摘要
目的:观察康莱特联合顺铂胸腔注入前后I型纤溶酶原激活物抑制剂(PAI-1)、转化生长因子β(TGF-β)、肿瘤坏死因子α(TNF-α)指标的变化,为明确其发生作用机制提供实验理论。方法:将患者随机分为联合用药组、康莱特组和顺铂组,在胸腔注药前及注药24、48h后取胸水标本,采用酶联免疫方法测定胸水中PAI-1、TGF-β和TNF-α的含量。结果:3组在注药24、48h后PAI-1、TGF-β、TNF-α含量均比治疗前升高,差别有统计学意义(P<0.05)。注药24h后PAI-1、TGF-β水平在3组间比较差别无统计学意义,而TNF-α在联合组要高于康莱特组和顺铂组,差别有统计学意义(P<0.05)。注药48h后PAI-1、TGF-β、TNF-α含量在联合组要高于康莱特组,差别有统计学意义(P<0.05)。结论:康莱特和顺铂联合用药后激活PAI-1、TGF-β、TNF-α等细胞因子,产生炎症反应并抑制纤溶活性,促进纤维蛋白生成和沉积并诱导胸膜粘连,其作用效果要优于单纯用康莱特或顺铂。
Objective: To detect the levels of plasminogen activator inhibitor-1 (PAI-1), transforming growth factor-β (TGF-β)and tumor necrosis factor-α (TNF-α) in the pleural fluid before and after intrapleural injection of Kanglaite combined with Cisplatin, and the mechanisms thereof. Methods: Patients were randomly divided into three groups, the Kanglaite combined with Cisplatin group (combination treatment group), Kangkaite group and Cisplatin group. The levels of PAI-1, TGF-β and TNF-α were determined by ELISA in pleural effusion 24 h and 48 h before and after intrapleural injection of medicine. Results: The levels of PAI-1, TGF-β and TNF-α were higher 24 h and 48 h after treatment compared with those of pre-treatment in three groups (P 〈 0.05). There were no statistical significances in levels of PAI-1 and TGF-β 24 h after injection medicine in three groups. But the level of TNF-α was higher in the combination treatment group than that in Kangkaite and Cisplatin groups(P 〈 0.05). After injection medicine 48 h, the levels of PAI-1, GF-β and TNF-α were higher in the combination treatment group than those in Kangkaite group (P 〈 0.05). Conclusion: The treatment of Kanglaite combined with Cisplatin activates PAI-1, TGF-β and TNF-α cytokines and causes inflammatory, suppresses fibrinolytic activity. These cytokines promote fibrin and induce pleural adhesion.
出处
《天津医药》
CAS
北大核心
2009年第7期538-540,共3页
Tianjin Medical Journal
基金
天津市教委科研课题(项目编号:20060316)
关键词
抗肿瘤药
顺铂
胸水
纤溶酶原激活物抑制物1
转化生长因子β
肿瘤坏死因子α
antineoplastic agents cisplatin hydrothorax plasminogen activator inhibitor 1 transforming growth factor beta tumor necrosis factor-alpha