Evidence map›Paper›PMID 23108548›Full record

ReviewPhilosophical transactions of the Royal Society of London. Series B, Biological sciences2012

Dynamic changes to the endocannabinoid system in models of chronic pain.

Devi Rani Sagar, James J Burston, Stephen G Woodhams, Victoria Chapman

Open access · bronzeAbstract readReview
In one paragraph

Review in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.7field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 76 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. The Endocannabinoid System and Physical Exercise.International journal of molecular sciences · 2023
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Interactions ofFrontiers in pharmacology · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. ΔJournal of lipid research · 2018
    Article
  17. Article
  18. The cannabinoid system and pain.Neuropharmacology · 2017
    Review
  19. Article
  20. Palmitoylethanolamide Reverses Paclitaxel-Induced Allodynia in Mice.The Journal of pharmacology and experimental therapeutics · 2016
    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

4 authors at 3 institutions in 2 countries.

Devi Rani SagarArthritis Research UK Pain Centre, University of Nottingham, School of Biomedical Sciences, Queen's Medical Centre, Nottingham NG7 2UH, UK.
James J Burston
Stephen G Woodhams
Victoria Chapman
University of Nottingham · GBHUN-REN Institute of Experimental Medicine · HUQueen's Medical Centre · GB

Funding

Arthritis Research UK 18769Medical Research Council MR/K00414X/1
6 · The paper itself

Abstract

The analgesic effects of cannabinoid ligands, mediated by CB1 receptors are well established. However, the side-effect profile of CB1 receptor ligands has necessitated the search for alternative cannabinoid-based approaches to analgesia. Herein, we review the current literature describing the impact of chronic pain states on the key components of the endocannabinoid receptor system, in terms of regionally restricted changes in receptor expression and levels of key metabolic enzymes that influence the local levels of the endocannabinoids. The evidence that spinal CB2 receptors have a novel role in the modulation of nociceptive processing in models of neuropathic pain, as well as in models of cancer pain and arthritis is discussed. Recent advances in our understanding of the spinal location of the key enzymes that regulate the levels of the endocannabinoid 2-AG are discussed alongside the outcomes of recent studies of the effects of inhibiting the catabolism of 2-AG in models of pain. The complexities of the enzymes capable of metabolizing both anandamide (AEA) and 2-AG have become increasingly apparent. More recently, it has come to light that some of the metabolites of AEA and 2-AG generated by cyclooxygenase-2, lipoxygenases and cytochrome P450 are biologically active and can either exacerbate or inhibit nociceptive signalling.

Indexed as

AnalgesicsAnimalsArachidonic AcidsArthritisCannabinoid Receptor AgonistsChronic PainDisease Models, AnimalEndocannabinoidsGlyceridesHumansNeoplasmsNeuralgiaPolyunsaturated AlkamidesReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2AnalgesicsanandamideArachidonic AcidsCannabinoid Receptor AgonistsEndocannabinoidsGlyceridesglyceryl 2-arachidonatePolyunsaturated AlkamidesReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2

Identifiers

PMID23108548
PMCPMC3481532
OpenAlexW2106929220

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.