Intracellular interaction and biotransformation of arsenite in rats and rabbits.

The accumulation of arsenic with time in tissues of rats and rabbits was determined by neutron activation analysis (NAA). Rats showed a steady increase in the As-concentrations with age, whereas in rabbits it was nearly the same for adults and in young animals. The metabolism of arsenic was studied in both animal species after i.p. injection of 50/micrograms As/kg b.w. as 74As labelled arsenite. Eight tissues, as well as blood and urine, were analysed for 74As content after 16 and 48 hours. The binding of 74As to hematic and intracellular components and the chemical forms of arsenic in tissues and urine were investigated. In the plasma and the RBC-fraction of the rabbit, the As concentration decreased during the first two days, while in the rats it only disappeared from the plasma, but was retained in the RBC-fraction. Liver, kidney and lung of rabbits with the highest As concentrations at 16 and 48 hours showed a rapid clearance of As in the first 48 hours. In the corresponding tissues of the rats, the rate of decline was significantly lower, due to the higher binding of 74As to tissue constituents. Poor binding of As to plasma proteins was seen in rabbits while in rats it was totally bound to this fraction. In the RBC, liver and kidney cytosols, however, the affinity of As for intracellular proteins was higher in both animal species but characterized by a rate of binding different between the two animal species. The amount of dimethylarsinic acid (DMA) in the tissues was significantly lower in the rat than in the rabbit, reflecting the total amount of diffusible arsenic, which was also much lower in the tissues of rats than in rabbits.