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作 者:董春玲[1] 鲁继荣[2] 王桂芳[1] 李波[1] 肖奎[1] 陈智鸿[1] 白春学[1]
机构地区:[1]复旦大学附属中山医院呼吸内科,上海200032 [2]吉林大学第一医院儿科,长春130021
出 处:《第二军医大学学报》2008年第2期126-130,共5页Academic Journal of Second Military Medical University
基 金:国家自然科学基金(30370611);上海市重点学科建设项目(B115)~~
摘 要:目的:探讨支气管哮喘(哮喘)小鼠肺组织中水通道蛋白5(aquaporin 5,AQP5)和黏蛋白5AC(MUC5AC)的变化及地塞米松对其的调节作用。方法:雌性C57BL/6小鼠48只,随机分为对照组、哮喘组和地塞米松干预组,每组16只。测定各组小鼠肺组织病理变化及湿/干质量比值,应用实时定量PCR法测定其肺组织中AQP5和MUC5AC mRNA的表达,应用免疫组化法测定各组AQP5蛋白在肺组织中的分布,免疫印迹法测定AQP5蛋白在肺组织中的表达。ELISA法测定各组支气管肺泡灌洗液中MUC5AC的含量。结果:哮喘组小鼠肺组织中AQP5表达较对照组明显降低[mRNA减少(42.5±3.6)%,蛋白质减少(64.3±8.2)%]。而MUC5AC表达显著升高[mRNA升高(93.3±8.1)%;蛋白质水平升高(98.3±7.2)%]。地塞米松分别负调节其表达(与模型组比较P<0.05)。结论:哮喘小鼠肺组织中AQP5表达明显降低可能与气道MUC5AC表达的升高有关,地塞米松对其显著负调节从而改善气道黏液高分泌、炎性浸润和肺水渗出的病理生理过程。Objective:To investigate the expression of aquaporin 5 (AQPS) and MUCSAC in lung of bronchial asthmatic murine model and the regulatory effect of dexamethasone on the expression. Methods.. Forty-eight female C57BL/6 mice were evenly randomized into control group, asthma group and dexamethasone group. The pathological changes of the lungs and the wet/dry weight ratios of the lungs were determined in mice of each group. The expression of AQP5 and MUCSAC mRNA in the lung was determined by real-time poly-merase chain reaction (real-time PCR); the AQP5 protein was examined by Western blotting assay; the distribution of AQP5 protein in the pulmonary tissue was studied immunohistochemically; and the content of MUCSAC in the bronchial alveolar lavage fluid (BALF) was determined by ELISA. Results: Compared with the control group, the pulmonary expression of AQP5 in asthma group was obviously decreased (mRNA by[42. 5 ± 3.6] %, protein by [64.3±8.21%) ,while the expression of MUCSAC was increased (mRNA by[93.3±8. 1]% ,protein by[98.3% ±7.21%) . Dexamethasone significantly decreased the pulmonary expression of AQP5 and MUCSAC compared with the asthma group (P〈0.05). Conclusion: The decreased pulmonary expression of AQP5 in asthmatic mice might be related to the elevation of MUCSAC expression in the airway; dexamethasone can decrease AQP5 expression and therefore alleviate the overproduction of airway mucus, pulmonary inflammation and lung edema.
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