Brandon J. Henderson, Stephen Grant, Betty W. Chu, Rezvan Shahoei, Stephanie M.
Huard, Shyam S. M. Saladi, Emad Tajkhorshid, Dennis A. Dougherty, and
Henry A. Lester.
Menthol stereoisomers exhibit different effects on α4β2
nAChR upregulation and dopamine neuron spontaneous firing.
eNeuro, 5:ENEURO.0465-18.2018, 2018.
(PMC: PMC6325563)
HEND2018-ET
Menthol contributes to poor cessation rates among smokers, in part
because menthol enhances nicotine reward and reinforcement. Mentholated
tobacco products contain menthol and menthol, in varying
proportions. We examined these two menthol stereoisomers for their ability
to upregulate nAChRs and to alter dopamine neuron firing
frequency using long-term, low-dose ( 500 nM) exposure that is
pharmacologically relevant to smoking. We found that menthol
upregulates nAChRs while menthol does not. We
also found that menthol decreases dopamine neuron baseline firing
and dopamine neuron excitability, while menthol exhibits no effect.
We then examined both stereoisomers for their ability to inhibit
nAChR function at higher concentrations (10 M)
using the Xenopus oocyte expression system. To probe for the
potential binding site of menthol, we conducted flooding simulations and
site-directed mutagenesis. We found that menthol likely binds to the
9 position on the TM2 helix. We found that menthol inhibition is
dependent on the end-to-end distance of the side chain at the 9
residue. Additionally, we have found that menthol is only modestly
(25%) more potent than menthol at inhibiting wildtype
nAChRs and a series of L9 mutant nAChRs.
These data reveal that menthol exhibits a stereoselective effect on nAChRs
and that the stereochemical effect is much greater for long-term,
sub M exposure in mice than for acute, higher level exposure. We
hypothesize that of the two menthol stereoisomers, only menthol
plays a role in enhancing nicotine reward through nAChRs on dopamine
neurons.
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