Extracorporeal shock wave treatment protects skin flaps against ischemia-reperfusion injury

被引:28
|
作者
Reichenberger, Matthias A. [1 ]
Heimer, Sina [1 ]
Schaefer, Amelia [1 ]
Lass, Ulrike [4 ]
Gebhard, Martha Maria [3 ]
Germann, Guenter [1 ]
Engel, Holger [1 ]
Koellensperger, Eva [1 ]
Leimer, Uwe [1 ]
Mueller, Wolf [2 ]
机构
[1] Univ Heidelberg Hosp, ETHIANUM Clin Plast & Reconstruct Surg Aesthet &, D-69115 Heidelberg, Germany
[2] Heidelberg Univ, Inst Pathol, Dept Neuropathol, D-6900 Heidelberg, Germany
[3] Heidelberg Univ, Dept Expt Surg, D-6900 Heidelberg, Germany
[4] German Canc Res Ctr, Clin Cooperat Unit Neuropathol, D-6900 Heidelberg, Germany
关键词
Shock wave treatment; Ischemia-reperfusion injury; Skin flap; ENDOTHELIAL GROWTH-FACTOR; NITRIC-OXIDE DONOR; ISCHEMIA/REPERFUSION INJURY; EXPRESSION; SURVIVAL; THERAPY; MECHANISMS; CHEMOKINES; NECROSIS;
D O I
10.1016/j.injury.2011.11.019
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Advances in the treatment of ischemia-reperfusion injury have created an opportunity for plastic surgeons to apply these treatments to flaps and implanted tissues. Using an extended inferior epigastric artery skin flap as a flap ischemia-reperfusion injury (IRI) model, we examined the capability of extracorporeal shock wave treatment (ESWT) to protect tissue against IRI in a rat flap model. Twenty-four rats were used and randomly divided into three groups (n = 8 for each group). Group I was the sham group and did not undergo ischemic insult; rather, the flap was raised and immediately sutured back (non-ischemic control group). Group II (ischemia control) and Group III (ESWT) underwent 3 h of ischemic insult. During reperfusion Group III was treated with ESWT and Group II was left untreated. Histological evaluation was made to investigate treatment induced tissue alterations. Survival areas were assessed at 5 d postoperatively. Skin flap survival and perfusion improved significantly in the ischemic animals following ESWT (p < 0.001, respectively). The tissue protecting effect of ESWT resulted in flap survival areas and perfusion data equal to non-ischemic, sham operated flaps. In line with the observation of better flap perfusion, tissue from ESWT-treated animals (Group III) revealed a significantly increased frequency of CD31-positive vessels compared to both the ischemic (Group II; p = 0.003) and the non-ischemic, sham operated control (Group I; p < 0.005) and an enhanced expression of pro-angiogenic genes. This was accompanied by a mild suppression of pro-inflammatory genes. Our study suggests that ESWT improves flap survival in IRI by promoting angiogenesis and inhibiting tissue inflammation. The study identifies ESWT as a low-cost and easy to use technique for surgical techniques that aim at reducing ischemia-reperfusion-induced tissue injury (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:374 / 380
页数:7
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