Wei Yuan, Liao Yi, Zavilowitz Beth, Ren Jin, Liu Wen, Chan Pokman, Rohatgi Rajeev, Estilo Genevieve, Jackson Edwin K, Wang Wen-Hui, Satlin Lisa M
Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, New York; Department of Pharmacology, New York Medical College, Valhalla, New York; Department of Cell Biology, New York University Medical Center, New York, New York
Department of Cell Biology, New York University Medical Center, New York, New York.
Am J Physiol Renal Physiol. 2014 Oct 1;307(7):F833-43. doi: 10.1152/ajprenal.00141.2014. Epub 2014 Aug 6.
The kidney adjusts K⁺ excretion to match intake in part by regulation of the activity of apical K⁺ secretory channels, including renal outer medullary K⁺ (ROMK)-like K⁺ channels, in the cortical collecting duct (CCD). ANG II inhibits ROMK channels via the ANG II type 1 receptor (AT1R) during dietary K⁺ restriction. Because AT1Rs and ANG II type 2 receptors (AT2Rs) generally function in an antagonistic manner, we sought to characterize the regulation of ROMK channels by the AT2R. Patch-clamp experiments revealed that ANG II increased ROMK channel activity in CCDs isolated from high-K⁺ (HK)-fed but not normal K⁺ (NK)-fed rats. This response was blocked by PD-123319, an AT2R antagonist, but not by losartan, an AT1R antagonist, and was mimicked by the AT2R agonist CGP-42112. Nitric oxide (NO) synthase is present in CCD cells that express ROMK channels. Blockade of NO synthase with N-nitro-l-arginine methyl ester and free NO with 2-(4-carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide potassium salt completely abolished ANG II-stimulated ROMK channel activity. NO enhances the synthesis of cGMP, which inhibits phosphodiesterases (PDEs) that normally degrade cAMP; cAMP increases ROMK channel activity. Pretreatment of CCDs with IBMX, a broad-spectrum PDE inhibitor, or cilostamide, a PDE3 inhibitor, abolished the stimulatory effect of ANG II on ROMK channels. Furthermore, PKA inhibitor peptide, but not an activator of the exchange protein directly activated by cAMP (Epac), also prevented the stimulatory effect of ANG II. We conclude that ANG II acts at the AT2R to stimulate ROMK channel activity in CCDs from HK-fed rats, a response opposite to that mediated by the AT1R in dietary K⁺-restricted animals, via a NO/cGMP pathway linked to a cAMP-PKA pathway.
肾脏通过调节皮质集合管(CCD)顶端钾分泌通道的活性,包括肾外髓质钾(ROMK)样钾通道,来部分调节钾排泄以匹配摄入量。在饮食钾限制期间,血管紧张素II(ANG II)通过1型血管紧张素II受体(AT1R)抑制ROMK通道。由于AT1R和2型血管紧张素II受体(AT2R)通常以拮抗方式发挥作用,我们试图研究AT2R对ROMK通道的调节作用。膜片钳实验表明,ANG II增加了从高钾(HK)喂养而非正常钾(NK)喂养大鼠分离的CCD中ROMK通道的活性。这种反应被AT2R拮抗剂PD - 123319阻断,但未被AT1R拮抗剂氯沙坦阻断,并且被AT2R激动剂CGP - 42112模拟。一氧化氮(NO)合酶存在于表达ROMK通道的CCD细胞中。用N - 硝基 - l - 精氨酸甲酯阻断NO合酶以及用2 -(4 - 羧基苯基)- 4,4,5,5 - 四甲基咪唑啉 - 1 - 氧基 - 3 - 氧化物钾盐清除游离NO,完全消除了ANG II刺激的ROMK通道活性。NO增强cGMP的合成,cGMP抑制通常降解cAMP的磷酸二酯酶(PDE);cAMP增加ROMK通道活性。用广谱PDE抑制剂异丁基甲基黄嘌呤(IBMX)或PDE3抑制剂西洛他唑预处理CCD,消除了ANG II对ROMK通道的刺激作用。此外,蛋白激酶A(PKA)抑制剂肽,但不是由cAMP直接激活的交换蛋白(Epac)的激活剂,也阻止了ANG II的刺激作用。我们得出结论,ANG II通过与cAMP - PKA途径相关的NO / cGMP途径作用于AT2R,以刺激HK喂养大鼠的CCD中ROMK通道活性,这一反应与饮食钾限制动物中AT1R介导的反应相反。