Upregulation of endothelial nitric oxide synthase and endothelin-1 in pulmonary hypertension secondary to heart failure in aorta-banded rats

被引:30
作者
Dai, ZK
Tan, MS
Chai, CY
Yeh, JL
Chou, SH
Chiu, CC
Jeng, AY
Chen, IJ
Wu, JR
机构
[1] Kaohsiung Med Univ, Dept Pediat, Div Cardiol & Pulmonol, Kaohsiung, Taiwan
[2] Kaohsiung Med Univ, Sch Biol, Kaohsiung, Taiwan
[3] Kaohsiung Med Univ, Dept Pathol, Kaohsiung, Taiwan
[4] Kaohsiung Med Univ, Dept Pharmacol, Kaohsiung, Taiwan
[5] Kaohsiung Med Univ, Dept Thorac Surg, Kaohsiung, Taiwan
[6] Kaohsiung Med Univ, Dept Cardiac Surg, Kaohsiung, Taiwan
[7] Novartis Inst Biomed Res, Metab & cardiovasc Dis Res, Summit, NJ USA
关键词
endothelial nitric oxide synthase; endothelin-1; pulmonary vascular remodeling; pulmonary hypertension; aortic banding; heart failure;
D O I
10.1002/ppul.10413
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
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. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:249 / 256
页数:8
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