Evidence map›Paper›PMID 18040803›Full record

ReviewJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology2006

Opioid receptors and signaling on cells from the immune system.

Jean M Bidlack, Maxim Khimich, Amy L Parkhill, Sarah Sumagin, Baoyong Sun, Christopher M Tipton

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Expression of Opioid Receptors in Cells of the Immune System.International journal of molecular sciences · 2020
    Review
  11. Review
  12. Immunomodulation Associated with Sustained-release Buprenorphine in Female CD1 Mice Challenged with Ovalbumin.Journal of the American Association for Laboratory Animal Science : JAALAS · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Is the experience of thermal pain genetics dependent?BioMed research international · 2015
    Review
  18. Article
  19. Review
  20. 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

6 authors at 2 institutions in 1 country.

Jean M BidlackDepartment of Pharmacology and Physiology, School of Medicine and Dentistry, University of Rochester, P.O. Box 711, 601 Elmwood Ave., Rochester, NY 14642-8711, USA. Jean_Bidlack@urmc.rochester.edu
Maxim Khimich
Amy L Parkhill
Sarah Sumagin
Baoyong Sun
Christopher M Tipton
University of Rochester · USUniversity of Rochester Medical Center · US

Funding

OPIOID RECEPTORS ON LYMPHOCYTES AND BRAINK05DA000360 · NIDA · UNIVERSITY OF ROCHESTER · PI BIDLACK, JEAN M · 1998 to 2007
$893k
OPIOID MODULATION OF IMMUNOCOMPETENCER01DA004355 · NIDA · UNIVERSITY OF ROCHESTER · PI BIDLACK, JEAN M · 1989 to 2003
$837k
NIDA NIH HHS K05-DA00360NIDA NIH HHS K05-DA04355
6 · The paper itself

Abstract

This review discusses the criteria for determining whether a binding site or functional response is directly mediated by either the mu, delta, or kappa opioid receptors. In 1988, Sibinga and Goldstein published the first review that addressed whether cells from the immune system express opioid receptors. The criteria that they used, namely, structure-activity relationships, stereoselectivity, dose- and concentration-dependence, and saturability are still relevant criteria today for determining if an immunological response is mediated by either the mu, delta or kappa opioid receptors. Radioligand receptor binding studies and functional studies that clearly show the presence of an opioid receptor on immunocytes are presented. Selective agonists and antagonists for the mu, delta, and kappa opioid receptors are discussed, and the need for their use in experiments is emphasized. Conditions used in functional assays are very important. Receptor desensitization and downregulation occur within minutes after the application of an agonist. However, many immunological assays are applying an agonist for days before measuring an immunological effect. The results obtained may reflect changes that are results of receptor desensitization and/or downregulation instead of changes that are observed with acute activation of the receptor. The future of receptor pharmacology lies in the crosstalk and dimerization of G protein-coupled receptors. In transfected systems, opioid receptors have been shown to dimerize with chemokine and cannabinoid receptors, resulting in crosstalk between different types of receptors.

Indexed as

AnimalsHumansImmune SystemLeukocytes, MononuclearReceptors, OpioidSignal TransductionReceptors, Opioid

Identifiers

PMID18040803
OpenAlexW2003623943

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.