Chin T A, Templeton D M
Department of Clinical Biochemistry, University of Toronto, Canada.
Toxicology. 1993 Jan 29;77(1-2):145-56. doi: 10.1016/0300-483x(93)90145-i.
Exposure of cultured rat mesangial cells to CdCl2 caused a dose- and time-dependent increase in intracellular glutathione that was significant at 0.5 microM and maximal at 1 microM Cd2+. The effect depended on glutathione synthesis and was masked by inhibiting synthesis with buthionine sulfoximine. The cells responded to slightly higher concentrations of Cd with a marked decrease in DNA synthesis, and reversible depletion of glutathione enhanced this sensitivity. Pre-induction of the thiol-rich protein metallothionein with ZnCl2 afforded a degree of protection to the glutathione-depleted cells. We conclude that the Cd-dependent elevation of glutathione in these cells may be protective at concentrations of Cd that can arise during acute environmental and occupational exposures.
将培养的大鼠系膜细胞暴露于氯化镉中,会导致细胞内谷胱甘肽呈剂量和时间依赖性增加,在0.5微摩尔时显著增加,在1微摩尔镉离子时达到最大值。这种效应依赖于谷胱甘肽的合成,用丁硫氨酸亚砜胺抑制合成会掩盖该效应。细胞对略高浓度的镉反应是DNA合成显著减少,而谷胱甘肽的可逆耗竭会增强这种敏感性。用氯化锌预先诱导富含硫醇的金属硫蛋白,可为谷胱甘肽耗竭的细胞提供一定程度的保护。我们得出结论,在急性环境和职业暴露可能出现的镉浓度下,这些细胞中镉依赖性谷胱甘肽升高可能具有保护作用。