CBG shows early promise against schizophrenia-like behaviors

Cannabigerol, a minor phytocannabinoid, prevents behavioral changes induced by psychotomimetic drugs.

Progress in neuro-psychopharmacology & biological psychiatry • • Highly Relevant
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AI Summary

Cannabigerol (CBG), a non-intoxicating cannabinoid from Cannabis sativa, reduced several schizophrenia-like behavioral changes in male mice. The researchers tested whether CBG could counteract effects produced by d-amphetamine and MK-801, drugs commonly used to model aspects of psychosis in animals.

CBG lessened drug-related disruptions in sensory filtering, movement, social interaction, and recognition memory across different behavioral tests. The benefits appeared at reduced concentrations, leading the authors to describe CBG as a promising candidate for future translational and clinical research. However, these results come from animal experiments and do not show that CBG treats schizophrenia or psychosis in people; the abstract also provides no quantitative results.

💡 Key Findings

1
CBG attenuated d-amphetamine-induced disruptions in prepulse inhibition and open-field behavioral tests in mice.
Moderate
50%
2
Pretreatment with CBG reduced MK-801-related impairments in social interaction, recognition memory, and prepulse inhibition tests.
Moderate
50%
3
The authors conclude that CBG shows a promising antipsychotic-like profile for future research, with effects observed at reduced concentrations; this remains preclinical evidence.
Moderate
45%

📄 Original Abstract

Cannabigerol (CBG) is a phytocannabinoid present in the plant Cannabis sativa that, similar to cannabidiol (CBD), does not cause psychotomimetic effects. It has shown potential therapeutic effects for relieving pain, inflammation, and anxiety, and it possesses antioxidant and neuroprotective properties. To date, few studies have investigated the potential of CBG in animal models of schizophrenia. Previous studies have demonstrated the antipsychotic-like profile of CBD in clinical and preclinical studies, with a lower induction of side effects when compared to conventional therapy. Although the pharmacological properties of CBG partially resemble those of CBD, some important differences could result in distinct clinical potential. In the present work, we investigated whether CBG could also show an antipsychotic-like profile in animal models of schizophrenia. Male Swiss mice received intraperitoneal injections of CBG followed by d-amphetamine (AMPH) or MK-801 and were exposed to different behavioral assays, including the open field, novel object recognition (NOR), social interaction, and prepulse inhibition (PPI) tests. CBG attenuated the disruptive effects of AMPH in the PPI and open field tests. In addition, pre-treatment with this compound also attenuated the impairments in the social interaction test, NOR, and PPI induced by MK-801. These results suggest that CBG therapeutic profile in behavioral assays. Notably, these benefits were observed at reduced concentrations, indicating that this compound represents a promising candidate for future translational and clinical investigations.

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