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Protective effect of metallothionein on cadmium toxicity in isolated rat hepatocytes.

机译:金属硫蛋白对离体大鼠肝细胞中镉毒性的保护作用。

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摘要

An isolated rat hepatocyte preparation was used to study the cellular toxicity of cadmium and the protective effects of metallothionein on cadmium-induced toxicity. Exposure of primary suspension cultures of isolated rat hepatocytes to Cd2+ (0-35.7 microM) for 15 min resulted in a dose-dependent reduction in the synthesis of cellular proteins during a subsequent 6 h incubation. Such inhibition could not be correlated with cellular lethality or gross membrane damage. Pre-induction of metallothionein in hepatocytes by zinc treatment in vivo of donor rats protected hepatocytes in vitro from cadmium-induced inhibition of protein synthesis. The protective effects in zinc-pre-induced hepatocytes are not due to alterations in the level of total cellular cadmium, but could be accounted for by the redistribution of intracellular cadmium in the presence of high levels of zinc-metallothionein. The data suggest that metallothionein exerts its protective effect by a kinetic detoxification mechanism, i.e. a decrease in reactive intracellular cadmium.
机译:使用分离的大鼠肝细胞制剂研究镉的细胞毒性以及金属硫蛋白对镉诱导的毒性的保护作用。将分离的大鼠肝细胞的原始悬浮培养物暴露于Cd2 +(0-35.7 microM)15分钟,导致随后6 h孵育过程中细胞蛋白合成的剂量依赖性降低。这种抑制作用与细胞致死率或总膜破坏无关。供体大鼠体内通过锌处理在肝细胞中预先诱导金属硫蛋白可保护肝细胞在体外免受镉诱导的蛋白质合成抑制。锌预诱导的肝细胞中的保护作用不是由于细胞总镉水平的改变,而是由于在高水平的锌-金属硫蛋白存在下细胞内镉的重新分布造成的。数据表明金属硫蛋白通过动力学解毒机制发挥其保护作用,即反应性细胞内镉的减少。

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