Evidence map›Paper›PMID 25552431›Full record

ArticleThe international journal of neuropsychopharmacology2014

Acute nicotine administration increases BOLD fMRI signal in brain regions involved in reward signaling and compulsive drug intake in rats.

Adrie W Bruijnzeel, Jon C Alexander, Pablo D Perez, Rayna Bauzo-Rodriguez, Gabrielle Hall, Rachel Klausner, Valerie Guerra, Huadong Zeng, Moe Igari, Marcelo Febo

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
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

24 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. Nicotine Increases Activation to Anticipatory Valence Cues in Anterior Insula and Striatum.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2018
    Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Development of Dependence in Smokers and Rodents With Voluntary Nicotine Intake: Similarities and Differences.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2023
    Review
  8. Putative neurochemical and cell type contributions to hemodynamic activity in the rodent caudate putamen.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
    Review
  9. Article
  10. Article
  11. Article
  12. The Effects of Nicotine and Tobacco Use on Brain Reward Function: Interaction With Nicotine Dependence Severity.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2019
    Article
  13. Neurobiological Considerations for Tobacco Use Disorder.Current behavioral neuroscience reports · 2018
    Article
  14. Neuregulin 3 Signaling Mediates Nicotine-Dependent Synaptic Plasticity in the Orbitofrontal Cortex and Cognition.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Adrie W BruijnzeelDepartment of Psychiatry, University of Florida, Gainesville, FL (Drs Bruijnzeel, Alexander, Perez, Bauzo-Rodriguez, Hall, Klausner, Guerra, Igari, and Febo); Advanced Magnetic Resonance Imaging and Spectroscopy Facility (AMRIS), University of Florida, Gainesville, FL (Dr Zeng). awbruijn@ufl.edu.
Jon C AlexanderDepartment of Psychiatry, University of Florida, Gainesville, FL (Drs Bruijnzeel, Alexander, Perez, Bauzo-Rodriguez, Hall, Klausner, Guerra, Igari, and Febo); Advanced Magnetic Resonance Imaging and Spectroscopy Facility (AMRIS), University of Florida, Gainesville, FL (Dr Zeng).
Pablo D PerezDepartment of Psychiatry, University of Florida, Gainesville, FL (Drs Bruijnzeel, Alexander, Perez, Bauzo-Rodriguez, Hall, Klausner, Guerra, Igari, and Febo); Advanced Magnetic Resonance Imaging and Spectroscopy Facility (AMRIS), University of Florida, Gainesville, FL (Dr Zeng).
Rayna Bauzo-RodriguezDepartment of Psychiatry, University of Florida, Gainesville, FL (Drs Bruijnzeel, Alexander, Perez, Bauzo-Rodriguez, Hall, Klausner, Guerra, Igari, and Febo); Advanced Magnetic Resonance Imaging and Spectroscopy Facility (AMRIS), University of Florida, Gainesville, FL (Dr Zeng).
Gabrielle HallDepartment of Psychiatry, University of Florida, Gainesville, FL (Drs Bruijnzeel, Alexander, Perez, Bauzo-Rodriguez, Hall, Klausner, Guerra, Igari, and Febo); Advanced Magnetic Resonance Imaging and Spectroscopy Facility (AMRIS), University of Florida, Gainesville, FL (Dr Zeng).
Rachel KlausnerDepartment of Psychiatry, University of Florida, Gainesville, FL (Drs Bruijnzeel, Alexander, Perez, Bauzo-Rodriguez, Hall, Klausner, Guerra, Igari, and Febo); Advanced Magnetic Resonance Imaging and Spectroscopy Facility (AMRIS), University of Florida, Gainesville, FL (Dr Zeng).
Valerie GuerraDepartment of Psychiatry, University of Florida, Gainesville, FL (Drs Bruijnzeel, Alexander, Perez, Bauzo-Rodriguez, Hall, Klausner, Guerra, Igari, and Febo); Advanced Magnetic Resonance Imaging and Spectroscopy Facility (AMRIS), University of Florida, Gainesville, FL (Dr Zeng).
Huadong ZengDepartment of Psychiatry, University of Florida, Gainesville, FL (Drs Bruijnzeel, Alexander, Perez, Bauzo-Rodriguez, Hall, Klausner, Guerra, Igari, and Febo); Advanced Magnetic Resonance Imaging and Spectroscopy Facility (AMRIS), University of Florida, Gainesville, FL (Dr Zeng).
Moe IgariDepartment of Psychiatry, University of Florida, Gainesville, FL (Drs Bruijnzeel, Alexander, Perez, Bauzo-Rodriguez, Hall, Klausner, Guerra, Igari, and Febo); Advanced Magnetic Resonance Imaging and Spectroscopy Facility (AMRIS), University of Florida, Gainesville, FL (Dr Zeng).
Marcelo FeboDepartment of Psychiatry, University of Florida, Gainesville, FL (Drs Bruijnzeel, Alexander, Perez, Bauzo-Rodriguez, Hall, Klausner, Guerra, Igari, and Febo); Advanced Magnetic Resonance Imaging and Spectroscopy Facility (AMRIS), University of Florida, Gainesville, FL (Dr Zeng).
University of Florida · US

