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ETA-receptor antagonist prevents and reverses chronic hypoxia-induced pulmonary hypertension in rat.

作者信息

DiCarlo V S, Chen S J, Meng Q C, Durand J, Yano M, Chen Y F, Oparil S

机构信息

Department of Medicine, University of Alabama at Birmingham School of Medicine 35294, USA.

出版信息

Am J Physiol. 1995 Nov;269(5 Pt 1):L690-7. doi: 10.1152/ajplung.1995.269.5.L690.

DOI:10.1152/ajplung.1995.269.5.L690
PMID:7491990
Abstract

The selective endothelin-A (ETA)-receptor antagonist BQ-123 has been shown to prevent chronic hypoxia-induced pulmonary hypertension in the rat. Therefore in the current study we utilized BQ-123 to test the hypothesis that blockade of the ETA receptor can reverse as well as prevent the increase in mean pulmonary artery pressure, right ventricle-to-left ventricle plus septum ratio, and percent wall thickness in small (50-100 microns) pulmonary arteries observed in male Sprague-Dawley rats exposed to normobaric hypoxia (10% O2, 2 wk). Infusion of BQ-123 (0.4 mg.0.5 microliter-1.h-1 for 2 wk in 10% O2) begun after 2 wk of hypoxia significantly reversed the established pulmonary hypertension and prevented further progression of right ventricular hypertrophy during the third and fourth week of hypoxia. BQ-123 infusion instituted before exposure to hypoxia completely prevented the hypoxia-induced pulmonary hypertension, right ventricular hypertrophy, and pulmonary vascular remodeling. These findings suggest that, in the lung, hypoxia induced an increase synthesis of endothelin-1, which acts locally on ETA receptors to cause pulmonary hypertension, right heart hypertrophy, and pulmonary vascular remodeling, while ETA-receptor blockade can both prevent and reverse these processes.

摘要

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