Evidence map›Paper›PMID 27105831›Full record

ArticleBiological psychiatry2016

Gamma-Aminobutyric Acidergic Projections From the Dorsal Raphe to the Nucleus Accumbens Are Regulated by Neuromedin U.

James M Kasper, David L McCue, Adrianna J Milton, Angelia Szwed, Catherine M Sampson, Mei Huang, Susan Carlton, Herbert Y Meltzer, Kathryn A Cunningham, Jonathan D Hommel

Abstract read
In one paragraph

Article in Biological psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Role of neuropeptide neuromedin U in the nucleus accumbens shell in cocaine self-administration in male rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Article
  6. The role of microglia in neuropsychiatric disorders and suicide.European archives of psychiatry and clinical neuroscience · 2022
    Review
  7. Neuromedin U, a Key Molecule in Metabolic Disorders.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

10 authors.

James M KasperCenter for Addiction Research, Department of Pharmacology & Toxicology, University of Texas Medical Branch, Galveston, Texas.
David L McCueCenter for Addiction Research, Department of Pharmacology & Toxicology, University of Texas Medical Branch, Galveston, Texas.
Adrianna J MiltonCenter for Addiction Research, Department of Pharmacology & Toxicology, University of Texas Medical Branch, Galveston, Texas.
Angelia SzwedCenter for Addiction Research, Department of Pharmacology & Toxicology, University of Texas Medical Branch, Galveston, Texas.
Catherine M SampsonCenter for Addiction Research, Department of Pharmacology & Toxicology, University of Texas Medical Branch, Galveston, Texas.
Mei HuangDepartment of Psychiatry and Behavioral Sciences, Northwestern Feinberg School of Medicine, Chicago, Illinois.
Susan CarltonDepartment of Neuroscience and Cell Biology, University of Texas Medical Branch, Galveston, Texas.
Herbert Y MeltzerDepartment of Psychiatry and Behavioral Sciences, Northwestern Feinberg School of Medicine, Chicago, Illinois.
Kathryn A CunninghamCenter for Addiction Research, Department of Pharmacology & Toxicology, University of Texas Medical Branch, Galveston, Texas.
Jonathan D HommelCenter for Addiction Research, Department of Pharmacology & Toxicology, University of Texas Medical Branch, Galveston, Texas. Electronic address: jdhommel@utmb.edu.

Funding

UTMB Clinical and Translational Science AwardUL1TR001439 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI URBAN, RANDALL J · 2015 to 2024
$40.0M
Translational Explorations in Substance Use DisordersT32DA007287 · NIDA · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI Kathryn A. Cunningham, Jonathan Dean Hommel · 1994 to 2026
$4.7M
UTMB Clinical and Translational Science AwardKL2TR001441 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI AMEREDES, BILL T · 2015 to 2024
$4.0M
Core Center for Translational Addiction SciencesP30DA028821 · NIDA · UNIVERSITY OF TEXAS MED BR GALVESTON · PI CUNNINGHAM, KATHRYN A. · 2009 to 2010
$1.5M
Addiction and the Neuropharmacology of PsychostimulantsK05DA020087 · NIDA · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI CUNNINGHAM, KATHRYN A. · 2005 to 2015
$1.3M
Neuromedin U as a Novel Mechanism Underlying Cocaine AddictionR03DA033437 · NIDA · UNIVERSITY OF TEXAS MED BR GALVESTON · PI HOMMEL, JONATHAN DEAN · 2013 to 2013
$116k
NCATS NIH HHS KL2 TR001441NCATS NIH HHS UL1 TR001439NIDA NIH HHS K05 DA020087NIDA NIH HHS P30 DA028821NIDA NIH HHS R03 DA033437NIDA NIH HHS T32 DA007287
6 · The paper itself

Abstract

backgroundNeuromedin U (NMU) is a neuropeptide enriched in the nucleus accumbens shell (NAcSh), a brain region associated with reward. While NMU and its receptor, NMU receptor 2 (NMUR2), have been studied for the ability to regulate food reward, NMU has not been studied in the context of drugs of abuse (e.g., cocaine). Furthermore, the neuroanatomical pathways that express NMUR2 and its ultrastructural localization are unknown.

methodsImmunohistochemistry was used to determine the synaptic localization of NMUR2 in the NAcSh and characterize which neurons express this receptor (n = 17). The functional outcome of NMU on NMUR2 was examined using microdialysis (n = 16). The behavioral effects of NMU microinjection directly to the NAcSh were investigated using cocaine-evoked locomotion (n = 93). The specific effects of NMUR2 knockdown on cocaine-evoked locomotion were evaluated using viral-mediated RNA interference (n = 40).

resultsNMUR2 is localized to presynaptic gamma-aminobutyric acidergic nerve terminals in the NAcSh originating from the dorsal raphe nucleus. Furthermore, NMU microinjection to the NAcSh decreased local gamma-aminobutyric acid concentrations. Next, we evaluated the effects of NMU microinjection on behavioral sensitization to cocaine. When repeatedly administered throughout the sensitization regimen, NMU attenuated cocaine-evoked hyperactivity. Additionally, small hairpin RNA-mediated knockdown of presynaptic NMUR2 in the NAcSh using a retrograde viral vector potentiated cocaine sensitization.

conclusionsTogether, these data reveal that NMUR2 modulates a novel gamma-aminobutyric acidergic pathway from the dorsal raphe nucleus to the NAcSh to influence behavioral responses to cocaine.

Indexed as

AnimalsBehavior, AnimalCocaineDopamine Uptake InhibitorsDorsal Raphe Nucleusgamma-Aminobutyric AcidMaleNeuronsNeuropeptidesNucleus AccumbensRatsRats, Sprague-DawleyReceptors, NeurotransmitterSignal TransductionCocaineDopamine Uptake Inhibitorsgamma-Aminobutyric Acidneuromedin Uneuromedin U receptorNeuropeptidesReceptors, NeurotransmitterAAV6CocaineGABANeuropeptideNonserotonergicRNAi

Identifiers

PMID27105831
PMCPMC5016225

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Registered trials

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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.