Acta Med. 2007, 50: 203-206
https://doi.org/10.14712/18059694.2017.83
Evaluation of Potency of Known Oximes (Pralidoxime, Trimedoxime, HI-6, Methoxime, Obidoxime) to in vitro Reactivate Acetylcholinesterase Inhibited by Pesticides (Chlorpyrifos and Methylchlorpyrifos and Nerve Agent (Russian VX)
References
1. Adv Clin Chem 2004; 38:151–216.
< J. Organophosphates/nerve agent poisoning: mechanism of action, diagnosis, prophylaxis, and treatment. https://doi.org/10.1016/S0065-2423(04)38006-6>
2. Biochemistry. 2006; 45:74–81.
< F, Akfur C, Tunemalm K, Lundberg S. Structural changes of phenylalanine 338 and histidine 447 revealed by the crystal structures of tabun-inhibited murine acetylcholinesterase. https://doi.org/10.1021/bi051286t>
3. Gupta R. Toxicology of organophosphate & carbamate compounds. In: Global epidemiology of organophosphate and carbamate poisonings. Elsevier Academic Press, London, pp. 89–102.
4. J Toxicol Clin Toxicol. 2002; 40:803–816.
< J. Review of oximes in the antidotal treatment of poisoning by organophosphorus nerve agents. https://doi.org/10.1081/CLT-120015840>
5. Biologia 2005; 60:79–81.
J, Kuča K, Cabal J. Comparison of the efficacy of currently available oximes against tabun in rats.
6. J Appl Biomed. 2003; 1:207–11.
K, Patočka J, Cabal J. Reactivation of organophosphate inhibited acetylcholinesterase activity by α,ω-bis-(4-hydroxyiminomethylpyridinium)alkanes in vitro.
7. J Appl Biomed. 2004; 2:51–56.
K, Pícha J, Cabal J, Liška F. Synthesis of the three monopyridinium oximes and evaluation of their potency to reactivate acetylcholinesterase inhibited by nerve agents.
8. Toxicol Mech Method. 2005; 15: 247–52.
< K, Cabal J. Evaluation of newly synthesized reactivators of the brain cholinesterase inhibited by sarin-nerve agent. https://doi.org/10.1080/15376520590968770>
9. J Appl Toxicol. 2005; 25:491–5.
< K, Cabal J, Musílek K, Jun D, Bajgar J. Effective bisquaternary reactivators of tabun-inhibited AChE. https://doi.org/10.1002/jat.1084>
10. J Appl Toxicol. 2005; 25:296–300.
< K, Cabal J, Jun D, Kassa J, Bartošová L, Kunešová G. In vitro reactivation potency of some acetylcholinesterase reactivators against sarin- and cyclosarin-induced inhibitions. https://doi.org/10.1002/jat.1065>
11. Mini-Rev Med Chem. 2006; 6:269–77.
< K, Jun D, Musílek K. Structural requirements of acetylcholinesterase reactivators. https://doi.org/10.2174/138955706776073510>
12. Pharmacol Ther. 1993; 58:51–66.
< TC. Organophosphate poisoning. https://doi.org/10.1016/0163-7258(93)90066-M>
13. J Enzym Inhib Med. Chem. 2005; 20:409–15.
< K, Kuča K, Jun D, Dohnal V. Doležal M. Synthesis of a novel series of bispyridinium compounds bearing a xylene linker and evaluation of their reactivation activity against chlorpyrifos-inhibited acetylcholinesterase. https://doi.org/10.1080/14756360500179762>
14. Bioorg Med Chem Lett. 2006; 16:622–7.
< K, Kuča K, Jun D, Dohnal V, Doležal M. Synthesis of the novel series of bispyridinium compounds bearing (E)-but-2–ene linker and evaluation of their reactivation activity against chlorpyrifos-inhibited acetylcholinesterase. https://doi.org/10.1016/j.bmcl.2005.10.059>
15. Chem Pap. 2006; 60:48–51.
< K., Lipka L., Račáková V., Kuča K., Jun D., Dohnal V., Doležal M. New methods in synthesis of acetylcholinesterase reactivators and evaluation of their potency to reactivate cyclosarin-inhibited AChE. https://doi.org/10.2478/s11696-006-0008-x>
16. Br J Pharmacol. 1993; 108:1006–15.
< JE. Ion channel blockade by oximes and recovery of diaphragm muscle from soman poisoning in vitro. https://doi.org/10.1111/j.1476-5381.1993.tb13498.x>
<PubMed>
17. Taylor P. Anticholinergic agents. In: The Pharmacological Basis of Therapeutics. 2001;Hill, New York, pp. 175–91.
18. Toxicol Lett. 1999; 107:233–9.
< H, Szinicz L, Eyer F, Worek F, Eyer P, Felgenhauer N, Zilker T. Modern strategies in therapy of organophosphate poisoning. https://doi.org/10.1016/S0378-4274(99)00052-1>
19. Biochem Pharmacol. 2004; 68:2237–48.
< F, Thiermann H, Szinicz L, Eyer P. Kinetic analysis of interactions between human acetylcholinesterase, structurally different organophosphorus compounds and oximes. https://doi.org/10.1016/j.bcp.2004.07.038>