Evidence map›Paper›PMID 27660244›Full record

ArticleThe Journal of pharmacology and experimental therapeutics2016

Constitutive Desensitization of Opioid Receptors in Peripheral Sensory Neurons.

Laura C Sullivan, Teresa S Chavera, Raehannah J Jamshidi, Kelly A Berg, William P Clarke

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of pharmacology and experimental therapeutics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Making Sense of Pharmacology: Inverse Agonism and Functional Selectivity.The international journal of neuropsychopharmacology · 2018
    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

5 authors at 1 institution in 1 country.

Laura C SullivanDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
Teresa S ChaveraDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
Raehannah J JamshidiDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
Kelly A BergDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, Texas berg@uthscsa.edu.
William P ClarkeDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, Texas.
The University of Texas Health Science Center at San Antonio · US

Funding

Institutional Research Training GrantT32DE014318 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Kenneth M Hargreaves · 2002 to 2026
$12.1M
Training in Drug Abuse Research: Behavior and NeurobiologyT32DA031115 · NIDA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CHARLES P FRANCE · 2011 to 2026
$5.2M
Regulation of opioid receptor function in trigeminal ganglionR01DA024865 · NIDA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARKE, WILLIAM P · 2009 to 2012
$1.3M
Regulation of Kappa opioid receptor-mediated signaling and peripheral analgesiaR01GM106035 · NIGMS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARKE, WILLIAM P · 2014 to 2017
$1.2M
NIDA NIH HHS R01 DA024865NIDA NIH HHS T32 DA031115NIDCR NIH HHS T32 DE014318NIGMS NIH HHS R01 GM106035
6 · The paper itself

Abstract

Opioid receptors expressed by peripheral pain-sensing neurons are functionally inactive for antinociceptive signaling under most basal conditions; however, tissue damage or exposure to inflammatory mediators (e.g., bradykinin) converts these receptors from a nonresponsive state to a functionally competent state. Here we tested the hypothesis that the basal, nonresponsive state of the mu- and delta-opioid receptors (MOR and DOR, respectively) is the result of constitutive receptor activity that activates desensitization mechanisms, resulting in MOR and DOR receptor systems that are constitutively desensitized. Consistent with our previous findings, under basal conditions, neither the MOR agonist [d-Ala

Indexed as

Animalsbeta-Arrestin 2BradykininDrug Inverse AgonismGene Expression RegulationGene SilencingMaleNaloxoneNociceptionRatsRats, Sprague-DawleyReceptors, Opioid, deltaReceptors, Opioid, muRNA, Small InterferingSensory Receptor Cellsbeta-Arrestin 2BradykininNaloxoneReceptors, Opioid, deltaReceptors, Opioid, muRNA, Small Interfering

Identifiers

PMID27660244
PMCPMC5118646
OpenAlexW2523434565

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.