A noninvasive murine model of hind limb ischemia-reperfusion injury

被引:59
作者
Bonheur, JA
Albadawi, H
Patton, GM
Watkins, MT
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Surg, Boston, MA 02114 USA
[2] VA Boston Healthcare Syst, Dept Surg, Boston, MA 02114 USA
[3] Boston Univ, Sch Med, Dept Surg, Boston, MA 02114 USA
关键词
ischemia; reperfusion; laser Doppler imager; myeloperoxidase; controlled tension tourniquet;
D O I
10.1016/S0022-4804(03)00232-4
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. This study describes a novel murine method of the Controlled Tension Tourniquet (CTT). The CTT applies a measured circumferential tension to hind limbs using a tourniquet attached to digital strain gauges, and is useful for investigating hind limb ischemia reperfusion (IR). Materials and methods. Mice were subjected to 1, 3, or 6 h of unilateral hind limb ischemia followed by either 4 or 24 h of reperfusion. Blood flow in the ischemic, reperfused, and contralateral limbs was monitored using a Laser Doppler Imager. Edema in the IR limbs was documented by changes in the wet weight to dry weight ratio. Myeloperoxidase and tetrazolium based mitochondrial activity assays indicated neutrophil infiltration and tissue viability, respectively. Results. During reperfusion following 1, 4, or 6 h, flow stabilized at 100%, 53%, and 23% of baseline levels, respectively. Edema was present all in IR limbs after 4 h of reperfusion, but increased with the duration of ischemia. After 24 h of reperfusion neutrophil infiltration was equivalent in all IR limbs after all intervals of ischemia. After 24 h of reperfusion, tissue viability after 1 h of ischemia was equivalent to sham or contralateral limbs. At 3 or 6 h of ischemia and 24 h reperfusion decreased tissue viability to 40% of sham and contralateral limbs. Conclusions. The CTT provides a reproducible, non-invasive model of acute limb ischemia, which reflects the biochemical indices of microvascular injury, inflammation and flow characteristic of reperfusion injury. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:55 / 63
页数:9
相关论文
共 28 条
[1]  
AMES A, 1968, AM J PATHOL, V52, P437
[2]   ILOPROST INFUSION DECREASES SKELETAL-MUSCLE ISCHEMIA-REPERFUSION INJURY [J].
BELKIN, M ;
WRIGHT, JG ;
HOBSON, RW .
JOURNAL OF VASCULAR SURGERY, 1990, 11 (01) :77-83
[3]   A NEW QUANTITATIVE SPECTROPHOTOMETRIC ASSAY OF ISCHEMIA-REPERFUSION INJURY IN SKELETAL-MUSCLE [J].
BELKIN, M ;
BROWN, RD ;
WRIGHT, JG ;
LAMORTE, WW ;
HOBSON, RW .
AMERICAN JOURNAL OF SURGERY, 1988, 156 (02) :83-86
[4]   INTRAARTERIAL UROKINASE INCREASES SKELETAL-MUSCLE VIABILITY AFTER ACUTE-ISCHEMIA [J].
BELKIN, M ;
VALERI, CR ;
HOBSON, RW .
JOURNAL OF VASCULAR SURGERY, 1989, 9 (01) :161-168
[5]   The pathophysiology of skeletal muscle ischemia and the reperfusion syndrome: a review [J].
Blaisdell, FW .
CARDIOVASCULAR SURGERY, 2002, 10 (06) :620-630
[6]   ILOPROST ATTENUATES THE INCREASED PERMEABILITY IN SKELETAL-MUSCLE AFTER ISCHEMIA AND REPERFUSION [J].
BLEBEA, J ;
CAMBRIA, RA ;
DEFOUW, D ;
FEINBERG, RN ;
HOBSON, RW ;
DURAN, WN .
JOURNAL OF VASCULAR SURGERY, 1990, 12 (06) :657-666
[7]  
Couffinhal T, 1998, AM J PATHOL, V152, P1667
[8]   Systemic inflammation induced by lipopolysaccharide increases neointimal formation after balloon and stent injury in rabbits [J].
Danenberg, HD ;
Welt, FGP ;
Walker, M ;
Seifert, P ;
Toegel, GS ;
Edelman, ER .
CIRCULATION, 2002, 105 (24) :2917-2922
[9]   NEUTROPHIL (PMN) PHAGOCYTOSIS AND CHEMOTAXIS AFTER 2 HR OF ISCHEMIA [J].
FREISCHLAG, JA ;
HANNA, D .
JOURNAL OF SURGICAL RESEARCH, 1991, 50 (06) :648-652
[10]   Attenuation of skeletal muscle ischemia/reperfusion injury by inhibition of tumor necrosis factor [J].
Gaines, GC ;
Welborn, MB ;
Moldawer, LL ;
Huber, TS ;
Harward, TRS ;
Seeger, JM .
JOURNAL OF VASCULAR SURGERY, 1999, 29 (02) :370-376