Pagel H, Jelkmann W, Weiss C
Institut für Physiologie, Medizinische Universität, Lübeck, F.R.G.
Biomed Biochim Acta. 1990;49(2-3):S271-4.
In order to further investigate the dependency of the production of erythropoietin (Epo) on the renal O2 supply, experiments were carried out in the isolated perfused rat kidney (IPRK). The kidneys were perfused with a substrate enriched Krebs-Henseleit solution containing 60 g/l bovine serum albumin at a constant perfusion pressure of 100 mmHg. When the kidneys were perfused at an arterial pO2 of 720 or 150 mmHg (hematocrit 5%), Epo production measured by RIA was very low (0.1-0.2 U/g kidney after 3 h of perfusion). At a pO2 of 20 mmHg, Epo production increased markedly up to 0.9 U/g kidney. However, the production of Epo was little affected by changes in the hematocrit of the perfusion medium from zero to 40%, even if severe anemia was mimicked. These results indicate that Epo production in the IPRK is mainly under the control of the arterial pO2.
为了进一步研究促红细胞生成素(Epo)产生对肾脏氧气供应的依赖性,在离体灌注大鼠肾脏(IPRK)中进行了实验。肾脏用含有60 g/l牛血清白蛋白的富含底物的克雷布斯 - 亨泽莱特溶液在100 mmHg的恒定灌注压力下进行灌注。当肾脏在动脉血氧分压为720或150 mmHg(血细胞比容5%)下灌注时,通过放射免疫分析测定的Epo产生非常低(灌注3小时后为0.1 - 0.2 U/g肾脏)。在血氧分压为20 mmHg时,Epo产生显著增加至0.9 U/g肾脏。然而,即使模拟了严重贫血,灌注介质的血细胞比容从零到40%的变化对Epo的产生影响很小。这些结果表明,IPRK中Epo的产生主要受动脉血氧分压的控制。