CBG or cannabigerol
CBG is one cannabinoid compound found in hemp that has been studied more than ever in recent years. The phytocannabinoid CBG is non-narcotic, meaning it does not cause intoxication to the user. CBG acts on the same receptors as CBD (1).
Despite the fact that coverage of cannabiger is still significantly lower than that of the best-known CBD and THCAccording to new studies, it has similar effects to CBD in addition to its unique properties. CBG is also classified as safe for daily use. Thus, CBG could very well be a new rising and trendy cannabinoid product.
CBG increases serotonin secretion
CBG, like other cannabinoids, acts on the body’s internal cannabinoid system through cannabinoid receptors (CB1 and CB2). Studies show that CBG increases serotonin, the so-called well-being hormone secretion, which has a mood-boosting effect.
CB1 and CB2 receptors play an active role in the regulation of cognitive functions such as appetite, pain response, mood, and internal balance. By acting on cannabinoid receptors, cannabinoids can alter the signals that neurotransmitters send to the body to maintain the balance of vital functions (2).
Use of CBG in various diseases
According to the latest research, CBG has versatile effects on well-being. It is used especially for certain diseases.
According to research, the cannabinoid CBG (cannabigerol) can reduce pain because it is a potent alpha-2-adrenoceptor agonist and also a moderately potent 5HT1A receptor antagonist. (3)
A 2014 study looked at colon cancer in rats and concluded that CBG may reduce the growth of cancer cells and other tumors. (4)
CBG has neuroprotective properties. A 2015 study looked at mice with a neurodegenerative disease called Huntington’s disease. The study concluded that CBG may also be promising in the treatment of other neurodegenerative diseases. (5)
IBD (Inflammatory Bowel Disease)
According to a 2013 study, CBG appears to reduce IBD symptoms. In summary, the study shows that CBG attenuated colitis in mice, reduced nitric oxide production in macrophages, and reduced ROS formation in intestinal epithelial cells. CBG could be considered for clinical trials in IBD patients. (6)
The study found that CBG can kill bacteria, especially methicillin-resistant Staphylococcus aureus (MRSA), which causes drug-resistant infections. These infections can be difficult to treat and also sometimes dangerous. (7)
In addition to the benefits listed above, CBG has been found to have an effect on improving appetite and many other ailments, which need further research for confirmation.
The CBG was discovered as early as 1964
CBG is not in itself a new discovery. The CBG was first identified from hemp in 1964. The compound was discovered together by researchers Raphael Mechoulam and Yehil Gaoni (8).
However, isolating CBG from hemp is not as easy as isolating CBD, which has made the launch of CBG products slower and more laborious. Now, several manufacturers have invented ways to extract CBG efficiently. At the moment, there are e.g. CBG oil, CBG capsules, CBG cosmetics, CBG candies, CBG flowers and more. CBG products.
CBG is the mother of all cannabinoids
CBG is called the mother of all cannabinoids, as CBG forms all other hemp cannabinoids. CBG is also known as the cannabinoid stem cell and the “Rolls Royce” of cannabis.
Like all other cannabinoids, CBG is present in hemp in acid form (CBG-A). Enzymes allow cannabigeric acid (CBG-A) to form other better-known cannabinoid acids such as THC-A and CBD-A, which in turn transform over time into THC, CBD and other non-acidic cannabinoid compounds (9). Finally, the remaining CBG-A (approximately 1%) decarboxylated CBG. A total of at least 120 different cannabinoids have been found in hemp.
What effect does CBG have in combination with other medicines?
It is not yet known what interactions CBG may have with other medicines.
If you are taking any medications, it is best to check compatibility with your doctor before trying CBG oil. This is especially important if you are taking a medicine that contains so-called grapefruit warning. In the same way as grapefruit juice, CBG can also increase the effectiveness of the effects of several drugs.
Medicines that often have this warning include:
- antibiotics and antimicrobials
- anticancer drugs
- antiepileptics (AEDs)
- antihypertensive drugs
- blood thinners
- cholesterol drugs
- erectile dysfunction drugs
- gastrointestinal (GI) medicines such as gastroesophageal reflux disease (GERD) or nausea
- antidepressants such as for anxiety, depression or mood disorders
- prostate medications (10).
List of drugs with interactions
See a more detailed list of drugs commonly used in Finland that have been shown to interact with CBD.
CBD can affect how your body metabolises these medicines. It’s not clear if CBG has the same effect, but given how similar it is to CBD, it’s best to be cautious and carefully consider co-medications. (10)
Do not stop taking your medication to use CBG oil unless instructed to do so by your healthcare professional.
Require third-party analysis
When choosing CBG products, you should first check that the company’s products are tested and trusted by a third party. Check the cannabinoid profile and possible contaminations for analysis. All analyzes should be available on the vendors ’website or should at least be available via email upon request.
- G. Navarro et al. 2018. Cannabigerol Action at Cannabinoid CB1 and CB2 Receptors and at CB1 – CB2 Heteroreceptor Complexes. Front Pharmacol.
- M. Lee. 2012. The Discovery of the Endocannabinoid System. The Prop 215 Era.
- RG. Pertwee. 2010. British Journal of Pharmacology. Evidence that the plant cannabinoid cannabigerol is a highly potent a2-adrenoceptor agonist and moderately potent 5HT1A receptor antagonistbph_515 129..141. https://bpspubs.onlinelibrary.wiley.com/doi/pdf/10.1111/j.1476-5381.2009.00515.x. Referred to 31.01.2023
- F. Borrelli ym. 2014. Carcinogenesis. Colon carcinogenesis is inhibited by the TRPM8 antagonist cannabigerol, a Cannabis-derived non-psychotropic cannabinoid. ncbi.nlm.nih.gov/pubmed/25269802. Referred to 31.01.2023
- S. Valdeolivas etc. 2015. Neurotherapeutics. Neuroprotective properties of cannabigerol in Huntington’s disease: studies in R6/2 mice and 3-nitropropionate-lesioned mice. ncbi.nlm.nih.gov/pubmed/25252936. Referred to 31.01.2023
- F. Borrelli ym. 2013. Biochem Pharmacol. Beneficial effect of the non-psychotropic plant cannabinoid cannabigerol on experimental inflammatory bowel disease. https://pubmed.ncbi.nlm.nih.gov/23415610/. Referred to 31.01.2023
- A. Maya ym. 2020. Science Daily. Researchers uncover hidden antibiotic potential of cannabis. https://www.sciencedaily.com/releases/2020/02/200226131325.html. Referred to 31.01.2023
- Gaoni, Y., & Mechoulam, R. 1964. Isolation, Structure, and Partial Synthesis of an Active Constituent of Hashish. Journal of the American Chemical Society, 86 (8), 1646–1647. https://doi.org/10.1021/ja01062a046
- Tahir M. et al. 2021. The biosynthesis of the cannabinoids. Journal of Cannabis Research. https://jcannabisresearch.biomedcentral.com/articles/10.1186/s42238-021-00062-4 . Referenced on 19.11.2021
- S. Ferguson. 2020. Healthline. Meet the CBG, the New Cannabinoid on the Block.
https://www.healthline.com/health/cbg-oil#interactions. Referenced on 11/18/2021.