In vitro reactivation of sarin-inhibited brain acetylcholinesterase from different species by various oximes

J Enzyme Inhib Med Chem. 2005 Jun;20(3):227-32. doi: 10.1080/14756360500043208.

Abstract

In vitro as well as in vivo evaluation of the reactivating efficacy of various oximes against nerve agent-inhibited acetylcholinesterase has been usually done with the help of animal experiments. Nevertheless, previously published data indicate that the reactivation potency of oximes may be different in human and animal species, which may hamper the extrapolation of animal data to human data. Therefore, to better evaluate the efficacy of various oximes (pralidoxime, obidoxime, HI-6, K033) to reactivate brain acetylcholinesterase inhibited by sarin by in vitro methods, human, rat and pig brain acetylcholinesterase were used to calculate kinetic parameters for the reactivation. Our results show differences among the species, depending on the type of oxime, and indicate that data from animal experiments needs to be carefully evaluated before extrapolation to humans.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / metabolism*
  • Animals
  • Brain / drug effects*
  • Brain / enzymology
  • Cholinesterase Inhibitors / pharmacology*
  • Cholinesterase Reactivators / pharmacology
  • Humans
  • Kinetics
  • Obidoxime Chloride / metabolism
  • Obidoxime Chloride / pharmacology
  • Oximes / metabolism
  • Oximes / pharmacology*
  • Pralidoxime Compounds / metabolism
  • Pralidoxime Compounds / pharmacology
  • Pyridinium Compounds / metabolism
  • Pyridinium Compounds / pharmacology
  • Rats
  • Sarin / pharmacology*
  • Species Specificity
  • Structure-Activity Relationship
  • Swine

Substances

  • 1,4-bis(2-hydroxyiminomethylpyridinium)butane
  • Cholinesterase Inhibitors
  • Cholinesterase Reactivators
  • Oximes
  • Pralidoxime Compounds
  • Pyridinium Compounds
  • Obidoxime Chloride
  • Sarin
  • Acetylcholinesterase
  • asoxime chloride
  • pralidoxime