Lee Kyung Sun, Kim So Ri, Park Seoung Ju, Park Hee Sun, Min Kyung Hoon, Lee Min Hee, Jin Sun Mi, Jin Gong Yong, Yoo Wan Hee, Lee Yong Chul
Department of Internal Medicine, Chonbuk National University Medical School, San 2-20 Geumam-dong, Jeonju, Jeonbuk 561-180, South Korea.
Am J Respir Cell Mol Biol. 2006 Aug;35(2):190-7. doi: 10.1165/rcmb.2005-0482OC. Epub 2006 Mar 30.
Oxidative stress plays critical roles in initiation and/or worsening of respiratory disease process. Although reactive oxygen species (ROS) are shown to cause vascular leakage, the mechanisms by which ROS induce an increase in vascular permeability are not clearly understood. In this study, we have used a murine model to evaluate the effect of hydrogen peroxide (H(2)O(2)) to examine roles of ROS and the molecular mechanism in vascular permeability. The results have revealed that ROS levels, vascular endothelial growth factor (VEGF) expression, hypoxia-inducible factor-1alpha protein level, airway hyperresponsiveness, and vascular permeability are increased after inhalation of H(2)O(2). Administration of antioxidants markedly reduced plasma extravasation and VEGF levels in lungs treated with H(2)O(2). These results indicate that ROS may modulate vascular permeability via upregulation of VEGF expression.
氧化应激在呼吸系统疾病进程的起始和/或恶化中起关键作用。尽管活性氧(ROS)已被证明可导致血管渗漏,但ROS诱导血管通透性增加的机制尚不清楚。在本研究中,我们使用小鼠模型评估过氧化氢(H₂O₂)的作用,以研究ROS的作用及血管通透性的分子机制。结果显示,吸入H₂O₂后,ROS水平、血管内皮生长因子(VEGF)表达、缺氧诱导因子-1α蛋白水平、气道高反应性和血管通透性均升高。给予抗氧化剂可显著降低H₂O₂处理的肺组织中的血浆外渗和VEGF水平。这些结果表明,ROS可能通过上调VEGF表达来调节血管通透性。