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作 者:陈乾坤[1] 姜格宁[1] 丁嘉安[1] 谢博雄[1] 陈晓峰[1]
机构地区:[1]同济大学附属上海市肺科医院胸外科,200433
出 处:《中华器官移植杂志》2008年第8期464-467,共4页Chinese Journal of Organ Transplantation
摘 要:目的探讨早期生长反应因子-1(EGR-1)在移植肺缺血再灌注过程中的炎症损伤作用。方法选择SD大鼠作为供、受者,建立左肺移植模型。实验分为4组:再灌注1h组、再灌注2h组和再灌注4h组,移植后对移植肺分别进行1、2和4h的再灌注;选取未进行移植和再灌注的供肺作为对照组。采用荧光定量实时聚合酶链法检测各组肺组织中EGR-1和白细胞介素(IL)-1βmRNA的相对表达量,并检测支气管肺泡灌洗液(BAL)中性粒细胞数、肺组织湿/干质量比(W/D)及髓过氧化物酶(MPO)活性等指标。结果各再灌注组EGR-1和IL-1βmRNA的相对表达量均高于对照组,并且随着再灌注时间的延长而明显增高.4组间比较,差异均有统计学意义(P〈0.05)。各组肺组织W/D、BAL中性粒细胞数以及MPO活性也均高于对照组,并且随着再灌注时间的延长而显著增高,4组间比较,差异均有统计学意义(P〈0.05),各组EGR-1mRNA与IL-1βmRNA的表达呈显著的正相关(r=0.921,P〈0.01)。各组EGR-1mRNA的表达与BAL中性粒细胞数呈显著的正相关(r=0.876,P〈0.01)。结论EGR-1由肺缺血诱导产生和表达;在肺缺血再灌注过程中,通过IL-1β的参与,EGR-1发挥重要的炎症损伤作用。Objective To investigate the inflammatory injury role of early growth response factor (EGR-1) in lung ischemia-reperfusion injury in rat lung transplant model. Methods Rat left lung transplant models were used in our study, and divided into following groups: 1 h after reperfusion, 2 h after reperfusion and 4 h after reperfusion. The nomal lung tissure served as a control group. Quantitative real-time RT-PCR was used to detect the expression of EGR-1 and IL-1β mRNA in lung tissures. Myeloperoxidase (MPO) activity, bronchoalveolar lavage (BAL) neutrophil count and the wetto-dry (W/D) lung weight ratio were recorded in every group. Results The expression of EGR-1 and IL-1β mRNA was obviously increased in groups of 1 h, 2 h and 4 h after reperfusion, and significantly higher than in nomal control group (P〈0.05). The values of MPO activity, BAL neutrophil count and the W/D lung weight ratio were increased obviously in groups of 1 h, 2 h and 4 h after reperfusion as compared with those in the normal control group and there was significant difference between these 4 groups (P〈0. 05). The expression of EGR-1 mRNA was significantly correlated with the IL-1β mRNA expression in every group (r= 0. 921, P〈0. 01 ). The EGR-1 mRNA expression had a strong correlation with BAL neutrophil count (r = 0. 876, P〈0. 01). Conclusion EGR-1 is induced by lung tissure ischemia, and may play an important role in the inflammatory injury mediated by IL-1β in lung ischemia-reperfusion injury in the rat lung transplant model.
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