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Delta-9-tetrahydrocannabinol increases striatal glutamate levels in healthy individuals: implications for psychosis

Abstract:
Research evidence suggests a dose-response relationship for the association between cannabis use and risk of psychosis. Such relationship seems to reflect an increased risk of psychosis not only as a function of frequent cannabis use, but also of high-potency cannabis use in terms of concentration of Δ-9-tetrahydrocannabinol (Δ9-THC), its main psychoactive component. This finding would be in line with the evidence that Δ9-THC administration induces transient psychosis-like symptoms in otherwise healthy individuals. Conversely, low-potency varieties would be less harmful because of their lower amount of Δ9-THC and potential compresence of another cannabinoid, cannabidiol (CBD), which seems to mitigate Δ9-THC detrimental effects. A growing body of studies begins to suggest that CBD may have not only protective effects against the psychotomimetic effects of Δ9-THC but even therapeutic properties on its own, opening new prospects for the treatment of psychosis. Despite being more limited, evidence of the effects of cannabis on cognition seems to come to similar conclusions, with increasing Δ9-THC exposure being responsible for the cognitive impairments attributed to recreational cannabis use while CBD preventing such effects and, when administered alone, enhancing cognition. Molecular evidence indicates that Δ9-THC and CBD may interact with cannabinoid receptors with almost opposite mechanisms, with Δ9-THC being a partial agonist and CBD an inverse agonist/antagonist. With the help of imaging techniques, pharmacological studies in vivo have been able to show opposite effects of Δ9-THC and CBD also on brain function. Altogether, they may account for the intoxicating and therapeutic effects of cannabis on psychosis and cognition
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41380-019-0374-8

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Role:
Author
ORCID:
0000-0001-6139-1920
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Role:
Author
ORCID:
0000-0002-9596-8000
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0003-4381-0532
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Role:
Author
ORCID:
0000-0002-5078-9025
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Role:
Author
ORCID:
0000-0003-4299-1941


Publisher:
Springer Nature [academic journals on nature.com]
Journal:
Molecular Psychiatry More from this journal
Volume:
25
Issue:
12
Pages:
3231-3240
Publication date:
2019-02-15
DOI:
EISSN:
1476-5578
ISSN:
1359-4184


Language:
English
Keywords:
Pubs id:
2359257
Local pid:
pubs:2359257
Source identifiers:
W2911748025
Deposit date:
2026-01-15
ARK identifier:
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