Cholinesterase-like organocatalysis by imidazole and imidazole-bearing molecules

Sci Rep. 2017 Apr 3:8:45760. doi: 10.1038/srep45760.

Abstract

Organocatalysis, which is mostly explored for its new potential industrial applications, also represents a chemical event involved in endogenous processes. In the present study, we provide the first evidence that imidazole and imidazole derivatives have cholinesterase-like properties since they can accelerate the hydrolysis of acetylthiocholine and propionylthiocholine in a concentration-dependent manner. The natural imidazole-containing molecules as L-histidine and histamine show a catalytic activity, comparable to that of imidazole itself, whereas synthetic molecules, as cimetidine and clonidine, were less active. In the experimental conditions used, the reaction progress curves were sigmoidal and the rational of such unexpected behavior as well as the mechanism of catalysis is discussed. Although indirectly, findings of the present study suggests that imidazolic compounds may interfere with the homeostasis of the cholinergic system in vivo.

MeSH terms

  • Catalysis
  • Cholinesterases / chemistry*
  • Cholinesterases / metabolism
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Histamine / chemistry
  • Histamine / pharmacology*
  • Histidine / chemistry
  • Histidine / pharmacology*
  • Humans
  • Imidazoles / chemistry
  • Imidazoles / pharmacology*

Substances

  • Enzyme Inhibitors
  • Imidazoles
  • Histidine
  • imidazole
  • Histamine
  • Cholinesterases
  • 4-methylimidazole
  • 1-ethyl-3-methylimidazolium