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Journal ArticleDOI

Dmsa and dmps-water soluble antidotes for heavy metal poisoning

H V Aposhian
- 01 Jan 1983 - 
- Vol. 23, Iss: 1, pp 193-215
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TLDR
This article reviews the pharmacological properties and the uses of two important antidotes for heavy metal poisoning, DMSA and DMPS, water soluble chemical analogs of dimercaprol, which have less toxicity, greater water solubility, and lim­ ited lipid solubilities, and are effective when given orally.
Abstract
This article reviews the pharmacological properties and the uses of two important antidotes for heavy metal poisoning. Meso-dimercaptosuccinic acid (DMSA) and 2,3-dimercapto-l-propanesulfonic acid, Na salt (DMPS) are relatively new antidotes-new, that is, to the western world. Although DMSA was introduced originally by Friedheim et al (1) to increase uptake of antimony during schistosomiasis therapy, Liang et al (77) at Shanghai in 1957 were the first to report its effectiveness as an antidote for heavy metal poisoning. The synthesis and some of the metal binding properties of DMPS were reported in 1956 by Petrunkin from Kiev (3). Shortly thereaf­ ter, DMPS became an official drug in the Soviet Union, where it is known as Unithiol (4). Between 1956 and 1975, DMSA and DMPS were studied extensively, at both the basic science and clinical levels, in the People's Republic of China, the Soviet Union, and Japan. Some of these investigations have been cited and can be found in an earlier review (5). In the USA and western Europe, however, these two compounds received very little attention until recently. A paper by Friedheim & Corvi (6) in 1975, dealing with DMSA for the treatment of mercury poisoning, and the recent production and availability of DMPS from Heyl & Co., Berlin, stimulated investigators to "rediscover" and study these two metal-binding agents. DMSA and DMPS are water soluble chemical analogs of dimercaprol (British Anti-Lewisite, BAL). In contrast to BAL, they have less toxicity, greater water solubility, and lim­ ited lipid solubility, and are effective when given orally.

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Mercury Toxicity and Treatment: A Review of the Literature

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Mercury: major issues in environmental health.

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References
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Journal ArticleDOI

The mouse metallothionein-I gene is transcriptionally regulated by cadmium following transfection into human or mouse cells

TL;DR: Recombinant vectors containing the mouse metallothionein-I gene (MT-I) and the Escherichia coli xanthine-guanine phosphoribosyltransferase gene (gpt) were used to transfect human hgprt- HeLa cells, finding that transcripts from transfected MT-I genes begin at the correct transcription initiation site.
Journal ArticleDOI

Inducible plasmid-determined resistance to arsenate, arsenite, and antimony (III) in escherichia coli and Staphylococcus aureus.

TL;DR: Mutants and a cloned deoxyribonucleic acid fragment from plasmid pI258 in S. aureus have lost arsenate resistance but retained resistances to arsenite and antimony, demonstrating that separate genes are involved.
Journal ArticleDOI

Comparison of the effectiveness of several chelators after single administration on the toxicity, excretion, and distribution of cadmium.

TL;DR: DTPA appears to be the most effective agent of those tested in the prevention of acute Cd intoxication, with significant increases in survival were noted with DMSA, EDTA, and DTPA.
Journal Article

Tests of efficacy of antidotes for removal of methylmercury in human poisoning during the Iraq outbreak

TL;DR: Three complexing agents and a thiolated resin were tested for their ability to reduce the T 1/2 of methylmercury in blood during an outbreak of human poisoning and it was concluded that agents that reduce blood levels and accelerate excretion are probably clinically useful if given before irreversible damage has occurred.
Journal ArticleDOI

Treatment of lead poisoning by 2,3-dimercaptosuccinic acid

TL;DR: D.M.S. seems to be safe and effective for the treatment of lead poisoning and has no effect on urinary zinc, calcium, magnesium, or iron excretion.
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