Disposition and metabolism of two acetylcholinesterase reactivators, pyrimidoxime and HI6, in rats submitted to organophosphate poisoning
- 1 January 1990
- journal article
- research article
- Published by Taylor & Francis in Xenobiotica
- Vol. 20 (7) , 699-709
- https://doi.org/10.3109/00498259009046886
Abstract
1. The dispositions of two acetylcholinesterase reactivators, pyrimidoxime and HI6, labelled with 14C on the oxime group, have been studied in normal rats and rats poisoned by the organophosphates Soman and A4. 2. For both compounds, and for healthy and poisoned rats, radioactivity was eliminated essentially in the urine (85% dose in 24 h). Faecal elimination was low (4% in 72 h). 3. Both compounds were concentrated in kidney and mucopolysaccharide-containing tissues such as cartilage and intervertebral disc. Soman and A4 poisoning do not modify the kinetic parameters of pyrimidoxime, but A4 poisoning increases HI6 tissue concentration. 4. Chromatography of urine and plasma showed only unchanged pyrimidoxime in both healthy and poisoned animals. In contrast, HI6 in plasma and urine was strongly degraded by scission of the quarternary ammonium bond, and formation of 2-pyridine aldoxime.This publication has 17 references indexed in Scilit:
- Effect of poisoning by soman (pinacolyl methylphosphono‐fluoridate) on the serum half‐life of the cholinesterase reactivator hi‐6 in miceBiopharmaceutics & Drug Disposition, 1988
- Separation and identification of substituted pyridine analogues in heat labile solutions of HI-6 dichlorideJournal of Chromatography A, 1986
- Sarin intoxication elevates plasma pralidoximeToxicology Letters, 1985
- Stability study of HI-6 dichloride in various anticholinergic formulationsJournal of Chromatography A, 1984
- HI-6: Reactivation of central and peripheral acetylcholinesterase following inhibition by soman, sarin and tabun in vivo in the ratBiochemical Pharmacology, 1982
- Toxicology and pharmacology of bispyridinium oximes insight into the mechanism of action vs Soman poisoning in vivoFundamental and Applied Toxicology, 1981
- The effects of atropine-oxime therapy on cholinesterase activity and the survival of animals poisoned with O,O-diethyl-O-(2-isopropyl-6-methyl-4-pyrimidinyl) phosphorothioateToxicology and Applied Pharmacology, 1969
- OXIME MIXTURES AND ATROPINE IN THE PROTECTION OF MICE AND RATS FROM SARIN POISONINGCanadian Journal of Biochemistry and Physiology, 1960
- Chemotherapeutic Effectiveness of 1,1'-Trimethylene Bis (4-Formylpyridinium Bromide) Dioxime (TMB-4) in Experimental Anticholinesterase PoisoningExperimental Biology and Medicine, 1958
- Reactivation of phosphorylated acetocholinesterase by pyridine-2-aldoxime methiodideBiochimica et Biophysica Acta, 1957