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AQP-1、AQP-4、VEGF、sE-选择素在肺低氧代谢中的表达

发布时间:2018-02-27 09:31

  本文关键词: 低氧代谢 水通道蛋白-1 水通道蛋白-4 低氧代谢 血管内皮生长因子 可溶性E选择素 出处:《广西医科大学》2012年硕士论文 论文类型:学位论文


【摘要】:目的:研究肺低氧代谢中大鼠肺组织水通道蛋白1、4(AQP-1、4)的表达,探讨低氧代谢与其相关性。 方法:将30只SD大鼠随机分成对照组和实验组A、B、C、D组,即1/2h单肺低氧组、1h单肺低氧组、2h单肺低氧组、4h单肺低氧组。对照组采用气管切开插管行双肺通气,实验组采用气管切开插管行单肺通气,建立急性低氧性肺损伤模型。分别于通气1/2h、1h、2h、4h后取非通气侧肺组织,光镜下观察肺组织病理变化情况;免疫组化观察AQP-1、AQP-4蛋白表达与分布;采用实时荧光定量PCR测定大鼠AQP-1、AQP-4mRNA表达。 结果:光镜下可见实验组随着低氧时间延长,肺组织毛细血管充血,腔内充满较多红细胞,肺泡隔增宽,炎性细胞浸润,而对照组未见明显病理变化。肺组织免疫组化观察到随着低氧时间延长AQP-1表达明显减少,而AQP-4变化不大。单肺低氧4h组AQP-lmRNA的表达较对照组显著减少(P0.05),且随着低氧时间延长呈下降趋势:ABCD,而AQP-4的表达没有明显变化。 结论:长时间低氧代谢导致大鼠肺组织结构发生改变,AQP-1表达下调,且与低氧代谢时间呈负相关,而AQP-4与肺低氧代谢无相关性。 目的:研究肺低氧代谢中大鼠血管内皮生长因子(VEGF)、可溶性E选择素(sE-Selectin)的表达,探讨低氧代谢与其相关性。 方法:将30只SD大鼠随机分成对照组和实验组A、B、C、D组,即1/2h单肺低氧组、1h单肺低氧组、2h单肺低氧组、4h单肺低氧组。对照组采用气管切开插管行双肺通气,实验组采用气管切开插管行单肺通气,建立急性低氧性肺损伤模型。分别于通气1/2h、1h、2h、4h后取非通气侧大鼠肺组织及血清。光镜下观察肺组织病理变化情况,采用ELISA法测定血清中sE-选择素、肺组织和血清中VEGF的含量,免疫组化观察VEGF蛋白表达与分布,采用实时荧光定量PCR测定大鼠VEGFmRNA表达。 结果:HE观察到实验组随着低氧时间延长,肺组织毛细血管充血,腔内充满较多红细胞,肺泡隔增宽,炎性细胞浸润,而对照组未见明显病理变化。ELISA法观察到sE-选择素在大鼠单肺低氧1h、2h、4h血清中的表达较对照组显著升高(P0.05),且随着时间延长,含量增加;VEGF在大鼠单肺低氧4h组肺组织中的表达较正常组显著降低(P0.05),而在该组血清中的表达较对照组显著升高(P0.05)。肺组织免疫组化观察到随着低氧时间延长VEGF表达减少。单肺低氧4h组VEGF mRNA的表达较对照组显著减少(P0.05),且随着低氧时间延长呈下降趋势:ABCD。 结论:长时间低氧代谢导致大鼠肺组织结构发生改变,sE-选择素表达上调,且与低氧代谢时间呈正相关;而肺组织中VEGF与低氧代谢时间呈负相关。
[Abstract]:Aim: to study the expression of aquaporin 1 (aquaporin 1) in rat lung tissue during hypoxic metabolism, and to explore the correlation between hypoxia metabolism and AQP-4. Methods: thirty Sprague-Dawley rats were randomly divided into two groups: control group and experimental group, namely 1 / 2 h one-lung hypoxia group, 1 / 2 h single lung hypoxia group, 1 h single lung hypoxia group and 4 h single lung hypoxia group, the control group was treated with tracheotomy and intubation to perform double lung ventilation. The model of acute hypoxic lung injury was established by using tracheotomy and intubation to establish acute hypoxic lung injury model. The lung tissues of the non-ventilated side were taken for 4 h after 1 / 2 h of ventilation, and the pathological changes of lung tissue were observed under light microscope, and the expression and distribution of AQP-1AQP-4 protein were observed by immunohistochemistry. The expression of AQP-4 mRNA in rat AQP-1 was measured by real-time fluorescence quantitative PCR. Results: with the prolongation of hypoxic time, pulmonary capillary congestion, more red blood cells, wider alveolar septum and inflammatory cell infiltration were observed under light microscope in the experimental group. In the control group, there was no obvious pathological change. The expression of AQP-1 decreased with the prolongation of hypoxic time by immunohistochemistry. Compared with the control group, the expression of AQP-lmRNA in single lung hypoxia group decreased significantly (P 0.05), and decreased with the increase of hypoxia time, but the expression of AQP-4 did not change significantly. Conclusion: the expression of AQP-1 is down-regulated and negatively correlated with hypoxic metabolic time due to long-term hypoxic metabolism in rats, but AQP-4 has no correlation with hypoxic metabolism. Aim: to study the expression of vascular endothelial growth factor (VEGF) in rat hypoxic metabolism and its correlation. Methods: thirty Sprague-Dawley rats were randomly divided into two groups: control group and experimental group, namely 1 / 2 h one-lung hypoxia group, 1 / 2 h single lung hypoxia group, 1 h single lung hypoxia group and 4 h single lung hypoxia group, the control group was treated with tracheotomy and intubation to perform double lung ventilation. The model of acute hypoxic lung injury was established by tracheotomy and intubation in the experimental group. Lung tissue and serum of the non-ventilated side were taken after 1 / 2 h / 1 h and 2 h / 4 h of ventilation respectively. The pathological changes of lung tissue were observed under light microscope. The content of sE- selectin in serum, VEGF in lung tissue and serum were measured by ELISA method. The expression and distribution of VEGF protein were observed by immunohistochemistry. The expression of VEGFmRNA in rats was measured by real-time fluorescence quantitative PCR. Results with the prolongation of hypoxic time, the blood capillaries of lung tissue in the experimental group were congested, the cavity was filled with more red blood cells, the alveolar septum widened, and the inflammatory cells infiltrated. The expression of sE- selectin in the serum of rats with single lung hypoxia for 1 h or 2 h was significantly higher than that in the control group (P 0.05), and the expression of sE-selectin in the serum of rats with single lung hypoxia for 1 h or 2 h was significantly higher than that in the control group, and the expression of sE-selectin was prolonged with time. The expression of VEGFin in lung tissue of single lung hypoxia group for 4 hours was significantly lower than that in normal group, but the expression in serum of this group was significantly higher than that in control group. The expression of VEGF in lung tissue was observed by immunohistochemistry with the prolongation of hypoxic time. The expression of VEGF mRNA in single lung hypoxia group for 4 h was significantly lower than that in control group (P 0.05), and the expression of VEGF mRNA decreased with the prolongation of hypoxia time. Conclusion: Long-term hypoxic metabolism leads to the changes of lung tissue structure in rats, and the expression of sE- selectin is up-regulated and positively correlated with hypoxic metabolic time, while VEGF is negatively correlated with hypoxic metabolic time.
【学位授予单位】:广西医科大学
【学位级别】:硕士
【学位授予年份】:2012
【分类号】:R363

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