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机构地区:[1]天津医科大学第二医院感染性疾病研究所,300211 [2]天津医科大学总医院呼吸科
出 处:《天津医药》2016年第1期14-18,共5页Tianjin Medical Journal
基 金:国家自然科学基金资助项目(81270144,30800507,81170071)
摘 要:目的建立间歇低氧(IH)-肺气肿大鼠模型,探讨其引起炎症和免疫反应的特点。方法 60只Wistar大鼠随机分成对照组、肺气肿组、IH组和重叠组(肺气肿合并IH组)。每组15只。造模成功后使用流式细胞仪测定各组外周血中性粒细胞(PMN)、CD3^+CD8^+T细胞、CD3^+CD4^+T细胞凋亡率水平。酶联免疫吸附试验(ELISA)法测定血浆中肿瘤坏死因子(TNF)-α、白细胞介素(IL)-6水平。取大鼠肺泡灌洗液(BALF),在光镜下计算巨噬细胞、外周血PMN和淋巴细胞比例。采集肺、肝脏、胰腺组织和右颈动脉并进行病理评分。结果重叠组中PMN、CD3^+CD8^+T细胞凋亡率与其他3组相比较低,CD3^+CD4^+T细胞凋亡率、TNF-α、IL-6表达水平最高(均P<0.05)。BALF中,肺气肿组巨噬细胞和PMN百分比高于其余3组(均P<0.05)。重叠组中肺、肝脏、胰腺、右颈动脉内中膜厚度的病理评分高于其他3组(均P<0.05)。结论肺气肿合并IH可产生更严重的系统性多器官炎症和免疫反应。Objective To develop an "overlap syndrome (OS)" rat model by intermittent hypoxia (IH) exposure on the base of pre-existing emphysema, and to explore its characters of severe systemic inflammation and immune responses. Methods Sixty Wistar rats were put into four groups: control group, IH group, emphysema group and overlap (emphysema+ IH) group. The peripheral blood samples were collected for detecting apoptosis of CD3+CD4+, CD3+CD8+ T lymphocytes and ueutrophils (PMN). Tumor necrosis factor (TNF)-α and interleukin (IL)-6 were evaluated by ELISA. The bronehoalveolar la- vage fluid (BALF) was taken to calculate the ratio of macrophages, neutrophils and lymphocytes under light microscope. Tis- sue blocks of lung, liver, pancreas, and right carotid artery were taken for pathologic scoring. Results The apoptotie rates of PMN and CD3 + CD8 + T cells were significantly lower in overlap group than those of other three groups (P 〈 0.05). Pro-in- flammatory factor IL-6, TNF-α and peripheral blood CD3 + CD4 + T cell apoptosis were the highest in overlap group com- pared to those of other three groups (P 〈 0.05). The ratio of PMN and maerophages in BALF were significantly higher in em- physema group than those of other three groups (P 〈 0.05) and the pathology scores of lung, liver, pancreas, the ratio of carot- id artery intima-media thickness of whole thickness of vascular were significantly higher in overlap group than those of other three groups (P 〈 0.05).Conclusion In rat model of intermittent hypoxia-emphysema there are more serious systemic multi-organ inflammation and immune responses.
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