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Myocardial elements content and cardiac function after repeated i.v. administration of DMPS in rabbitsDepartment of Pharmacology and Toxicology, Faculty of Pharmacy, Charles University, Hradec Králové
Department of Pharmacology, Faculty of Medicine, Charles University, Hradec Králové
Institute of Clinical Biochemistry and Diagnostics, University Hospital, Hradec Králové
Institute of Clinical Biochemistry and Diagnostics, University Hospital, Hradec Králové
Institute of Clinical Biochemistry and Diagnostics, University Hospital, Hradec Králové
Department of Clinical Hematology, University Hospital, Hradec Králové
Department of Histology, Faculty of Medicine, Charles University, Hradec Králové
Military Medical Academy, Hradec Králové, Czech Republic 1 A dithiol chelating agent-2,3-dimercapto-1-propane-sulphonate (DMPS)- may be administered in acute or chronic intoxication with certain heavy metals (e.g. cadmium, cobalt, lead) that may cause cardiotoxicity. 2 DMPS can act as a depleter of physiologically important elements (e.g. potassium, magnesium, calcium) in various tissues including cardiac one. The possibility of subsequent alteration in cardiac function cannot be excluded. 3 Changes in the myocardial concentration of the abovementioned elements at the end of the experiment and cardiac function were studied during repeated I.V. administration of DMPS as single doses of 50 mg/kg/ week for 10 weeks in rabbits. Biochemical, haemato-logical and histological examinations were also performed. 4 Most of the measured parameters were not affected by the repeated administration of DMPS. A significant decrease in magnesium and a near significant decrease in calcium in cardiac muscle was not accompanied by functional or morphological changes. It is still suggested, however, that care should be taken in using DMPS for treating patients with cardiotoxicity as a result of poisoning with heavy metals.
Key Words: 2,3-dimercapto-1-propanesulphonate DMPS cardiac function elements heavy metals chelating agents
Human & Experimental Toxicology, Vol. 17, No. 4,
221-224 (1998) |
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