Kudo N, Nakagawa Y, Waku K
Faculty of Pharmaceutical Sciences, Teikyo University, Kanagawa, Japan.
Arch Toxicol. 1996;70(12):801-8. doi: 10.1007/s002040050342.
One major role of alveolar macrophages is the production of eicosanoids, which modulate immune and inflammatory processes in the lung. In this study, the effects were investigated of cadmium ions on the secretion of leukotriene (LT)B4 and prostaglandin (PG)E2, predominant products of lipoxygenase and cyclooxygenase, respectively. Cd2+ had an inhibitory effect on the secretion of LTB4 and PGE2 in response to A23187 stimulation at concentrations > 3 x 10(-5)M. This effect can be explained by the inhibition of arachidonic acid (20:4) liberation from membrane phospholipids by Cd2+, because Cd2+ inhibits both [3H] arachidonic acid (20:4) liberation from [3H]20:4-prelabeled macrophages and the cytosolic phospholipase A2 activity. At concentrations < 3 x 10(-5)M, Cd2+ had no effect on PGE2 secretion but showed an augmentation of LTB4 secretion. In vitro study using macrophage lysate showed enhanced LTB4 synthesis from arachidonic acid by Cd2+, which could be responsible for the augmentation of LTB4 secretion in cells. These results indicate that Cd2+ may increase inflammation by increasing LTB4 production in lung.
肺泡巨噬细胞的一个主要作用是产生类花生酸,其可调节肺部的免疫和炎症过程。在本研究中,研究了镉离子对白三烯(LT)B4和前列腺素(PG)E2分泌的影响,它们分别是脂氧合酶和环氧化酶的主要产物。在浓度>3×10⁻⁵M时,Cd²⁺对A23187刺激引起的LTB4和PGE2分泌具有抑制作用。这种作用可以通过Cd²⁺抑制膜磷脂中花生四烯酸(20:4)的释放来解释,因为Cd²⁺既抑制[³H]花生四烯酸(20:4)从[³H]20:4预标记的巨噬细胞中的释放,也抑制胞质磷脂酶A2的活性。在浓度<3×10⁻⁵M时,Cd²⁺对PGE2分泌没有影响,但显示LTB4分泌增加。使用巨噬细胞裂解物的体外研究表明,Cd²⁺可增强花生四烯酸合成LTB4,这可能是细胞中LTB4分泌增加的原因。这些结果表明,Cd²⁺可能通过增加肺部LTB4的产生来加重炎症。