This research proposal will investigate the metabolism and toxicity of cadmium in mammalian systems. The role of metallothionein in metal metabolism and toxicity will also be evaluated. Three types of mammalian systems will be utilized: Populations environmentally or occupationally exposed to cadmium, rats and mice experimentally exposed to the metal, and primary cultures of adult rat hepatocytes and renal tubular epithelial cells pulsed with the metal. The studies in humans will evaluate whether urinary metallothionein is related to the tissue cadmium levels and whether its concentrations in urine is also related to the renal function. Metallothionein levels in human and animal tissues, cells, and biological fluids will be determined using the radio-immunoassay developed in this laboratory. Improvements in the assay will be made to further increase its sensitivity. Studies in rats will be carried out to understand the role of metallothionein in metal-induced renal dysfunction. Mice will be used to address the issue of strain differences in susceptibility to testicular and hepatic damage induced by acute cadmium exposure. The cell culture studies are planned to gain insight about the mechanism of metal uptake, metallothionein induction and its toxicity. There is a need to identify a specific biological indicator of cadmium exposure since blood and urinary cadmium levels are only indicative of recent exposure. It is expected that as a result of the studies proposed in this application the assay of metallothionein in biological fluids may evolve as the much needed routine screening procedure for assessing the extent of exposure and hence toxicity of the metal in human populations that may be at risk.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES003187-03
Application #
3250341
Study Section
Toxicology Study Section (TOX)
Project Start
1983-02-01
Project End
1986-07-31
Budget Start
1985-08-01
Budget End
1986-07-31
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Rhode Island
Department
Type
Schools of Pharmacy
DUNS #
135531015
City
Kingston
State
RI
Country
United States
Zip Code
Tang, Weifeng; Xie, Jianxun; Shaikh, Zahir A (2006) Protection of renal tubular cells against the cytotoxicity of cadmium by glycine. Toxicology 223:202-8
Tang, W; Shaikh, Z A (2001) Renal cortical mitochondrial dysfunction upon cadmium metallothionein administration to Sprague-Dawley rats. J Toxicol Environ Health A 63:221-35
Limaye, D A; Shaikh, Z A (1999) Cytotoxicity of cadmium and characteristics of its transport in cardiomyocytes. Toxicol Appl Pharmacol 154:59-66
Shaikh, Z A; Zaman, K; Tang, W et al. (1999) Treatment of chronic cadmium nephrotoxicity by N-acetyl cysteine. Toxicol Lett 104:137-42
Shaikh, Z A; Northup, J B; Vestergaard, P (1999) Dependence of cadmium-metallothionein nephrotoxicity on glutathione. J Toxicol Environ Health A 57:211-22
Shaikh, Z A; Tang, W (1999) Protection against chronic cadmium toxicity by glycine. Toxicology 132:139-46
Tang, W; Kido, T; Gross, W A et al. (1999) Measurement of cadmium-induced metallothionein in urine by ELISA and prevention of overestimation due to polymerization. J Anal Toxicol 23:153-8
Shaikh, Z A; Jordan, S A; Tang, W (1999) Protection against chronic cadmium toxicity by caloric restriction. Toxicology 133:93-103
Shaikh, Z A; Vu, T T; Zaman, K (1999) Oxidative stress as a mechanism of chronic cadmium-induced hepatotoxicity and renal toxicity and protection by antioxidants. Toxicol Appl Pharmacol 154:256-63
Tang, W; Sadovic, S; Shaikh, Z A (1998) Nephrotoxicity of cadmium-metallothionein: protection by zinc and role of glutathione. Toxicol Appl Pharmacol 151:276-82

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