内皮素-1在大鼠缺氧性肺动脉高压易感性中的作用

M.R. Karamsetty , L. Pietras , J.R. Klinger , J.J. Lanzillo , J.C. Leiter , L.-C. Ou , N.S. Hill
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引用次数: 5

摘要

Hilltop (H)毒株与Madison (M)毒株相比,Sprague-Dawley大鼠对慢性缺氧的反应出现严重的肺动脉高压。我们检验了内皮素-1 (ET-1)导致这些菌株相关差异的假设。血浆ET-1含量均未因慢性缺氧而改变。缺氧2周和3周时,两组小鼠肺ET-1肽和preproET-1 mRNA含量均显著升高至相同水平。缺氧3周时,H大鼠肺内ETA受体mRNA表达明显高于M大鼠,其他时间点无明显差异。两种菌株的ETB受体mRNA均未被缺氧修饰。缺氧2周后正常恢复3天后,两种大鼠的ET-1蛋白和mRNA水平均降至基线水平。我们得出结论,ET-1不促进H和M菌株对缺氧反应的心肺差异的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of endothelin-1 in strain-related susceptibility to develop hypoxic pulmonary hypertension in rats

The Hilltop (H) strain compared to the Madison (M) strain of Sprague–Dawley rats develops severe pulmonary hypertension in response to chronic hypoxia. We tested the hypothesis that endothelin-1 (ET-1) contributes to these strain-related differences. Plasma ET-1 content was not modified by chronic hypoxia in either strain. The lung ET-1 peptide and preproET-1 mRNA content were significantly increased to the same magnitude in both strains at 2 and 3 weeks of hypoxia. The ETA receptor mRNA increased more at 3 weeks of hypoxia in the lungs of H rats than in M rats, but not at other time points. The ETB receptor mRNA was not modified by hypoxia in either strain. After 3 days of normoxic recovery following 2 weeks of hypoxia, ET-1 protein and mRNA levels decreased to baseline levels in both rat strains. We conclude that ET-1 does not contribute to the development of cardiopulmonary differences between the H and M strains in response to hypoxia.

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