世界中医药
文章摘要
引用本文:李言1,梁俊清2,张高峰1,李佳1,杨锡兰1,陈前芬1,赵士弟1.基于络病学探讨内毒素“二次打击”急性肺损伤大鼠的Rho/ROCK机制及川芎嗪的保护作用[J].世界中医药,2016,(01):.  
基于络病学探讨内毒素“二次打击”急性肺损伤大鼠的Rho/ROCK机制及川芎嗪的保护作用
A Modified Lipolysaccharide “Two hit” Induced Acute Lung Injury Model in Rats via Rho/ROCK Mechanism and Protective Effects of Tetramethylpyrazine on Injury Based on Collateral Disease Theory
投稿时间:2015-07-23  
DOI:10.3969/j.issn.1673-7202.2016.01.033
中文关键词:  络病学  内毒素血症  急性肺损伤  川芎嗪  Rho/ROCK
English Keywords:Collateral Disease Theory  Endotoxemia  Acute lung injury (ALI)  Tetramethylpyrazine (TMP)  Rho/ROCK
基金项目:国家自然科学基金项目(编号:81202833);安徽省自然科学基金项目(编号:1308085MH140)
作者单位
李言1,梁俊清2,张高峰1,李佳1,杨锡兰1,陈前芬1,赵士弟1 1 蚌埠医学院病理生理学教研室蚌埠233030 2 河北以岭医药研究院有限公司石家庄050035 
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中文摘要:
      目的:研究内毒素血症“瘀滞络脉”急性肺损伤大鼠的Rho/ROCK机制及川芎嗪的保护作用。方法:以内毒素“二次打击”建立大鼠内毒素血症“瘀滞络脉”急性肺损伤模型,分别设正常对照组、模型组、川芎嗪低剂量组、高剂量组,测定呼吸频率、肺泡灌洗液中性粒细胞(PMN)百分率、肺湿/干重比、肺组织髓过氧化物酶(Myeloperoxidase,MPO)活性、ROCK mRNA表达量,并观察、评估肺组织损伤严重程度。结果:与模型组相比,川芎嗪显著降低呼吸频率、PMN百分率、肺湿/干重比、MPO活性、ROCK mRNA表达量,减轻大鼠急性肺损伤病理改变。结论:川芎嗪可能通过抑制Rho/ROCK通路对内毒素血症“瘀滞络脉”大鼠急性肺损伤有较好的保护作用。
English Summary:
      To investigate the protective effect of tetramethylpyrazine (TMP) on acute lung injury (ALI) in endotoxemia rats with “Collaterals Damaged by Toxic Stasis” (YuZhiLuoMai) and its mechanism of Rho/ROCK. Methods:Endotoxemia rats model in ALI with YuZhiLuoMai were established through lipolysaccharide “two hit”. Rats were randomized into 4 groups: G1 (normal control group), G2 (“two hit” group), G3 (low dosage TMP group) and G4 (high dosage TMP group). Measure the respiratory rate, lung wet/dry weight ratio, BALF PMN percentage, pulmonary MPO activity, ROCK2 mRNA expression quantity, observe and evaluate the severity of lung tissue injury. Results:Compared with the G2 rats, TMP significantly reduced respiratory rate, PMN percentage and lung wet/dry weight ratio, MPO activity and ROCK mRNA expression quantity, and reduced the pathological changes in endotoxemia rats with ALI.Conclusion:We found TMP might have better protection against ALI in endotoxemia rats with YuZhiLuoMai through inhibiting RhoA/ROCK pathway.
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