Antonipillai I
Section of Endocrinology, USC Medical Center, Los Angeles 90033.
Proc Soc Exp Biol Med. 1990 Jul;194(3):224-30. doi: 10.3181/00379727-194-43083.
In isolated human or rat glomeruli, arachidonic acid can be metabolized by the cyclooxygenase pathway to prostaglandins or by the lipoxygenase pathway to hydroxyeicosatetraenoic acids (HETES). We have recently shown that 12-lipoxygenase products are potent inhibitors of renin release. Since prostacyclin (PGI2) is a potential renin secretagogue, we studied the direct effects of 12-lipoxygenase products on prostacyclin-induced renin secretion. Treatment of rat renal cortical slices with picomolar concentrations of 12-hydroperoxyeicosatetraenoic acid (12-HPETE) and 12-HETE blocked the prostacyclin- or iloprost (an analog of PGI2)-induced renin secretion. The inhibitory effects of 12-lipoxygenase products were not exhibited by the 5-lipoxygenase-derived products, leukotriene B4 and 5-HPETE. These results suggest that HETES are not only potent modulators of prostacyclin actions on renin, but that the concerted actions of these compounds in cells may be critical determinants of the juxtaglomerular cell secretion of renin.
在分离的人或大鼠肾小球中,花生四烯酸可通过环氧化酶途径代谢为前列腺素,或通过脂氧合酶途径代谢为羟基二十碳四烯酸(HETEs)。我们最近发现,12-脂氧合酶产物是肾素释放的有效抑制剂。由于前列环素(PGI2)是一种潜在的肾素分泌刺激剂,我们研究了12-脂氧合酶产物对前列环素诱导的肾素分泌的直接影响。用皮摩尔浓度的12-氢过氧二十碳四烯酸(12-HPETE)和12-HETE处理大鼠肾皮质切片,可阻断前列环素或伊洛前列素(PGI2的类似物)诱导的肾素分泌。5-脂氧合酶衍生产物白三烯B4和5-HPETE未表现出12-脂氧合酶产物的抑制作用。这些结果表明,HETEs不仅是前列环素对肾素作用的有效调节剂,而且这些化合物在细胞中的协同作用可能是肾小球旁细胞肾素分泌的关键决定因素。