Zhu Xin-yong, Fang Chi-hua, Zhang Li-yun, Zuo Da-ming, Chen Zheng-liang
Department of General Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou 510282, China.
Di Yi Jun Yi Da Xue Xue Bao. 2005 Jul;25(7):844-6.
To investigate the expression of endogenetic matrix metalloproteinases-9 (MMP-9) and transforming growth factor-beta(TGF-beta) and their role in the wound healing of blast injury.
Rat models of blast injury under a humid and hot environment were established and the effusion from the wound surface was collected at 4, 24, 48 h and 5, 7, 14, 21 and 28 days after injury, respectively. The contents of MMP-9 and TGF-beta in the effusion of the wound were measured by zymography and enzyme-linked immunosorbent assay (ELISA), respectively.
During the wound healing of blast injury, MMP-9 and TGF-beta exhibited changes that followed a regular pattern, both reaching the peak value at 48 h after the injury. TGF-beta content reached the another peak on day 7. TGF-beta value and MMP-9 contents decreased in the second week after injury and their reduction was no longer parallel. Administration of tissue inhibitor of metalloproteinase (TIMP) in the early phase of injury showed no obvious effect, but during the 2 weeks after the injury, its administration caused decrease in MMP-9 content and increase in TGF-beta content in the effusion.
In the early phase of wound healing, the elevation of MMP-9 and TGF-beta accelerated cell migration to promote the clearance of the inflammatory necrosis tissues, which might be one of the wound healing mechanisms. But overexpression of MMP-9 in the wound may hinder wound healing, and appropriate use of TIMP can accelerate the delayed wound healing.
探讨内源性基质金属蛋白酶-9(MMP-9)和转化生长因子-β(TGF-β)的表达及其在冲击伤创面愈合中的作用。
建立湿热环境下大鼠冲击伤模型,分别于伤后4、24、48 h及5、7、14、21和28 d收集创面渗出液。分别采用酶谱法和酶联免疫吸附测定(ELISA)法检测创面渗出液中MMP-9和TGF-β的含量。
冲击伤创面愈合过程中,MMP-9和TGF-β呈规律性变化,均于伤后48 h达峰值。TGF-β含量于伤后第7天出现另一个峰值。伤后第2周TGF-β值和MMP-9含量下降,且二者下降不再平行。伤后早期给予金属蛋白酶组织抑制剂(TIMP)无明显效果,但伤后2周内给予TIMP可使创面渗出液中MMP-9含量降低,TGF-β含量升高。
创面愈合早期,MMP-9和TGF-β升高可加速细胞迁移,促进炎性坏死组织清除,这可能是创面愈合机制之一。但创面MMP-9过表达可能阻碍创面愈合,适当使用TIMP可加速延迟愈合的创面愈合。