Volume 80, Issue 4 pp. 182-186

Comparative in vivo Lead Mobilization of meso- and rac-2,3-Dimercaptosuccinic Acids in Albino Wistar Rats

Mark M. Jones

Corresponding Author

Mark M. Jones

1 Department of Chemistry, Vanderbilt University, Nashville, TN 37235, U. S. A.

Author for correspondence: Mark M. Jones, Box 1583, Station B, Department of Chemistry, Vanderbilt University, Nashville, TN 37235, U.S.A. (fax +1 (615) 322–4936).Search for more papers by this author
Pramod K. Singh

Pramod K. Singh

1 Department of Chemistry, Vanderbilt University, Nashville, TN 37235, U. S. A.

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Krista Kostial

Krista Kostial

Department of Mineral Metabolism, Institute for Medical Research and Occupational Health, Ksaverska cesta 2, 10000 Zagreb, Republic of Croatia

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Maja Blanuša

Maja Blanuša

Department of Mineral Metabolism, Institute for Medical Research and Occupational Health, Ksaverska cesta 2, 10000 Zagreb, Republic of Croatia

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Martina Piasek

Martina Piasek

Department of Mineral Metabolism, Institute for Medical Research and Occupational Health, Ksaverska cesta 2, 10000 Zagreb, Republic of Croatia

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Nada Restek-Samarožija

Nada Restek-Samarožija

Department of Mineral Metabolism, Institute for Medical Research and Occupational Health, Ksaverska cesta 2, 10000 Zagreb, Republic of Croatia

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First published: 25 March 2009
Citations: 12

Abstract

Abstract: Comparison of the racemic and meso forms of 2,3-dimercaptosuccinic acid (DMSA) in lead mobilization from lead-loaded albino Wistar rats demonstrates that the racemic form is significantly more effective in reducing femur lead levels. After four oral doses at 0.5 mmol/kg, femur lead levels were reduced to 87% of control values by meso-DMSA and to 50% of control levels by rac-DMSA. Similarly, when the dose was increased to 1.0 mmol/kg, femur lead levels were reduced to 69% of control levels by meso-DMSA and to 45% of control levels by rac-DMSA. A similar pattern was found for renal lead levels. Brain lead concentrations were significantly lower in treated groups than in control groups, but no differences were found between rac- and meso-DMSA. Rac-DMSA is more soluble than meso-DMSA in acetonitrile, ethyl acetate, and ethyl ether. The partition coefficient of rac-DMSA in the n-octanol/water system was found to be about 2.8. These results indicate that rac-DMSA deserves further attention as a possible substitute for meso-DMSA.

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