Nüsing Rolf M, Treude Antje, Weissenberger Christian, Jensen Boye, Bek Martin, Wagner Charlotte, Narumiya Shuh, Seyberth Hannsjörg W
Institute of Clinical Pharmacology, Johann Wolfgang Goethe-University, Theodor Stern Kai 7, Frankfurt 60590, Germany.
J Am Soc Nephrol. 2005 Aug;16(8):2354-62. doi: 10.1681/ASN.2004070556. Epub 2005 Jun 23.
Increased formation of prostaglandin E2 (PGE2) is a key part of hyperprostaglandin E syndrome/antenatal Bartter syndrome (HPS/aBS), a renal disease characterized by NaCl wasting, water loss, and hyperreninism. Inhibition of PGE2 formation by cyclo-oxygenase inhibitors significantly lowers patient mortality and morbidity. However, the pathogenic role of PGE2 in HPS/aBS awaits clarification. Chronic blockade of the Na-K-2Cl co-transporter NKCC2 by diuretics causes symptoms similar to HPS/aBS and provides a useful animal model. In wild-type (WT) mice and in mice lacking distinct PGE2 receptors (EP1-/-, EP2-/-, EP3-/-, and EP4-/-), the effect of chronic furosemide administration (7 d) on urine output, sodium and potassium excretion, and renin secretion was determined. Furthermore, furosemide-induced diuresis and renin activity were analyzed in mice with defective PGI2 receptors (IP-/-). In all animals studied, furosemide stimulated a rise in diuresis and electrolyte excretion. However, this effect was blunted in EP1-/-, EP3-/-, and EP4-/- mice. Compared with WT mice, no difference was observed in EP2-/- and IP-/- mice. The furosemide-induced increase in plasma renin concentration was significantly decreased in EP4-/- mice and to a lesser degree also in IP-/- mice. Pharmacologic inhibition of EP4 receptors in furosemide-treated WT mice with the specific antagonist ONO-AE3-208 mimicked the changes in renin mRNA expression, plasma renin concentration, diuresis, and sodium excretion seen in EP4-/- mice. The GFR in EP4-/- mice was not changed compared with that in WT mice, which indicated that blunted diuresis and salt loss seen in EP4-/- mice were not a consequence of lower GFR. In summary, these findings demonstrate that the EP4 receptor mediates PGE2-induced renin secretion and that EP1, EP3, and EP4 receptors all contribute to enhanced PGE2-mediated salt and water excretion in the HPS/aBS model.
前列腺素E2(PGE2)生成增加是高前列腺素E综合征/产前巴特综合征(HPS/aBS)的关键环节,这是一种以氯化钠耗竭、水分丢失和高肾素血症为特征的肾脏疾病。环氧化酶抑制剂抑制PGE2生成可显著降低患者的死亡率和发病率。然而,PGE2在HPS/aBS中的致病作用尚待阐明。利尿剂对钠-钾-2氯协同转运蛋白NKCC2的慢性阻断会导致与HPS/aBS相似的症状,并提供了一个有用的动物模型。在野生型(WT)小鼠和缺乏不同PGE2受体(EP1-/-、EP2-/-、EP3-/-和EP4-/-)的小鼠中,测定了慢性给予呋塞米(7天)对尿量、钠和钾排泄以及肾素分泌的影响。此外,还分析了具有缺陷的前列环素I2受体(IP-/-)的小鼠中呋塞米诱导的利尿和肾素活性。在所有研究的动物中,呋塞米刺激了尿量和电解质排泄的增加。然而,这种作用在EP1-/-、EP3-/-和EP4-/-小鼠中减弱。与WT小鼠相比,EP2-/-和IP-/-小鼠中未观察到差异。呋塞米诱导的血浆肾素浓度升高在EP4-/-小鼠中显著降低,在IP-/-小鼠中也有一定程度的降低。用特异性拮抗剂ONO-AE3-208对呋塞米处理的WT小鼠进行EP4受体的药理抑制,模拟了EP4-/-小鼠中肾素mRNA表达、血浆肾素浓度、尿量和钠排泄的变化。与WT小鼠相比,EP4-/-小鼠的肾小球滤过率(GFR)没有变化,这表明EP4-/-小鼠中尿量减少和盐丢失不是GFR降低的结果。总之,这些发现表明EP4受体介导PGE2诱导的肾素分泌,并且EP1、EP3和EP4受体均有助于在HPS/aBS模型中增强PGE2介导的盐和水排泄。