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作 者:周凤桐[1] 陶国才[2] 王松柏[3] 曹怀宇[3] 刘俊堂[3]
机构地区:[1]解放军251医院肝胆外科,张家口075000 [2]第三军医大学西南医院麻醉科,重庆400038 [3]解放军251医院麻醉科,张家口075000
出 处:《第三军医大学学报》2006年第15期1585-1587,共3页Journal of Third Military Medical University
摘 要:目的探讨Janus激酶/信号转导和转录激活子(janus kinase/signal transducer and activator of transcription,JAK/STAT)通路对严重腹腔感染肝、肺中干扰素-γ(interferon-,γIFN-γ)表达的调节作用。方法采用盲肠结扎穿孔(CLP)模型,大鼠分为CLP组、JAK激酶抑制剂(AG490)处理组和STAT抑制剂(RPM)处理组。采用RT-PCR技术和ELISA检测试剂盒检测肝、肺IFN-γmRNA表达水平和蛋白含量。结果与CLP 0时相点相比,CLP后各时相点IFN-γmRNA表达水平和蛋白含量不同程度升高(P<0.05,P<0.01)。经JAK和STATA抑制剂预处理后,与CLP组相应时相点相比,CLP后多个时相点IFN-γmRNA表达水平和蛋白含量显著下降(P<0.05,P<0.01)。结论腹腔脓毒症时肝、肺IFN-γ表达明显升高,抑制JAK/STAT通路的活化可下调肝、肺IFN-γ的表达,这可能是防止及治疗多器官功能衰竭的一个新的干预途径。Objective To determine the effect of janus kinase/signal transducer and activator of transcription (JAK/STAT) pathway on the expressions of interferon-γ (IFN-γ) in vital organs of rats with sepsis. Methods A sepsis model was induced by cecal ligation puncture (CLP) in 60 male Wistar rats, and randomly divided into CLP group ( n = 24), AG490 group in which inhibitor of JAK-AG490 at dose of 8 mg/kg was subcutaneously injected 30 min before CLP (n = 18), and rapamycin group in which inhibitor of STAT-rapamycin at dose of 0.4 mg/kg was subcutaneously injected 30 min before CLP (n = 18). On 2, 6, 24 h after CLP, all rats were sacrificed, then hepatic and pulmonary tissue samples were harvested to determine IFN-γmRNA expression levels by reverse transcription polymerase chain reaction (RT-PCR) and its protein expression levels by enzyme-linked immunosorbent assay (ELISA). Results As compared with normal rats without CLP, IFN-γ mRNA and protein levels in hepatic and pulmonary tissues at 2, 6, 24 h after CLP significantly elevated (P 〈 0.05, P 〈0.01 ). AG490 or rapamycin could markedly reduce IFN-γmRNA and protein expression levels at 2 or 6 h after CLP (P 〈0.05, P〈0.01 ). Conclusion Our data suggest that severe intra-abdominal infection can elevate IFN-γexpressions in vital organs, which might be involved in JAK/STAT pathway. Inhibiting the activation of JAK/STAT pathway can reduce IFN-γexpressions.
关 键 词:脓毒症 干扰素-Γ 信号转导 JAK/STAT通路
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