Evidence map›Paper›PMID 25637601›Full record

ArticleThe Journal of pharmacology and experimental therapeutics2015

Dual regulation of δ-opioid receptor function by arachidonic acid metabolites in rat peripheral sensory neurons.

Laura C Sullivan, Kelly A Berg, William P Clarke

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of pharmacology and experimental therapeutics, 2015. 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
2.3field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Making Sense of Pharmacology: Inverse Agonism and Functional Selectivity.The international journal of neuropsychopharmacology · 2018
    Review
  10. Allosterism withinMolecular pharmacology · 2018
    Article
  11. Article
  12. Constitutive Desensitization of Opioid Receptors in Peripheral Sensory Neurons.The Journal of pharmacology and experimental therapeutics · 2016
    Article
  13. Article
  14. Article
  15. Molecular Pharmacology of δ-Opioid Receptors.Pharmacological reviews · 2016
    Review
  16. Review
  17. Functional selectivity of kappa opioid receptor agonists in peripheral sensory neurons.The Journal of pharmacology and experimental therapeutics · 2015
    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

3 authors at 1 institution in 1 country.

Laura C SullivanDepartment 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.
William P ClarkeDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, Texas clarkew@uthscsa.edu.
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
NIDA NIH HHS R01 DA024865NIDA NIH HHS R01-DA24865NIDA NIH HHS T32 DA031115NIDA NIH HHS T32-DA031115NIDCR NIH HHS T32 DE014318NIDCR NIH HHS T32-DE14318
6 · The paper itself

Abstract

The regulation of opioid receptor system function in peripheral sensory neurons is not well understood. Opioid agonist efficacy to inhibit nociceptor function and to promote antinociception is generally weak under basal conditions and frequently no response occurs. However, in response to a cyclooxygenase-dependent metabolite of arachidonic acid (AA) after exposure to inflammatory mediators, such as bradykinin (BK) or exogenous AA, peripheral opioid receptor systems become much more responsive to opioid agonists. In this study, we examined the time course for the induction and maintenance of functional competence of the δ-opioid receptor (DOR) system in adult rat nociceptors in culture and in vivo. We found that the responsive state of DOR after pretreatment with BK or exogenous AA is transient (30-60 minutes) and persists for 15-30 minutes after a 15-minute exposure of nociceptors to BK or AA. Interestingly, whereas functional competence of the DOR system could be reinduced with a second application of BK 60 minutes after the first, responsiveness of the DOR system could not be reinduced after an initial exposure to AA. This nonresponsive state of DOR after exogenous AA was mediated by a lipoxygenase (LOX)-dependent metabolite of AA. Intraplantar carrageenan also produced transient DOR functional competence and responsiveness was also reinduced by inhibition of LOX. Thus, the DOR system expressed by peripheral sensory neurons is under dual regulation by cyclooxygenase- and LOX-dependent metabolites of AA.

Indexed as

AnimalsArachidonic AcidBradykininCells, CulturedCyclic AMPCyclooxygenase 1Cyclooxygenase 2DinoprostoneEnkephalin, D-Penicillamine (2,5)-HyperalgesiaLipoxygenaseLipoxygenase InhibitorsMaleRats, Sprague-DawleyReceptors, Opioid, deltaSensory Receptor CellsArachidonic AcidBradykininCyclic AMPCyclooxygenase 1Cyclooxygenase 2DinoprostoneEnkephalin, D-Penicillamine (2,5)-LipoxygenaseLipoxygenase InhibitorsReceptors, Opioid, delta

Identifiers

PMID25637601
PMCPMC4366754
OpenAlexW2107482793

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.