Department of Pharmacology, New York Medical College, Valhalla, New York 10595, USA.
Am J Physiol Renal Physiol. 2010 Jun;298(6):F1515-22. doi: 10.1152/ajprenal.00502.2009. Epub 2010 Mar 31.
We previously demonstrated that K depletion inhibited ROMK-like small-conductance K channels (SK) in the cortical collecting duct (CCD) and that the effect was mediated by superoxide anions that stimulated Src family protein tyrosine kinase (PTK) and mitogen-activated protein kinase (MAPK) (51). However, because animals on a K-deficient diet had a severe hypokalemia, superoxide-dependent signaling may not regulate ROMK channels under physiological conditions with a normal plasma K concentration. In the present study, we used the patch-clamp technique and Western blot to examine the effect of a moderate K restriction on ROMK-like SK channels and the role of PTK and MAPK in regulating apical K channels in the CCD of animals on a low-K diet (LK; 0.1% K). Rats and mice fed a LK diet for 7 days had a normal plasma K concentration. However, a LK intake increased the expression of angiotensin II type 1 receptor in the kidney. Moreover, patch-clamp experiments demonstrated that LK intake decreased the probability finding SK channels and channel activity defined by NP(o) (a product of channel number and open probability) in the CCD of both rat and mouse kidneys. Also, LK intake significantly stimulated the production of superoxide anions in the renal cortex and outer medulla in both rats and mice and increased superoxide level in the rat CCD. Moreover, LK intake augments the phosphorylation of p38 and ERK MAPK, the expression of c-Src and tyrosine phosphorylation of ROMK channels. However, treatment of animals with tempol abolished the effect of LK intake on MAPK and c-Src and increased ROMK channel activity in comparing with those of nontreated rats on a LK diet. Inhibiting p38 and ERK with SB202190 and PD98059 significantly stimulated SK in the CCD in rats on a LK diet. In addition, inhibition of PTK with herbimycin A activated SK channels in the CCD from rats on a LK diet. We conclude that LK intake stimulates the generation of superoxide anion and related products and that MAPK and Src family PTK play a physiological role in inhibiting apical K channels in the principal cells in response to LK intake.
我们之前已经证明,在皮质集合管(CCD)中,钾缺乏会抑制 ROMK 样小电导钾通道(SK),这种作用是由超氧阴离子介导的,超氧阴离子会刺激原癌基因 Src 家族蛋白酪氨酸激酶(PTK)和丝裂原活化蛋白激酶(MAPK)(51)。然而,由于低钾饮食的动物患有严重的低钾血症,因此在正常血浆钾浓度的生理条件下,超氧阴离子依赖性信号可能不会调节 ROMK 通道。在本研究中,我们使用膜片钳技术和 Western blot 检测了中度钾限制对 CCD 中 ROMK 样 SK 通道的影响,以及 PTK 和 MAPK 在调节低钾饮食(LK;0.1%K)动物的顶端钾通道中的作用。喂养 LK 饮食 7 天的大鼠和小鼠具有正常的血浆钾浓度。然而,LK 摄入增加了肾脏中血管紧张素 II 型 1 受体的表达。此外,膜片钳实验表明,LK 摄入降低了大鼠和小鼠肾脏 CCD 中 SK 通道的概率发现和通道活性(由通道数量和开放概率的乘积 NP(o)定义)。此外,LK 摄入显著刺激了大鼠和小鼠肾脏皮质和外髓质中超氧阴离子的产生,并增加了大鼠 CCD 中的超氧水平。此外,LK 摄入增加了 p38 和 ERK MAPK 的磷酸化、c-Src 的表达和 ROMK 通道的酪氨酸磷酸化。然而,与 LK 饮食的未处理大鼠相比,用 tempol 处理动物可消除 LK 摄入对 MAPK 和 c-Src 的影响,并增加 ROMK 通道活性。用 SB202190 和 PD98059 抑制 p38 和 ERK 可显著刺激 LK 饮食大鼠 CCD 中的 SK。此外,用 herbimycin A 抑制 PTK 可激活 LK 饮食大鼠 CCD 中的 SK 通道。我们得出结论,LK 摄入刺激超氧阴离子和相关产物的产生,MAPK 和 Src 家族 PTK 在响应 LK 摄入抑制主细胞顶端钾通道方面发挥生理作用。