Evidence map›Paper›PMID 28485408›Full record

ArticleMolecular psychiatry2018

Genetic and pharmacological antagonism of NK

A J Sandweiss, M I McIntosh, A Moutal, R Davidson-Knapp, J Hu, A K Giri, T Yamamoto, V J Hruby, R Khanna, T M Largent-Milnes and 1 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Functional evaluation of NKDrug and alcohol dependence · 2021
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
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

11 authors.

A J SandweissDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.
M I McIntoshDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.
A MoutalDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.
R Davidson-KnappDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.
J HuDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.
A K GiriDepartment of Chemistry, University of Arizona, Tucson, AZ, USA.
T YamamotoDepartment of Chemistry, University of Arizona, Tucson, AZ, USA.
V J HrubyDepartment of Chemistry, University of Arizona, Tucson, AZ, USA.
R KhannaDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.
T M Largent-MilnesDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA.
T W VanderahDepartment of Pharmacology, College of Medicine, University of Arizona, Tucson, AZ, USA. vanderah@email.arizona.edu.

Funding

THERAPEUTIC PROFILES OF OPIOID DELTA RECEPTORS--NEW MODALITIESP01DA006284 · NIDA · UNIVERSITY OF ARIZONA · PI HRUBY, VICTOR J · 1989 to 2015
$14.8M
NIDA NIH HHS P01 DA006284
6 · The paper itself

Abstract

Development of an efficacious, non-addicting analgesic has been challenging. Discovery of novel mechanisms underlying addiction may present a solution. Here we target the neurokinin system, which is involved in both pain and addiction. Morphine exerts its rewarding actions, at least in part, by inhibiting GABAergic input onto substance P (SP) neurons in the ventral tegmental area (VTA), subsequently increasing SP release onto dopaminergic neurons. Genome editing of the neurokinin 1 receptor (NK

Indexed as

Acute PainAnalgesicsAnimalsCRISPR-Cas SystemsDisease Models, AnimalDopamineEscherichia coliGene Knockdown TechniquesMaleMice, Inbred ICRMorphineNeurokinin-1 Receptor AntagonistsNociceptive PainOpioid-Related DisordersRats, Sprague-DawleyReceptors, Neurokinin-1AnalgesicsDopamineMorphineNeurokinin-1 Receptor AntagonistsReceptors, Neurokinin-1Receptors, Opioid, deltaReceptors, Opioid, muSubstance P

Identifiers

PMID28485408
PMCPMC5680162

What OpenQuestion holds

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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.