Department of Pharmacology, Midwestern University, Downers Grove, IL 60515, USA.
Biometals. 2010 Oct;23(5):793-809. doi: 10.1007/s10534-010-9288-2. Epub 2010 Jan 27.
As the risks of cadmium (Cd)-induced kidney disease have become increasingly apparent, much attention has been focused on the development and use of sensitive biomarkers of Cd nephrotoxicity. The purpose of this review is to briefly summarize the current state of Cd biomarker research. The review includes overviews of the toxicokinetics of Cd, the mechanisms of Cd-induced proximal tubule injury, and mechanistic summaries of some of the biomarkers (N-acetyl-β-D-glucosamidase; β(2)-microglubulin, metallothionein, etc.) that have been most widely used in monitoring of human populations for Cd exposure and nephrotoxicity. In addition, several novel biomarkers (kidney injury molecule-1, α-glutathione-S-transferase and insulin) that offer the potential for improved biomonitoring of Cd-exposed populations are discussed.
随着镉(Cd)诱导的肾脏疾病的风险日益明显,人们越来越关注开发和使用镉肾毒性的敏感生物标志物。本文旨在简要总结 Cd 生物标志物研究的现状。本文综述了 Cd 的毒代动力学、Cd 诱导的近端肾小管损伤的机制以及一些已被广泛用于监测人群 Cd 暴露和肾毒性的生物标志物(N-乙酰-β-D-氨基葡萄糖苷酶;β(2)-微球蛋白、金属硫蛋白等)的机制总结。此外,还讨论了几种具有潜在改善 Cd 暴露人群生物监测能力的新型生物标志物(肾损伤分子-1、α-谷胱甘肽-S-转移酶和胰岛素)。