机构地区:[1]解放军第二军医大学附属长海医院胸外科,上海市200433
出 处:《中国组织工程研究与临床康复》2008年第50期9862-9865,共4页Journal of Clinical Rehabilitative Tissue Engineering Research
摘 要:背景:肺缺血再灌注时,大量聚集在肺内的白细胞被激活,释放多种细胞因子如肿瘤坏死因子α、白细胞介素1β等,进而介导再灌注损伤。新近研究发现,转化生长因子β1对犬移植肺组织缺血再灌注损伤有保护作用。目的:观察转化生长因子β1干预后,肺缺血再灌注损伤肺组织肿瘤坏死因子α和白细胞介素1β的含量变化。设计、时间及地点:随机对照动物实验,于2007-08/10在解放军第二军医大学附属长海医院胸心外科实验室完成。材料:清洁级SD大鼠30只,随机分为假手术组、缺血再灌注组、转化生长因子β1组,10只/组。转化生长因子β1为PeprotechINC.公司产品。方法:缺血再灌注组与转化生长因子β1组大鼠通过结扎肺门阻断肺循环1h、再灌注2h建立原位肺缺血再灌注损伤模型,假手术组大鼠仅以10#丝线绕过肺门后不结扎。肺循环阻断前15min,各组颈静脉注射肝素抗凝,转化生长因子β1组同时注射10μg/kg转化生长因子β1。主要观察指标:再灌注2h后摘取左肺组织,光镜下观察肺组织形态变化,测定湿干重比及肺泡损伤指数,ELISA法检测肺组织匀浆中肿瘤坏死因子α和白细胞介素1β的含量。结果:30只大鼠均进入结果分析。假手术组肺组织无明显病理改变;缺血再灌注组可见明显的组织水肿及中性粒细胞浸润;转化生长因子β1组轻微组织水肿,少量中性粒细胞浸润。与假手术组比较,缺血再灌注组湿干重比及肺泡损伤指数均显著升高(P<0.01);与缺血再灌注组比较,转化生长因子β1组上述两项指标均明显降低(P<0.05)。与假手术组比较,缺血再灌注组肿瘤坏死因子α及白细胞介素1β含量均显著升高(P<0.01);与缺血再灌注组比较,转化生长因子β1组上述两项指标均明显降低(P<0.05,P<0.01)。结论:转化生长因子β1能够明显改善肺缺血再灌注损伤,该作用与其有效抑制肿瘤坏死因子α及白细胞介素1β的表BACKGROUND: When leucocytes were activated in the process of lung ischemia-reperfusion, various cell factors will be released, including tumor necrosis factor α (TNF-α ) and interleukin 1β (1L-Iβ ), which lead to ischemia-reperfusion injury. Recent research demonstrates that transforming growth factor- β 1 plays a protective role in ischemia-reperfusion injury after lung transplantation OBJECTIVE: To investigate the level changes of TNF-α and IL-1β after interfered with transforming growth factor- β 1 after lung ischemic-reperfusion injury DESIGN, TIME AND SETTING: The randomized controlled experiment of animal was performed in the Cardiothoracic Surgery Laboratory of Changhai Hospital, Second Military Medical University of Chinese PLA from August to October 2007. MATERIALS: Thirty Sprague-Dawley rats with clean grade, were randomly divided into the sham operation, ischemia-reperfusion and transforming growth factor β1 groups, with 10 animal in each group. The transforming growth factor β1 was phuchased from Peprotech INC. METHODS: The left lung of rat in the ischemia-reperfusion and transforming growth factor β1 groups was prepared for to ischemia-reperfusion model by blocking pulmonary circulation with hilar vessels ligation for 60 minutes, followed by reperfusion for 2 hours. Animals in the sham operation group were crossed hilar with 10# silk thread. Heparin was administered intravenously through vena cervicalis at 15 minutes before ischemia in each group. Concurrently, 10μg/kg transforming growth factor β1 was administered in transforming growth factor β1 group. MAIN OUTCOME MEASURES: After 2 hours of ischemia-reperfusion, the tissues of left lung were removed, histomorphological changes, wet-dry weight ratio, the index of histological lung injury and the content of TNF- α and IL-1β were determined by light microscope, enzyme-linked immunosorbent assay (ELISA), respectively. RESULTS: A total of 30 animals were enrolled in the result analysis. There was no obvious pat
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