Skip to main content
Log in

Two models for screening chelating agents for cadmium removal

  • Published:
Cell Biology and Toxicology Aims and scope Submit manuscript

Abstract

The effectiveness of some chelating agents to mobilize cadmium from Chinese hamster ovary cells after chronic exposure (20 hr), as well as from cytosolic metallothionein, was studied. In the first protocol, the most effective substance was 2,3-dimercaptopropanol, followed by 2,3-dimercaptopropane-1-sulfonate and 2,3-dimercaptosuccinic acid, whereas CaNa33-diethylenetriamine pentaacetic acid × 5H2O showed less effect. Simultaneous incubation of cells with cadmium and the chelating agent resulted in a different order of effectiveness: CaNa3 DTPA prevented cadmium uptake almost totally, 2,3-mercaptopropanol by 75% and 2,3-dimercaptopropane-1-sulfonate by 35%. Neither CaNa3-diethylenetriamine pentaacetic acid × 5H2O nor 2,3-dimercaptosuccinic acid had altered the distribution of cadmium between the cytosolic protein fractions after a 2 hr incubation of cells, whereas after this period, 2,3-dimercaptopropanol had removed all cadmium from metallothionein, and 2,3-dimercaptopropane-1-sulfonate about 50%. None of the chelating agents had reduced the amount of Cd bound to high molecular weight proteins. In the cell free system, 2,3-dimercaptopropanol and 2,3-dimercaptopropane-1-sulfonate were equally effective and removed all cadmium from metallothionein within ten minutes. CaNa3-diethylenetriamine pentaacetic acid × 5H2O, however, even after 60 min, had removed only 50% of the cadmium. The remaining cadmium was found distributed to the high molecular weight and lower molecular weight protein fractions.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

BAL:

2,3-dimercaptopropanol

CHO:

Chinese hamster ovary cells

DMPS:

2,3-dimercaptopropane-1-sulfonate

DMSA:

2,3-dimercaptosuccinic acid

DTPA:

CaNa3-diethylenetriaminepentaacetic acid × 5 H2O

HMW proteins:

high molecular weight proteins

MT:

metallothionein

References

  • BAKKA, A., AASETH, J. and RUGSTAD, E. (1981). Influence of certain chelating agents on egress of cadmium from cultured epithelial cells containing high amounts of metallothionein: A screening of Cd-releasing and toxic effects. Acta Pharmacol. et Toxicol. 49:432–437.

    Google Scholar 

  • CANTILENA, L.R., JR. and KLAASSEN, C.D. (1981). Comparison of the effectiveness of several chelators after single administration on the toxicity, excretion and distribution of cadmium. Toxicol. and Appl. Pharmacol. 5:452–460.

    Google Scholar 

  • CANTILENA, L.R., JR. and KLAASSEN, C.D. (1982a). Decreased effectiveness of chelating therapy with time after acute cadmium poisoning. Toxicol. and Appl. Pharmacol. 63:173–180.

    Google Scholar 

  • CANTILENA, L.R., JR. and KLAASSEN, C.D. (1982b). The effect of repeated administration of several chelators on the distribution and excretion of cadmium. Toxicol. and Appl. Pharmacol. 66:361–367.

    Google Scholar 

  • CANTILENA, L.R., JR., STACEY, N.H. and KLAASSEN, C.D. (1983). Isolated rat hepatocytes as a model system for screening chelators for use in cadmium intoxication. Toxicol. and Appl. Pharmacol. 66:257–263.

    Google Scholar 

  • CHERIAN, M.G. (1980). Chelation of cadmium with BAL and DTPA in rats. Nature (London) 287:871–872.

    Google Scholar 

  • CHERIAN, M.G. and RODGERS, K. (1982). Chelation of cadmium from metallothionein in vivo and its excretion in rats repeatedly injected with cadmium chloride. J. of Pharmacol. and Exp. Therapeutics 222:699–704.

    Google Scholar 

  • FISCHER, A.B. (1982). Uptake of 115mCd by mammalian cells (in vitro). Effects of chelating agents and of other heavy metals. In: Trace Metals in Environmental Health. Columbia, MO, XVI:244–251.

  • FISCHER, A.B. and SEIBOLD, G. (1985). Antidotal effects of chelating agents against cadmium induced cytotoxicity tested in vitro. International Conference of Heavy Metals in Environment 2:110–112.

    Google Scholar 

  • MAY, P.M., SMITH, G.L. and WILLIAMS, D.R. (1981). Speciation studies for cadmiumin vivo and an assessment of cadmium chelating drugs. In: Proceedings of International Conference on Heavy Metals in the Environment. Amsterdam, pp. 632–634.

  • PAGE, A.L., El-AMAMY, M.M. and CHANG, A.C. (1986). Cadmium in the environment and its entry into terrestrial food chain crops. In: Cadmium, Handbook of Experimental Pharmacology (E.C. Foulkes ed.), Vol. 80, pp. 33–74. Springer Verlag, Berlin. Heidelberg, New York, Tokyo.

    Google Scholar 

  • PLANAS-BORNE, F. and LEHMANN, M. (1983). Influence of chelating agents on the distribution and excretion of cadmium in rats. Toxicol. and Appl. Pharmacology. 67:408–416.

    Google Scholar 

  • RAU, W. and TAYLOR, D.M. (1985). A comparison of in vitro and in vivo models for screening chelating agents for cadmium removal. Plzen, Lek. Sborn., Suppl. 49:19–23.

    Google Scholar 

  • RAU, W. (1986). Die Bedeutung der biochemischen Bindung von Cadmium in der Zelle fur seine Mobilisierung. University of Heidelberg; Doctoral thesis.

  • RAU, W., PLANAS-BORNE, F. and TAYLOR, D.M. (1987). Influence of several chelating agents on the distribution and binding of cadmium in rats. Human Toxicol. 6:451–458.

    Google Scholar 

  • STACEY, N.H.A, CANTILENA, L.R., JR. and KLAASSEN, C.D. (1980). Cadmium toxicity and lipid peroxidation in isolated rat hepatocytes. Toxicol. and Appl. Pharmacol. 53:470–480.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Rau, W., Planas-Borne, F. & Taylor, D.M. Two models for screening chelating agents for cadmium removal. Cell Biol Toxicol 5, 91–99 (1989). https://doi.org/10.1007/BF00141067

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00141067

Key words

Navigation