Cargando…
T145. EFFECTS OF CANNABIDIOL ON EMOTION PROCESSING IN PSYCHOSIS RISK: AN FMRI INVESTIGATION
BACKGROUND: There is currently a lack of effective pharmacological treatment for people at Clinical High Risk of Psychosis (CHR), who present with emotional dysregulation and high levels of anxiety. These individuals also show altered neural responses to emotional stimuli in key brain regions implic...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234570/ http://dx.doi.org/10.1093/schbul/sbaa029.705 |
_version_ | 1783535794273648640 |
---|---|
author | Davies, Cathy Wilson, Robin Appiah-Kusi, Elizabeth Brammer, Michael Perez, Jesus Murray, Robin Allen, Paul Bossong, Matthijs McGuire, Philip Bhattacharyya, Sagnik |
author_facet | Davies, Cathy Wilson, Robin Appiah-Kusi, Elizabeth Brammer, Michael Perez, Jesus Murray, Robin Allen, Paul Bossong, Matthijs McGuire, Philip Bhattacharyya, Sagnik |
author_sort | Davies, Cathy |
collection | PubMed |
description | BACKGROUND: There is currently a lack of effective pharmacological treatment for people at Clinical High Risk of Psychosis (CHR), who present with emotional dysregulation and high levels of anxiety. These individuals also show altered neural responses to emotional stimuli in key brain regions implicated in psychosis onset, including the striatum and medial temporal lobe. Cannabidiol (CBD), a non-intoxicating constituent of the cannabis plant, is thought to have antipsychotic and anxiolytic properties. The effects of CBD on brain function in CHR individuals during emotion processing has not been tested before. METHODS: In a randomised, double-blind, placebo-controlled, parallel-group design, 33 CHR individuals received a single oral 600mg dose of CBD or matched placebo, while 19 healthy controls did not receive any drug. Participants were studied using an emotion processing functional magnetic resonance imaging (fMRI) paradigm. Using a region-of-interest approach, we examined the differences in brain activation related to the CHR state and the effects of CBD, indexed using the blood oxygen level-dependent haemodynamic response fMRI signal. RESULTS: Compared to controls (n=19), CHR participants receiving placebo (n=15) showed significantly greater activation in the medial temporal lobe and less activation in the striatum during emotion processing. Within these same regions, activation in the CBD group (n=15) was (significantly) intermediate between that of the placebo and control groups. That is, CBD attenuated medial temporal and enhanced striatal activation in CHR participants. DISCUSSION: These findings suggest that CBD modulates the function of brain regions strongly implicated in psychosis onset and altered emotion processing. Further research is required to examine whether these neurofunctional effects translate into clinical efficacy after a period of treatment. |
format | Online Article Text |
id | pubmed-7234570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72345702020-05-23 T145. EFFECTS OF CANNABIDIOL ON EMOTION PROCESSING IN PSYCHOSIS RISK: AN FMRI INVESTIGATION Davies, Cathy Wilson, Robin Appiah-Kusi, Elizabeth Brammer, Michael Perez, Jesus Murray, Robin Allen, Paul Bossong, Matthijs McGuire, Philip Bhattacharyya, Sagnik Schizophr Bull Poster Session III BACKGROUND: There is currently a lack of effective pharmacological treatment for people at Clinical High Risk of Psychosis (CHR), who present with emotional dysregulation and high levels of anxiety. These individuals also show altered neural responses to emotional stimuli in key brain regions implicated in psychosis onset, including the striatum and medial temporal lobe. Cannabidiol (CBD), a non-intoxicating constituent of the cannabis plant, is thought to have antipsychotic and anxiolytic properties. The effects of CBD on brain function in CHR individuals during emotion processing has not been tested before. METHODS: In a randomised, double-blind, placebo-controlled, parallel-group design, 33 CHR individuals received a single oral 600mg dose of CBD or matched placebo, while 19 healthy controls did not receive any drug. Participants were studied using an emotion processing functional magnetic resonance imaging (fMRI) paradigm. Using a region-of-interest approach, we examined the differences in brain activation related to the CHR state and the effects of CBD, indexed using the blood oxygen level-dependent haemodynamic response fMRI signal. RESULTS: Compared to controls (n=19), CHR participants receiving placebo (n=15) showed significantly greater activation in the medial temporal lobe and less activation in the striatum during emotion processing. Within these same regions, activation in the CBD group (n=15) was (significantly) intermediate between that of the placebo and control groups. That is, CBD attenuated medial temporal and enhanced striatal activation in CHR participants. DISCUSSION: These findings suggest that CBD modulates the function of brain regions strongly implicated in psychosis onset and altered emotion processing. Further research is required to examine whether these neurofunctional effects translate into clinical efficacy after a period of treatment. Oxford University Press 2020-05 2020-05-18 /pmc/articles/PMC7234570/ http://dx.doi.org/10.1093/schbul/sbaa029.705 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Poster Session III Davies, Cathy Wilson, Robin Appiah-Kusi, Elizabeth Brammer, Michael Perez, Jesus Murray, Robin Allen, Paul Bossong, Matthijs McGuire, Philip Bhattacharyya, Sagnik T145. EFFECTS OF CANNABIDIOL ON EMOTION PROCESSING IN PSYCHOSIS RISK: AN FMRI INVESTIGATION |
title | T145. EFFECTS OF CANNABIDIOL ON EMOTION PROCESSING IN PSYCHOSIS RISK: AN FMRI INVESTIGATION |
title_full | T145. EFFECTS OF CANNABIDIOL ON EMOTION PROCESSING IN PSYCHOSIS RISK: AN FMRI INVESTIGATION |
title_fullStr | T145. EFFECTS OF CANNABIDIOL ON EMOTION PROCESSING IN PSYCHOSIS RISK: AN FMRI INVESTIGATION |
title_full_unstemmed | T145. EFFECTS OF CANNABIDIOL ON EMOTION PROCESSING IN PSYCHOSIS RISK: AN FMRI INVESTIGATION |
title_short | T145. EFFECTS OF CANNABIDIOL ON EMOTION PROCESSING IN PSYCHOSIS RISK: AN FMRI INVESTIGATION |
title_sort | t145. effects of cannabidiol on emotion processing in psychosis risk: an fmri investigation |
topic | Poster Session III |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234570/ http://dx.doi.org/10.1093/schbul/sbaa029.705 |
work_keys_str_mv | AT daviescathy t145effectsofcannabidiolonemotionprocessinginpsychosisriskanfmriinvestigation AT wilsonrobin t145effectsofcannabidiolonemotionprocessinginpsychosisriskanfmriinvestigation AT appiahkusielizabeth t145effectsofcannabidiolonemotionprocessinginpsychosisriskanfmriinvestigation AT brammermichael t145effectsofcannabidiolonemotionprocessinginpsychosisriskanfmriinvestigation AT perezjesus t145effectsofcannabidiolonemotionprocessinginpsychosisriskanfmriinvestigation AT murrayrobin t145effectsofcannabidiolonemotionprocessinginpsychosisriskanfmriinvestigation AT allenpaul t145effectsofcannabidiolonemotionprocessinginpsychosisriskanfmriinvestigation AT bossongmatthijs t145effectsofcannabidiolonemotionprocessinginpsychosisriskanfmriinvestigation AT mcguirephilip t145effectsofcannabidiolonemotionprocessinginpsychosisriskanfmriinvestigation AT bhattacharyyasagnik t145effectsofcannabidiolonemotionprocessinginpsychosisriskanfmriinvestigation |