Escalante B, Falck J R, Yadagiri P, Sun L M, Laniado-Schwartzman M
Department of Pharmacology, New York Medical College, Valhalla 10595.
Biochem Biophys Res Commun. 1988 May 16;152(3):1269-74. doi: 10.1016/s0006-291x(88)80422-4.
Omega- and omega-1 hydroxylations are the major pathways by which arachidonic acid is metabolized in cortical and outer medullary microsomes of rat and rabbit kidneys. It is a cytochrome P450-dependent oxidation leading to the formation of 20-hydroxy- and 19-hydroxyeicosatetraenoic acids. In this study, we compared the effects of the synthetically prepared omega- and omega-1 metabolites of arachidonic acid on the activity of the renal Na+-K+-ATPase partially purified from rat renal cortical microsomes. 19(S)-hydroxyeicosatetraenoic acid caused a dose related stimulation of Na+-K+-ATPase activity with an EC50 of 3 x 10(-7) M. In contrast, neither 19(R)-hydroxyeicosatetraenoic acid, 20-hydroxyeicosatetraenoic acid nor arachidonic acid at 10(-6) M had any effect on Na+-K+-ATPase activity. In the same preparation, ouabain at 10(-3) M and 12(R)-hydroxyeicosatetraenoic acid at 10(-6) M inhibited the enzyme activity by 75% and 60%, respectively. We conclude that 19(S)-hydroxyeicosatetraenoic acid is a specific stimulator of renal Na+-K+-ATPase. Therefore, the formation of 19(S)-hydroxyeicosatetraenoic acid by renal cortical cytochrome P450 omega-1-hydroxylase may contribute to the regulation of renal function by regulating Na+-K+-ATPase which is essential for transtubular transport processes.
ω-羟化和ω-1羟化是花生四烯酸在大鼠和兔肾脏皮质及外髓质微粒体中代谢的主要途径。这是一种细胞色素P450依赖性氧化反应,可导致生成20-羟基-和19-羟基二十碳四烯酸。在本研究中,我们比较了人工合成的花生四烯酸ω-和ω-1代谢产物对从大鼠肾皮质微粒体中部分纯化的肾Na+-K+-ATP酶活性的影响。19(S)-羟基二十碳四烯酸引起Na+-K+-ATP酶活性呈剂量依赖性刺激,半数有效浓度(EC50)为3×10(-7)M。相比之下,19(R)-羟基二十碳四烯酸、20-羟基二十碳四烯酸以及10(-6)M的花生四烯酸对Na+-K+-ATP酶活性均无任何影响。在同一制剂中,10(-3)M的哇巴因和10(-6)M的12(R)-羟基二十碳四烯酸分别使该酶活性抑制了75%和60%。我们得出结论,19(S)-羟基二十碳四烯酸是肾Na+-K+-ATP酶的特异性刺激剂。因此,肾皮质细胞色素P450 ω-1-羟化酶生成19(S)-羟基二十碳四烯酸可能通过调节对肾小管转运过程至关重要的Na+-K+-ATP酶来参与肾功能的调节。