Effects of Insecticidal Ketones Present in Mint Plants on GABA Receptor from Mammalian Neurons.

Background: The genus , an important member of the family, is represented by many species commonly known as mint. The insecticidal activity of oil and its main components has been tested and established against various insects/pests. Among these, the ketone monoterpenes that are most common in different species demonstrated insect toxicity, with pulegone being the most active, followed by carvone and menthone. Considering that the GABA receptor (GABA-R) is one of the main insecticide targets on neurons, and that pulegone would modulate the insect GABA system, it may be expected that the insecticidal properties of ketones are mediated by their interaction with this receptor.

Objective: In order to discern the pharmacological actions of these products when used as insecticides on mammalian organisms, we evaluated the pharmacologic activity of ketones, commonly present in plants, on native GABA-R from rats.

Materials And Methods: Determination of ketones effects on allosterically enhanced benzodiazepine binding, using primary cultures of cortical neurons, which express functional receptors and MTT assay to evaluate their cell toxicity.

Results: Our results seem to indicate that ketone components of , with proven repellent or insecticide activity, were able to behave as GABA-R negative allosteric modulators in murine cells and consequently could exhibit convulsant activity in mammalians. Only pulegone at the highest assayed concentration (2 mM) showed a significant reduction in cell viability after exposure for 24 hr.

Conclusion: The present results strongly suggest that the ketone components of are able to exhibit convulsant activity in mammalian organisms, but functional assays and experiments would be necessary to corroborate this proposed action.

Summary: The pharmacological activity of insecticide ketones, commonly present in plants, was evaluated on native GABA receptor from mammalian neurons.All studied compounds: pulegone, menthone and dihydrocarvone, were able to behave as negative allosteric modulators and could exhibit convulsant activity in mammalian organisms.Citotoxicity assays demonstrated that only pulegone affected the cell viability. GABA: gamma aminobutyric acid, GABAA-R: GABAA receptor, MTT: 1-(4,5-dimethylthiazol-2-yl)-3,5-diphenylformazam, DMEM: Dulbecco's modified minimum essential mèdium, [3H]TBOB: [3H] t-Butylbicycloorthobenzoate.