Evidence map›Paper›PMID 24732880›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2014

Transient receptor potential vanilloid type 1 channel may modulate opioid reward.

Thi-Lien Nguyen, Seung-Hwan Kwon, Sa-Ik Hong, Shi-Xun Ma, Yang-Hee Jung, Ji-Young Hwang, Hyoung-Chun Kim, Seok-Yong Lee, Choon-Gon Jang

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 45 citations in OpenAlex.

  1. The Role of TRPV1/CGRP Pathway Activated byInternational journal of molecular sciences · 2025
    Article
  2. Review
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  6. Repeated Morphine Administration IncreasesBiomolecules & therapeutics · 2022
    Article
  7. Review
  8. Side Effects of Opioids Are Ameliorated by Regulating TRPV1 Receptors.International journal of environmental research and public health · 2022
    Review
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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

9 authors at 2 institutions in 1 country.

Thi-Lien NguyenDepartment of Pharmacology, School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Seung-Hwan KwonDepartment of Pharmacology, School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Sa-Ik HongDepartment of Pharmacology, School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Shi-Xun MaDepartment of Pharmacology, School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Yang-Hee JungDepartment of Pharmacology, School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Ji-Young HwangDepartment of Pharmacology, School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Hyoung-Chun KimNeurotoxicology Program, College of Pharmacy, Korea Institute of Drug Abuse, Kangwon National University, Chuncheon, Republic of Korea.
Seok-Yong LeeDepartment of Pharmacology, School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Choon-Gon JangDepartment of Pharmacology, School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
Sungkyunkwan University · KRKangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transient receptor potential vanilloid type 1 (TRPV1), a nonselective cation channel, is a well-known pain-related receptor. TRPV1 involvement in morphine-induced antinociception, tolerance, and withdrawal symptoms has been previously reported. Emerging evidence indicates that TRPV1 may be related to both the cellular and behavioral effects of addictive drugs. In the present study, we investigated the role of TRPV1 in morphine reward using the conditioned place preference (CPP) paradigm in mice. Repeated morphine treatments upregulated TRPV1 expression in the dorsal striatum (DSt). Treatment with a TRPV1 agonist potentiated morphine reward, and pretreatment with TRPV1 antagonists attenuated these effects. Microinjection of a selective TRPV1 antagonist into the DSt significantly inhibited morphine-CPP. In addition, treatment with a TRPV1 antagonist suppressed morphine-induced increases in μ-opioid receptor binding, adenylyl cyclase 1 (AC1), p38 mitogen-activated protein kinase (p38 MAPK), and nuclear factor kappa B (NF-κB) expression in the DSt. Administering a p38 inhibitor not only prevented morphine-CPP, but also prevented morphine-induced NF-κB and TRPV1 activation in the DSt. Furthermore, injecting an NF-κB inhibitor significantly blocked morphine-CPP. Our findings suggest that TRPV1 in the DSt contribute to morphine reward via AC1, p38 MAPK, and NF-κB. Brain TRPV1 may serve as a novel therapeutic target to treat morphine-addictive disorders.

Indexed as

RewardAdenylyl CyclasesAnalgesics, OpioidAnimalsConditioning, PsychologicalCorpus StriatumMaleMice, Inbred ICRMorphineNF-kappa Bp38 Mitogen-Activated Protein KinasesReceptors, Opioid, muSpace PerceptionTRPV Cation Channelsadenylyl cyclase 1Adenylyl CyclasesAnalgesics, OpioidMorphineNF-kappa Bp38 Mitogen-Activated Protein KinasesReceptors, Opioid, muTRPV1 protein, mouseTRPV Cation Channels

Identifiers

PMID24732880
PMCPMC4138752
OpenAlexW1965146708

What OpenQuestion holds

Textmetadata
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.