Are the current commercially available oximes capable of reactivating acetylcholinesterase inhibited by the nerve agents of the A-series?
Language English Country Germany Media print-electronic
Document type Journal Article
PubMed
35666269
DOI
10.1007/s00204-022-03316-z
PII: 10.1007/s00204-022-03316-z
Knihovny.cz E-resources
- Keywords
- A-242, AChE, Commercial reactivators, Novichoks, Surrogates,
- MeSH
- Acetylcholinesterase MeSH
- Antidotes pharmacology MeSH
- Cholinesterase Inhibitors toxicity MeSH
- Humans MeSH
- Nerve Agents * toxicity MeSH
- Oximes pharmacology MeSH
- Cholinesterase Reactivators * pharmacology MeSH
- Molecular Docking Simulation MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Acetylcholinesterase MeSH
- Antidotes MeSH
- Cholinesterase Inhibitors MeSH
- Nerve Agents * MeSH
- Oximes MeSH
- Cholinesterase Reactivators * MeSH
The misuse of novichok agents in assassination attempts has been reported in the international media since 2018. These relatively new class of neurotoxic agents is claimed to be more toxic than the agents of the G and V series and so far, there is no report yet in literature about potential antidotes against them. To shed some light into this issue, we report here the design and synthesis of NTMGMP, a surrogate of A-242 and also the first surrogate of a novichok agent useful for experimental evaluation of antidotes. Furthermore, the efficiency of the current commercial oximes to reactivate NTMGMP-inhibited acetylcholinesterase (AChE) was evaluated. The Ellman test was used to confirm the complete inhibition of AChE, and to compare the subsequent rates of reactivation in vitro as well as to evaluate aging. In parallel, molecular docking, molecular dynamics and MM-PBSA studies were performed on a computational model of the human AChE (HssAChE)/NTMGMP complex to assess the reactivation performances of the commercial oximes in silico. Experimental and theoretical studies matched the exact hierarchy of efficiency and pointed to trimedoxime as the most promising commercial oxime for reactivation of AChE inhibited by A-242.
Chemical Engineering Department Military Institute of Engineering Rio de Janeiro Brazil
Federal University of Espírito Santo Unit Goiabeiras Vitória ES Brazil
Institute of Chemical Biological Radiological and Nuclear Defense Rio de Janeiro Brazil
Université de Québec INRS Centre Armand Frappier Santé Biotechnologie Laval Québec H7V 1B7 Canada
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A-agents, misleadingly known as "Novichoks": a narrative review