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作 者:陈天狮[1] 乔玉宏[1] 冀小玲[1] 马珂[1]
出 处:《山西职工医学院学报》2010年第4期1-3,共3页Journal of Shanxi Medical College for Continuing Education
摘 要:目的:通过研究地塞米松对大鼠肺泡巨噬细胞吞噬功能的影响,探讨地塞米松治疗急性肺损伤的作用机理。方法:健康雄性Wistar大鼠放血处死后全肺灌洗获取肺泡巨噬细胞(PAMs),贴壁纯化,在预培养20 h后重悬PAMs,分3组分别处理4 h。正常对照(C)组:不做任何干预;脂多糖(LPS)组:按10μg/mL的剂量加入LPS刺激;脂多糖加地塞米松(LPS+Dex)组:将含Dex终浓度1×10 mmol/L^1×6 mmol/L的RPMI 1640培养基加入LPS。收集PAMs,与1%鸡红细胞悬液培育后制片,瑞氏染色观察并计算吞噬率和吞噬指数,对两者做相关回归分析并采用单因素方差分析比较组间差异。结果:各组AM的吞噬率和吞噬指数呈线性相关性关系,从高到低依次为:C组(12.50±2.07)%,2.29±0.08;LPS+Dex组(8.25±1.67)%,1.73±0.18;LPS组(3.50±1.20)%,1.16±0.19;各组间的差异均具有统计学意义(P<0.05)。结论:LPS可抑制体外培养PAMs的吞噬活性;Dex对LPS抑制的PAMs吞噬活性有一定的活化作用。Objective: To investigate the mechanism of dexamethasone in treatment of acute lung injury by studying the effect of dexamethasone on phagocytic function of rat alveolar macrophages. Methods: After the healthy male Wistar rats were sacrificed to carry out whole lung lavage so as to take pulmonary alveolar macrophages and perform adherent purification, PAMs were resuspended after 20 h pre-culture and divided into 3 groups for intervention treatment for 4 hours respectively. The normal control(C) group was not interventioned. Lipopolysaccharide (LPS)group was stimulated by 10 μg/mL and LPS. LPS and Dex (LPS + Dex) group was treated by contained Dex final concentration 1 - 10 mmol/L - 1×6 mmol/L RPMI 1 640 medium and LPS. PAMs were collected and incubated with 1% chicken eryth-rocyte suspension to make slice. Wright's staining was implemented for calculating the ratio and index of phagocytosis. The two targets were treated with correlation-regression analysis and the disparity of 3 groups were compared with one- factor analysis of variance. Results: The phagocytic ratio and index of AM in each group showed linear correlation . The ratio and index of phagocytosis from descending order of the 3 groups were ( 12.50 ±2.07) % ,2.29±0.08 in group C, (8.25±1.67)% ,1.73±0.18 in group LPS and Dex and (3.50±1.20)% ,1.16±0.19 in group LPS respectively. There were statistically significant differences between the 3 groups (P 〈 0.05). Conclusion: LPS could inhibit the phagocytic activity of PAMs cuhured in vitro. Dex has some activation for the PAMs phagocytic activity inhibited by LPS.
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