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Development of small bisquaternary cholinesterase inhibitors as drugs for pre-treatment of nerve agent poisonings
K. Kuca, JZ. Karasova, O. Soukup, J. Kassa, E. Novotna, V. Sepsova, A. Horova, J. Pejchal, M. Hrabinova, E. Vodakova, D. Jun, E. Nepovimova, M. Valis, K. Musilek,
Language English Country New Zealand
Document type Journal Article
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PubMed
29563775
DOI
10.2147/dddt.s133038
Knihovny.cz E-resources
- MeSH
- Acetylcholinesterase metabolism MeSH
- Cell Line MeSH
- Cholinesterase Inhibitors chemistry pharmacology MeSH
- HeLa Cells MeSH
- Small Molecule Libraries chemistry pharmacology MeSH
- Humans MeSH
- Models, Molecular MeSH
- Molecular Structure MeSH
- Nerve Agents adverse effects MeSH
- Soman adverse effects MeSH
- Cell Survival drug effects MeSH
- Dose-Response Relationship, Drug MeSH
- Structure-Activity Relationship MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Background: Intoxication by nerve agents could be prevented by using small acetylcholinesterase inhibitors (eg, pyridostigmine) for potentially exposed personnel. However, the serious side effects of currently used drugs led to research of novel potent molecules for prophylaxis of organophosphorus intoxication. Methods: The molecular design, molecular docking, chemical synthesis, in vitro methods (enzyme inhibition, cytotoxicity, and nicotinic receptors modulation), and in vivo methods (acute toxicity and prophylactic effect) were used to study bispyridinium, bisquinolinium, bisisoquinolinium, and pyridinium-quinolinium/isoquinolinium molecules presented in this study. Results: The studied molecules showed non-competitive inhibitory ability towards human acetylcholinesterase in vitro that was further confirmed by molecular modelling studies. Several compounds were selected for further studies. First, their cytotoxicity, nicotinic receptors modulation, and acute toxicity (lethal dose for 50% of laboratory animals [LD50]; mice and rats) were tested to evaluate their safety with promising results. Furthermore, their blood levels were measured to select the appropriate time for prophylactic administration. Finally, the protective ratio of selected compounds against soman-induced toxicity was determined when selected compounds were found similarly potent or only slightly better to standard pyridostigmine. Conclusion: The presented small bisquaternary molecules did not show overall benefit in prophylaxis of soman-induced in vivo toxicity.
Biomedical Research Center University Hospital Hradec Kralove
Department of Neurology University Hospital Hradec Kralove Hradec Kralove Czech Republic
References provided by Crossref.org
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