Schweda F, Blumberg F C, Schweda A, Kammerl M, Holmer S R, Riegger G A, Pfeifer M, Krämer B K
Klinik und Poliklinik für Innere Medizin II, Klinikum der Universität Regensburg, Regensburg, Germany.
Nephrol Dial Transplant. 2000 Jan;15(1):11-5. doi: 10.1093/ndt/15.1.11.
The effects of hypoxia on renin secretion and renin gene expression have been controversial. In recent studies, we have demonstrated that acute hypoxia of 6 h duration caused a marked stimulation of renin secretion and renal renin gene expression. This hypoxia-induced stimulation of the renin-angiotensin system might contribute, for example, to the progression of chronic renal failure and to the development of hypertension in the sleep-apnoea syndrome. For this reason, we were interested in the more chronic effects of hypoxia on renal renin gene expression and its possible regulation.
Male rats were exposed to chronic normobaric hypoxia (10% O(2)) for 2 and 4 weeks. Additional groups of rats were treated with an endothelin ET(A) receptor antagonist, LU135252, or a NO donor, molsidomine, respectively. Systolic blood pressure and right ventricular pressures were measured. Renal renin, endothelin-1 and endothelin-3 gene expression were quantitated using RNAase protection assays.
During chronic hypoxia, haematocrit increased to 72+/-2%, and right ventricular pressure increased by a mean of 26 mmHg. Renal renin gene expression was halved during 4 weeks of chronic hypoxia. This decrease was reversed by endothelin receptor blockade (105 or 140% of baseline values after treatment for weeks 3-4 or 1-4). Furthermore, there was a trend of increasing renal endothelin-1 gene expression (to 173% of baseline values) after 4 weeks of hypoxia. Systolic blood pressure increased moderately during 4 weeks of chronic hypoxia from 129+/-2 to 150+/-4 mmHg. This blood pressure increase was higher in rats treated for 4 weeks with an endothelin receptor antagonist (196+/-11 mmHg).
Chronic hypoxia (in contrast to acute hypoxia) suppresses renal renin gene expression. This inhibition presumably is mediated by endothelins.
缺氧对肾素分泌及肾素基因表达的影响一直存在争议。在最近的研究中,我们已经证明,持续6小时的急性缺氧会显著刺激肾素分泌及肾脏肾素基因表达。这种缺氧诱导的肾素 - 血管紧张素系统的刺激可能会导致,例如,慢性肾衰竭的进展以及睡眠呼吸暂停综合征中高血压的发展。因此,我们对缺氧对肾脏肾素基因表达的更长期影响及其可能的调节感兴趣。
雄性大鼠暴露于慢性常压缺氧(10%氧气)环境中2周和4周。另外几组大鼠分别用内皮素ET(A)受体拮抗剂LU135252或一氧化氮供体吗多明进行治疗。测量收缩压和右心室压力。使用核糖核酸酶保护分析法对肾脏肾素、内皮素 - 1和内皮素 - 3基因表达进行定量。
在慢性缺氧期间,血细胞比容增加到72±2%,右心室压力平均增加26 mmHg。慢性缺氧4周期间,肾脏肾素基因表达减半。这种下降通过内皮素受体阻断得以逆转(治疗3 - 4周或1 - 4周后为基线值的105%或140%)。此外,缺氧4周后,肾脏内皮素 - 1基因表达有增加的趋势(达到基线值的173%)。慢性缺氧4周期间,收缩压从129±2 mmHg适度增加到150±4 mmHg。在用内皮素受体拮抗剂治疗4周的大鼠中,血压升高幅度更大(196±11 mmHg)。
慢性缺氧(与急性缺氧相反)会抑制肾脏肾素基因表达。这种抑制作用可能是由内皮素介导的。