Some people are more sensitive to cannabis than others. Specific genetic variations have recently been linked to THC metabolism and cannabis sensitivity.

The field that studies how your genes affect your response to drugs is called pharmacogenetics – and it is exploding!

There are so many different proteins that affect how you can respond to cannabis:

  • Drug metabolizing enzymes control how quickly cannabinoids like THC and CBD are eliminated from your body
  • Drug transporters control how much THC penetrates into your brain
  • Cannabinoid CB1 and CB2 receptors and their downstream cellular signaling systems control the effect of cannabinoids

Every one of these proteins is encoded by a gene. Each gene has variations at specific locations called genetic polymorphisms.

Today we will explore a polymorphism in the CYP2C9 gene which can significantly affect your sensitivity to cannabis. If you know someone who gets high really easily, this may explain why!


THC Metabolism by CYP2C9

It is worth reading more about how your body metabolizes cannabinoids such as THC. However, here is a summary:

Your body (specifically your GI tract and your liver) express drug metabolizing enzymes. These enzymes chemically modify drugs in an attempt to detoxify them and remove them from your body.

Below is the main metabolic pathway of THC. THC is metabolized to the psychoactive metabolite 11-OH-THC. 11-OH-THC is further metabolized to the inactive metabolite THC-COOH.


THC metabolism CYP2C9


Both of these metabolic steps are performed primarily by the same drug metabolizing enzyme called CYP2C9. Therefore, any difference in activity of the CYP2C9 enzyme may cause a change in THC metabolism.


Genetics of CYP2C9

The gene for CYP2C9 has more than 50 polymorphisms, some of which change enzyme activity. The wild-type version (i.e. the most common version) of the gene is called CYP2C9*1. There is a specific polymorphism that has significance for drug metabolism called CYP2C9*3. The CYP2C9*3 variant has significantly decreased enzyme activity.

Because every person has two versions of each gene (one inherited from your mother and one from your father), you may have two copies of the *1 variant, two copies of the *3 variant, or one copy of each.



The CYP2C9*3 polymorphism is relatively common in people of European descent. It is estimated to be 3.3 – 16.2% of all genes in this population (this is called the allele frequency). It is much more rare in other populations. For example, the allele frequency is 0 – 2.3% in Africans and 1.1 – 3.6% in Asians.

[If you want to know which version of the CYP2C9 gene you have, you can use 23andMe to find out.] 


Effect of CYP2C9*3 on THC Metabolism

The first study to assess the effect of CYP2C9*3 on THC metabolism used isolated enzymes in a lab. They showed that the ability of the *3 version of CYP2C9 to metabolize THC was only 27% of the *1 version.


CYP2C9 genetic variant THC metabolism

The decreased metabolism of THC by CYP2C9*3 brought up many questions. Would people who were homozygous for the *3 version (meaning they had two copies of the *3 gene) have much higher levels of THC in their body because of slower metabolism? The answer came 4 years later when a clinical study was published.


Effect of CYP2C9*3 on THC Pharmacokinetics and Pharmacodynamics

This clinical study investigated the pharmacokinetics (blood levels) and pharmacodynamics (sleepiness) of 43 subjects administered a single oral dose of 15 mg THC. All subjects were genotyped to determine their CYP2C9 polymorphisms.

As was expected from the above lab data, subjects with the *3/*3 genotype had 3-fold higher THC levels in their blood than subjects with the *1/*1 genotype. Those subjects with one copy of each gene (*1/*3) had intermediate THC levels that were about 2-fold higher than subjects with *1/*1.


THC pharmacokinetics CYP2C9

Interestingly, 11-OH-THC levels were not significantly different in subjects of different CYP2C9 genotypes. This is probably because 11-OH-THC is both formed by CYP2C9, but also metabolized by CYP2C9. So any change in CYP2C9 activity may cancel itself out.

Given the higher THC blood levels, it is not surprising that subjects with the *3/*3 genotype also had a significantly greater pharmacodynamic effect. Subjects with the *3/*3 genotype felt  more drowsy and this feeling lasted for a longer time than wild-type subjects.

[If you want to know which version of the CYP2C9 gene you have, you can use 23andMe to find out.] 


