Evidence map›Paper›PMID 30275151›Full record

ArticleThe Journal of pharmacology and experimental therapeutics2018

Brain-Permeant and -Impermeant Inhibitors of Fatty Acid Amide Hydrolase Synergize with the Opioid Analgesic Morphine to Suppress Chemotherapy-Induced Neuropathic Nociception Without Enhancing Effects of Morphine on Gastrointestinal Transit.

Richard A Slivicki, Shahin A Saberi, Vishakh Iyer, V Kiran Vemuri, Alexandros Makriyannis, Andrea G Hohmann

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of pharmacology and experimental therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Efficacy of GABA aminotransferase inactivator OV329 in models of neuropathic and inflammatory pain without tolerance or addiction.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Negative allosteric modulation of CBNeuropharmacology · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Negative allosteric modulation of CBPharmacological research · 2022
    Article
  14. Fatty acid amide hydrolase activity in the dorsal periaqueductal gray attenuates neuropathic pain and associated dysautonomia.American journal of physiology. Regulatory, integrative and comparative physiology · 2022
    Article
  15. Review
  16. Article
  17. Review
  18. The cannabinoid CBEuropean journal of pharmacology · 2020
    Article
  19. Article
  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.

Richard A SlivickiProgram in Neuroscience (R.A.S., V.I., A.G.H.), Department of Psychological and Brain Sciences (R.A.S., S.A.S., V.I., A.G.H.), and Gill Center for Biomolecular Science (A.G.H.), Indiana University, Bloomington, Indiana; and Center for Drug Discovery, Northeastern University, Boston, Massachusetts (V.K.V., A.M.).
Shahin A SaberiProgram in Neuroscience (R.A.S., V.I., A.G.H.), Department of Psychological and Brain Sciences (R.A.S., S.A.S., V.I., A.G.H.), and Gill Center for Biomolecular Science (A.G.H.), Indiana University, Bloomington, Indiana; and Center for Drug Discovery, Northeastern University, Boston, Massachusetts (V.K.V., A.M.).
Vishakh IyerProgram in Neuroscience (R.A.S., V.I., A.G.H.), Department of Psychological and Brain Sciences (R.A.S., S.A.S., V.I., A.G.H.), and Gill Center for Biomolecular Science (A.G.H.), Indiana University, Bloomington, Indiana; and Center for Drug Discovery, Northeastern University, Boston, Massachusetts (V.K.V., A.M.).
V Kiran VemuriProgram in Neuroscience (R.A.S., V.I., A.G.H.), Department of Psychological and Brain Sciences (R.A.S., S.A.S., V.I., A.G.H.), and Gill Center for Biomolecular Science (A.G.H.), Indiana University, Bloomington, Indiana; and Center for Drug Discovery, Northeastern University, Boston, Massachusetts (V.K.V., A.M.).
Alexandros MakriyannisProgram in Neuroscience (R.A.S., V.I., A.G.H.), Department of Psychological and Brain Sciences (R.A.S., S.A.S., V.I., A.G.H.), and Gill Center for Biomolecular Science (A.G.H.), Indiana University, Bloomington, Indiana; and Center for Drug Discovery, Northeastern University, Boston, Massachusetts (V.K.V., A.M.).
Andrea G HohmannProgram in Neuroscience (R.A.S., V.I., A.G.H.), Department of Psychological and Brain Sciences (R.A.S., S.A.S., V.I., A.G.H.), and Gill Center for Biomolecular Science (A.G.H.), Indiana University, Bloomington, Indiana; and Center for Drug Discovery, Northeastern University, Boston, Massachusetts (V.K.V., A.M.) hohmanna@indiana.edu.
Indiana University Bloomington · USNortheastern University · US

Funding

Project 3 - In vivo pharmacology of cannabinoid receptor probesP01DA009158 · NIDA · UNIVERSITY OF CONNECTICUT STORRS · PI Alexandros Makriyannis · 1994 to 2026
$26.0M
INTEGRATIVE PREDOCTORAL TRAINING IN DRUG ABUSE RESEARCH AT INDIANA UNIVERSITYT32DA024628 · NIDA · TRUSTEES OF INDIANA UNIVERSITY · PI Andrea Grace Hohmann, Kenneth Mackie · 2008 to 2026
$3.1M
Role of CB2 in Analgesic MechanismsR01DA041229 · NIDA · TRUSTEES OF INDIANA UNIVERSITY · PI HOHMANN, ANDREA GRACE, MACKIE, KENNETH · 2016 to 2020
$1.8M
NOS1AP as a novel target for treating pathological painR01CA200417 · NCI · TRUSTEES OF INDIANA UNIVERSITY · PI COURTNEY, MICHAEL, HOHMANN, ANDREA GRACE · 2016 to 2020
$1.4M
A Novel Mechanism for Decreasing Opioid RewardR21DA042584 · NIDA · TRUSTEES OF INDIANA UNIVERSITY · PI HOHMANN, ANDREA GRACE, REBEC, GEORGE VINCENT · 2016 to 2017
$392k
NCI NIH HHS R01 CA200417NIDA NIH HHS P01 DA009158NIDA NIH HHS R01 DA041229NIDA NIH HHS R21 DA042584NIDA NIH HHS T32 DA024628
6 · The paper itself

Abstract

Opioid-based therapies remain a mainstay for chronic pain management, but unwanted side effects limit therapeutic use. We compared efficacies of brain-permeant and -impermeant inhibitors of fatty acid amide hydrolase (FAAH) in suppressing neuropathic pain induced by the chemotherapeutic agent paclitaxel. Paclitaxel produced mechanical and cold allodynia without altering nestlet shredding or marble burying behaviors. We compared FAAH inhibitors that differ in their ability to penetrate the central nervous system for antiallodynic efficacy, pharmacological specificity, and synergism with the opioid analgesic morphine. (3'-(aminocarbonyl)[1,1'-biphenyl]- 3-yl)-cyclohexylcarbamate (URB597), a brain-permeant FAAH inhibitor, attenuated paclitaxel-induced allodynia via cannabinoid receptor 1 (CB

Indexed as

AmidohydrolasesAnalgesics, OpioidAnimalsAntineoplastic AgentsArachidonic AcidsBenzamidesBrainCannabinoidsCarbamatesFatty Acid Amide HydrolasesGastrointestinal TransitHyperalgesiaIndolesMiceMice, Inbred C57BLMorphineAM 251AM6545AmidohydrolasesAnalgesics, OpioidAntineoplastic AgentsArachidonic AcidsBenzamidesCannabinoidsCarbamatescarbamic acidcyclohexyl carbamic acid 3'-carbamoylbiphenyl-3-yl esterFatty Acid Amide HydrolasesIndolesiodopravadolineMorphineMorpholinesPiperidinesPyrazolesReceptor, Cannabinoid, CB1Receptor, Cannabinoid, CB2URB937

Identifiers

PMID30275151
PMCPMC6246979
OpenAlexW2895741321

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.