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PLoS One. 2013 Jul 23;8(7):e67674. doi: 10.1371/journal.pone.0067674. Print 2013.

Menthol binding and inhibition of α7-nicotinic acetylcholine receptors.

Author information

1
Department of Pharmacology Laboratory of Functional Lipidomics, College of Medicine and Health Sciences, UAE University, Al Ain, United Arab Emirates.

Abstract

Menthol is a common compound in pharmaceutical and commercial products and a popular additive to cigarettes. The molecular targets of menthol remain poorly defined. In this study we show an effect of menthol on the α7 subunit of the nicotinic acetylcholine (nACh) receptor function. Using a two-electrode voltage-clamp technique, menthol was found to reversibly inhibit α7-nACh receptors heterologously expressed in Xenopus oocytes. Inhibition by menthol was not dependent on the membrane potential and did not involve endogenous Ca(2+)-dependent Cl(-) channels, since menthol inhibition remained unchanged by intracellular injection of the Ca(2+) chelator BAPTA and perfusion with Ca(2+)-free bathing solution containing Ba(2+). Furthermore, increasing ACh concentrations did not reverse menthol inhibition and the specific binding of [(125)I] α-bungarotoxin was not attenuated by menthol. Studies of α7- nACh receptors endogenously expressed in neural cells demonstrate that menthol attenuates α7 mediated Ca(2+) transients in the cell body and neurite. In conclusion, our results suggest that menthol inhibits α7-nACh receptors in a noncompetitive manner.

PMID:
23935840
PMCID:
PMC3720735
DOI:
10.1371/journal.pone.0067674
[Indexed for MEDLINE]
Free PMC Article

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