Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

A comprehensive evaluation of novel oximes in creation of butyrylcholinesterase-based nerve agent bioscavengers

Journal Article · · Toxicology and Applied Pharmacology
;  [1]; ; ; ; ; ;  [2];  [1];  [3];  [1];  [2];  [1]
  1. Institute for Medical Research and Occupational Health, POB 291, HR-10001 Zagreb (Croatia)
  2. Department of Chemistry, Faculty of Science, University of Zagreb, HR-10001 Zagreb (Croatia)
  3. Fidelta Ltd., HR-10001 Zagreb (Croatia)

A well-considered treatment of acute nerve agents poisoning involves the exogenous administration of butyrylcholinesterase (BChE, EC 3.1.1.8) as a stoichiometric bioscavenger efficient in preventing cholinergic crises caused by acetylcholinesterase (AChE, EC 3.1.1.7) inhibition. An additional improvement in medical countermeasures would be to use oximes that could reactivate BChE as well to upgrade bioscavenging from stoichiometric to oxime-assisted catalytic. Therefore, in this paper we investigated the potency of 39 imidazolium and benzimidazolium oximes (36 compounds synthesized for the first time) to be considered as the reactivators specifically designed for reactivation of phosphylated human BChE. Their efficiency in the reactivation of paraoxon-, VX-, and tabun-inhibited human BChE, as well as human AChE was tested and compared with the efficiencies of HI-6 and obidoxime, used in medical practice today. A comprehensive analysis was performed for the most promising oximes defining kinetic parameters of reactivation as well as interactions with uninhibited BChE. Furthermore, experimental data were compared with computational studies (docking, QSAR analysis) as a starting point in future oxime structure refinement. Considering the strict criteria set for in vivo applications, we determined the cytotoxicity of lead oximes on two cell lines. Among the tested oxime library, one imidazolium compound was selected for preliminary in vivo antidotal study in mice. The obtained protection in VX poisoning outlines its potential in development oxime-assisted OP-bioscavenging with BChE. - Highlights: • 36 new imidazolium and benzimidazolium oximes were designed and synthesized. • In vitro reactivation kinetics of phosphylated butyrylcholinesterase was studded. • The modes of actions were elucidated by QSAR and docking simulations. • Protection in VX poisoning was 6.3 × LD{sub 50} in in vivo antidotal study in mice. • Imidazolium oxime-assisted catalysis is feasible for OP-bioscavenging with BChE.

OSTI ID:
22690841
Journal Information:
Toxicology and Applied Pharmacology, Journal Name: Toxicology and Applied Pharmacology Vol. 310; ISSN TXAPA9; ISSN 0041-008X
Country of Publication:
United States
Language:
English

Similar Records

Reactivation of organophosphate-inhibited human, Cynomolgus monkey, swine and guinea pig acetylcholinesterase by MMB-4: A modified kinetic approach
Journal Article · Tue Dec 14 23:00:00 EST 2010 · Toxicology and Applied Pharmacology · OSTI ID:21529107

A comprehensive evaluation of the efficacy of leading oxime therapies in guinea pigs exposed to organophosphorus chemical warfare agents or pesticides
Journal Article · Sun Dec 14 23:00:00 EST 2014 · Toxicology and Applied Pharmacology · OSTI ID:22439929

Recent advances in evaluation of oxime efficacy in nerve agent poisoning by in vitro analysis
Journal Article · Thu Mar 15 00:00:00 EDT 2007 · Toxicology and Applied Pharmacology · OSTI ID:20976889