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At least 433 records · Page 24Linked to original sources
PubMed1976

The excretion and distribution of inorganic mercury in the rat as influenced by several chelating agents.

Among 15 chelating agents tested, sodium-2,3-dimercaptopropane 1 sulfonate (DMPS), 2,3-dimercaptopropanol (BAL), sodium-mercaptoethyliminodiacetate (MEIDA), and D-penicillamine (PA) exerted an influence on the excretion of Hg and its distribution in the organs. The excretion pattern however, is different for these compounds, and, from the practical point of view, a favourable effect is exhibited only by DMPS which enhances the urinary excretion rate and lowers the Hg-concentration in all organs.

Animals↗
PubMed1984

The effect of 2,3-dimercaptopropane sodium sulfonate on mercury retention in rats in relation to age.

The effectiveness of DMPS (sodium 2,3-dimercaptopropane-1-sulfonate) in reducing inorganic mercury retention was studied in 2-, 6-, and 28-week-old albino rats. 203Hg was administered IP. The chelating agent DMPS was administered by IP injection at a dose of 250 mumol/kg body weight three times, 1 day after 203Hg administration and at 24 h intervals thereafter. The whole body retention determined 1, 2, 3, and 6 days after 203Hg administration showed that DMPS decreased the body retention of mercury in all age groups, being about twice as effective in adult compared to suckling rats. The reduced effectiveness was due to the reduced efficacy of DMPS in reducing kidney retention in young animals. In other organs the effectiveness of DMPS was not age dependent. These and previous results obtained with different chelating agents and other metals indicate that age might be an important factor in chelation therapy in general.

Age Factors↗
PubMed1975

Influence of chelation therapy on acute lead intoxication in rats.

The intraperitoneal administration of Pb acetate (5 x 20 mg Pb/kg per day) evokes a moderate and transient hypochromic anemia, a long-lasting enhanced urinary excretion of delta-aminolevulinic acid whereas the urinary excretion of alkaline phosphatase is not affected and that of lactic dehydrogenase only marginally. It is concluded that neither the hematologic response nor the slight nephrotoxicity are responsible for the lethal action of Pb. Chelate treatment started 3 days after the last Pb dose and was continued over 7 weeks. The daily intraperitoneal dose was 25, 50, and 100 mumol/kg, respectively. The efficacy in promoting the urinary excretion of Pb decreased in the following order: Ca diethylenetriaminepentaacetate greater than 2,3-dimercaptopropane-1-sulfonate greater than Zn diethylenetriaminepentaacetate greater than D-penicillamine. This effect was mainly due to the mobilization of skeletal Pb. The chelating agents also lowered the excretion of delta-aminolevulinic acid but failed to exert a beneficial influence on the anemia and the lethal action of Pb. These negative results raise questions about the usefulness of chelation therapy in cases of acute Pb poisoning.

Acute Disease↗
PubMed1978

The influence of unithiol and spironolactone on the biliary excretion of 203Hg in rat.

Rats with cannulated bile ducts were intravenously given 203HgCl2 in the dose of 120 microgram of Hg2+ per rat. Intramuscular administration of Unithiol (sodium 2,3-dimercaptopropanosulphonate) 4 and 7 h after 203Hg injection markedly increased both biliary and urinary excretion of 203Hg. In rats with Spironolactone (17-Hydroxy-7alpha-mercapto-3-oxo-17alpha-pregn-4-ene-21-carboxylic acid, gamma-lactone, acetate) pretreatment the effect of Unithiol on the biliary excretion of 203Hg was enhanced. Urinary excretion of mercury was lowest in comparison with Unithiol treated group.

Animals↗
PubMed1975

[Quantitative determination of supplemental vitamin C in mineral salt mixtures (author's transl)].

Supplemental vitamin C in mineral salt mixtures is extracted without destruction by diluted ethanol under the reducing and stabilizing protection of 2,3-dimercaptopropanol-(1) (BAL). After removal of heavy metal ions in form of mercaptides and by means of cation exchange BAL is extracted and vitamin C (ascorbic plus dehydroascorbic acid) titrated with dichlorophenolindophenol. Recovery 98-100%.

Ascorbic Acid↗
PubMed1995

Prebiotic polymerization: oxidative polymerization of 2,3-dimercapto-1-propanol on the surface of iron(III) hydroxide oxide.

The oxidation of 2,3-dimercapto-1-propanol by ferric ions on the surface of iron(III) hydroxide oxide (Fe(OH)O) yielded polydisulfide oligomers. This polymerization occurred readily at low dithiol concentration under mild aqueous conditions. Polydisulfide polymers up to the 15-mer were synthesized from 1 mM dithiol in 5 ml water reacted with iron(III) hydroxide oxide (20 mg, 160 micromoles Fe) for 3 days under anaerobic conditions at 40 degrees C and pH 4. About 91% of the dithiol was converted to short soluble oligomers and 9% to insoluble larger oligomers that were isolated with the Fe(OH)O phase. Reactions carried out at the same ratio of dithiol to Fe(OH)O but at higher dithiol concentrations gave higher yields of the larger insoluble oligomers. The relationship of these results to prebiotic polymer synthesis is discussed.

Dimercaprol↗