TY - JOUR
T1 - Cannabidiol inhibits THC-elicited paranoid symptoms and hippocampal-dependent memory impairment
AU - Englund, Amir
AU - Morrison, Paul D.
AU - Nottage, Judith
AU - Hague, Dominic
AU - Kane, Fergus
AU - Bonaccorso, Stefania
AU - Stone, James M.
AU - Reichenberg, Avi
AU - Brenneisen, Rudolf
AU - Holt, David
AU - Feilding, Amanda
AU - Walker, Lucy
AU - Murray, Robin M.
AU - Kapur, Shitij
N1 - Funding Information:
This study was supported by the MRC (UK) G0800462, G0701748.
Funding Information:
PDM has received an unrestricted grant from GW Pharmaceuticals and honoraria from Valeant Pharmaceuticals and STI Pharmaceuticals. SK and RM receive salary support from the National Institute for Health Research (NIHR) Mental Health Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King’s College London. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health.
PY - 2013/1
Y1 - 2013/1
N2 - Community-based studies suggest that cannabis products that are high in δ 9-tetrahydrocannabinol (THC) but low in cannabidiol (CBD) are particularly hazardous for mental health. Laboratory-based studies are ideal for clarifying this issue because THC and CBD can be administered in pure form, under controlled conditions. In a between-subjects design, we tested the hypothesis that pre-treatment with CBD inhibited THC-elicited psychosis and cognitive impairment. Healthy participants were randomised to receive oral CBD 600mg (n=22) or placebo (n=26), 210 min ahead of intravenous (IV) THC (1.5 mg). Post-THC, there were lower PANSS positive scores in the CBD group, but this did not reach statistical significance. However, clinically significant positive psychotic symptoms (defined a priori as increases ≥ 3 points) were less likely in the CBD group compared with the placebo group, odds ratio (OR)=0.22 (2=4.74, p<0.05). In agreement, post-THC paranoia, as rated with the State Social Paranoia Scale (SSPS), was less in the CBD group compared with the placebo group (t=2.28, p<0.05). Episodic memory, indexed by scores on the Hopkins Verbal Learning Task-revised (HVLT-R), was poorer, relative to baseline, in the placebo pre-treated group (-10.6±18.9%) compared with the CBD group (-0.4%±9.7 %) (t=2.39, p<0.05). These findings support the idea that high-THC/low-CBD cannabis products are associated with increased risks for mental health.
AB - Community-based studies suggest that cannabis products that are high in δ 9-tetrahydrocannabinol (THC) but low in cannabidiol (CBD) are particularly hazardous for mental health. Laboratory-based studies are ideal for clarifying this issue because THC and CBD can be administered in pure form, under controlled conditions. In a between-subjects design, we tested the hypothesis that pre-treatment with CBD inhibited THC-elicited psychosis and cognitive impairment. Healthy participants were randomised to receive oral CBD 600mg (n=22) or placebo (n=26), 210 min ahead of intravenous (IV) THC (1.5 mg). Post-THC, there were lower PANSS positive scores in the CBD group, but this did not reach statistical significance. However, clinically significant positive psychotic symptoms (defined a priori as increases ≥ 3 points) were less likely in the CBD group compared with the placebo group, odds ratio (OR)=0.22 (2=4.74, p<0.05). In agreement, post-THC paranoia, as rated with the State Social Paranoia Scale (SSPS), was less in the CBD group compared with the placebo group (t=2.28, p<0.05). Episodic memory, indexed by scores on the Hopkins Verbal Learning Task-revised (HVLT-R), was poorer, relative to baseline, in the placebo pre-treated group (-10.6±18.9%) compared with the CBD group (-0.4%±9.7 %) (t=2.39, p<0.05). These findings support the idea that high-THC/low-CBD cannabis products are associated with increased risks for mental health.
KW - CBD
KW - Delta-9-tetrahydrocannabinol
KW - THC
KW - cannabidiol
KW - psychosis
UR - https://www.scopus.com/pages/publications/84871534813
U2 - 10.1177/0269881112460109
DO - 10.1177/0269881112460109
M3 - Article
C2 - 23042808
AN - SCOPUS:84871534813
SN - 0269-8811
VL - 27
SP - 19
EP - 27
JO - Journal of Psychopharmacology
JF - Journal of Psychopharmacology
IS - 1
ER -