Literature DB >> 28743602

Menthol disrupts nicotine's psychostimulant properties in an age and sex-dependent manner in C57BL/6J mice.

Benjamin W Fait1, David C Thompson1, Tenna N Mose1, Peter Jatlow2, Sven E Jordt3, Marina R Picciotto1, Yann S Mineur4.   

Abstract

Menthol is a commonly used flavorant in tobacco and e-cigarettes, and could contribute to nicotine sensitivity. To understand how menthol could contribute to nicotine intake and addiction, it is important to determine whether specific mechanisms related to sex and age could underlie behavioral changes induced by menthol-laced nicotinic products. Using a validated paradigm of nicotine-dependent locomotor stimulation, adolescent and adult C57BL/6J mice of both sexes were exposed to nicotine, or nicotine laced with menthol, as their sole source of fluid, and psychostimulant effects were evaluated by recording home cage locomotor activity for ten days. Nicotine and cotinine blood levels were measured following exposure. Results show an interaction between treatment, age, and sex on liquid consumption, indicating that mice responded differently to menthol and nicotine based on their age and sex. Adult male mice greatly increased their nicotine intake when given menthol. In female mice of both age groups, menthol did not have this effect. Despite an increase in nicotine intake promoted by menthol, adult male mice showed a significant decrease in locomotion, suggesting that menthol blunted nicotine-induced psychostimulation. This behavioral response to menthol was not detected in adolescent mice of either sex. These data confirm that menthol is more than a flavorant, and can influence both nicotine intake and its psychostimulant effects. These results suggest that age- and sex-dependent mechanisms could underlie menthol's influence on nicotine intake and that studies including adolescent and adult menthol smokers of both sexes are warranted.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Age difference; Locomotion; Menthol; Nicotine; Sex difference

Mesh:

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Year:  2017        PMID: 28743602      PMCID: PMC5580257          DOI: 10.1016/j.bbr.2017.07.027

Source DB:  PubMed          Journal:  Behav Brain Res        ISSN: 0166-4328            Impact factor:   3.332


  34 in total

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5.  Quit attempts and quit rates among menthol and nonmenthol smokers in the United States.

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Journal:  Am J Public Health       Date:  2011-05-12       Impact factor: 9.308

6.  Modification of aftertaste with a menthol mouthwash reduces food wanting, liking, and ad libitum intake of potato crisps.

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7.  Menthol Alone Upregulates Midbrain nAChRs, Alters nAChR Subtype Stoichiometry, Alters Dopamine Neuron Firing Frequency, and Prevents Nicotine Reward.

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8.  Beta2-subunit-containing nicotinic acetylcholine receptors are critical for dopamine-dependent locomotor activation following repeated nicotine administration.

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9.  Voluntary oral nicotine intake in mice down-regulates GluR2 but does not modulate depression-like behaviors.

Authors:  Patricia Vieyra-Reyes; Marina R Picciotto; Yann S Mineur
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10.  Adolescent menthol smokers: will they be a harder target for cessation?

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Journal:  Environ Sci Pollut Res Int       Date:  2018-01-09       Impact factor: 4.223

2.  Effect of menthol on nicotine intake and relapse vulnerability in a rat model of concurrent intravenous menthol/nicotine self-administration.

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3.  Cotinine inhibits TLR4/NF-κB signaling pathway and improves deep vein thrombosis in rats.

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Review 5.  Chemosensory Contributions of E-Cigarette Additives on Nicotine Use.

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6.  The Intergenerational Transmission of Developmental Nicotine Exposure-Induced Neurodevelopmental Disorder-Like Phenotypes is Modulated by the Chrna5 D397N Polymorphism in Adolescent Mice.

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  6 in total

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