History of cannabis use is not associated with alterations in striatal dopamine D2/D3 receptor availability.
J Psychopharmacol. 2012 Jan; 26(1):144-9.JP

Abstract

Cannabis use in adolescence is emerging as a risk factor for the development of psychosis. In animal studies, Δ9-tetrahydrocannabinol (THC), the psychoactive component of cannabis, modulates striatal dopaminergic neurotransmission. Alterations in human striatal dopaminergic function have also been reported both in psychosis and in stimulant use. We sought to examine whether striatal dopamine D(2)/D(3) receptor availability was altered in volunteers with a history of cannabis use using a database of previously acquired [(11)C]-raclopride positron emission tomography (PET) scans. Ten [(11)C]-raclopride scans from volunteers with a history of cannabis use were compared to ten control scans using a functional striatal subdivision region of interest (ROI) analysis. No significant differences in either overall striatal BP(ND) values or BP(ND) values in any functional striatal subdivision were found between the two groups. There was also no correlation between lifetime frequency of cannabis use and BP(ND) values. Limbic striatal BP(ND) values were ten percent lower in current nicotine cigarette smokers. These findings suggest that, unlike other drugs of abuse, a history of cannabis use is not associated with alterations in striatal dopamine D(2)/D(3) receptor availability.

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Authors+Show Affiliations

Stokes PR
Psychiatric Imaging Group, MRC Clinical Sciences Centre, Imperial College London, London, UK. paul.stokes@imperial.ac.uk
Egerton A
No affiliation info available
Watson B
No affiliation info available
Reid A
No affiliation info available
Lappin J
No affiliation info available
Howes OD
No affiliation info available
Nutt DJ
No affiliation info available
Lingford-Hughes AR
No affiliation info available

MeSH

AdultAlcohol DrinkingCannabisCarbon IsotopesCorpus StriatumFemaleHumansLimbic SystemMaleMarijuana AbuseNicotinePositron-Emission TomographyPsychotic DisordersRacloprideReceptors, Dopamine D2Receptors, Dopamine D3Synaptic Transmission

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

21890594