Evidence map›Paper›PMID 30483833›Full record

ArticlePsychopharmacology2019

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

Tanseli Nesil, Syeda Narmeen, Anousheh Bakhti-Suroosh, Wendy J Lynch

Abstract read
In one paragraph

Article in Psychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

  1. Article
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  3. Review
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  6. Review
  7. Differences in Cognitive Task Performance, Reinforcement Enhancement, and Nicotine Dependence Between Menthol and Nonmenthol Cigarette Smokers.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2021
    Article
  8. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Tanseli NesilDepartment of Psychiatry and Neurobehavioral Sciences, University of Virginia, Charlottesville, VA, 22902, USA.
Syeda NarmeenDepartment of Psychiatry and Neurobehavioral Sciences, University of Virginia, Charlottesville, VA, 22902, USA.
Anousheh Bakhti-SurooshDepartment of Psychiatry and Neurobehavioral Sciences, University of Virginia, Charlottesville, VA, 22902, USA.
Wendy J LynchDepartment of Psychiatry and Neurobehavioral Sciences, University of Virginia, Charlottesville, VA, 22902, USA. wlynch@virginia.edu.

Funding

Dopaminergic and Glutamatergic Mechanisms of Cocaine Addiction: Sex DifferencesR01DA024716 · NIDA · UNIVERSITY OF VIRGINIA · PI Wendy Jean Lynch · 2008 to 2026
$6.1M
Exercise as a Sex-Specific Intervention Strategy for Cocaine AddictionR01DA039093 · NIDA · UNIVERSITY OF VIRGINIA · PI LYNCH, WENDY JEAN · 2015 to 2019
$1.7M
NIDA NIH HHS R01 DA024716NIDA NIH HHS R01DA024716NIDA NIH HHS R01 DA039093
6 · The paper itself

Abstract

rationaleEpidemiological data suggest that menthol may increase vulnerability to cigarette/nicotine use and relapse. While menthol's sensory properties are often attributed as the underlying cause of the enhanced vulnerability, an alternative possibility is that they are mediated via pharmacological interactions with nicotine.

objectiveThis study addressed the possibility that menthol enhances nicotine intake and relapse vulnerability via pharmacological interactions with nicotine using a concurrent intravenous menthol/nicotine self-administration procedure.

methodsFollowing acquisition, adolescent rats were given 23-h/day access to nicotine (0.01 mg/kg/infusion), nicotine plus menthol (0.16, 0.32, or 0.64 mg/kg/infusion), or menthol alone (0.16, 0.32, 0.64 mg/kg/infusion) for a total of 10 days. Nicotine-seeking was assessed using an extinction/cue-induced reinstatement procedure following 10 days of forced abstinence. We also assessed the effect of menthol (0.32 mg/kg/infusion) on progressive ratio responding for nicotine (0.01 mg/kg/infusion).

resultsMenthol decreased PR responding for nicotine but did not affect self-administration under extended access conditions. The low dose of menthol tended to decrease subsequent extinction responding, and was not different from menthol alone, whereas the high dose decreased reinstatement responding. Although not significant, the highest levels of extinction responding were observed in a minority of rats in the moderate and high menthol-nicotine groups; rats in these groups also took longer to extinguish.

conclusionsTaken together, these results demonstrate that pharmacological interactions of menthol with nicotine reduce, rather than increase, nicotine's reinforcing effects and some measures of relapse vulnerability. Importantly, however, moderate and high menthol doses may increase some aspects of relapse vulnerability in a minority of individuals.

Indexed as

Reinforcement, PsychologyAnimalsBehavior, AddictiveBehavior, AnimalConditioning, OperantExtinction, PsychologicalInfusions, IntravenousMaleMentholNicotineNicotinic AgonistsRatsRats, Sprague-DawleyRecurrenceSelf AdministrationMentholNicotineNicotinic AgonistsExtended accessMentholNicotine-seekingProgressive-ratioReinstatementSelf-administration

Identifiers

PMID30483833
PMCPMC6536373

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.