Evidence map›Paper›PMID 30238130›Full record

ArticlePsychopharmacology2018

Cannabidiol modulation of antinociceptive tolerance to Δ

Nicholas Z Greene, Jenny L Wiley, Zhihao Yu, Brian H Clowers, Rebecca M Craft

Open access · greenAbstract read
In one paragraph

Article in Psychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Cannabidiol for moderate-severe insomnia: a randomized controlled pilot trial of 150 mg of nightly dosing.Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2024
    Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Sex differences and the endocannabinoid system in pain.Pharmacology, biochemistry, and behavior · 2021
    Review
  13. Review
  14. Review
  15. Interactions between cannabidiol and ΔBritish journal of pharmacology · 2020
    Article
  16. Review
  17. Article
  18. Vaporized Cannabis Extracts Have Reinforcing Properties and Support Conditioned Drug-Seeking Behavior in Rats.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  19. Article
  20. 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

5 authors at 2 institutions in 1 country.

Nicholas Z GreeneDepartment of Psychology, Washington State University, Pullman, WA, 99164-4820, USA.
Jenny L WileyRTI International, Research Triangle Park, NC, USA.
Zhihao YuDepartment of Chemistry, Washington State University, Pullman, WA, USA.
Brian H ClowersDepartment of Chemistry, Washington State University, Pullman, WA, USA.
Rebecca M CraftDepartment of Psychology, Washington State University, Pullman, WA, 99164-4820, USA. craft@wsu.edu.ORCID http://orcid.org/0000-0003-4768-2160
Washington State University · USRTI International · US

Funding

Sex Differences in Cannabinoid Dependence and Analgesia (parent grant)R01DA016644 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI WILEY, JENNY L. · 2004 to 2016
$3.9M
National Institute on Drug Abuse DA-016644NIDA NIH HHS R01 DA016644
6 · The paper itself

Abstract

rationaleHumans typically self-administer cannabidiol (CBD) and delta-9-tetrahydrocannabinol (THC) together repeatedly (as in cannabis, cannabis extract, or Sativex®) to relieve pain. It has been suggested that one benefit of the drug combination may be decreased tolerance development.

objectiveThe present study compared the development of tolerance to the antinociceptive effects of THC given alone versus combined with CBD, in rats.

methodsTHC dose-effect curves on tail withdrawal and paw pressure tests were obtained before and after twice-daily treatment with vehicle or CBD (10 mg/kg), plus vehicle or THC (3.6 mg/kg females; 9.3 mg/kg males) for 4 days.

resultsOn the first day, THC was more potent in females than males on both nociceptive tests. From pre- to post-chronic (day 1 to day 6), THC potency on the tail withdrawal test decreased more in females than males, and rats that had been treated with CBD + THC repeatedly showed greater rightward/downward shifts of the THC dose-effect curve than rats that had been treated with THC alone. Analysis of blood samples taken after day 6 testing showed that serum THC levels were higher in CBD + THC-treated females than in vehicle + THC-treated females, and THC's active metabolite 11-OH-THC and its inactive metabolite THC-COOH were lower in CBD + THC-treated rats than in vehicle + THC-treated rats of both sexes. CBD also increased serum levels of the active metabolite cannabinol in both sexes.

conclusionThe decrease in THC's antinociceptive effects after repeated CBD exposure may be due to CBD-induced inhibition of THC metabolism, and/or antagonism of THC effects that emerges with repeated CBD treatment.

Indexed as

Drug ToleranceAnalgesics, Non-NarcoticAnimalsCannabidiolDose-Response Relationship, DrugDronabinolDrug Therapy, CombinationFemaleMaleMotor ActivityPain MeasurementRatsRats, Sprague-DawleyAnalgesics, Non-NarcoticCannabidiolDronabinolCannabinoidsPainSex differences

Identifiers

PMID30238130
PMCPMC6454895
OpenAlexW2890513701

What OpenQuestion holds

Textmetadata
LicenceTDM
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.