Sakamoto H, Kitahara J, Nakagawa Y
School of Pharmaceutical Sciences, Kitasato University, Minato-ku, Tokyo, 108-8641, Japan.
J Biochem. 1999 Jan;125(1):90-5. doi: 10.1093/oxfordjournals.jbchem.a022274.
The liberation of arachidonic acid and the production of prostaglandin D2 (PGD2) were significantly influenced by peroxide and the level of intracellular glutathione (GSH). The productions of free arachidonic acid and PGD2 in RBL-2H3 cells were enhanced considerably by exposure to tert-butyl hydroperoxide (t-BHP). The liberation of arachidonic acid induced by t-BHP was not inhibited by EGTA. The productions of PGD2 and arachidonic acid induced by t-BHP were significantly facilitated by the depletion of intracellular GSH using buthionine sulfoximine (BSO) or diethyl maleate (DEM), although the depletion of GSH had no effect on the production of PGD2 induced by A23187. t-BHP failed to activate the conversion of free arachidonic acid to PGD2, since the formation of PGD2 from exogenously added arachidonic acid was not enhanced by treatment with t-BHP. The level of lipid hydroperoxides in t-BHP-treated cells was significantly elevated by treatment with DEM. These results suggest that hydroperoxides increase the free arachidonic acid available for the synthesis of PGD2 by activating phospholipase A2 (PLA2) and that the depletion of GSH by DEM accelerates the activation of PLA2 by raising peroxide levels in cells. Thus, the observed alterations in GSH levels are large enough to cause increased PGD2 synthesis in RBL-2H3 cells exposed to oxidative stress.
花生四烯酸的释放和前列腺素D2(PGD2)的产生受到过氧化物和细胞内谷胱甘肽(GSH)水平的显著影响。用叔丁基过氧化氢(t-BHP)处理可显著增强RBL-2H3细胞中游离花生四烯酸和PGD2的产生。EGTA不能抑制t-BHP诱导的花生四烯酸释放。用丁硫氨酸亚砜胺(BSO)或马来酸二乙酯(DEM)消耗细胞内GSH可显著促进t-BHP诱导的PGD2和花生四烯酸的产生,尽管GSH的消耗对A23187诱导的PGD2产生没有影响。t-BHP未能激活游离花生四烯酸向PGD2的转化,因为用t-BHP处理并未增强外源性添加花生四烯酸生成PGD2的过程。用DEM处理可显著提高t-BHP处理细胞中脂质氢过氧化物的水平。这些结果表明,氢过氧化物通过激活磷脂酶A2(PLA2)增加了可用于合成PGD2的游离花生四烯酸,并且DEM消耗GSH通过提高细胞内过氧化物水平加速了PLA2的激活。因此,观察到的GSH水平变化足以导致暴露于氧化应激的RBL-2H3细胞中PGD2合成增加。