Tsan M F, Danis E H, Del Vecchio P J, Rosano C L
Biochem Biophys Res Commun. 1985 Feb 28;127(1):270-6. doi: 10.1016/s0006-291x(85)80154-6.
We studied the role of glutathione in the endothelial cell defense against H2O2 damage. Treatment of endothelial cells with buthionine sulfoximine, an irreversible inhibitor of gamma-glutamylcysteine synthetase, depleted the cells of GSH, while L-2-oxothiazolidine-4-carboxylate, an effective intracellular cysteine delivery agent, markedly enhanced endothelial cell GSH concentration. Depletion of intracellular GSH sensitized the endothelial cells to injury by H2O2 either preformed or generated by the glucose-glucose oxidase system. In contrast, an increase of intracellular GSH protected the cells from H2O2 damage. There was an inverse, linear relationship between the intracellular GSH concentrations and killing of endothelial cells by H2O2. Our results suggest that enhancement of endothelial cell GSH may be an alternative approach toward the prevention of oxidant-induced endothelial damage such as adult respiratory distress syndrome.
我们研究了谷胱甘肽在内皮细胞抵御过氧化氢损伤中的作用。用丁硫氨酸亚砜胺(γ-谷氨酰半胱氨酸合成酶的不可逆抑制剂)处理内皮细胞,会耗尽细胞内的谷胱甘肽(GSH),而L-2-氧代噻唑烷-4-羧酸(一种有效的细胞内半胱氨酸递送剂)则显著提高内皮细胞的GSH浓度。细胞内GSH的耗尽使内皮细胞对预先形成的或由葡萄糖-葡萄糖氧化酶系统产生的过氧化氢损伤敏感。相反,细胞内GSH的增加可保护细胞免受过氧化氢损伤。细胞内GSH浓度与过氧化氢对内皮细胞的杀伤之间存在反比线性关系。我们的结果表明,提高内皮细胞GSH水平可能是预防诸如成人呼吸窘迫综合征等氧化应激诱导的内皮损伤的另一种方法。