Document Detail


Combined early treatment with chelating agents DMSA and CaDTPA in acute oral cadmium exposure.
MedLine Citation:
PMID:  15049341     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The influence of chelating agents: meso-2,3-dimercaptosuccinic acid (DMSA); calcium trisodium diethylenetriaminepentaacetate (CaDTPA) and their combination on mobilisation of cadmium (Cd) was compared in female albino rats. After oral Cd administration chelators were applied either orally (DMSA) or intraperitoneally (CaDTPA) at various short time intervals after Cd. Three experiments were carried out with four treatment groups in each: 1) Cd (control); 2) Cd+DMSA; 3) Cd+CaDTPA; 4) Cd+DMSA+CaDTPA. Time intervals for chelator treatment after Cd administration were: immediate application in the first, half an hour in the second and one hour in the third experiment. At the end of each experiment cadmium was analysed in kidney and liver. Additionally in experiment 3 essential elements (Fe, Cu, Zn) were also determined in the same organs. In experiment 2 the effect of the treatment on urinary elimination of cadmium, copper and zinc were analysed. Results showed that the efficiency of Cd removal from the body (kidneys and liver) is lower when the time between Cd and chelating agents administration is longer. The two chelators differ in efficiency in mobilizing Cd, with DMSA being more efficient than CaDTPA. The combined therapy with the two chelators gave generally better results. It seems that DMSA which is given orally after oral Cd administration removes this element very efficiently from the gastrointestinal tract. CaDTPA, however, which is given parenterally removes absorbed Cd less efficiently, Organs are not significantly depleted in iron and copper after chelation treatment. Only zinc concentration was, however, significantly lower in the liver and higher in kidneys only after CaDTPA and combined DMSA+CaDTPA chelation.
Authors:
Marijana Matek Sarić; Maja Blanusa; Dijana Juresa; Marija Sarić; Veda Marija Varnai; Krista Kostial
Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Basic & clinical pharmacology & toxicology     Volume:  94     ISSN:  1742-7835     ISO Abbreviation:  Basic Clin. Pharmacol. Toxicol.     Publication Date:  2004 Mar 
Date Detail:
Created Date:  2004-03-29     Completed Date:  2004-06-25     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  101208422     Medline TA:  Basic Clin Pharmacol Toxicol     Country:  Denmark    
Other Details:
Languages:  eng     Pagination:  119-23     Citation Subset:  IM    
Affiliation:
Mineral Metabolism Unit, Institute for Medical Research and Occupational Health, Zagreb, Croatia.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Administration, Oral
Animals
Cadmium / analysis,  toxicity*
Chelating Agents / therapeutic use*
Copper / analysis
Drug Therapy, Combination
Female
Glycine / analogs & derivatives*,  therapeutic use*
Injections, Intraperitoneal
Kidney / chemistry
Liver / chemistry
Organometallic Compounds / therapeutic use*
Pentetic Acid
Rats
Rats, Wistar
Succimer / therapeutic use*
Zinc / analysis
Chemical
Reg. No./Substance:
0/Chelating Agents; 0/Organometallic Compounds; 304-55-2/Succimer; 56-40-6/Glycine; 67-43-6/Pentetic Acid; 7440-43-9/Cadmium; 7440-50-8/Copper; 7440-66-6/Zinc

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  In vivo and in vitro effects of cadmium on adult rat brain total antioxidant status, acetylcholinest...
Next Document:  Cytoprotection following endoplasmic reticulum stress protein induction in continuous cell lines.