Heart Disease – Cannabis Research

Heart Disease Research Dashboard


Primary Studies


Related Studies


Total Studies

Clinical Studies


Clinical Meta-analyses


Double-blind human trials


Clinical human trials

Pre-Clinical Studies




Animal studies


Laboratory studies

What am I missing as a non-subscriber?

To see a full dashboard with study details and filtering, go to our DEMO page.

As a subscriber, you will be able to access dashboard insights including chemotype overviews and dosing summaries for medical conditions and organ system and receptor breakdowns for cannabinoid and terpene searches. Study lists present important guidance including dosing and chemotype information with the ability to drill down to the published material. And all outputs are fully filterable, to help find just the information you need. Stay up-to-date with the science of cannabis and the endocannabinoid system with CannaKeys.

CannaKeys has 149 studies associated with Heart Disease.

Here is a small sampling of Heart Disease studies by title:

Components of the Heart Disease Research Dashboard

  • Dosing information available for Heart Disease
  • Chemotype guidance for treating Heart Disease with cannabis
  • Synopsis of cannabis research for Heart Disease
  • Individual study details for Heart Disease

Ready to become a subscriber? Go to our PRICING page.

Select New Condition

Search By Keyword

Filter Condition

Members can filter by the following criteria:

  • Study Type
  • Chemotype
  • Cannabinoids & Endocannabinoids
  • Terpenes
  • Receptors
  • Ligands
  • Study Result
  • Year of Publication

Overview - Heart Disease

Description of Heart Disease

The heart is a unique muscle that gets its own nourishment from three main vessels called the coronary arteries. In Western medicine's model, when one or more of these coronary arteries is slowly or suddenly blocked (as in the case of a blood clot) or gradually narrows (as in the case of atherosclerosis, a build-up of plaque), the heart muscle begins to ache. If not corrected, this "ache" can progress to tissue death called a myocardial infarction or heart attack. The size of the infarct determines survivability. Other common causes of damaged hearts or contributing factors include high blood pressure, metabolic syndrome (insulin resistance), excess weight, drug use (especially "uppers" such as cocaine, crack, methamphetamine), stress (especially chronic stress), mineral imbalances, pharmaceutical drugs including those designed to prevent irregular heartbeats, surgical procedures such as bypass or angioplasty, build-up of toxins (such as lead, mercury, etc.), and degeneration from chronic overexposure to free radicals. Whatever the underlying sudden or chronic cause for acute heart pain, in orthodox medicine it boils down to a lack of oxygen. Allopathic treatments include supplemental oxygen, pharmaceuticals, emergency interventions, and surgery.

Disease Classification

Condition: Heart Disease
Disease Family: Cardiovascular Disease
Organ System: Cardiovascular System
ICD-10 Chapter: Diseases of the Circulatory System
ICD-10 Code: I51

Heart Disease Symptoms:

Chest pain (esp. pressure, tightness, pain does not change when moving), shortness of breath, irregular heartbeat (e.g. tachycardia, bradycardia, palpitations), nausea/vomiting, pale, diaphoresis, pain radiating down the left arm, dizzyness, confusion, loss of consiousness, swelling of legs

Also known as:

HD, Cardiovasular Disease, Cardiac Dysfunction

Drug Interactions

THC Interaction with Pharmaceutical Drugs

  • THC can enhance the effects of drugs that cause sedation and depress the central nervous system, such as benzodiazepines, barbiturates, and alcohol, for example. 
  • THC is metabolized by and an inhibitor of a number of enzymatic liver pathways referred to as cytochrome P450. There are more than 50 enzymes belonging to this enzyme family, a number of which are responsible for the breakdown of common drugs such as antidepressants (e.g. amitriptyline, doxepine, fluvoxamine), antipsychotics (haloperidol, clozapine, stelazine), beta-blockers (e.g. propranolol), bronchodilators (e.g. theophylline), or bloodthinners (e.g. warfarin).  Thus patients taking these classes of medication may find that THC increases the concentration and effects of these drugs as well as the duration of their effects.
  • Clinical observation suggests no likely interactions with other pharmaceuticals at a total daily dose of up to 20mg THC.

CBD Interaction with Pharmaceutical Drugs

  • CBD may alter action on metabolic enzymes (certain drug-transport mechanisms), and as such may alter interactions with other drugs, some of which may produce therapeutic or adverse effects. For instance, CBD interacts with the enzyme cytochrome P450 3A4 and cytochrome P450 2C19, increasing the bioavailability of anti-epileptic drugs such as clobazam (a benzodiazepine). This makes it possible to achieve the same results at significantly lower dosages, reducing treatment costs and risks of adverse effects. 
  • Groups of drugs affected include: anti-epileptic drugs, psychiatric drugs, and drugs affecting metabolic enzymes, for example.
  • Clinical observations suggest no likely interactions with other pharmaceuticals at a total daily dose of up to 100mg CBD

Dosing Considerations

THC Dosage Considerations

  • THC micro dose:  0.1 mg to 0.4 mg
  • THC low dose:  0.5 mg to 5 mg
  • THC medium dose:  6 mg to 20 mg
  • THC high dose:  21 mg to 50+ mg

CBD Dosage Considerations

  • CBD low dose:  0.4 mg to 19 mg
  • CBD medium dose: 20 mg to 99 mg
  • CBD high dose:  100 mg to 800+ mg (upper limits tested ~1,500mg)

Disclaimers: Information on this site is provided for informational purposes only and is not meant to substitute for the advice provided by your own physician or other medical professional. You should not use the information contained herein for diagnosing a health problem or disease. If using a product, you should read carefully all product packaging. If you have or suspect that you have a medical problem, promptly contact your health care provider.

Information on this site is based on scientific studies (human, animal, or in vitro), clinical experience, or traditional usage as cited in each article. The results reported may not necessarily occur in all individuals. For many of the conditions discussed, treatment with prescription or over-the-counter medication is also available. Consult your physician, nutritionally oriented health care practitioner, and/or pharmacist for any health problem and before using any supplements or before making any changes in prescribed medications.