Deneke S M, Steiger V, Fanburg B L
Pulmonary Division, New England Medical Center Hospitals, Boston, Massachusetts.
J Appl Physiol (1985). 1987 Nov;63(5):1966-71. doi: 10.1152/jappl.1987.63.5.1966.
Intracellular glutathione was increased by 80% after exposure of bovine pulmonary arterial endothelial cells to 80% O2 (hyperoxia) for 24 h. No change in glutathione occurred in cells exposed to hypoxia (3% O2) for a corresponding period of time. The rate of uptake of [3H]glutamic acid also increased by 35-55% after 24 h of exposure of cells to hyperoxia, whereas exposure to hypoxia had no effect on the [3H]glutamic acid uptake. The increase in glutamic acid uptake reflected a specific effect on amino acid transport systems rather than a change in cell membrane permeability. The major portion of the increased uptake was inhibited by the elimination of sodium and the addition of the competitive inhibitor, cystine, to the incubation medium. Thus increases in glutamic acid uptake parallel increases in cellular glutathione, and glutamic acid may be a regulating factor in the increase in glutathione after exposure to hyperoxia.
将牛肺动脉内皮细胞暴露于80%氧气(高氧)24小时后,细胞内谷胱甘肽增加了80%。在相应时间段内,将细胞暴露于低氧(3%氧气)环境中,谷胱甘肽没有变化。细胞暴露于高氧24小时后,[3H]谷氨酸的摄取率也增加了35 - 55%,而暴露于低氧对[3H]谷氨酸的摄取没有影响。谷氨酸摄取的增加反映了对氨基酸转运系统的特异性作用,而非细胞膜通透性的改变。摄取增加的主要部分可通过去除钠并在孵育培养基中添加竞争性抑制剂胱氨酸来抑制。因此,谷氨酸摄取的增加与细胞内谷胱甘肽的增加平行,并且谷氨酸可能是暴露于高氧后谷胱甘肽增加的调节因子。