Evidence map›Paper›PMID 41874416›Full record

ArticleNicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco2026

The role of the gut microbiome in nicotine withdrawal and dependence.

Eda Koseli, Katarzyna M Tyc, Belle Buzzi, Hamid I Akbarali, M Imad Damaj

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Article in Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Eda KoseliDepartment of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond VA 23298, United States.
Katarzyna M TycDepartment of Biostatistics, Virginia Commonwealth University, Richmond VA 23298, United States.
Belle BuzziDepartment of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond VA 23298, United States.
Hamid I AkbaraliDepartment of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond VA 23298, United States.
M Imad DamajDepartment of Pharmacology and Toxicology, Virginia Commonwealth University, Richmond VA 23298, United States.ORCID 0000-0002-8859-029X

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Renato Martins · 1985 to 2026
$51.0M
VCU Center for Drug Addiction ResearchP30DA033934 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI JOLENE J WINDLE · 2014 to 2026
$13.8M
NCI NIH HHS P30 CA016059NIDA NIH HHS P30 DA033934NIDA NIH HHS P30DA033934NIH-NCI Cancer Center Support P30 CA016059
6 · The paper itself

Abstract

introductionSmoking is considered a global pandemic, with more than 1.3 billion people being active smokers. Increasing evidence suggests that nicotine exposure can lead to changes in the gut microbiome, increases in permeability, and impaired mucosal immune responses in the gastrointestinal tract. However, the literature on behavioral aspects of nicotine-microbiome interaction, such as dependence and withdrawal, is limited. In this study, we used homologous fecal material transplants (FMT) to modify the gut microbiome and its impact on the intensity of nicotine withdrawal in mice.

methodsWe used osmotic minipumps (MPs) as an application of chronic nicotine for 15 days and orally gavaged FMT 2x a day to the mice. We assessed the nicotine withdrawal by measuring the number of somatic signs and anxiety-like behaviors at 24 h and 1 week after the mini pump removal. Fecal samples were also collected points to identify the gut microbiome changes.

resultsFecal transplants reduced the number of somatic signs and anxiety-like behaviors in nicotine-treated mice up to a week after the removal of MPs. The shotgun metagenomic results of the fecal samples from 24 h after MP removal time point show altered gut microbiome with a significant shift in the species composition between the nicotine-treated and its homologous FMT treatment.

conclusionsOur results indicate that under our experimental conditions, fecal transplant can reduce the severity of nicotine withdrawal. This suggests that interactions along the gut-brain axis are important for the development of nicotine dependence and might help lower the risk of cancer and other serious health problems in humans. IMPLICATIONS: This report shows for the first time that the gut microbiome may modulate nicotine withdrawal intensity in mice. Homologous fecal material transplants (FMT) prevented nicotine-induced gut microbiome dysbiosis and consequently reduced withdrawal severity in mice. These results may have important implications in the management of smoking cessation.

Indexed as

Gastrointestinal MicrobiomeNicotineSubstance Withdrawal SyndromeTobacco Use DisorderAnimalsFecal Microbiota TransplantationFecesMaleMiceMice, Inbred C57BLNicotinebehavioralpharmacology (non-clinical)withdrawal symptoms

Identifiers

PMID41874416
PMCPMC13500348

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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.