Evidence map›Paper›PMID 26602173›Full record

ArticleScientific reports2015

A new animal model of placebo analgesia: involvement of the dopaminergic system in reward learning.

In-Seon Lee, Bombi Lee, Hi-Joon Park, Håkan Olausson, Paul Enck, Younbyoung Chae

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Convergent state-control of endogenous opioid analgesia.bioRxiv : the preprint server for biology · 2025
    Article
  3. Haloperidol for Pain Management: A Narrative Review.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
  4. Article
  5. Review
  6. Placebo: a brief updated review.Naunyn-Schmiedeberg's archives of pharmacology · 2022
    Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. The Placebo Effect in Pain Therapies.Annual review of pharmacology and toxicology · 2019
    Review
  13. Role of placebo effects in pain and neuropsychiatric disorders.Progress in neuro-psychopharmacology & biological psychiatry · 2018
    Review
  14. Article
  15. Article
  16. Placebo Analgesia in Rodents: Current and Future Research.International review of neurobiology · 2018
    Review
  17. Article
  18. Article
  19. Article
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

6 authors at 3 institutions in 3 countries.

In-Seon LeeAcupuncture and Meridian Science Research Center, College of Korean Medicine, Kyung Hee University, Seoul, Korea.
Bombi LeeAcupuncture and Meridian Science Research Center, College of Korean Medicine, Kyung Hee University, Seoul, Korea.
Hi-Joon ParkAcupuncture and Meridian Science Research Center, College of Korean Medicine, Kyung Hee University, Seoul, Korea.
Håkan OlaussonCenter for Social and Affective Neuroscience, Linköping University.
Paul EnckDepartment of Internal Medicine: Psychosomatic Medicine and Psychotherapy, University of Tübingen, Tübingen, Germany.
Younbyoung ChaeAcupuncture and Meridian Science Research Center, College of Korean Medicine, Kyung Hee University, Seoul, Korea.
Kyung Hee University · KRUniversity of Tübingen · DELinköping University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We suggest a new placebo analgesia animal model and investigated the role of the dopamine and opioid systems in placebo analgesia. Before and after the conditioning, we conducted a conditioned place preference (CPP) test to measure preferences for the cues (Rooms 1 and 2), and a hot plate test (HPT) to measure the pain responses to high level-pain after the cues. In addition, we quantified the expression of tyrosine hydroxylase (TH) in the ventral tegmental area (VTA) and c-Fos in the anterior cingulate cortex (ACC) as a response to reward learning and pain response. We found an enhanced preference for the low level-pain paired cue and enhanced TH expression in the VTA of the Placebo and Placebo + Naloxone groups. Haloperidol, a dopamine antagonist, blocked these effects in the Placebo + Haloperidol group. An increased pain threshold to high-heat pain and reduced c-Fos expression in the ACC were observed in the Placebo group only. Haloperidol blocked the place preference effect, and naloxone and haloperidol blocked the placebo analgesia. Cue preference is mediated by reward learning via the dopamine system, whereas the expression of placebo analgesia is mediated by the dopamine and opioid systems.

Indexed as

AnalgesiaAnimalsDopamine AntagonistsGyrus CinguliHaloperidolImmunohistochemistryMaleModels, AnimalNaloxoneNarcotic AntagonistsPainPain ThresholdPlacebo EffectProto-Oncogene Proteins c-fosRatsRats, Sprague-DawleyDopamine AntagonistsHaloperidolNaloxoneNarcotic AntagonistsProto-Oncogene Proteins c-fosTyrosine 3-Monooxygenase

Identifiers

PMID26602173
PMCPMC4658539
OpenAlexW2343718497

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.