Literature DB >> 1653637

Effects of chelating agents on the cadmium burden of cells in culture.

F Planas-Bohne1, M M Jones, P K Singh.   

Abstract

The effects of some new chelating agents on the cadmium burden of CHO cells in culture were investigated. The chelators were sodium-N-(4-methoxybenzyl)-D-glucamine-dithiocarbamate (MeOBG-DTC), sodium-N-benzyl-D-glucaminedithiocarbamate (BG-DTC) and diisopropylmeso-2,3-dimercapto succinate (DiP-DMSA). The results were compared with the effect of the well known dimercaptopropanol (BAL). The derivates of dithiocarbamate are much less toxic than DiP-DMSA and BAL. All chelators effectively prevent Cd uptake into the cells. Mobilization of intracellular Cd, however, is more effective by the DTC-derivatives than by DiP-DMSA or BAL. Within the cell the major fraction of Cd after 48 hours incubation is found in the nuclei and cytosol and very little in the peroxisomes. The chelating agents remove the metal mostly from nuclei and cytosol. Incubation of the cells with cadmium leads to the induction of a Cd binding protein of an apparent molecular weight of 12500 Da, presumably metallothionein. MeOBG-DTC is more effective in removing the metal from this protein than BG-DTC.

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Year:  1991        PMID: 1653637     DOI: 10.1007/bf00122829

Source DB:  PubMed          Journal:  Cell Biol Toxicol        ISSN: 0742-2091            Impact factor:   6.691


  18 in total

1.  The effect of repeated administration of several chelators on the distribution and excretion of cadmium.

Authors:  L R Cantilena; C D Klaassen
Journal:  Toxicol Appl Pharmacol       Date:  1982-12       Impact factor: 4.219

2.  Determination and metabolism of dithiol chelating agents: X. In humans, meso-2,3-dimercaptosuccinic acid is bound to plasma proteins via mixed disulfide formation.

Authors:  R M Maiorino; J M Akins; K Blaha; D E Carter; H V Aposhian
Journal:  J Pharmacol Exp Ther       Date:  1990-08       Impact factor: 4.030

3.  Effect of N-benzyl-D-glucamine dithiocarbamate on the renal toxicity produced by subacute exposure to cadmium in rats.

Authors:  S Kojima; H Ono; M Kiyozumi; T Honda; A Takadate
Journal:  Toxicol Appl Pharmacol       Date:  1989-03-15       Impact factor: 4.219

4.  Two models for screening chelating agents for cadmium removal.

Authors:  W Rau; F Planas-Bohne; D M Taylor
Journal:  Cell Biol Toxicol       Date:  1989-01       Impact factor: 6.691

5.  Chelation of cadmium from metallothionein in vivo and its excretion in rats repeatedly injected with cadmium chloride.

Authors:  M G Cherian; K Rodgers
Journal:  J Pharmacol Exp Ther       Date:  1982-09       Impact factor: 4.030

6.  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.

Authors:  A Bakka; J Aaseth; H E Rugstad
Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1981-11

7.  Influence of chelating agents on the distribution and excretion of cadmium in rats.

Authors:  F Planas-Bohne; M Lehmann
Journal:  Toxicol Appl Pharmacol       Date:  1983-03-15       Impact factor: 4.219

8.  Use of the Topliss scheme for the design of more effective chelating agents for cadmium decorporation.

Authors:  S G Jones; P K Singh; M M Jones
Journal:  Chem Res Toxicol       Date:  1988 Jul-Aug       Impact factor: 3.739

9.  Roles of metallothionein and related proteins in metal metabolism and toxicity: problems and perspectives.

Authors:  D H Petering; B A Fowler
Journal:  Environ Health Perspect       Date:  1986-03       Impact factor: 9.031

10.  Chelation of cadmium.

Authors:  O Andersen
Journal:  Environ Health Perspect       Date:  1984-03       Impact factor: 9.031

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