Iversen L, Fogh K, Kragballe K
Department of Dermatology, Marselisborg Hospital, University of Aarhus, Denmark.
Arch Dermatol Res. 1992;284(4):222-6. doi: 10.1007/BF00375798.
The purpose of the present study was to determine the effect of the n-6 fatty acid, dihomogammalinolenic acid (DGLA, 20: 3, n-6) on arachidonic acid (AA) (C20: 4) metabolism by human peripheral mononuclear leukocytes (HPML). After incubation of HPML with A23187 (5 microM) and DGLA, the cyclooxygenase (CO) and lipoxygenase (LO) products were separated and quantified by reversed-phase high-performance liquid chromatography (RP-HPLC) combined with radioimmunoassay. DGLA led to no change in PGE2 formation, but at similar concentrations there was a dose-dependent decrease in LTB4 formation (IC50 = 45.0 microM). The inhibition of LTB4 formation by DGLA was associated with a dose-dependent increase in its 15-LO metabolite 15-hydroxyeicosatraenoic acid (15-HETrE) and its CO metabolite prostaglandin E1 (PGE1). Incubation of HPLM with 15-HETrE (0-1.5 microM) alone did not result in a change in PGE2 formation, whereas 15-HETrE was a much more potent inhibitor of LTB4 formation (IC50 = 0.5 microM) than DGLA. These results show that the addition of DGLA to HPML results in a selective inhibition of LTB4 formation, presumably via its metabolite (15-HETrE).
本研究的目的是确定n-6脂肪酸二高γ-亚麻酸(DGLA,20:3,n-6)对人外周血单个核白细胞(HPML)花生四烯酸(AA,C20:4)代谢的影响。在用A23187(5微摩尔)和DGLA孵育HPML后,通过反相高效液相色谱(RP-HPLC)结合放射免疫测定法分离并定量环氧化酶(CO)和脂氧化酶(LO)产物。DGLA对PGE2的生成没有影响,但在相似浓度下,LTB4的生成呈剂量依赖性降低(IC50 = 45.0微摩尔)。DGLA对LTB4生成的抑制作用与其15-LO代谢产物15-羟基二十碳四烯酸(15-HETrE)及其CO代谢产物前列腺素E1(PGE1)的剂量依赖性增加有关。单独用15-HETrE(0 - 1.5微摩尔)孵育HPML不会导致PGE2生成的变化,而15-HETrE对LTB4生成的抑制作用(IC50 = 0.5微摩尔)比DGLA更强。这些结果表明,向HPML中添加DGLA会导致LTB4生成的选择性抑制,可能是通过其代谢产物(15-HETrE)实现的。