Implications of CYP2C9 Pharmacogenetics for Cannabis Consumption

CYP2C9 is probably the most important enzyme for the metabolism of THC. A solid scientific study has shown that people with CYP2C9*3 genotypes have higher blood levels of THC and experience a stronger effect after cannabis consumption. This polymorphism helps explain why some people are naturally more sensitive to cannabis than others. 

This study was performed with an oral dose of THC and there may be a different effect after smoking cannabis. After an oral THC dose, metabolism starts in the GI tract and liver before THC makes it to the general circulation, so CYP2C9 variants will affect both how high you get as well as the duration. After smoking cannabis, CYP2C9 variants will have little effect on how high you get since the lungs deliver THC directly to the blood. However, the CYP2C9 variants will still have an effect on the duration of the high.



[Flickr/ Dorli photography]

CYP2C9 polymorphisms should not affect CBD metabolism. CBD is metabolized by a related enzyme called CYP2C19. CYP2C19 has its own genetic polymorphisms, which may affect metabolism of CBD. I will cover this in a future article.

[If you want to know which version of the CYP2C9 gene you have, you can use 23andMe to find out.] 

[Featured image:]

Last modified: September 11, 2017

6 Responses to " How Your Genes Affect Your Cannabis High – The Case of CYP2C9 "

  1. J says:

    Do you think that consuming food/substances (such as St. John’s Wart) to induce the up regulation of CYP2C9 as well as the enzymes and substrates responsible for glucuronidation would help to clear out the stored metabolite in adipose tissue?

    up-regulating CYP2C9 and glucuronidation (either just CYP2C9 or both 2C9 and gluc.) as well as starting an activated charcoal regimen with adequate time seems to be an efficient and potent method of clearing out adipose-dwelling metabolites and simultaneously break up the vicious hepatic cycling to clear out the metabolites and pass a urine test (at least on paper).

    I’d love to hear your thoughts on this plan, Thank you for your time and insight

    • Prof of Pot says:

      You are definitely on the right track. I have been working on a side project on this very topic for the last year. I will be releasing more details very soon! And I can give a full explanation about optimal induction/inhibition at that time.

  2. Johannes says:

    Interesting article. Still waiting for the followup on how to analyse one’s own genes regarding THC metabolism 🙂

    I’m wondering right now, if it’s possible to somehow trick my body to induce the production of the CYP2C9 enzyme?
    Would this speed up the removal of THC metabolites from the system?

    According to some sources(see below) there are several prescription (Modafinil, Anti-Epileptic) drugs as well as OTC supplements (Saint John’s Wort) that do seem to induce said enzymes.

    From my own experience I can report, that Modafinil seems to reduce the effect of orally consumed Cannabis drastically. Vaporizing weed while using Modafinil produces a better yet still somehow reduced effect. The reduced effect seems to persist even on the next day.

    Looking forward to your opinion!

    My sources:
    – “Enzyme induction with antiepileptic drugs: Cause for concern?”
    – “In vitro inhibition and induction of human hepatic cytochrome P450 enzymes by modafinil ”

    • Prof of Pot says:

      There are several drugs that induce CYP2C9 (see Table 3-3 here: As you point out, some herbs do the same, but they are rarely selective (meaning that they induce other CYP enzymes as well).

      If you are taking an inducer after you have stopped smoking, it may work. I wouldn’t start taking it while still smoking, because this would make more THC go down the metabolite pathway that gets detected in urine. I will be writing an article about this eventually.

      The first link actually says that modafinil decreases CYP2C9 activity (although only at concentrations so high that it probably doesn’t happen in people). If anything, this should raise THC levels, so interesting that it would block the high. It sounds like people have had mixed experiences with this though: I’ll keep an eye out in case I come across something that would explain it.

      • Johannes says:

        My personal explanation for my experience with Moda + THC:
        I’ve been using THC for years and usually in high dosages. So I think that because of the entourage effect it triggers a lot of receptors in my brain. Some of those who might be antagonized by the Moda, which I am quite new to. That’s just speculation though, because nobody really knows how Moda works.

        • Johannes says:

          Oh and I’ve also found that Moda the day after THC clears all of the brainfog very quickly and effectively, making me again think there is some kind of opposite action going on. Sorry for off-topic spam though 🙂

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