Antonipillai I, Nadler J, Horton R
Section of Endocrinology, University of Southern California School of Medicine, Los Angeles 90033.
Endocrinology. 1988 Apr;122(4):1277-81. doi: 10.1210/endo-122-4-1277.
Angiotensin II (AII) action on adrenal and smooth muscle cells is mediated via mechanisms that include changes in calcium flux and phosphoinositide hydrolysis. Phosphoinositide metabolism results in the release of arachidonic acid, a precursor of both the cyclooxygenase (CO) and lipoxygenase (LO) pathway. The effects of both LO and CO inhibitors on AII action were studied using both static incubations and perifusions of rat renal cortical slices. 12-Hydroperoxyeicosatetraenoic acid and its stable metabolite 12-hydroxyacid mimicked the inhibitory actions of AII on renin. A specific CO blocker did not alter AII inhibition of renin and a 5-LO blocker U60,257 was also ineffective, whereas the LO blockers BW755c, phenidone, and baicalein all eliminated or interfered with the action of AII on renin. All inhibition in the presence of a LO blocker was restored by adding nanomolar concentrations of 12-hydroperoxyeicosatetraenoic acid. LO inhibitors were specific for blocking AII, as they did not interfere with potassium (K+)-induced renin inhibition. These results imply that 12 and/or 15 products of the LO pathway are involved in AII action.
血管紧张素II(AII)对肾上腺和平滑肌细胞的作用是通过包括钙通量变化和磷酸肌醇水解在内的机制介导的。磷酸肌醇代谢导致花生四烯酸的释放,花生四烯酸是环氧化酶(CO)和脂氧化酶(LO)途径的前体。使用大鼠肾皮质切片的静态孵育和灌流研究了LO和CO抑制剂对AII作用的影响。12-氢过氧化二十碳四烯酸及其稳定代谢产物12-羟基酸模拟了AII对肾素的抑制作用。一种特异性CO阻滞剂不会改变AII对肾素的抑制作用,5-LO阻滞剂U60,257也无效,而LO阻滞剂BW755c、非那吡啶和黄芩苷均消除或干扰了AII对肾素的作用。通过添加纳摩尔浓度的12-氢过氧化二十碳四烯酸,在存在LO阻滞剂的情况下的所有抑制作用均得以恢复。LO抑制剂对阻断AII具有特异性,因为它们不会干扰钾(K+)诱导的肾素抑制作用。这些结果表明,LO途径的12和/或15产物参与了AII的作用。