Sud'ina G F, Barskiĭ O A, Varfolomeev S D
Biokhimiia. 1990 Sep;55(9):1655-9.
By using high performance liquid chromatography with simultaneous detection of unlabeled and radiolabeled product of lipoxygenase oxidation of arachidonic acid, the mechanism of exogenous arachidonate involvement in leukotriene synthesis in human neutrophils induced by the Ca2+ ionophore A23187 was studied. It was found that after addition of labeled arachidonate the specific radioactivity of the reaction product (leukotriene B4) does not change on a time scale, i.e., the free arachidonic acid exchange between the cell and extracellular space is a very rapid process. Exogenous arachidonic acid was found to be the substrate of the lipoxygenase reaction which acts in parallel with the endogenous one. The dependence of specific radioactivity of leukotriene B4 in added arachidonic acid concentration is described by a hyperbolic curve with saturation. When exogenous arachidonate is used at a concentration of 10.8 +/- 3.9 microM, that of intracellular arachidonic acid increases twofold at the expense of the exogenously added acid.
通过使用高效液相色谱法同时检测花生四烯酸脂氧合酶氧化的未标记和放射性标记产物,研究了外源性花生四烯酸参与钙离子载体A23187诱导的人中性粒细胞白三烯合成的机制。研究发现,添加标记的花生四烯酸后,反应产物(白三烯B4)的比放射性在时间尺度上没有变化,即细胞与细胞外空间之间的游离花生四烯酸交换是一个非常快速的过程。外源性花生四烯酸被发现是脂氧合酶反应的底物,它与内源性底物并行起作用。白三烯B4的比放射性与添加的花生四烯酸浓度的关系由一条具有饱和度的双曲线描述。当以10.8±3.9微摩尔的浓度使用外源性花生四烯酸时,细胞内花生四烯酸的浓度以外源性添加的酸为代价增加了两倍。