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机构地区:[1]咸宁学院附属第一医院内科,湖北咸宁437100
出 处:《咸宁学院学报(医学版)》2008年第5期373-375,共3页Journal of Xianning Univarsity(medical Sciences)
摘 要:目的探讨脂多糖(LPS)诱导急性肺损伤(ALI)大鼠肺组织磷酸化p38 MAPK表达的变化以及黄芪对其之影响。方法静脉注射LPS复制大鼠ALI模型。随机分成3组:正常对照组、ALI组和黄芪组。采用蛋白质印迹检测肺组织磷酸化p38 MAPK的表达,并观察大鼠动脉血氧分压(PaO2)、肺湿/干重比(W/D)、支气管肺泡灌洗液(BALF)白蛋白、血清TNF-α的变化以及肺组织病理学改变。结果LPS诱导大鼠ALI时肺组织磷酸化p38 MAPK的表达较正常对照组显著增加(P<0.01)。黄芪注射液可显著抑制大鼠肺组织磷酸化p38MAPK表达,降低W/D、BALF白蛋白以及血清TNF-α含量,使下降的PaO2回升,减轻肺组织病理学损伤。结论ALI时肺组织p38 MAPK磷酸化表达增加;黄芪注射液对内毒素性肺损伤有保护作用,其机制可能与抑制磷酸化p38 MAPK的表达有关。Objective To study the expression of p^38 protein kinase in LPS-induecd acute lung injury (ALI) and the intervention effect of astragalus. Methods LPS was injected intravenously to prepare ALI model. The rats were divided into three groups randomly: control group, LPS group and astragalus group. The expression of phospho-p^38 protein kinase was analyzed by western blot. Changes of Pa02, wet/dried lung weight( W/ D), albumin in BALF,TNF-α in serum and histopathology were observed. Results Resting rat lung expressed a little phospho-p^38; the expression of phospho-p^38 was up-regulated significantly in the lung after rats were injected with LPS ( P 〈 0.01). Compared with LPS group, astragalus significantly inhibited the expression of phospho-p^38, decreased PaO2, W/D, albumin in BALF and TNF-α in serum (P 〈0.01 ), and alleviated histropathologic damage alleviated. Conclusion The expression of phospho-p^38 is up-regulated in rat lung with LPS-induecd ALI. Astragalus injection has a protective effect on ALI and its therapeutic mechanism may be related to inhibition of the phosphorylation of p^38 MAPK.
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