Wang Jian-Rong, Zhou Ying, Sang Kui, Li Ming-Xia
Department of Neonatology, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2013 Feb;15(2):138-44.
To investigate the association between pulmonary vascular remodeling and expression of hypoxia-inducible factor-1α (HIF-1α), endothelin-1 (ET-1) and inducible nitric oxide synthase (iNOS) in pulmonary vessels in neonatal rats with hypoxic pulmonary hypertension (HPH).
A neonatal rat model of HPH was established as an HPH group, and normal neonatal rats were enrolled as a control group. The mean pulmonary arterial pressure (mPAP) was measured. The percentage of medial thickness to outer diameter of the small pulmonary arteries (MT%) and the percentage of medial cross-section area to total cross-section area of the pulmonary small arteries (MA%) were measured as the indicators for pulmonary vascular remodeling. The immunohistochemical reaction intensities for HIF-1α, ET-1 and iNOS and their mRNA expression in lung tissues of neonatal rats were measured. Correlation analysis was performed to determine the relationship between pulmonary vascular remodeling and mRNA expression of HIF-1α, ET-1 and iNOS.
The mPAP of the HPH group kept increasing on days 3, 5, 7, 10, 14, and 21 of hypoxia, with a significant difference compared with the control group (P<0.05). The HPH group had significantly higher MT% and MA% than the control group from day 7 of hypoxia (P<0.05). HIF-1α protein expression increased significantly on days 3, 5, 7 and 10 days of hypoxia, and HIF-1α mRNA expression increased significantly on days 3, 5 and 7 days of hypoxia in the HPH group compared with the control group (P<0.05). ET-1 protein expression increased significantly on days 3, 5 and 7 days of hypoxia and ET-1 mRNA expression increased significantly on day 3 of hypoxia in the HPH group compared with the control group (P<0.05). Both iNOS protein and mRNA expression were significantly higher on days 3, 5 and 7 days of hypoxia than the control group (P<0.05). Both MT% and MA% were positively correlated with HIF-1α mRNA expression (r=0.835 and 0.850 respectively; P<0.05).
Pulmonary vascular remodeling is developed on day 7 of hypoxia in neonatal rats. HIF-1α, ET-1 and iNOS are all involved in the occurrence and development of HPH in neonatal rats.
探讨低氧性肺动脉高压(HPH)新生大鼠肺血管重塑与缺氧诱导因子-1α(HIF-1α)、内皮素-1(ET-1)及诱导型一氧化氮合酶(iNOS)在肺血管中表达的相关性。
建立新生大鼠HPH模型作为HPH组,选取正常新生大鼠作为对照组。测量平均肺动脉压(mPAP)。测量小肺动脉中膜厚度与外径百分比(MT%)以及肺小动脉中膜横截面积与总横截面积百分比(MA%)作为肺血管重塑指标。检测新生大鼠肺组织中HIF-1α、ET-1和iNOS的免疫组化反应强度及其mRNA表达。进行相关性分析以确定肺血管重塑与HIF-1α、ET-1和iNOS mRNA表达之间的关系。
HPH组在缺氧第3、5、7、10、14和21天mPAP持续升高,与对照组相比差异有统计学意义(P<0.05)。从缺氧第7天起HPH组MT%和MA%显著高于对照组(P<0.05)。与对照组相比HPH组在缺氧第3、5、7和10天HIF-1α蛋白表达显著增加,在缺氧第3、5和7天HIF-1α mRNA表达显著增加(P<0.05)。与对照组相比HPH组在缺氧第3、5和7天ET-1蛋白表达显著增加,在缺氧第3天ET-1 mRNA表达显著增加(P<0.05)。在缺氧第3、5和7天iNOS蛋白和mRNA表达均显著高于对照组(P<0.05)。MT%和MA%均与HIF-1α mRNA表达呈正相关(分别为r=0.835和0.850;P<0.05)。
新生大鼠在缺氧第7天发生肺血管重塑。HIF-1α、ET-1和iNOS均参与新生大鼠HPH的发生发展。