Schewe C, Schewe T, Rohde E, Diezel W, Czarnetzki B M
Institute of Biochemistry, University Clinics Charité, Humboldt University of Berlin, Germany.
Arch Dermatol Res. 1994;286(3-4):137-41. doi: 10.1007/BF00374208.
The two commercial pharmaceutical preparations of ammonium bituminosulphonates, Leukichthol and Dark Ichthyol, were shown to inhibit the formation of 5S-hydroxy-6E,8Z,11Z,14Z-eicosatetraenoic acid (5-HETE) from external arachidonic acid by human polymorphonuclear leukocytes stimulated by ionophore A-23187 in a dose-dependent manner. Pure arachidonate 15-lipoxygenases from rabbit reticulocytes and soya beans, and the particulate prostaglandin endoperoxide synthase from sheep vesicular glands, were also inhibited. With the reticulocyte lipoxygenase, the Ichthyols suppressed the enzyme activity by two different mechanisms: (1) a prolongation of the lag period typical of lipoxygenase catalysis, and (2) by a lowering of the maximal enzymatic activity after the end of lag period. As expected, the first effect was reversed by the addition of the lipoxygenase product 13S-hydroperoxy-9Z,11E-octadecadienoic acid (13-HpODE). Ammonium bituminosulphonates are thus universal inhibitors of lipoxygenase activities, and the latter are of potential importance in inflammatory dermatoses.
两种商业药用的氨基磺酸铵盐制剂,即白鱼石脂和黑鱼石脂,已被证明能剂量依赖性地抑制离子载体A - 23187刺激的人多形核白细胞从外源性花生四烯酸形成5S - 羟基 - 6E,8Z,11Z,14Z - 二十碳四烯酸(5 - HETE)。兔网织红细胞和大豆中的纯花生四烯酸15 - 脂氧合酶以及绵羊精囊中的微粒体前列腺素内过氧化物合酶也受到抑制。对于网织红细胞脂氧合酶,鱼石脂通过两种不同机制抑制酶活性:(1)延长脂氧合酶催化典型的延迟期,(2)在延迟期结束后降低最大酶活性。正如预期的那样,添加脂氧合酶产物13S - 氢过氧 - 9Z,11E - 十八碳二烯酸(13 - HpODE)可逆转第一种效应。因此,氨基磺酸铵盐是脂氧合酶活性的通用抑制剂,而脂氧合酶在炎症性皮肤病中具有潜在重要性。