Insect pheromones as reversible competitive inhibitors of acetylcholinesterase

Summary

Structural aspects of insect pheromones, especially their hydrophobicity, prompted the examination of them by in vitro and in vivo experiments as inhibitors of acetylcholinesterase. All 17 pheromones assayed in sufficient detail were reversible, competitive inhibitors of acetylcholinesterase: K_i values ranged from 0.27 mM for frontalin to 9.3 mM for ipsenol, both aggregation pheromones. All seven pheromones assayed with Tribolium castaneum immobilised this species with an effect that was weakly dose-responsive over the range of concentrations tested. Concentrations eliciting 25% immobility (IC₂₅) ranged from 2.0x10³ ppm for 3-methy 1–2-cyclohexenone to 2.0x10⁴ ppm for cis-7, cis-11-hexadecadien-1-yl acetate, both sex attractants. Such efficacies suggest that the pheromones tested would be effective as defence agents only in species living in a confined area, as under bark, or in aggregations.