Many people turn to marijuana or cannabidiol to ease their achy joints and help them sleep, but a new study suggests that could wreak havoc with any other medications they’re taking.
Why? Because the body uses the same set of enzymes to process them all, scientists report.
The chemicals in marijuana — THC, cannabidiol (CBD), cannabinol (CBN) — are metabolized in the body by at least two families of enzymes that also help process and eliminate more than 70% of the most commonly used prescription drugs from the body, the researchers say.
That means there’s a risk that pot might dangerously amp up the effects of some prescription drugs, or cause other medications to flush through your system so quickly that they do you no good, lead researcher Philip Lazarus says. He’s a professor of pharmaceutical sciences at Washington State University, in Spokane.
“We saw some significant inhibitions,” Lazarus adds. “The concentrations we see in the lab are probably an indicator there is at least some inhibition of these enzymes in real-time.”
Some drugs that could be affected by pot use include the blood thinner warfarin, the breast cancer drug tamoxifen, and painkillers like acetaminophen (Tylenol) or ibuprofen (Motrin), Lazarus and Ed Bednarczyk, a clinical associate professor of pharmacy practice at the University at Buffalo, in New York say.
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In two lab reports published in the December issue of the journal Drug Metabolism and Disposition, Lazarus served as senior author. One study looked at a family of enzymes known as cytochrome P450s (CYPs), and the other analyzed the enzyme group UDP-glucuronosyltransferases (UGTs).
The CYPs are involved in the early stages of metabolizing THC and CBD, while the UGTs are involved in the later stages.
THC and CBD stay in your body for only about 30 minutes before the enzymes break them down, but the chemicals that result from the process can linger in your body for up to two weeks, the study authors said in background notes.
In the lab, the researchers tested how the pot chemicals might interfere with these enzymes’ ability to break down other drugs, using cultured human kidney cells to test a single enzyme at a time.
The investigators found that the major THC metabolites inhibited key CYP enzymes, including several that serve key roles in the liver.
And all three cannabis chemicals, but especially CBD, inhibited two of the primary UGT enzymes in the liver.
CBD was also found to block three enzymes that account for about 95% of UGT metabolism in the kidney, which helps clear toxins and some drugs from the body.
“It’s a very, very good reminder that these interactions are real,” Bednarczyk says. “It’s important for physicians and pharmacists who are working with patients to explore this.”
This is the first research effort to demonstrate the potential effects of pot on UGT enzymes, the researchers say. The study also sheds more light on marijuana’s effect on CYP enzymes.
It’s been known for some time that pot could interact with other drugs, Paul Armentano, deputy director of NORML, a group that advocates for the reform of marijuana laws shares.
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The U.S. Food and Drug Administration’s labeling of a form of synthetic THC called dronabinol, which has been available as a prescription drug for more than 30 years, indicates that it might influence CYP levels, Armentano notes. And the agency’s warning for Epidiolex, a plant-based prescription CBD drug, also addresses how the substance could affect the liver, he adds.
But Armentano questioned how powerful these interactions could be, given how long marijuana has been used both recreationally and medicinally.
“Adults — and patients in particular — have been consuming cannabinoids medicinally for centuries, and this practice has become quite commonplace over the past few decades,” Armentano says. “Many of these patients are older and many of them may also be prescribed other medications. Were cannabinoids to be significantly contraindicated among this population, one would presume that there would be ample empirical evidence already available substantiating this concern.”
Pot’s effect on metabolism wouldn’t likely affect someone who takes a recreational toke or three on the weekend, according to Lazarus.
“Even though it probably inhibits these enzymes, it doesn’t inhibit them enough to interfere with your everyday metabolism,” Lazarus acknowledges.
The problem comes when you mix regular pot use with other drugs, or if you’re taking a marijuana-derived product alongside your prescription.
“Generally,” Bednarczyk says, “CBD is thought to inhibit metabolic pathways, and THC is thought to induce metabolic pathways. THC can make your blood levels of other drugs fall, and CBD can make your blood levels rise.”
One well-known example is warfarin, “a very, very potent blood thinner,” Bednarczyk says.
A case study published a couple of years ago says one warfarin patient “had the effects of this drug go way up into the danger zone shortly after starting CBD.” “That one, you don’t mess with. The effects of having too high a level even transiently for a few days can be lethal,” he warns.
“That’s the king of the hill for risk, because it’s all over the map in terms of patient-to-patient variability,” Bednarczyk says of warfarin and pot. “One patient can need a bucket of this stuff to have the same effect as another patient who’s on the lowest dose manufactured.”
The opposite occurs when you mix pot with tamoxifen, a hormone therapy drug used to treat breast cancer by blocking the effects of estrogen, Lazarus adds.
For tamoxifen to work, he notes, it must be broken down by the body into another chemical called endoxifen, which is 100 times more active than tamoxifen.
If pot interferes with the processing of tamoxifen, it could cause the breast cancer patient to receive little to no benefit from the drug, Lazarus explains.
Lazarus says he’s also concerned about the interaction pot might have with over-the-counter pain medications.
Ibuprofen is toxic to your liver and your kidney anyway, but if you start taking marijuana on top of that, then you’re going to see some significant effects,” Lazarus says. “It would probably cause toxicity because you’re slowing down its metabolism, so that means you’re not excreting the stuff and you have more of it sitting in your body.”
However, all these concerns are based on lab studies. What’s needed now are clinical trials to establish the true effects of pot on other drugs, Lazarus notes.
“We have to do some clinical studies to show in people that if you’re taking a specific drug and then you also smoke a marijuana cigarette that morning, you see higher or lower levels of that drug in your body,” Lazarus said.
In the meantime, people should discuss their use of pot products with their doctor and their pharmacist to make sure they aren’t putting their health at risk, Lazarus and Bednarczyk suggest.
“This should not be a roll-your-own process,” Bednarczyk concludes.
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