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
Hauptverfasser: VOSKUIL, Michiel, VAN ROYEN, Niels, HOEFER, Imo E, SEIDLER, Randolph, GUTH, Brian D, BODE, Christoph, SCHAPER, Wolfgang, PIEK, Jan J, BUSCHMANN, Ivo R
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container_issue 4
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container_title American journal of physiology. Heart and circulatory physiology
container_volume 53
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 &lt; 0.05). 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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 &lt; 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 &lt; 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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source American Physiological Society; EZB-FREE-00999 freely available EZB journals
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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