Evidence map›Paper›PMID 40812200›Full record

ArticleThe Journal of pharmacology and experimental therapeutics2025

Nicotine enhances the ability of cues to control behavior and evoke dopamine release in the dorsolateral striatum.

Michael Z Leonard, Hannah B Elam, Hye Jean Yoon, Sofia H Lago, Megan E Altemus, Shemuel Roberts, Maxime Chevée, Erin S Calipari

Abstract read
In one paragraph

Article in The Journal of pharmacology and experimental therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Michael Z LeonardDepartment of Pharmacology, Vanderbilt University, Nashville, Tennessee; Vanderbilt Center for Addiction Research, Vanderbilt University, Nashville, Tennessee.
Hannah B ElamDepartment of Pharmacology, Vanderbilt University, Nashville, Tennessee; Vanderbilt Center for Addiction Research, Vanderbilt University, Nashville, Tennessee.
Hye Jean YoonDepartment of Pharmacology, Vanderbilt University, Nashville, Tennessee; Vanderbilt Center for Addiction Research, Vanderbilt University, Nashville, Tennessee.
Sofia H LagoDepartment of Pharmacology, Vanderbilt University, Nashville, Tennessee; Vanderbilt Center for Addiction Research, Vanderbilt University, Nashville, Tennessee.
Megan E AltemusDepartment of Pharmacology, Vanderbilt University, Nashville, Tennessee; Vanderbilt Center for Addiction Research, Vanderbilt University, Nashville, Tennessee.
Shemuel RobertsDepartment of Pharmacology, Vanderbilt University, Nashville, Tennessee; Vanderbilt Center for Addiction Research, Vanderbilt University, Nashville, Tennessee.
Maxime ChevéeDepartment of Pharmacology, Vanderbilt University, Nashville, Tennessee; Vanderbilt Center for Addiction Research, Vanderbilt University, Nashville, Tennessee.
Erin S CalipariDepartment of Pharmacology, Vanderbilt University, Nashville, Tennessee; Vanderbilt Center for Addiction Research, Vanderbilt University, Nashville, Tennessee. Electronic address: erin.calipari@vanderbilt.edu.

Funding

Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Lea K Davis · 2020 to 2026
$10.3M
Mechanisms of dopaminergic dysfunction in substance use disorderR01DA052317 · NIDA · VANDERBILT UNIVERSITY · PI CALIPARI, ERIN · 2021 to 2025
$2.4M
Making and breaking opioid memories to prevent relapseDP1DA048931 · NIDA · VANDERBILT UNIVERSITY · PI CALIPARI, ERIN · 2019 to 2023
$2.4M
Circuit control of motivation to take and seek alcoholR01AA030931 · NIAAA · VANDERBILT UNIVERSITY · PI Erin Calipari · 2023 to 2026
$2.3M
Defining the Role of D1 and D2 Medium Spiny Neurons in Relapse to Cocaine SeekingR00DA042111 · NIDA · VANDERBILT UNIVERSITY · PI CALIPARI, ERIN · 2018 to 2020
$747k
Circuit mechanisms underlying inflexible habitual behaviors following chronic cocaine useK99DA060930 · NIDA · VANDERBILT UNIVERSITY · PI Maxime F. Chevee · 2025 to 2026
$311k
Cocaine effects on spatial patterns of striatal dopamine releaseF32DA061606 · NIDA · VANDERBILT UNIVERSITY · PI Hannah Reiley · 2024 to 2026
$227k
Defining the cell-type specific control of alcohol drinkingF31AA030916 · NIAAA · VANDERBILT UNIVERSITY · PI Hye Jean Yoon · 2023 to 2026
$152k
Defining Disruptions to Dopaminergic Control of Striatal Activity after Chronic Cocaine UseF32DA060662 · NIDA · VANDERBILT UNIVERSITY · PI LEONARD, MICHAEL Z. · 2024 to 2024
$77k
NIAAA NIH HHS F31 AA030916NIAAA NIH HHS R01 AA030931NICHD NIH HHS P50 HD103537NIDA NIH HHS DP1 DA048931NIDA NIH HHS F32 DA060662NIDA NIH HHS F32 DA061606NIDA NIH HHS K99 DA060930NIDA NIH HHS R00 DA042111NIDA NIH HHS R01 DA052317
6 · The paper itself

Abstract

Nicotine is one of the most widely used addictive substances, yet its primary reinforcing effects are relatively weak. Nicotine's ability to potentiate responding for conditioned reinforcers is thought to drive persistent drug use. Here, we show that nicotine failed to alter responding maintained by a primary sucrose reinforcer (under a variable-ratio [VR] 11 schedule) across a broad dose range (0.01-1.0 mg/kg). Yet, nicotine enhanced operant behavior under a second-order reinforcement schedule in which responses produced sucrose-associated cues and were only intermittently reinforced by sucrose itself. Together, we demonstrate that nicotine selectively augments behavior maintained by conditioned reinforcers (sucrose-associated cues) in a rate-dependent manner, increasing responding only in mice with low rates of reinforcement behavior at baseline. Using fiber photometry, we demonstrate that nicotine selectively amplified cue-evoked dopamine release in the dorsolateral striatum-but only in low baseline responders-while having no effect on dopamine signaling in the nucleus accumbens. These effects were blocked by the nicotinic receptor antagonist mecamylamine. Further, nicotine's influence on behavior was abolished when the contingency between action and conditioned stimuli was disrupted, indicating that nicotine strengthens cue control of behavior rather than increasing motivation generally. Collectively, these findings reveal that nicotine's behavioral actions emerge through an interaction between pharmacological mechanisms, behavioral contingencies, and individual differences in baseline behavioral control. SIGNIFICANCE STATEMENT: Nicotine strengthens the impact of environmental cues on behavior by amplifying dopamine signals in specific projection targets, but only in individuals with specific behavioral traits. This reveals how nicotine hijacks learning processes to promote persistent, cue-driven actions.

Indexed as

Behavior, AnimalCorpus StriatumCuesDopamineNicotineAnimalsConditioning, OperantMaleMiceMice, Inbred C57BLNicotinic AgonistsReinforcement, PsychologyDopamineNicotineNicotinic AgonistsConditioned reinforcementCueReinforcerSecond order schedule

Identifiers

PMID40812200
PMCPMC12597647

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.