Literature DB >> 2539660

Influence of 2,3-dimercaptopropane-1-sulfonate and dimercaptosuccinic acid on the mobilization of mercury from tissues of rats pretreated with mercuric chloride, phenylmercury acetate or mercury vapors.

J P Buchet1, R R Lauwerys.   

Abstract

The efficiency of the sodium salt of 2,3-dimercaptopropanesulfonic acid (DMPS) and meso-dimercaptosuccinic acid (DMSA) to mobilize mercury from tissues has been assessed in rats pretreated with different doses of HgCl2, phenylmercury acetate or exposed to different concentrations of mercury vapors. These pretreatments increase the mercury concentration in the kidney and to a lower extent in the liver. Only exposure to metallic mercury vapor leads to mercury accumulation in the brain. Both chelators mobilize mercury stored in the kidney and the amount of metal excreted in urine following a single administration of DMSA is a good indicator of the renal burden of mercury. The rate of removal is greater after DMPS administration than after DMSA but repeated administration of either agents eventually leads to the same total amount of mercury mobilized from the kidney. The loss of mercury from the liver can be slightly accelerated by repeated administration of the chelators. However, the chelators are inefficient in removing mercury from the brain.

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Year:  1989        PMID: 2539660     DOI: 10.1016/0300-483x(89)90067-x

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  8 in total

Review 1.  The role of chelation in the treatment of arsenic and mercury poisoning.

Authors:  Michael J Kosnett
Journal:  J Med Toxicol       Date:  2013-12

2.  Chronic elemental mercury intoxication: clinical and field studies in lampsocket manufacturers.

Authors:  Y J Yang; C C Huang; T S Shih; S S Yang
Journal:  Occup Environ Med       Date:  1994-04       Impact factor: 4.402

3.  Clearance half life of mercury in urine after the cessation of long term occupational exposure: influence of a chelating agent (DMPS) on excretion of mercury in urine.

Authors:  G Sällsten; L Barregård; A Schütz
Journal:  Occup Environ Med       Date:  1994-05       Impact factor: 4.402

4.  Urinary excretion of mercury after occupational exposure to mercury vapour and influence of the chelating agent meso-2,3-dimercaptosuccinic acid (DMSA).

Authors:  H A Roels; M Boeckx; E Ceulemans; R R Lauwerys
Journal:  Br J Ind Med       Date:  1991-04

5.  Evaluation of the protective activity of 2,3-dimercaptopropanol and sodium 2,3-dimercaptopropane-1-sulfonate on methylmercury-induced developmental toxicity in mice.

Authors:  M Gomez; D J Sanchez; M T Colomina; J L Domingo; J Corbella
Journal:  Arch Environ Contam Toxicol       Date:  1994-01       Impact factor: 2.804

6.  Diagnostic chelation challenge with DMSA: a biomarker of long-term mercury exposure?

Authors:  H Frumkin; C C Manning; P L Williams; A Sanders; B B Taylor; M Pierce; L Elon; V S Hertzberg
Journal:  Environ Health Perspect       Date:  2001-02       Impact factor: 9.031

7.  Intravenous injection of elemental mercury: A report of two cases.

Authors:  A Gopalakrishna; T V Pavan Kumar
Journal:  Indian J Plast Surg       Date:  2008-07

8.  Mercury exposure aboard an ore boat.

Authors:  Richard R Roach; Stephanie Busch
Journal:  Environ Health Perspect       Date:  2004-06       Impact factor: 9.031

  8 in total

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