Evidence map›Paper›PMID 41920974›Full record

ArticleThe international journal of neuropsychopharmacology2026

Effects of nicotinic receptor antagonism on nicotine and THC self-administration in a model of polysubstance use.

Mary M Torregrossa, Tamara Racic, Samantha L Baglot, Sierra J Stringfield, Matthew N Hill, Alan Sved

Abstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Mary M TorregrossaDepartment of Psychiatry, University of Pittsburgh, Pittsburgh, PA 15219, United States.ORCID 0000-0003-2083-0231
Tamara RacicDepartment of Neuroscience, University of Pittsburgh, Pittsburgh, PA 15213, United States.
Samantha L BaglotDepartments of Cell Biology and Anatomy & Psychiatry, Cumming School of Medicine, Hotchkiss Brain Institute and The Mathison Centre for Mental Health Research and Education, University of Calgary, Calgary, Canada.
Sierra J StringfieldDepartment of Neuroscience, University of Pittsburgh, Pittsburgh, PA 15213, United States.ORCID 0000-0003-4840-0866
Matthew N HillDepartments of Cell Biology and Anatomy & Psychiatry, Cumming School of Medicine, Hotchkiss Brain Institute and The Mathison Centre for Mental Health Research and Education, University of Calgary, Calgary, Canada.
Alan SvedDepartment of Neuroscience, University of Pittsburgh, Pittsburgh, PA 15213, United States.

Funding

Subject Management and BiobankingP50DA046346 · NIDA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Daniel J. Buysse, Colleen A McClung · 2020 to 2026
$23.4M
Investigating mechanisms mediating enhanced THC reinforcement by nicotineR01DA058955 · NIDA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Mary M Torregrossa · 2023 to 2026
$2.1M
Investigating the bidirectional relationship between circadian rhythms and cannabinoid useR01DA061227 · NIDA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Kyle Ketchesin, Marianne L Seney · 2024 to 2026
$1.3M
Canadian Institute of Health Research CIHR TCP-431510NIDA NIH HHS P50DA046346NIDA NIH HHS R01DA058955NIDA NIH HHS R01DA061227United States Public Health Services
6 · The paper itself

Abstract

backgroundMost substance users are polysubstance users; however, little is known about how the combined use of different drugs affects the course of substance use disorder or effectiveness of treatment. Notably, co-use of cannabis and nicotine is very common, and we previously demonstrated that nicotine enhances the self-administration of a synthetic cannabinoid receptor agonist and the primary psychoactive phytocannabinoid in cannabis, Δ-9-tetrahydrocannabinol (THC).

methodsHere we aimed to further investigate the patterns of nicotine and THC self-administration when available in a concurrent choice model, and to determine the effects of nicotinic acetylcholine receptor (nAchR) antagonists on nicotine-enhanced THC self-administration in male and female rats.

resultsDuring concurrent choice, nicotine availability increased THC self-administration in females without affecting THC metabolism, while THC availability decreased nicotine self-administration and preference in females relative to when nicotine and saline were concurrently available. In females, THC self-administration was reduced by the α4β2/4 subunit-containing nAchR antagonist dihydro-beta-erythroidine in both nicotine and saline concurrent availability groups; while nicotine self-administration was reduced in both sexes by the α7nAchR antagonist methylylcaconitine, but only in rats that had concurrent access to THC. The nonspecific nAchR antagonist mecamylamine had minimal effects in the concurrent choice model, but it prevented nicotine-induced enhancement of THC self-administration when nicotine was given prior to a single choice THC only self-administration session.

conclusionsThus, behavioral regulation of self-administration is differentially influenced by nAchR subtypes depending on the availability of other substances, which has implications for the efficacy of treatments in the context of polysubstance use. Significance statement Polysubstance use is extremely common, but very understudied in both clinical and preclinical research. The results presented here highlight that pharmacological modulators of drug reinforcement can differ when multiple drugs are available simultaneously, highlighting the importance of investigating potential treatments for substance use disorders in the context of polysubstance use.

Indexed as

Behavior, AnimalDronabinolNicotineNicotinic AgonistsNicotinic AntagonistsAnimalsChoice BehaviorDihydro-beta-ErythroidineDisease Models, AnimalFemaleMaleMecamylamineRatsRats, Sprague-DawleyReceptors, NicotinicSelf AdministrationDihydro-beta-ErythroidineDronabinolMecamylamineNicotineNicotinic AgonistsNicotinic AntagonistsReceptors, NicotinicnAchR antagonistnicotinepolysubstance useself-administrationTHC

Identifiers

PMID41920974
PMCPMC13127143

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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 Socratic graph.