Funding

Brain Imaging of Cocaine and Maternal RewardR01DA019946 · NIDA · UNIVERSITY OF FLORIDA · PI FEBO, MARCELO · 2007 to 2011
$1.6M
Upgrade of an 11T/40cm MRI/S SystemS10RR025671 · NCRR · UNIVERSITY OF FLORIDA · PI EDISON, ARTHUR S · 2009 to 2009
$500k
NCRR NIH HHS S10 RR025671NCRR NIH HHS S10RR025671NIDA NIH HHS DA019946NIDA NIH HHS R01 DA019946
6 · The paper itself

Abstract

backgroundAcute nicotine administration potentiates brain reward function and enhances motor and cognitive function. These studies investigated which brain areas are being activated by a wide range of doses of nicotine, and if this is diminished by pretreatment with the nonselective nicotinic receptor antagonist mecamylamine.

methodsDrug-induced changes in brain activity were assessed by measuring changes in the blood oxygen level dependent (BOLD) signal using an 11.1-Tesla magnetic resonance scanner. In the first experiment, nicotine naïve rats were mildly anesthetized and the effect of nicotine (0.03-0.6 mg/kg) on the BOLD signal was investigated for 10 min. In the second experiment, the effect of mecamylamine on nicotine-induced brain activity was investigated.

resultsA high dose of nicotine increased the BOLD signal in brain areas implicated in reward signaling, such as the nucleus accumbens shell and the prelimbic area. Nicotine also induced a dose-dependent increase in the BOLD signal in the striato-thalamo-orbitofrontal circuit, which plays a role in compulsive drug intake, and in the insular cortex, which contributes to nicotine craving and relapse. In addition, nicotine induced a large increase in the BOLD signal in motor and somatosensory cortices. Mecamylamine alone did not affect the BOLD signal in most brain areas, but induced a negative BOLD response in cortical areas, including insular, motor, and somatosensory cortices. Pretreatment with mecamylamine completely blocked the nicotine-induced increase in the BOLD signal.

conclusionsThese studies demonstrate that acute nicotine administration activates brain areas that play a role in reward signaling, compulsive behavior, and motor and cognitive function.

Indexed as

AnimalsBrainBrain MappingCerebrovascular CirculationCompulsive BehaviorDose-Response Relationship, DrugMagnetic Resonance ImagingMaleMecamylamineNicotineNicotinic AgonistsNicotinic AntagonistsOxygenRats, WistarRewardMecamylamineNicotineNicotinic AgonistsNicotinic AntagonistsOxygenaddictioncompulsive behaviornicotinepharmacological fMRIratsreward.

Identifiers

PMID25552431
PMCPMC4368882
OpenAlexW2395200172

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.