基质金属蛋白酶
医学
静脉曲张
发病机制
血栓形成
免疫组织化学
病理
免疫印迹
静脉
大隐静脉
炎症
内科学
外科
化学
生物化学
基因
作者
Guoting Yu,Kun Li,Yongbo Xu,Haibo Chu,Hanxiang Zhan,Yuxu Zhong
出处
期刊:Phlebology
[SAGE Publishing]
日期:2021-09-08
卷期号:37 (1): 63-71
被引量:2
标识
DOI:10.1177/02683555211043332
摘要
Objectives Superficial venous thrombosis (SVT) is the complications of varicose great saphenous veins (VGSVs), but its pathogenesis remains unclear. This study was designed to measure the changes in expression of matrix metalloproteinases (MMPs) and the tissue inhibitor of metalloproteinases (TIMPs) from SVT, VGSVs, and great saphenous veins (GSVs). Methods In the venous walls of the three groups, the expression of MMP-2, MMP-9, TIMP-1, and TIMP-2 proteins, protein-positive expression ratios, mRNA expression, and protein expression were determined by immunohistochemistry, polymerase chain reaction, and western blot. Results The MMP-2, MMP-9, TIMP-1, and TIMP-2 protein-positive expression ratios, mRNA and protein expression in the SVT group were significantly higher than those in the VGSV and the GSV groups. The corresponding expression in the VGSV group were significantly higher than those in the GSV group. Conclusion Disequilibrium of MMPs and TIMPs in SVT wall occurs due to underlying high hydrostatic pressure and inflammation. These results suggested that MMPs and TIMPs participate in the process of venous wall remodeling.
科研通智能强力驱动
Strongly Powered by AbleSci AI