Wolf Sabine C, Schultze Michael, Risler Teut, Rieg Timo, Lang Florian, Schulze-Osthoff Klaus, Brehm Bernhard R
Medical Clinic IV, Section of Nephrology, Hypertension and Renal Failure, University of Tübingen, Germany.
Biochem Pharmacol. 2006 Apr 14;71(8):1175-83. doi: 10.1016/j.bcp.2006.01.001. Epub 2006 Feb 17.
The serum- and glucocorticoid-regulated kinase-1 (SGK1) participates in the regulation of sodium homeostasis and blood pressure by mineralocorticoids. Aldosterone rapidly induces SGK1 transcription, which contributes to the activation of renal epithelial sodium channels. Another important regulator of blood pressure is the vasoactive hormone endothelin-1 (ET-1) that is systemically upregulated in chronic renal failure. In the present study, we investigated whether ET-1 modulates SGK1 expression, and thereby might explain some of its hypertensive effects. As assessed by real-time PCR analysis, ET-1 triggered the rapid increase of SGK1 mRNA levels in A-10 smooth muscle cells and also in intact aortas of adult rats. In A-10 cells transcriptional activation was associated with a more than 6-fold upregulation of SGK1 protein expression and in similar range as found after treatment with aldosterone. A stimulatory effect of ET-1 was not only observed in isolated cells, but also in an animal model. Upon subtotal nephrectomy (SNX) of rats, myocardial ET-1 levels strongly increased, which was followed by a more than 2-fold induction of SGK1 expression in the left ventricle. The myocardial upregulation of SGK1 was completely abrogated by a specific ET(A) receptor antagonist, thereby substantiating the in vivo role of ET-1 in SGK1 expression. Thus, these data demonstrate that ET-1 increases expression of SGK1 in vivo and in vitro, and therefore indicate that SGK1 upregulation might be involved in ET-1-dependent regulation of blood pressure and cardiac modelling during mild renal failure.
血清和糖皮质激素调节激酶-1(SGK1)参与盐皮质激素对钠稳态和血压的调节。醛固酮可迅速诱导SGK1转录,这有助于肾上皮钠通道的激活。另一个重要的血压调节因子是血管活性激素内皮素-1(ET-1),其在慢性肾衰竭时会全身性上调。在本研究中,我们调查了ET-1是否调节SGK1表达,从而可能解释其一些高血压效应。通过实时PCR分析评估,ET-1可使A-10平滑肌细胞以及成年大鼠完整主动脉中SGK1 mRNA水平迅速升高。在A-10细胞中,转录激活与SGK1蛋白表达上调超过6倍相关,且上调幅度与醛固酮处理后相似。ET-1的刺激作用不仅在分离的细胞中观察到,在动物模型中也观察到。大鼠进行次全肾切除(SNX)后,心肌ET-1水平大幅升高,随后左心室中SGK1表达诱导增加超过2倍。SGK1在心肌中的上调被特异性ET(A)受体拮抗剂完全消除,从而证实了ET-1在SGK1表达中的体内作用。因此,这些数据表明ET-1在体内和体外均可增加SGK1的表达,因此表明SGK1上调可能参与轻度肾衰竭期间ET-1依赖性血压调节和心脏重塑。