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机构地区:[1]吉林大学第一医院呼吸内科,吉林长春130021 [2]吉林大学基础医学院病理生理教研室,吉林长春130021
出 处:《中国病理生理杂志》2008年第12期2402-2406,共5页Chinese Journal of Pathophysiology
基 金:吉林省科委自然科学基金资助项目(No.20030551-3)
摘 要:目的:通过失血性休克复合脂多糖(LPS)二次打击建立稳定的急性肺损伤模型并研究人参二醇组皂苷(PDS)的抗损伤作用。方法:40只成龄Wistar大鼠随机分为假手术组(S)、二次打击模型组(HL)、地塞米松(Dex)预治疗组(HLD)和人参二醇组皂苷预治疗组(HLP)。观察各组大鼠的平均动脉压(MABP)的变化及肺脏病理学改变,通过血清酶学检测分析各主要脏器功能变化,采用放射免疫分析法(RIA)测定了血清炎症介质TNF-α和IL-6水平。结果:失血性休克-LPS二次打击造成了大鼠MABP明显下降,血清酶学指标AST、ALT、ALP、LDH、CK水平升高,血清TNF-α和IL-6的含量增高;肺组织结构出现破坏,出现明显炎症反应。与HL比较,HLD及HLP二次打击1 h后MABP逐渐回升,血清酶学指标及TNF-α和IL-6含量明显降低,肺间质炎症明显减轻。结论:大鼠失血复合内毒素注射可成功建立稳定的急性肺损伤模型。与地塞米松作用相似,PDS可升高二次打击大鼠MABP,逆转血清酶水平变化并降低血清中TNF-α和IL-6含量,从而对抗失血及LPS导致的肺损伤。AIM: To establish the two- hit rat model with hemorrhage and lipopolysaccharide (LPS) and to study the effect of panaxadiol saponins (PDS) against acute lung injury. METHODS: Forty Wistar rats were divided randomly into 4 groups: sham operational group(S) ; two - hit groups with hemorrhagic shock - LPS (HL) ; dexamethasone pretreatment group (HLD) and PDS pretreatment group (HLP). The mean arterial blood pressure (MABP) was monitored dynamically by 4 - channel physiological meter RM - 6000, and pathological alteration of lung tissues was also observed. The leveLs of various serum enzymes, TNF-α and IL - 6 were detected. RESULTS : MABP decreased in two - hit rat model with hemorrhage - LPS. The serum levels of aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, lactate dehydrogenase, creatine kinase, TNF-α and IL- 6 increased significantly. Severe inflammatory change of pulmonary interstitium in HL group was also observed. CONCLUSION: Endotoxin injection following hemorrhage can be used to establish the animal model of acute lung injury. Similar with dexamethasone, PDS prevents lung tissue from serious- ly damage through increasing MABP and decreasing the level of serum enzymes, TNF-α and IL - 6 levels.
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