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Lipocalin-2 Test in Distinguishing Acute Lung Injury Cases from Septic Mice Without Acute Lung Injury

机译:Lipocalin-2试验用于区分无急性肺损伤的败血症小鼠的急性肺损伤

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Objective To explore whether the amount of lipocalin-2 in the biofluid could reflect the onset of sepsis-induced acute lung injury (ALI) in mice. Methods Lipopolysaccharide (LPS, 10 mg/kg) injection or cecal ligation and puncture (CLP) was performed to induce severe sepsis and ALI in C57 BL/6 male mice randomly divided into 5 groups (n=10 in each group):group A (intraperitoneal LPS injection), group B (intravenous LPS injection via tail vein), group C (CLP with 25%of the cecum ligated), group D (CLP with 75%of the cecum ligated), and the control group (6 sham-operation controls plus 4 saline controls). All the mice received volume resuscitation. Measurements of pulmonary morphological and functional alterations were used to identify the presence of experimental ALI. The expressions of lipocalin-2 and interleukin (IL)-6 in serum, bronchoalveolar lavage fluid (BALF), and lung tissue were quantified at both protein and mRNA levels. The overall abilities of lipocalin-2 and IL-6 tests to diagnose sepsis-induced ALI were evaluated by generating receiver operator characteristic curves (ROC) and computing area under curve (AUC). Results In both group B and group D, most of the“main features”of experimental ALI were reproduced in mice, while group A and group C showed septic syndrome without definite evidence for the presence of ALI. Compared with septic mice without ALI (group A+group C), lipocalin-2 protein expression in septic mice with ALI (group B+group D) was significantly up-regulated in BALF (P<0.01) and in serum (P<0.01), and mRNA expression boosted in lung tissues (all P<0.05). Lipocalin-2 tests performed better than IL-6 tests in recognizing sepsis-induced ALI cases, evidenced by the larger AUC of the former (BALF tests, 0.8800 versus 0.6625;serum tests, 0.8500 versus 0.7000). Using a dual cutoff system to diagnose sepsis-induced ALI, BALF lipocalin-2 test exhibited the highest positive likelihood ratio (13.000) and the lowest negative likelihood ratio (0.077) among the tests of lipocalin-2 and IL-6 in blood and BALF. A statistically significant correlation was found between lipocalin-2 concentration in BALF and that in serum (Spearman r=0.8803, P<0.0001). Conclusions Lipocalin-2 expression is significantly up-regulated in septic ALI mice compared with those without ALI. Lipocalin-2 tests with a dual cutoff system could be an effective tool in distinguishing experimental ALI cases.
机译:目的探讨生物流体中lipocalin-2的含量是否能反映败血症诱发的小鼠急性肺损伤(ALI)的发作。 方法脂多糖(LPS,10 mg / kg)注射或盲肠结扎穿刺(CLP)诱导C57 BL / 6雄性小鼠随机分为5组(每组n = 10)引起严重脓毒症和ALI。 :A组(腹膜内LPS注射),B组(经尾静脉静脉内LPS注射),C组(CLP结扎盲肠25%),D组(CLP结扎盲肠75%)和对照组(6个假手术控件和4个盐水控件)。所有小鼠均接受了体积复苏。肺形态和功能改变的测量被用于鉴定实验性ALI的存在。在蛋白质和mRNA水平上定量定量血清,支气管肺泡灌洗液(BALF)和肺组织中lipocalin-2和白介素(IL)-6的表达。通过生成接收者操作者特征曲线(ROC)和计算曲线下面积(AUC)来评估lipocalin-2和IL-6测试诊断败血症诱导的ALI的整体能力。 结果在B组和D组中,实验性ALI的大多数“主要特征”均在小鼠中复制,而A组和C组显示败血症综合征,而没有确切证据表明存在ALI。与没有ALI的脓毒症小鼠(A + C组)相比,有ALI的脓毒症小鼠(B + D组)的lipocalin-2蛋白表达在BALF和血清中显着上调(P <0.01)。 ),并在肺组织中增强mRNA表达(所有P <0.05)。在识别败血症诱导的ALI病例中,Lipocalin-2测试的表现优于IL-6测试,前者的AUC较大(BALF测试,0.8800对0.6625;血清测试,0.8500对0.7000)证明了这一点。使用双截止系统诊断败血症诱导的ALI,在血液和BALF中lipocalin-2和IL-6的测试中,BALF lipocalin-2测试表现出最高的阳性似然比(13.000)和最低的阴性似然比(0.077)。 。在BALF和血清中Calcal-2的浓度之间存在统计学意义的相关性(Spearman r = 0.8803,P <0.0001)。 结论与没有ALI的小鼠相比,脓毒症ALI小鼠的Lipocalin-2表达明显上调。具有双截止系统的Lipocalin-2测试可能是区分实验性ALI病例的有效工具。

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  • 来源
    《中国医学科学杂志(英文版)》 |2014年第2期|65-77|共13页
  • 作者单位

    Department of Emergency, Chinese Academy of Medical Sciences&Peking Union Medical College, Beijing 100730, China;

    Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences&Peking Union Medical College, Beijing 100730, China;

    Department of Emergency, Chinese Academy of Medical Sciences&Peking Union Medical College, Beijing 100730, China;

    Department of Emergency, Chinese Academy of Medical Sciences&Peking Union Medical College, Beijing 100730, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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