Li Yue-Jun, Cao Da-Yong, Chen Shao-Zong
Tangdu Hospital, Fourth Military Medical University, Xi'an 710038, China.
Zhonghua Zheng Xing Wai Ke Za Zhi. 2006 Jul;22(4):306-9.
To study the effect of vacuum-assisted closure (V.A.C) on the expression of Urokinase-type plasminogen activator (uPA) and Urokinase-type plasminogen activator receptor(uPAR) protein in margin tissue of pigs with acute wounds and patients with chronic wounds.
Acute wounds were created on the two side of five male pigs' back, the experiment wounds on one side received V. A. C treatment and the control side received traditional treatment. Punch biopsies were taken from margin tissue of the wounds in 0, 1, 3, 6, 9, 12, 18, 25 days after the V.A.C treatment. The uPA and uPAR positive cells were stained with immunohistochemical technique . Six human chronic wounds were also treated with the V. A. C treatment, and the samples of extravasate from those wounds were collected in 0, 1, 3, 5, 7 days after the treatment, and the levels of uPA and uPAR expression were examined by enzyme-linked immunosorbent assay (ELISA).
The expression of uPA and uPAR protein in margin tissues of pigs with acute wounds increased and peaked in 3 days after the treatment with V. A. C, then it presented rapidly downtrend, but the expression and staining in the experiment group were obviously higher than that of the control group. In the six chronic wounds, the high level expression of uPA and uPAR protein was decreased after the treatment with V. A. C.
The V. A. C may increase the expression of uPA and uPAR protein in acute wound keratinocytes and decrease the high expression of uPA and uPAR in chronic wounds.
研究封闭负压引流(V.A.C)对急性创伤猪及慢性创伤患者伤口边缘组织中尿激酶型纤溶酶原激活物(uPA)及尿激酶型纤溶酶原激活物受体(uPAR)蛋白表达的影响。
在5只雄性猪背部两侧制造急性伤口,一侧实验伤口采用V.A.C治疗,另一侧对照伤口采用传统治疗。在V.A.C治疗后0、1、3、6、9、12、18、25天从伤口边缘组织取打孔活检标本。采用免疫组化技术对uPA和uPAR阳性细胞进行染色。6例人类慢性伤口也采用V.A.C治疗,在治疗后0、1、3、5、7天收集这些伤口的渗出液样本,采用酶联免疫吸附测定(ELISA)检测uPA和uPAR表达水平。
急性创伤猪伤口边缘组织中uPA和uPAR蛋白表达在V.A.C治疗后升高,并在3天达到峰值,然后迅速下降,但实验组的表达和染色明显高于对照组。在6例慢性伤口中,V.A.C治疗后uPA和uPAR蛋白的高表达水平降低。
V.A.C可能增加急性伤口角质形成细胞中uPA和uPAR蛋白的表达,并降低慢性伤口中uPA和uPAR的高表达。