Metallothioneins and diseases with special reference to cadmium poisoning

G. Nordberg, T. Jin, P. Leffler, Mona Svensson, T. Zhou, M. Nordberg
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引用次数: 25

Abstract

Metallothionein (MT) a low molecular weight metal binding protein, is involved in several human diseases. Brain tissue from Alzheimers patients contains lower concentrations of Growth Inhibitory Factor or MT-3. Induction of MT by bismuth increases resistance to renal toxicity of cis-platinum and may be advantageous in can- cer therapy. Cadmium exposure induces MT-syn- thesis in liver, binding Cd and protecting against acute toxicity. Cd-MT is released from liver into plasma, filtered in renal glomerulus and absor- bed in tubules. Lysosomal breakdown of MT releases toxic Cd. This mechanism explains renal tubular damage after long-term exposure to Cd. Impaired tubular regulation of calcium and vita- min D metabolism contributes to the develop- ment of the adverse effects on the skeleton. Quantitative, specific polymerase chain reaction (PCR) studies showed increased expression of mRNA of MT in testicles after Cd exposure, sup- porting the notion that MT increases cellular resistance to metals and protects from Cd toxi- city. This idea was advanced by one of the pre- sent authors thirty years ago.
金属硫蛋白与镉中毒的疾病
金属硫蛋白(MT)是一种低分子量的金属结合蛋白,与多种人类疾病有关。阿尔茨海默病患者的脑组织含有较低浓度的生长抑制因子或MT-3。铋诱导MT增加顺铂对肾毒性的抵抗,可能有利于癌症治疗。镉暴露诱导肝脏mt合成,结合Cd,防止急性中毒。Cd-MT从肝脏释放进入血浆,在肾小球中过滤,并在小管中吸收。MT的溶酶体分解释放出有毒的Cd。这一机制解释了长期暴露于Cd后肾小管的损伤。小管对钙和维生素D代谢的调节受损有助于骨骼不良反应的发展。定量、特异性聚合酶链反应(PCR)研究显示,在镉暴露后,睾丸中MT mRNA的表达增加,支持MT增加细胞对金属的抵抗力并保护细胞免受镉中毒的观点。这个想法是由现在的一位作者在三十年前提出的。
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