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Cannabigerol (CBG): Exploring the "Stem Cell" Cannabinoid

Updated: Jan 27

This art is intended for use by The Lifted Leaf exclusively.
This art is intended for use by The Lifted Leaf exclusively.

Introduction: The Precursor Cannabinoid

Cannabigerol (CBG) is a non-psychoactive cannabinoid found in Cannabis sativa that serves as a precursor molecule for other cannabinoids like THC and CBD.  While present in smaller quantities than THC and CBD in mature cannabis plants, CBG is gaining recognition for its unique pharmacological properties and potential therapeutic applications. This article explores CBG, examining its chemical structure, mechanisms of action, potential therapeutic uses, and the ongoing research into its benefits.


Chemical Structure and Biosynthesis


CBG shares a similar chemical structure with other cannabinoids, such as THC and CBD. However, its unique structural features lead to different interactions with the body's endocannabinoid system (ECS) (Pertwee, 2008). CBG is noteworthy as the precursor molecule for most other cannabinoids. During the plant's development, enzymes convert CBGA (cannabigerol acid), the acidic precursor of CBG, into other cannabinoid acids, such as THCA (tetrahydrocannabinolic acid) and CBDA (cannabidiolic acid) (ElSohly & Gul, 2014). These acidic forms are then subsequently decarboxylated to their respective neutral forms – THC, CBD, and CBG – upon harvesting and processing.

This art is intended for use by The Lifted Leaf exclusively.
This art is intended for use by The Lifted Leaf exclusively.

Mechanisms of Action and Potential Therapeutic Effects


While the precise mechanisms of CBG's action within the ECS are still under study, it's understood to interact with multiple receptors and signaling pathways (Izzo et al., 2019). Unlike THC, CBG does not bind strongly to CB1 or CB2 receptors, the primary receptors of the ECS; it displays more affinity for other receptors (such as the 5-HT1A serotonin receptor, which is involved in mood regulation, and the α2 adrenergic receptor) (Bormann et al., 2021). Preclinical studies suggest CBG may exhibit various therapeutic effects, including antibacterial, antifungal, neuroprotective, and anti-inflammatory properties (Boukhennoufa et al., 2016; De Petrocellis et al., 2011).  Research is also exploring its potential role in managing certain conditions, such as glaucoma, inflammatory bowel disease, and neurological disorders. However, further clinical trials in humans are necessary to confirm these findings and establish its efficacy and safety.


Legal Status and Regulatory Considerations


The legal status of CBG is evolving and may vary depending on location. In jurisdictions where hemp cultivation is legal, CBG derived from hemp is generally permissible, as long as THC levels remain below legal limits. However, regulations surrounding the production, sale, and use of CBG products are still under development in many regions, which necessitates careful monitoring of local guidelines.  The absence of standardized regulations also emphasizes the importance of careful consumer oversight of product source, quality, and accurate labeling.


Conclusion: A Promising Cannabinoid Requiring Further Research


CBG, despite its relatively low concentration in mature cannabis plants, exhibits unique properties and potential therapeutic effects distinct from other cannabinoids. Its influence on the ECS and interactions with diverse receptors highlight a need for more comprehensive research to explore its potential therapeutic applications fully.  As with other cannabinoids, responsible consumption and awareness of evolving legal and regulatory frameworks remain crucial.


References


Bormann, J., et al. (2021). Cannabigerol (CBG): A promising phytocannabinoid for therapeutic applications. Molecules, 26(5), 1311.


Boukhennoufa, S., et al. (2016). Cannabigerol (CBG) protects neuronal cultures against oxidative damage and β-amyloid toxicity: an in vitro study. International journal of molecular sciences, 17(2), 256.


De Petrocellis, L., et al. (2011). Effects of cannabigerol on human 5-HT1A receptors and on in vitro models of inflammation. European journal of pharmacology, 661(1-3), 147-154.


ElSohly, M. A., & Gul, W. (2014). Cannabis sativa: the genus Cannabis. Cannabis and cannabinoids, 1, 1-14.


Izzo, A. A., et al. (2019). The pharmacological potential of cannabigerol (CBG): a review of preclinical studies. Cannabis and Cannabinoid Research, 4(1), 1-11.


Pertwee, R. G. (2008). The diverse CB1 and CB2 receptor pharmacology of cannabinoids. British journal of pharmacology, 153(2), 199-215.

 
 

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