NORMOBARIC HYPOXIA STIMULATES ENDOTHELIN-1 GENE-EXPRESSION IN THE RAT

被引:196
作者
ELTON, TS
OPARIL, S
TAYLOR, GR
HICKS, PH
YANG, RH
JIN, HK
CHEN, YF
机构
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1992年 / 263卷 / 06期
关键词
VASOCONSTRICTOR; PULMONARY HYPERTENSION; OXYGEN TENSION;
D O I
10.1152/ajpregu.1992.263.6.R1260
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The current study tested the hypothesis that exposure to hypoxia enhances endothelin-1 (ET-1) gene expression and elevates circulating ET-1 levels in the rat. Rats were exposed to normobaric hypoxia (10% O2) or room air for 24 or 48 h. ET-1 in arterial blood was measured by radioimmunoassay. ET-1 gene transcript levels were measured by the slot blot technique on total RNA isolated from lung, right and left atria, right and left ventricles, kidney, spleen, liver, brain, main trunk of pulmonary artery, and thoracic aorta. Blots were probed with a 0.5 kb rat prepro ET-1 cDNA that does not cross-hybridize with mRNA for ET-2 or ET-3. Plasma ET-1 levels were increased significantly at 24 (10.03 +/- 2.33 pg/ml) and 48 h (14.02 +/- 3.44 pg/ml) of hypoxia compared with air controls (4.14 +/- 0.66 pg/ml). ET-1 mRNA levels were increased significantly (2-fold) in lung and right atrium after 48 h of hypoxia; no change was seen in organs perfused by the systemic vascular bed. These findings suggest that the hypoxia-induced increase in circulating ET-1 levels is mainly of pulmonary origin. A paracrine effect of ET-1 produced by lung endothelial cells could account for hypoxic pulmonary hypertension.
引用
收藏
页码:R1260 / R1264
页数:5
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