Dai Zen-Kong, Tan Mian-Shin, Chai Chee-Yin, Yeh Jwu-Lai, Chou Shah-Hwa, Chiu Chaw-Chi, Jeng Arco Y, Chen Ing-Jun, Wu Jiunn-Ren
Division of Cardiology and Pulmonology, Department of Pediatrics, Kaohsiung Medical University, Kaohsiung, Taiwan.
Pediatr Pulmonol. 2004 Mar;37(3):249-56. doi: 10.1002/ppul.10413.
This study assessed alterations in expression of pulmonary endothelial nitric oxide synthase (eNOS) and endothelin-1 (ET-1) in rats with pulmonary hypertension (PH) after the ascending aorta had been banded. Rats were studied 12 weeks after banding, which resulted in left heart failure with elevated pulmonary arterial pressure (banded: 31.3 +/- 5.9 (mean +/- SD) mmHg; sham: 20.0 +/- 4.7 mmHg, P<0.05). Competitive reverse transcription-polymerase chain reaction demonstrated significant increases in pulmonary expression of preproET-1 mRNA and eNOS mRNA. Western blot analysis indicated increased pulmonary eNOS protein. Radioimmunoassays indicated increased plasma ET-1 concentrations in the pulmonary artery (banded: 12.4 +/- 1.5 pg/ml; sham: 9.0 +/- 1.3 pg/ml, P<0.01) and increased ET-1 content in lungs (banded: 240 +/- 21 ng/g protein; sham: 203 +/- 20 ng/g protein, P<0.05). There was increased immunohistochemical staining of eNOS and ET-1 in the pulmonary vascular endothelium of aorta-banded rats. Even in the presence of increased eNOS expression, it was not clear how nitric oxide (NO) production (decreased, unchanged, or increased) was involved in the compensatory mechanism to offset pulmonary vasoconstriction. Increased ET-1 expression may be important in mediating PH secondary to aortic banding, and may offer insights into the use of ET-1 antagonists in treating patients with PH secondary to heart failure.
本研究评估了升主动脉缩窄后肺动脉高压(PH)大鼠肺内皮型一氧化氮合酶(eNOS)和内皮素-1(ET-1)表达的变化。在缩窄术后12周对大鼠进行研究,结果导致左心衰竭伴肺动脉压升高(缩窄组:31.3±5.9(均值±标准差)mmHg;假手术组:20.0±4.7 mmHg,P<0.05)。竞争性逆转录-聚合酶链反应显示前体ET-1 mRNA和eNOS mRNA的肺表达显著增加。蛋白质印迹分析表明肺eNOS蛋白增加。放射免疫分析表明肺动脉血浆ET-1浓度升高(缩窄组:12.4±1.5 pg/ml;假手术组:9.0±1.3 pg/ml,P<0.01),肺中ET-1含量增加(缩窄组:240±21 ng/g蛋白;假手术组:203±20 ng/g蛋白,P<0.05)。在主动脉缩窄大鼠的肺血管内皮中,eNOS和ET-1的免疫组化染色增加。即使存在eNOS表达增加的情况,尚不清楚一氧化氮(NO)生成(减少、不变或增加)如何参与抵消肺血管收缩的代偿机制。ET-1表达增加可能在介导主动脉缩窄继发的PH中起重要作用,并且可能为ET-1拮抗剂用于治疗心力衰竭继发PH患者提供思路。