Evidence map›Paper›PMID 35252951›Full record

ArticleBiological psychiatry global open science2022

Cannabidiol Produces Distinct U-Shaped Dose-Response Effects on Cocaine-Induced Conditioned Place Preference and Associated Recruitment of Prelimbic Neurons in Male Rats.

Hermina Nedelescu, Grant E Wagner, Genna L De Ness, Ayla Carroll, Tony M Kerr, Jingjun Wang, Saiwen Zhang, Stephen Chang, Amy H Than, Nora E Emerson and 2 more

Open access · goldAbstract read
In one paragraph

Article in Biological psychiatry global open science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

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  8. A PAM of the αCurrent research in pharmacology and drug discovery · 2023
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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

12 authors at 1 institution in 1 country.

Hermina NedelescuDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Grant E WagnerDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Genna L De NessDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Ayla CarrollDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Tony M KerrDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Jingjun WangDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Saiwen ZhangDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Stephen ChangDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Amy H ThanDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Nora E EmersonDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Nobuyoshi SutoDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Friedbert WeissDepartment of Neuroscience (HN, GEW, GLD, AC, TMK, JW, SZ, SC, AHT, NEE, NS, FW), The Scripps Research Institute, La Jolla, California.
Scripps Research Institute · US

Funding

Neurpsychopharmacology-Multidisciplinary TrainingT32AA007456 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI MARISA ROBERTO · 1985 to 2026
$13.4M
The dark side of addiction: Significance of environmental conditioning to negative reinforcement by EtOH in subjects with a dependence historyR01AA027555 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI WEISS, FRIEDBERT · 2020 to 2024
$2.0M
Implementation of novel methodology to study the anti-relapse potential of cannabidiolR21DA039821 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI WEISS, FRIEDBERT · 2015 to 2016
$695k
Functional Epigenetic Profiling of Anti-Relapse CannabidiolR21DA043030 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI SUTO, NOBUYOSHI · 2017 to 2018
$529k
Cannabidiol: Lasting attenuation of ethanol seekingR21AA023648 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI WEISS, FRIEDBERT · 2016 to 2017
$505k
Transcriptional adaptations driving the intensification of alcohol-seeking in dependent rats undergoing prolonged abstinenceR21AA030184 · NIAAA · SCRIPPS RESEARCH INSTITUTE, THE · PI SANNA, PIETRO P, SUTO, NOBUYOSHI · 2022 to 2023
$470k
NIAAA NIH HHS R01 AA027555NIAAA NIH HHS R21 AA023648NIAAA NIH HHS R21 AA030184NIAAA NIH HHS T32 AA007456NIDA NIH HHS R21 DA039821NIDA NIH HHS R21 DA043030
6 · The paper itself

Abstract

backgroundCannabidiol (CBD) has received attention for the treatment of substance use disorders. In preclinical models of relapse, CBD attenuates drug seeking across several drugs of abuse, including cocaine. However, in these models CBD has not been consistently effective. This inconsistency in CBD effects may be related to presently insufficient information on the full spectrum of CBD dose effects on drug-related behaviors.

methodsWe address this issue by establishing a full dose-response profile of CBD's actions using expression of cocaine-induced conditioned place preference as a model for drug-motivated behavior in male rats and by concurrently identifying dose-dependent effects of CBD on underlying neuronal activation and distinct neuronal phenotypes showing dose-dependent activation changes. Additionally, we established CBD levels in plasma and brain samples.

resultsCBD produced linear increases in CBD brain/plasma concentrations but suppressed conditioned place preference in a distinct U-shaped manner. In parallel with its behavioral effects, CBD produced U-shaped suppressant effects on neuronal activation in the prelimbic but not infralimbic cortex or nucleus accumbens core and shell. RNAscope in situ hybridization identified suppression of glutamatergic and GABAergic (gamma-aminobutyric acidergic) signaling in the prelimbic cortex as a possible cellular mechanism for the attenuation of cocaine-induced conditioned place preference by CBD.

conclusionsThe findings extend previous evidence on the potential of CBD in preventing drug-motivated behavior. However, CBD's dose-response profile may have important dosing implications for future clinical applications and may contribute to the understanding of discrepant CBD effects on drug seeking reported in the literature.

Identifiers

PMID35252951
PMCPMC8896771
OpenAlexW3179851299

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.