Interaction of Chelating Agents with Cadmium in Mice and Rats

The influence of several chelating agents (CaDTPA, ZnDTPA, CaEDTA, ZnEDTA, DMSA, D-penicillamine and DMPS, DMP and DDC) on the acute toxicity of CdCl2and on the whole body retention and tissue distribution of cadmium after the IV application of115 mCdCl2was compared in mice. The chelating agents wer...

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Veröffentlicht in:Environ. Health Perspect.; (United States) 1984-03, Vol.54, p.267-273
Hauptverfasser: Eybl, Vladislav, Sýkora, Jindřich, Koutenský, Jaroslav, Caisová, Dagmar, Schwartz, Alexandr, Mertl, František
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Sprache:eng
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Zusammenfassung:The influence of several chelating agents (CaDTPA, ZnDTPA, CaEDTA, ZnEDTA, DMSA, D-penicillamine and DMPS, DMP and DDC) on the acute toxicity of CdCl2and on the whole body retention and tissue distribution of cadmium after the IV application of115 mCdCl2was compared in mice. The chelating agents were applied immediately after the application of cadmium. CaDTPA, ZnDTPA and DMSA appeared to be the most effective antidotes. However, DMSA increased the amount of cadmium retained in kidneys. The treatment of cadmium-poisoned mice with the combination of DMSA (IP) and ZnDTPA (SC) (all the compounds were injected in equimolar dose) decreased the toxicity of cadmium more than treatment with one chelating agents (given in a 2:1 dose). However, by studying the effect of these chelating agents and their combination of the retention and distribution of Cd in mice, it was demonstrated that the combined application of the antidotes showed little or no improvement over the results obtained with the most effective of the individual components. In the urine of rats injected with CdCl2and treated with the chelating agents (CaDTPA, ZnDTPA, DMSA), the presence of cadmium complexes was demonstrated. The formation of mixed ligand chelates in vivo was not proved. Experiments in mice given a single injection of115 mCd-labeled Cd complexes of DMPS, DMSA and DTPA showed a high retention of cadmium in the organisms after the IV application of CdDMPS and CdDMSA complexes.
ISSN:0091-6765
1552-9924
DOI:10.1289/ehp.8454267