Kroetz Deanna L, Zeldin Darryl C
Department of Biopharmaceutical Sciences, School of Pharmacy, University of California, San Francisco, USA.
Curr Opin Lipidol. 2002 Jun;13(3):273-83. doi: 10.1097/00041433-200206000-00007.
Cytochrome P450s metabolize arachidonic acid to hydroxyeicosatetraenoic acids and epoxyeicosatrienoic acids. These eicosanoids are formed in a tissue and cell-specific manner and have numerous biological functions. Of major interest are the opposing actions of hydroxyeicosatetraenoic and epoxyeicosatrienoic acids within the vasculature. Regio- and stereoisomeric epoxyeicosatrienoic acids have potent vasodilatory properties while 20-hydroxyeicosatetraenoic acid is a potent vasoconstrictor. Both effects are mediated through actions on large-conductance Ca2+-activated K+ channels. Cytochrome P450-derived eicosanoids are also important in the regulation of ion transport, and have recently been shown to influence a number of fundamental biological processes including cellular proliferation, apoptosis, inflammation, and hemostasis. The formation of these functionally relevant eicosanoids is tightly controlled by the expression and activity of the cytochrome P450 epoxygenases and hydroxylases. In addition, soluble epoxide hydrolase catalyzes the hydrolysis of epoxyeicosatrienoic acids to dihydroxyeicosatrienoic acids, and the activity of this enzyme is a critical determinant of tissue epoxyeicosatrienoic and dihydroxyeicosatrienoic acid levels. The intracellular balance between epoxyeicosatrienoic, dihydroxyeicosatrienoic and hydroxyeicosatetraenoic acids influences the biological response to these eicosanoids and alterations in their levels have recently been associated with certain pathological conditions. The involvement of the cytochrome P450-derived eicosanoids in a wide array of biological functions and the observation that levels are altered in pathological conditions suggest that the enzymes involved in the formation and degradation of these fatty acids may be novel therapeutic targets.
细胞色素P450将花生四烯酸代谢为羟基二十碳四烯酸和环氧二十碳三烯酸。这些类花生酸以组织和细胞特异性方式形成,并具有多种生物学功能。血管系统中羟基二十碳四烯酸和环氧二十碳三烯酸的相反作用是主要研究兴趣点。区域和立体异构的环氧二十碳三烯酸具有强大的血管舒张特性,而20-羟基二十碳四烯酸是一种强大的血管收缩剂。这两种作用均通过对大电导钙激活钾通道的作用介导。细胞色素P450衍生的类花生酸在离子转运调节中也很重要,并且最近已显示其会影响许多基本生物学过程,包括细胞增殖、凋亡、炎症和止血。这些功能相关类花生酸的形成受到细胞色素P450环氧化酶和羟化酶的表达和活性的严格控制。此外,可溶性环氧化物水解酶催化环氧二十碳三烯酸水解为二羟基二十碳三烯酸,该酶的活性是组织中环氧二十碳三烯酸和二羟基二十碳三烯酸水平的关键决定因素。环氧二十碳三烯酸、二羟基二十碳三烯酸和羟基二十碳四烯酸之间的细胞内平衡影响对这些类花生酸的生物学反应,并且它们水平的改变最近已与某些病理状况相关联。细胞色素P450衍生的类花生酸参与广泛的生物学功能,以及在病理状况下其水平会改变这一观察结果表明,参与这些脂肪酸形成和降解的酶可能是新的治疗靶点。