Center for Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic.
Kidney Blood Press Res. 2012;35(6):595-607. doi: 10.1159/000339883. Epub 2012 Aug 29.
The present study was performed to examine whether the blood pressure (BP)-lowering effects of soluble epoxide hydrolase (sEH) inhibition in two-kidney, one-clip (2K1C) Goldblatt hypertension are nitric oxide (NO) dependent.
Mice lacking the endothelial NO synthase (eNOS) gene (eNOS-/-) and their wild-type controls (eNOS+/+) underwent clipping of one renal artery. BP was monitored by radiotelemetry and the treatment with the sEH inhibitor cis-4-[4-(3-adamantan-1-yl-ureido)cyclohex-yloxy]-benzoic acid (c-AUCB) was initiated on day 25 after clipping and lasted for 14 days. Renal concentrations of epoxyeicosatrienoic acids (EETs) and their inactive metabolite dihydroxyeicosatrienoic acids (DHETs) were measured in the nonclipped kidney. Renal NO synthase (NOS) activity was determined by measuring the rate of formation of L-[(14)C]citruline from L-[(14)C]arginine.
Treatment with the sEH inhibitor elicited similar BP decreases that were associated with increases in daily sodium excretion in 2K1C eNOS+/+ as well as 2K1C eNOS-/- mice. In addition, treatment with the sEH inhibitor increased the ratio of EETs/DHETs in the nonclipped kidney of 2K1C eNOS+/+ as well as 2K1C eNOS-/- mice. Treatment with the sEH inhibitor did not alter renal NOS activity in any of the experimental groups.
Collectively, our present data suggest that the BP-lowering effects of chronic sEH inhibition in 2K1C mice are mainly associated with normalization of the reduced availability of biologically active EETs in the nonclipped kidney and their direct natriuretic actions.
本研究旨在探讨二肾一夹(2K1C)Goldblatt 高血压中可溶性环氧化物水解酶(sEH)抑制的降压作用是否依赖于一氧化氮(NO)。
缺乏内皮型一氧化氮合酶(eNOS)基因的小鼠(eNOS-/-)及其野生型对照(eNOS+/+)接受单侧肾动脉夹闭。通过无线电遥测监测血压,在夹闭后第 25 天开始用 sEH 抑制剂 cis-4-[4-(3-金刚烷-1-基-脲基)环己基氧基]-苯甲酸(c-AUCB)治疗,持续 14 天。在未夹闭的肾脏中测量环氧二十碳三烯酸(EETs)及其无活性代谢物二羟二十碳三烯酸(DHETs)的肾浓度。通过测量 L-[(14)C]精氨酸形成 L-[(14)C]瓜氨酸的速率来确定肾型一氧化氮合酶(NOS)活性。
sEH 抑制剂的治疗在 2K1C eNOS+/+以及 2K1C eNOS-/-小鼠中引起相似的血压降低,同时伴有每日钠排泄量增加。此外,sEH 抑制剂的治疗增加了 2K1C eNOS+/+以及 2K1C eNOS-/-小鼠未夹闭肾脏中 EETs/DHETs 的比值。在任何实验组中,sEH 抑制剂的治疗均未改变肾NOS 活性。
总的来说,我们目前的数据表明,2K1C 小鼠慢性 sEH 抑制的降压作用主要与未夹闭肾脏中生物活性 EETs 的可用性降低及其直接的利钠作用的正常化有关。