Evidence map›Paper›PMID 27501482›Full record

ArticleBritish journal of pharmacology2016

Robust anti-nociceptive effects of monoacylglycerol lipase inhibition in a model of osteoarthritis pain.

James J Burston, Paul I Mapp, Sarir Sarmad, David A Barrett, Micah J Niphakis, Benjamin F Cravatt, David A Walsh, Victoria Chapman

Open access · hybridAbstract read
In one paragraph

Article in British journal of pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

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  12. The Endocannabinoid System Alleviates Pain in a Murine Model of Cancer-Induced Bone Pain.The Journal of pharmacology and experimental therapeutics · 2020
    Article
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  16. The Endogenous Cannabinoid System: A Budding Source of Targets for Treating Inflammatory and Neuropathic Pain.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2018
    Review
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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

8 authors at 3 institutions in 2 countries.

James J BurstonArthritis Research UK Pain Centre, University of Nottingham, Medical School, Queen's Medical Centre, Nottingham, UK. james.burston@nottingham.ac.uk.
Paul I MappArthritis Research UK Pain Centre, University of Nottingham, Medical School, Queen's Medical Centre, Nottingham, UK.
Sarir SarmadCentre for Analytical Bioscience, School of Pharmacy, University of Nottingham, Nottingham, UK.
David A BarrettCentre for Analytical Bioscience, School of Pharmacy, University of Nottingham, Nottingham, UK.
Micah J NiphakisThe Skaggs Institute for Chemical Biology and Department of Chemical Physiology, The Scripps Research Institute, La Jolla, CA, USA.
Benjamin F CravattThe Skaggs Institute for Chemical Biology and Department of Chemical Physiology, The Scripps Research Institute, La Jolla, CA, USA.
David A WalshArthritis Research UK Pain Centre, University of Nottingham, Medical School, Queen's Medical Centre, Nottingham, UK.
Victoria ChapmanArthritis Research UK Pain Centre, University of Nottingham, Medical School, Queen's Medical Centre, Nottingham, UK. victoria.chapman@nottingham.ac.uk.
University of Nottingham · GBQueen's Medical Centre · GBScripps Research Institute · US

Funding

Arthritis Research UK 18769
6 · The paper itself

Abstract

background and purposeChronic pain is often a symptom of knee osteoarthritis (OA) for which current analgesics are either inadequate or are associated with serious side effects. The endocannabinoid system may offer alternative targets for pain relief. We evaluated the effects of a potent and selective monoacylglycerol (MAG) lipase inhibitor (MJN110) on OA pain behaviour, spinal mechanisms of action and joint histopathology in the rat. EXPERIMENTAL APPROACH: Intra-articular injection of monosodium iodoacetate (MIA) models OA pain and mimics clinical joint pathology. Effects of MJN110 on MIA-induced weight-bearing asymmetry and lowered paw withdrawal thresholds (PWTs), changes in spinal gene expression and brain levels of relevant lipids were determined. KEY

resultsAcute MJN110 (5 mg·kg CONCLUSIONS AND IMPLICATIONS: Our data support further assessment of the therapeutic potential of MAG lipase inhibitors for the treatment of OA pain.

Indexed as

AnalgesicsAnimalsDisease Models, AnimalEnzyme InhibitorsInjections, Intra-ArticularIodoacetic AcidMaleMonoacylglycerol LipasesOsteoarthritisPainPain MeasurementRatsRats, Sprague-DawleyAnalgesicsEnzyme InhibitorsIodoacetic AcidMonoacylglycerol Lipases

Identifiers

PMID27501482
PMCPMC5056226
OpenAlexW2528493014

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.