Evidence map›Paper›PMID 24236199›Full record

ArticlePloS one2013

Dopamine and pain sensitivity: neither sulpiride nor acute phenylalanine and tyrosine depletion have effects on thermal pain sensations in healthy volunteers.

Susanne Becker, Marta Ceko, Mytsumi Louis-Foster, Nathaniel M Elfassy, Marco Leyton, Yoram Shir, Petra Schweinhardt

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
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  7. Exploring Nepicastat Activity: Beyond DβH.International journal of molecular sciences · 2025
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  11. Research Progress on the Pharmacological Action of Schisantherin A.Evidence-based complementary and alternative medicine : eCAM · 2022
    Review
  12. Article
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  14. Article
  15. Article
  16. Chronic Back Pain Is Associated with Alterations in Dopamine Neurotransmission in the Ventral Striatum.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  17. Spinal dopaminergic projections control the transition to pathological pain plasticity via a D1/D5-mediated mechanism.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  18. Article
  19. 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

7 authors at 4 institutions in 3 countries.

Susanne BeckerAlan Edwards Centre for Research on Pain and Faculty of Dentistry, McGill University, Montreal, Quebec, Canada ; Department of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
Marta Ceko
Mytsumi Louis-Foster
Nathaniel M Elfassy
Marco Leyton
Yoram Shir
Petra Schweinhardt
McGill University · CAConcordia University · CAMontreal General Hospital · CANational Center for Complementary and Integrative Health · US

Funding

CIHR 102636-1CIHR MOP-102636
6 · The paper itself

Abstract

Based on animal studies and some indirect clinical evidence, dopamine has been suggested to have anti-nociceptive effects. Here, we investigated directly the effects of increased and decreased availability of extracellular dopamine on pain perception in healthy volunteers. In Study 1, participants ingested, in separate sessions, a placebo and a low dose of the centrally acting D2-receptor antagonist sulpiride, intended to increase synaptic dopamine via predominant pre-synaptic blockade. No effects were seen on thermal pain thresholds, tolerance, or temporal summation. Study 2 used the acute phenylalanine and tyrosine depletion (APTD) method to transiently decrease dopamine availability. In one session participants ingested a mixture that depletes the dopamine amino acid precursors, phenylalanine and tyrosine. In the other session they ingested a nutritionally balanced control mixture. APTD led to a small mood-lowering response following aversive thermal stimulation, but had no effects on the perception of cold, warm, or pain stimuli. In both studies the experimental manipulation of dopaminergic neurotransmission was successful as indicated by manipulation checks. The results contradict proposals that dopamine has direct anti-nociceptive effects in acute experimental pain. Based on dopamine's well-known role in reward processing, we hypothesize that also in the context of pain, dopamine acts on stimulus salience and might play a role in the initiation of avoidance behavior rather than having direct antinociceptive effects in acute experimental pain.

Indexed as

AdolescentAdultAffectAnxietyDopamineDopamine D2 Receptor AntagonistsFemaleHealthy VolunteersHumansMalePainPain PerceptionPain ThresholdPhenylalaninePresynaptic TerminalsReceptors, Dopamine D2DopamineDopamine D2 Receptor AntagonistsPhenylalanineReceptors, Dopamine D2SulpirideTyrosine

Identifiers

PMID24236199
PMCPMC3827462
OpenAlexW1990957056

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.