Kutsky P, Falck J R, Weiss G B, Manna S, Chacos N, Capdevila J
Prostaglandins. 1983 Jul;26(1):13-21. doi: 10.1016/0090-6980(83)90070-9.
The 5,6-; 8,9-; 11,12- and 14,15-epoxyeicosatrienoic acids and their respective hydration products, the vic-diols, recently reported as metabolites of arachidonic acid in rat liver microsomes, were examined for effect on release of 45Ca from canine aortic smooth muscle microsomes. At 10(-6) M, the diols had no effect, but the 5,6-; 11,12- and 14,15-epoxyacids increased the loss of 45Ca. Further studies with the 14,15-epoxyacid demonstrated a dose-dependent decrease of Ca++ uptake (ATP present) in canine aortic microsomes in 0.03 mM Ca++, whereas Ca++ binding (ATP absent) was not affected. Ca++ uptake, binding and release in rat liver microsomes was similarly affected by the 14,15-epoxyacid, the major epoxyeicosatrienoic acid derivative produced by rat liver microsomal incubations. It is suggested that alterations in Ca++ metabolism might be a possible mechanism of action for these derivatives of arachidonic acid.
5,6-;8,9-;11,12-和14,15-环氧二十碳三烯酸及其各自的水合产物即邻二醇,最近被报道为大鼠肝脏微粒体中花生四烯酸的代谢产物,研究了它们对犬主动脉平滑肌微粒体中45Ca释放的影响。在10(-6) M浓度下,邻二醇无作用,但5,6-;11,12-和14,15-环氧酸增加了45Ca的流失。对14,15-环氧酸的进一步研究表明,在0.03 mM Ca++条件下,犬主动脉微粒体中Ca++摄取(存在ATP)呈剂量依赖性降低,而Ca++结合(不存在ATP)不受影响。大鼠肝脏微粒体中的Ca++摄取、结合和释放同样受到14,15-环氧酸的影响,14,15-环氧酸是大鼠肝脏微粒体孵育产生的主要环氧二十碳三烯酸衍生物。提示Ca++代谢的改变可能是这些花生四烯酸衍生物的一种可能作用机制。