Evidence map›Paper›PMID 33221340›Full record

ArticleProgress in neuro-psychopharmacology & biological psychiatry2021

The contributions of the endocannabinoid system and stress on the neural processing of reward stimuli.

F M Filbey, D Beaton, S Prashad

Open access · hybridAbstract read
In one paragraph

Article in Progress in neuro-psychopharmacology & biological psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. 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 at 3 institutions in 2 countries.

F M FilbeyCenter for BrainHealth, School of Behavioral and Brain Sciences, University of Texas at Dallas, TX, USA. Electronic address: Francesca.Filbey@utdallas.edu.
D BeatonRotman Research Institute, Baycrest Health Sciences, Toronto, Ontario, Canada.
S PrashadDepartment of Kinesiology and Educational Psychology, Washington State University, Pullman, WA, United States of America.
Baycrest Hospital · CAThe University of Texas at Dallas · USWashington State University · US

Funding

The Role of Motivation and Control in Cannabis Use Disorders: A Cross-Cultural Longitudinal Neuroimaging StudyR01DA042490 · NIDA · UNIVERSITY OF TEXAS DALLAS · PI COUSIJN, JANNA, FILBEY, FRANCESCA · 2017 to 2021
$2.6M
Genetic and Environmental Modulators of the Brain's Response to Marijuana CuesR01DA030344 · NIDA · UNIVERSITY OF TEXAS DALLAS · PI FILBEY, FRANCESCA · 2012 to 2016
$2.4M
Implementing Appropriate Multivariate Methods for Higher Quality Results from GenF31DA035039 · NIDA · UNIVERSITY OF TEXAS DALLAS · PI BEATON, DEREK F. · 2013 to 2015
$125k
NIDA NIH HHS F31 DA035039NIDA NIH HHS R01 DA030344NIDA NIH HHS R01 DA042490
6 · The paper itself

Abstract

The brain's endocannabinoid system plays a crucial role in reward processes by mediating appetitive learning and encoding the reinforcing properties of substances. Evidence also suggests that endocannabinoids are an important constituent of neuronal substrates involved in emotional responses to stress. Thus, it is critical to understand how the endocannabinoid system and stress may affect reward processes given their importance in substance use disorders. We examined the relationship between factors that regulate endocannabinoid system signaling (i.e., cannabinoid receptor genes and prolonged cannabis exposure) and stress on fMRI BOLD response to reward cues using multivariate statistical analysis. We found that proxies for endocannabinoid system signaling (i.e., endocannabinoid genes and chronic exposure to cannabis) and stress have differential effects on neural response to cannabis cues. Specifically, a single nucleotide polymorphism (SNP) variant in the cannabinoid receptor 1 (CNR1) gene, early life stress, and current perceived stress modulated reward responsivity in long-term, heavy cannabis users, while a variant in the fatty acid amide hydrolase (FAAH) gene and current perceived stress modulated cue-elicited response in non-using controls. These associations were related to distinct neural responses to cannabis-related cues compared to natural reward cues. Understanding the contributions of endocannabinoid system factors and stress that lead to downstream effects on neural mechanisms underlying sensitivity to rewards, such as cannabis, will contribute towards a better understanding of endocannabinoid-targeted therapies as well as individual risks for cannabis use disorder.

Indexed as

RewardAdultEndocannabinoidsFemaleHumansMaleMarijuana AbusePolymorphism, Single NucleotideReceptor, Cannabinoid, CB1Stress, PsychologicalYoung AdultCNR1 protein, humanEndocannabinoidsReceptor, Cannabinoid, CB1CannabisCue-elicited cravingfMRIRewardStress

Identifiers

PMID33221340
PMCPMC8204292
OpenAlexW3101600261

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.