STRATEGY FOR THE DEVELOPMENT OF NEW ACETYLCHOLINESTERASE REACTIVATORS – ANTIDOTES USED FOR TREATMENT OF NERVE AGENT POISONINGS

The mechanism of intoxication with organophosphorus compounds, including highly toxic nerve agents, is based on the formation of irreversibly inhibited acetylcholinesterase (AChE; EC 3.1.1.7) that could be followed by a gener-alized cholinergic crisis. Nerve agent poisoning is conventionally treated using a combination of a cholinolytic drug (atropine mostly) to counteract the accumulation of acetylcholine at muscarinic receptors and AChE reactivators (pralidoxime or obidoxime) to reactivate inhibited AChE. At the Department of Toxicology, the strategy of the development of new more potent AChE reactivators consists of several steps: description of the nerve agent intoxication mechanism on the molecular basis (molecular design), prediction of the biological active structure of AChE reactivators (artificial neural networks), their synthesis, in vitro evaluation of their potencies (potentiometric titration and Ellman’s method), in vivo studies (therapeutic index, LD50 of newly synthesized reactivators, reactivation in different tissues, neuroprotective efficacy)