib><creatorcontrib>GUTH, Brian D</creatorcontrib><creatorcontrib>BODE, Christoph</creatorcontrib><creatorcontrib>SCHAPER, Wolfgang</creatorcontrib><creatorcontrib>PIEK, Jan J</creatorcontrib><creatorcontrib>BUSCHMANN, Ivo R</creatorcontrib><title>Modulation of collateral artery growth in a porcine hindlimb ligation model using MCP-1</title><title>American journal of physiology. Heart and circulatory physiology</title><description>For an appropriate extrapolation to patients with peripheral arterial obstructive disease, we tested the efficacy of monocyte chemoattractant protein 1 (MCP-1) treatment in a porcine hindlimb ligation model. In 40 minipigs, a femoral artery ligation was performed. Control animals were examined immediately after ligation (n = 4) or after 2 wk of intra-arterial infusion of PBS (n = 11). A second group of animals was evaluated after intra-arterial infusion of 2.0 mu g/h of MCP-1 for 48 h (followed by 12 days of PBS; n = 13) or 2 wk continuously (n = 12). In the terminal experiment after 2 wk, resting flow to the leg and peripheral arterial pressures were assessed without vasodilatation. Subsequently, vascular conductance was determined by using a pump-driven extracorporal circulation during maximal vasodilatation. The results showed that resting blood flow to the hindlimb was 53% of the normal after 2 wk of infusion of PBS, compared with 81% in both MCP-1 treatment groups (P < 0.05). Collateral conductance was 645 +/- 346 ml x min-1 x mmHg-1 after 2 wk of infusion with PBS, compared with 1,070 +/- 530 and 1,158 +/- 535 ml x min-1 x mmHg-1 after 48 h and 2 wk treatment with MCP-1, respectively (P < 0.05). Modulation of the process of arteriogenesis is feasible in this large animal model via intra-arterial infusion of the Cys-Cys-chemokine MCP-1. [PUBLICATION ABSTRACT]</description><subject>Biological and medical sciences</subject><subject>Blood vessels</subject><subject>Cardiovascular system</subject><subject>Circulatory system</subject><subject>Hogs</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Miscellaneous</subject><subject>Pharmacology. 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Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>VOSKUIL, Michiel</creatorcontrib><creatorcontrib>VAN ROYEN, Niels</creatorcontrib><creatorcontrib>HOEFER, Imo E</creatorcontrib><creatorcontrib>SEIDLER, Randolph</creatorcontrib><creatorcontrib>GUTH, Brian D</creatorcontrib><creatorcontrib>BODE, Christoph</creatorcontrib><creatorcontrib>SCHAPER, Wolfgang</creatorcontrib><creatorcontrib>PIEK, Jan J</creatorcontrib><creatorcontrib>BUSCHMANN, Ivo R</creatorcontrib><collection>Pascal-Francis</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><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>VOSKUIL, Michiel</au><au>VAN ROYEN, Niels</au><au>HOEFER, Imo E</au><au>SEIDLER, Randolph</au><au>GUTH, Brian D</au><au>BODE, Christoph</au><au>SCHAPER, Wolfgang</au><au>PIEK, Jan J</au><au>BUSCHMANN, Ivo R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulation of collateral artery growth in a porcine hindlimb ligation model using MCP-1</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><date>2003-04-01</date><risdate>2003</risdate><volume>53</volume><issue>4</issue><spage>1422</spage><epage>1428</epage><pages>1422-1428</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>For an appropriate extrapolation to patients with peripheral arterial obstructive disease, we tested the efficacy of monocyte chemoattractant protein 1 (MCP-1) treatment in a porcine hindlimb ligation model. In 40 minipigs, a femoral artery ligation was performed. Control animals were examined immediately after ligation (n = 4) or after 2 wk of intra-arterial infusion of PBS (n = 11). A second group of animals was evaluated after intra-arterial infusion of 2.0 mu g/h of MCP-1 for 48 h (followed by 12 days of PBS; n = 13) or 2 wk continuously (n = 12). In the terminal experiment after 2 wk, resting flow to the leg and peripheral arterial pressures were assessed without vasodilatation. Subsequently, vascular conductance was determined by using a pump-driven extracorporal circulation during maximal vasodilatation. The results showed that resting blood flow to the hindlimb was 53% of the normal after 2 wk of infusion of PBS, compared with 81% in both MCP-1 treatment groups (P < 0.05). Collateral conductance was 645 +/- 346 ml x min-1 x mmHg-1 after 2 wk of infusion with PBS, compared with 1,070 +/- 530 and 1,158 +/- 535 ml x min-1 x mmHg-1 after 48 h and 2 wk treatment with MCP-1, respectively (P < 0.05). Modulation of the process of arteriogenesis is feasible in this large animal model via intra-arterial infusion of the Cys-Cys-chemokine MCP-1. [PUBLICATION ABSTRACT]</abstract><cop>Bethesda, MD</cop><pub>American Physiological Society</pub><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Blood vessels Cardiovascular system Circulatory system Hogs Medical research Medical sciences Miscellaneous Pharmacology. Drug treatments |
title | Modulation of collateral artery growth in a porcine hindlimb ligation model using MCP-1 |
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