Ritthaler T, Göpfert T, Firth J D, Ratcliffe P J, Krämer B K, Kurtz A
Institute of Physiology, University of Regensburg, Germany.
Pflugers Arch. 1996 Feb;431(4):587-93. doi: 10.1007/BF02191907.
This study aimed to investigate the influence of different forms of tissue hypoxia on the expression of the endothelin genes in kidneys and livers. Tissue hypoxia in rats was induced by five different manoeuvres, namely hypoxia (8% O2), functional anaemia (0.1% CO), haemorrhage (haematocrit, hct = 0.12), cobalt treatment (60 mg/kg) for 6 h each and renal artery stenosis (0.2-mm clips) for 2 days. Endothelin-1 (ET-1) mRNA levels in the kidneys were increased by 200% with renal artery stenosis, 70% by hypoxia, 50% by anaemia, 30% by CO, but were not changed by cobalt. ET-3 mRNA in the kidneys decreased during renal artery clipping and cobalt treatment and were not significantly changed under the other conditions. ET-2 mRNA was not detected in the kidneys and livers. The abundance of ET-1 in the livers of normoxic animals was about 15% of that found in the kidney. Hypoxia increased ET-1 mRNA by 200%, haemorrhage by 400%, whilst CO and cobalt did not change hepatic ET-1 gene expression. The abundance of ET-3 mRNA in the livers of normoxic animals was about 6% of that found in the kidneys. The expression of the ET-3 gene in the livers was decreased by CO, but was not changed by any of the other experimental conditions used. These findings suggest that hyoxaemia and tissue hypoxia are moderate stimuli for the expression of the ET-1 gene but not for the ET-3 gene in the kidney and more potent stimuli in the liver, whilst cobalt does not activate ET-1 gene expression in the kidneys nor the livers.
本研究旨在探讨不同形式的组织缺氧对肾脏和肝脏中内皮素基因表达的影响。通过五种不同的操作诱导大鼠组织缺氧,即低氧(8%氧气)、功能性贫血(0.1%一氧化碳)、出血(血细胞比容,hct = 0.12)、钴处理(60毫克/千克),每种处理6小时,以及肾动脉狭窄(0.2毫米夹子)处理2天。肾动脉狭窄使肾脏中内皮素-1(ET-1)mRNA水平增加200%,低氧使其增加70%,贫血使其增加50%,一氧化碳使其增加30%,但钴处理未使其改变。肾动脉夹闭和钴处理期间肾脏中ET-3 mRNA减少,其他条件下无显著变化。在肾脏和肝脏中未检测到ET-2 mRNA。常氧动物肝脏中ET-1的丰度约为肾脏中的15%。低氧使肝脏中ET-1 mRNA增加200%,出血使其增加400%,而一氧化碳和钴未改变肝脏中ET-1基因表达。常氧动物肝脏中ET-3 mRNA的丰度约为肾脏中的6%。肝脏中ET-3基因的表达因一氧化碳而降低,但其他任何实验条件均未使其改变。这些发现表明,低氧血症和组织缺氧是肾脏中ET-1基因表达的中度刺激因素,但不是ET-3基因的刺激因素,在肝脏中是更强的刺激因素,而钴不会激活肾脏和肝脏中的ET-1基因表达。