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MODS大鼠外周血中PPARγ与TNF-α和IL-10动态变化的研究
引用本文:乔万海,屈莉,师猛,王立明.MODS大鼠外周血中PPARγ与TNF-α和IL-10动态变化的研究[J].第四军医大学学报,2009,30(8):690-693.
作者姓名:乔万海  屈莉  师猛  王立明
作者单位:西安交通大学第二附属医院急诊科,陕西,西安,710004  
摘    要:目的:探讨MODS大鼠外周血中过氧化物酶体增殖物激活受体γ(PPARγ)与TNF-α,IL-10动态变化的关系,并观察PPARγ能否调控炎症反应,即能否保持IL-10/TNF-α比值的稳定.方法:健康雄性SD大鼠96只,随机分为4组:①正常对照组;②LPS刺激组;③罗格列酮(ROSI)预处理组;④选择性拮抗剂2-氯-5-硝基苯胺(GW9662)预处理组.每组又分为1,3,5,7h组.免疫细胞化学结合图像分析检测外周血单个核细胞内PPARγ的表达,利用酶联免疫吸附剂测定法检测外周血中TNF-α及IL-10的水平.结果:①ROSI预处理组TNF-α各时间点的值较LPS刺激组低(P〈0.05).GW9662预处理组TNF-α各时间点的值较LPS刺激组高(P〈0.05).ROSI预处理组比同时相LPS刺激组IL-10的水平高(P〈0.05).GW9662预处理组与LPS刺激组IL-10的变化趋势基本相同,但5h及7h组IL-10的水平比同时相的LPS刺激组低(P〈0.05).②相关分析表明,外周血单个核细胞内PPARγ和TNF-α在ROSI预处理组、GW9662预处理组呈显著负相关ROSI预处理组(r=-0.635,P〈0.05);GW9662预处理组(r=-0.725,P〈0.05)].外周血单个核细胞内PPARγ和IL-10在ROSI预处理组、GW9662预处理组呈显著正相关ROSI预处理组(r=0.605,P〈0.05);GW9662预处理组(r=0.645,P〈0.05)].③ROSI预处理组IL-10/TNF-α值与同时相正常对照组相比无显著差异.GW9662预处理组IL-10/TNF-α值明显降低,与同时相LPS刺激组相比有显著差异(P〈0.05).结论:PPARγ可降低MODS大鼠外周血中TNF-α的水平,PPARγ升高MODS大鼠外周血中IL-10的水平,PPARγ对MODS大鼠有保护作用.

关 键 词:多器官功能衰竭  PPARγ  肿瘤坏死因子α  白细胞介素10

Relationship of dynamic changes between PPARγ and TNF-α and IL-10 in peripheral blood of MODS rats
QIAO Wan-Hai,QU Li,SHI Meng,WANG Li-Ming.Relationship of dynamic changes between PPARγ and TNF-α and IL-10 in peripheral blood of MODS rats[J].Journal of the Fourth Military Medical University,2009,30(8):690-693.
Authors:QIAO Wan-Hai  QU Li  SHI Meng  WANG Li-Ming
Institution:QIAO Wan-Hai,QU Li,SHI Meng,WANG Li-Ming Department of Emergency Medicine,Second Affiliated Hospital,Xi'an Jiaotong University,Xi'an 710004,China
Abstract:AIM:To investigate the relationship of dynamic changes between peroxisome proliferator-activated receptor γ (PPARγ) and TNF-α and IL-10 in peripheral blood of multiple organ dysfunction syndrome (MODS) rats. METHODS:Ninety-six male SD rats were divided randomly into 4 groups:Normal control group,endotoxin (LPS) group,rosiglitazone (ROSI) pretreatment group and PPARγ antagonist GW9662 pretreatment group. Each group was further divided into 4 groups according to different observation time point respectively of 1,3,5 and 7 h. Immunocytochemical detection and image analysis were used to detect the PPARγ expression in peripheral blood mononuclear cells. Levels of TNF-α and IL-10 were detected by enzyme-linked immunosorbent assay. RESULTS:The levels of PPARγ in each time-related subgroups in ROIS pretreatment group were all higher than those in LPS group (P〈0.05). The level of PPARγ was positively correlated to TNF-α (r=-0.635,P〈0.05) and negatively correlated to IL-10 (r=0.605,P〈0.05). The levels of PPARγ in each time-related subgroups of GW9662 pretreatment group were higher (P〈0.05) than those in LPS group. The level of PPARγ was negatively correlated to TNF-α (r=-0.725,P〈0.05)and positively correlated to IL-10 (r=0.645,P〈0.05). The ratio of IL-10/TNF-α in ROSI pretreatment group showed no significant difference (P〉0.05) compared with that in normal control group. In GW9662 pretreatment group,the ratio of IL-10/TNF-α was significantly reduced compared with that in LPS group (P〈0.05). CONCLUSION:PPARγ exerts some protective effect on MODS rats by the immune adjustment of anti-inflammatory/pro-inflammatory mechanism.
Keywords:multiple organ failure  PPAR garnma  tumornecrosis factor-alpha  interleukin-10  
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