| 张航 韩敬泉 夏恩迪 崔键△ 曹守强 赵桂彬 张凯 刘成 张翔宇.低血压灌注对无心跳大鼠肺支气管肺泡灌洗液中不同白细胞及HMGB1 的影响[J].,2016,16(24):4636-4639 |
| 低血压灌注对无心跳大鼠肺支气管肺泡灌洗液中不同白细胞及HMGB1 的影响 |
| Impact of Hypotension Perfusion on Different Leukocytes in BronchoalveolarLavage From Non-Heart-Beating Rat Lung and HMGB1 |
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| DOI： |
| 中文关键词: 无心跳供体 白细胞 HMGB1 肺泡灌洗液 |
| 英文关键词: Non-Heart-Beating donor Leukocytes HMGB1 Bronchoalveolar Lavage |
| 基金项目:哈尔滨市科技局基金项目（RC2011XK004053）;
黑龙江省科技厅应用技术研究与开发计划项目（GA14C101） |
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| 中文摘要: |
| 目的：研究低血压灌注对无心跳大鼠肺支气管肺泡灌洗液中不同白细胞及HMGB1 的影响。方法：将32只180-200gSD 雄性
大鼠随机分成对照组[sham]、缺血30min 组[30I]、缺血60 min 组[60I]和缺血90 min 组[90I]（n=8），4 组大鼠分别接受麻醉后持续
机械通气，测定并统计各组支气管肺泡灌洗液中总白细胞计数及不同白细胞计数，免疫印迹法检测支气管肺泡灌洗液中HMGB1
蛋白的表达。结果：总白细胞、巨噬细胞、淋巴细胞计数及HMGB1 蛋白表达均随着低血压灌注时间的延长而逐渐增加，尤其在
[60I]和[90I]两组，灌洗液中巨噬细胞和淋巴细胞计数有显著增高，并且巨噬细胞和淋巴细胞与HMGB1 蛋白表达呈正相关。结论：
本研究证实HMGB1 蛋白表达和巨噬细胞，淋巴细胞计数在低血压灌注缺血期内升高，提示HMGB1 蛋白可能具有驱动炎症反应
的作用。 |
| 英文摘要: |
| Objective:Hypotension perfusion study on different leukocytes in bronchoalveolar lavage from non-heart-beating rat
lung and HMGB1.Methods:32 SD rats (180g-200 g) that were randomly assigned to four groups that are control group[sham], ischemia
group for 30, 60, 90 minutes (Groups [30I], [60I], [90I], n=8, respectively), which were continuous ventilating for 90min [sham] after
anesthesia in order to determine and calculate the total and various number of Leukocytes in each Bronchoalveolar Lavage with Western
blot method to detect the expression of HMGB1 protein in bronchoalveolar lavage.Results:This study confirmed that the total cells,
macrophages, lymphocytes, Leukocytes and HMGB1 numbers increased progressively with the rising of hypotension perfusion.
Especially, a significant rise in macrophages and lymphocytes was observed between[60I] and [90I]. A positive correlation was found in
the number of macrophages and the number of lymphocytes and HMGB1 Protein Level.Conclusion:This study demonstrates for the
first time that HMGB1 Protein Level and macrophages and lymphocytes increase significantly during hypotension perfusion ischemia.
Prompting HMGB1 protein may have driven the role of inflammation. |
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