• Home
  • Blog
  • How CBD works: breaking down the substance's mechanism of action.

How CBD works: breaking down the substance's mechanism of action.

04/11/2022

The rapid growth in the global popularity of cannabidiol (CBD) is driven by a unique combination of its therapeutic potential and a high level of safety for the body [1]. The scientific community and proponents of preventive medicine are showing significant interest in this compound, as numerous studies confirm its ability to effectively counteract neuroinflammation, provide protection for nerve cells, and act as a powerful antioxidant [2]. 

A key advantage of CBD is that it helps minimize manifestations of anxiety, depressive states, and pain without causing the side effects that often accompany traditional pharmaceuticals with a similar focus [3].

The impact of CBD on the FAAH enzyme

A deep understanding of exactly how cannabidiol works requires an analysis of its interaction with numerous biological components of our body: from ion channels to specific enzymes and receptors [4].

Contrary to widespread myths, the primary endocannabinoid receptors CB1 and CB2 are not the main targets for this substance. In particular, CBD shows no activity toward CB1 receptors, which explains the absence of the psychoactive effects characteristic of THC. Similarly, cannabidiol does not directly activate CB2 receptors, which are mostly localized in immune system cells.

The primary therapeutic pathway of CBD lies in inhibiting the activity of the FAAH enzyme, which leads to a natural increase in anandamide levels in tissues. Since anandamide is an internal cannabinoid that independently stimulates CB1 and CB2 receptors, inhibiting its breakdown allows for the enhancement of the entire endocannabinoid system's performance. It is this mechanism that ensures mood improvement and sleep normalization.  

Additional mechanisms of CBD action 

Beyond its influence on the endocannabinoid system, CBD engages a number of additional physiological levers. Its sedative properties are partly explained by interaction with glycine receptors, which are responsible for inhibiting excess excitation in the brain [7].

 Significant relief from symptoms of depression and anxiety is achieved through its effect on 5-HT1a-type serotonin receptors, which also contributes to overall emotional recovery and analgesia [8].

The additional analgesic effect is achieved through the TRPV1 capsaicin receptors, which regulate our perception of temperature and pain stimuli [9].

 The ability of cannabidiol to modulate the function of sodium and calcium channels allows for the adjustment of the brain's electrical activity, which is the basis of its anti-epileptic action [4].

In addition, CBD comes into contact with opioid and dopamine receptors [10]. This allows the substance to be used to reduce symptoms of psychosis, which is currently being actively studied in the context of schizophrenia therapy using high doses of cannabidiol [12]. The specific impact on the reward system results in not only the absence of a risk of developing an addiction to CBD itself but also its ability to help overcome cravings for substances such as nicotine, cocaine, or alcohol [11]. 

Such a multifaceted interaction with various body systems makes CBD a promising subject for further clinical research, which will allow for an even fuller disclosure of its medical potential.


References :

1. https://www.singlecare.com/blog/news/cbd-statistics/

2. https://www.nature.com/articles/d41586-019-02524-5

3. https://www.mdpi.com/2218-273X/10/11/1575

4. https://bpspubs.onlinelibrary.wiley.com/doi/10.1002/prp2.682

5. https://bpspubs.onlinelibrary.wiley.com/doi/full/10.1111/bph.12944

6. https://www.frontiersin.org/journals/pharmacology/articles/10.3389/fphar.2017.00744/full

7. https://www.intechopen.com/chapters/50856

8. https://pmc.ncbi.nlm.nih.gov/articles/PMC6319597/

9. https://pmc.ncbi.nlm.nih.gov/articles/PMC1575333/

10. https://pmc.ncbi.nlm.nih.gov/articles/PMC5315552/

11. https://pmc.ncbi.nlm.nih.gov/articles/PMC4444130/

12. https://pmc.ncbi.nlm.nih.gov/articles/PMC6843725/




Related Articles