Sur l'inhibition sélective des acétylcholinestérasesin vivo chez le chien

Summary

3318 CT [bis(piperidinométhylcoumaranyl-5) cetone diméthiodide] a compound recently synthesized byA. Funke andK. von Däniken, is shown to be a potent and selective inhibitor, bothin vitro andin vivo, of the blood acetyl-cholinesterase (AcChE) of the dog. It produces acetylcholinomimetic symptoms in the animal and sensitizes different responses to acetylcholine and to stimulation of cholinergic nerves without inhibiting the blood non-specific cholinesterase (XChE). However, the action of 3318 CT appears to be limited, both in nature and in intensity, when compared to that of prostigmine, although the latter substance is a less potent inhibitor of AcChEin vitro than is 3318 CT. This difference is probably related to many factors, one of which may be the fact that prostigmine inhibits not only AcChE but also XChE; and it is not yet ascertained that XChE plays no role at all in the limitation of the effect of the stimulations of cholinergic nerves.