4.7 Article

Cannabigerolic acid, a major biosynthetic precursor molecule in cannabis, exhibits divergent effects on seizures in mouse models of epilepsy

期刊

BRITISH JOURNAL OF PHARMACOLOGY
卷 178, 期 24, 页码 4826-4841

出版社

WILEY
DOI: 10.1111/bph.15661

关键词

cannabinoids; CBGA; Dravet syndrome; epilepsy

资金

  1. National Health and Medical Research Council [1161571, 1185122]
  2. National Institutes of Health [R01 NS084959]
  3. Lambert Initiative for Cannabinoid Therapeutics
  4. National Health and Medical Research Council of Australia [1185122] Funding Source: NHMRC

向作者/读者索取更多资源

The study found that plant cannabinoids such as CBGA, CBDVA and CBGVA have anti-seizure properties which can be used to treat childhood epilepsy. However, there are also some limitations and challenges that need to be addressed before these cannabinoids can be widely used as alternative treatments.
Background and Purpose Cannabis has been used to treat epilepsy for millennia, with such use validated by regulatory approval of cannabidiol (CBD) for Dravet syndrome. Unregulated artisanal cannabis-based products used to treat children with intractable epilepsies often contain relatively low doses of CBD but are enriched in other phytocannabinoids. This raises the possibility that other cannabis constituents might have anticonvulsant properties. Experimental Approach We used the Scn1a(+/-) mouse model of Dravet syndrome to investigate the cannabis plant for phytocannabinoids with anticonvulsant effects against hyperthermia-induced seizures. The most promising, cannabigerolic acid (CBGA), was further examined against spontaneous seizures and survival in Scn1a(+/-) mice and in electroshock seizure models. Pharmacological effects of CBGA were surveyed across multiple drug targets. Key Results The initial screen identified three phytocannabinoids with novel anticonvulsant properties: CBGA, cannabidivarinic acid (CBDVA) and cannabigerovarinic acid (CBGVA). CBGA was most potent and potentiated the anticonvulsant effects of clobazam against hyperthermia-induced and spontaneous seizures, and was anticonvulsant in the MES threshold test. However, CBGA was proconvulsant in the 6-Hz threshold test and a high dose increased spontaneous seizure frequency in Scn1a(+/-) mice. CBGA was found to interact with numerous epilepsy-relevant targets including GPR55, TRPV1 channels and GABA(A) receptors. Conclusion and Implications These results suggest that CBGA, CBDVA and CBGVA may contribute to the effects of cannabis-based products in childhood epilepsy. Although these phytocannabinoids have anticonvulsant potential and could be lead compounds for drug development programmes, several liabilities would need to be overcome before CBD is superseded by another in this class.

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