Evidence map›Paper›PMID 31790682›Full record

ArticleBrain research2020

Soluble epoxide hydrolase inhibitor mediated analgesia lacks tolerance in rat models.

Karen M Wagner, Jogen Atone, Bruce D Hammock

Abstract read
In one paragraph

Article in Brain research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Soluble epoxide hydrolase inhibition alleviates chemotherapy induced neuropathic pain.Frontiers in pain research (Lausanne, Switzerland) · 2022
    Article
  8. Review
  9. 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.

Karen M WagnerDepartment of Entomology and Nematology and UC Davis Comprehensive, Cancer Center, University of California Davis, Davis, CA 95616, United States.
Jogen AtoneDepartment of Entomology and Nematology and UC Davis Comprehensive, Cancer Center, University of California Davis, Davis, CA 95616, United States.
Bruce D HammockDepartment of Entomology and Nematology and UC Davis Comprehensive, Cancer Center, University of California Davis, Davis, CA 95616, United States. Electronic address: bdhammock@ucdavis.edu.

Funding

Workshop on Environmental Technology Transfer and EntrepreneurshipP42ES004699 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI YOUNG, THOMAS MICHAEL · 1987 to 2021
$50.1M
Training and Education CoreU54NS079202 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEIN, PAMELA J · 2012 to 2021
$35.7M
ENVIRONMENTAL TOXICOLOGYT32ES007059 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI Laura S Van Winkle · 1985 to 2026
$7.9M
Training Program In Basic & Translational Cardiovascular ScienceT32HL086350 · NHLBI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Martin Cadeiras, David A. Liem · 2008 to 2026
$7.1M
HYDROLYTIC ENZYMES IN THE METABOLISM OF TOXINSR01ES002710 · NIEHS · UNIVERSITY OF CALIFORNIA DAVIS · PI HAMMOCK, BRUCE D · 1985 to 2018
$4.0M
sEH Inhibitors to Treat Neuropathic PainR44ES025598 · NIEHS · EICOSIS, LLC · PI BUCKPITT, ALAN R, HAMMOCK, BRUCE D · 2016 to 2017
$1.5M
Training Program in Basic and Clinical Communication ScienceT32DC008072 · NIDCD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI YAMOAH, EBENEZER N · 2008 to 2012
$939k
Development of an Oral Analgesic for Neuropathic PainUH2NS094258 · NINDS · EICOSIS, LLC · PI BUCKPITT, ALAN R, HAMMOCK, BRUCE D · 2016 to 2016
$274k
NHLBI NIH HHS T32 HL086350NIDCD NIH HHS T32 DC008072NIEHS NIH HHS P42 ES004699NIEHS NIH HHS R01 ES002710NIEHS NIH HHS R44 ES025598NIEHS NIH HHS T32 ES007059NINDS NIH HHS U54 NS079202NINDS NIH HHS UH2 NS094258
6 · The paper itself

Abstract

Effectively treating chronic pain remains a therapeutic challenge in the clinic. Recent evidence has shown the inhibition of the soluble epoxide hydrolase (sEH) to be an effective strategy to limit chronic pain in preclinical models, horses and companion animals. Determining the safety of sEH inhibition in addition to this demonstrated efficacy is a critical step to the further development of sEH inhibitors (sEHI) as analgesics. Here we describe a comparison of the sEHI TPPU with other first in class analgesics for human chronic pain. We assess the development of tolerance to the analgesia mediated by TPPU with extended use. We also assess for CNS effects by measuring changes in motor control and functioning. The sEHI are multimodal analgesics that have demonstrated potent efficacy against chronic pain. They have previously been tested and show no reward potential using operant methods. The results of the current experiments show that they lack motor function effects and also lack the development of tolerance with extended dosing.

Indexed as

Drug ToleranceAnalgesicsAnimalsChronic PainDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Diabetic NeuropathiesEnzyme InhibitorsEpoxide HydrolasesGait AnalysisMaleMorphinePhenylurea CompoundsPiperidinesPregabalinRats1-trifluoromethoxyphenyl-3-(1-propionylpiperidine-4-yl)ureaAnalgesicsEnzyme InhibitorsEPHX2 protein, ratEpoxide HydrolasesMorphinePhenylurea CompoundsPiperidinesPregabalinStreptozocinAnalgesiaEpoxy-fatty acids (EpFA)Motor functionOpioidsSoluble epoxide hydrolase (sEH)Tolerance

Identifiers

PMID31790682
PMCPMC6996511

What OpenQuestion holds

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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.