Enhanced endothelin-1 and endothelin receptor gene expression in chronic hypoxia

H Li, SJ Chen, YF Chen, QC Meng… - Journal of applied …, 1994 - journals.physiology.org
H Li, SJ Chen, YF Chen, QC Meng, J Durand, S Oparil, TS Elton
Journal of applied physiology, 1994journals.physiology.org
To test the hypothesis that endothelin (ET)-1 synthesis and ET receptor levels are increased
selectively in the lung of rats with chronic hypoxic pulmonary hypertension, the current study
examined the effects of exposure to chronic hypoxia (10% O2, 1 atm, 4 wk) on pulmonary
arterial pressure, ET-1 levels in plasma and lung, and ET-1 and ETA and ETB receptor
mRNA levels in lung, heart, pulmonary artery, aorta, kidney, spleen, and liver. Hypoxic
exposure was associated with increases in pulmonary arterial pressure, plasma ET-1 levels …
To test the hypothesis that endothelin (ET)-1 synthesis and ET receptor levels are increased selectively in the lung of rats with chronic hypoxic pulmonary hypertension, the current study examined the effects of exposure to chronic hypoxia (10% O2, 1 atm, 4 wk) on pulmonary arterial pressure, ET-1 levels in plasma and lung, and ET-1 and ETA and ETB receptor mRNA levels in lung, heart, pulmonary artery, aorta, kidney, spleen, and liver. Hypoxic exposure was associated with increases in pulmonary arterial pressure, plasma ET-1 levels, ET-1 mRNA in lung and pulmonary artery, and ET-1 stores and ETA and ETB receptor mRNA levels in lung. In thoracic aorta and the four heart chambers, ETA and ETB receptor mRNA levels were increased, but ET-1 mRNA levels were unchanged from air control levels. No change in ET-1 or ET receptor mRNA levels was seen in organs perfused by the systemic vascular bed, except in liver, where ETA receptor mRNA levels were decreased. The findings of concomitant increases in gene transcript levels for ET-1 and the ETA and ETB receptors in lung, but not in the great vessels or any other organ examined, are consistent with the hypothesis that increased ET-1 synthesis in the lung contributes to pulmonary vascular remodeling and the maintenance of chronic hypoxic pulmonary hypertension.
American Physiological Society