October 14, 1997
Journal Article

Pharmacokinetics and metabolism of dichloroacetate in the F344 rat after prior administration in drinking water

Abstract

The effect of chronic administration of dichloroacetate (DCA) in drinking water on the pharmacokinetics of DCA in male F344 rats was studied. Rats were provided with DCA in their drinking water at 0.2 and 2.0 g/l for 14 days and then given i.v. or gavage doses of 14C-DCA. The blood concentration-time profile of DCA and the disposition of 14C was characterized and compared with control rats. Additional experiments studied the effect of pretreatment on the in-vitro metabolism of DCA in hepatic cytosol. Pretreatment caused a significant increase in the blood concentration and AUCof DCA (433.3 vs. 2406 g ml-1 hr). Pharmacokinetic analysis indicated that pretreatment caused a significant decrease in total body clearance (267.4 vs. 42.7 ml hr-1 kg-1) which was largely due to decreased metabolism because only modest differences in the urinary clearance of DCA were observed. Pretreatment significantly decreased the formation of 14C-CO2 after both i.v. and oral doses of 14C-DCA. The decrease in CO2 formation was also observed after pretreatment with DCA at 0.2 g/l. Pretreatment increased the urinary elimination of DCA and several metabolites, especially glycollate. The results of the in-vitro experiments were consistent with the conclusion that DCA was inhibiting its metabolism as pretreatment significantly reduced the formation of glyoxylate-oxalate-glycollate in hepatic cytosol. These results indicate that DCA has an auto-inhibitory effect on its metabolism and that previous pharmacokinetic studies using single doses in naive rats may underestimate the elimination of DCA during chronic or repeated exposures.

Revised: February 12, 2020 | Published: October 14, 1997

Citation

Gonzalez-Leon A., I.R. Schultz, G.H. Xu, and R.J. Bull. 1997. Pharmacokinetics and metabolism of dichloroacetate in the F344 rat after prior administration in drinking water. Toxicology and Applied Pharmacology 146, no. 2:189-195. PNWD-SA-5221. doi:10.1006/taap.1997.8232