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Kava

Learn more about kava, a plant with indigenous roots gaining popularity in social consumption.

Overview

Common Nicknames

Ava, tonga, yangona

Drug Class

Depressant

Drug Form

Typically a drink, though can be in capsules, powders, or drops

Route of Administration

Oral

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What is the science of Kava?

Unlike most substances reviewed at Drug Science, kava is not simply a drug, but inclusive of wider cultural understandings including practice, therefore defying a narrow definition script.


Kava in its beverage form typically contains 20 kavalactones in combination with various other active ingredients, including flavokavains and alkaloids. Pharmacology reports that six of the 20 kavalactones as being responsible for its psychoactive effect.  These six lactones have each been allocated a number to aid chemotype classification, and are listed below with their chemotype number and standard abbreviation:


  1. demethoxy-yangonin (DMY)

  2. dihydro kavain (DHK)

  3. yangonin (YAN)

  4. kavain (KAV)

  5. dihydromethysticin (DHM)

  6. methysticin (METH).    


Pharmacology explains that kava acts on the brain and central nervous system by blocking the calcium ion channels, which leads to a reduction of neurotransmitter release excitation, and the potentiation of gamma-Aminobutyric acid (GABAA), through enhanced ligand binding to the GABA receptors. This creates a reduction in the neuronal re-uptake of noradrenaline responders and possibly dopamine, leading to a reversal of monoamine oxidase (MAO) B inhibition. Although this explanation would suggest there is a high level of knowledge regarding kavalactone psychopharmacology, researchers warn that kavalactone “modes of action are not fully understood”, with even less known about “the neurophysiological mechanisms associated with kavalactone metabolism”. Further confusing this knowledge gap is the psychopharmacology of Piper methysticum pharmaceuticals/nutraceuticals preparation, particularly extracts, containing selected or altered kavalactones.

What are the risks?

High kava use increases gamma-glutamyl transpeptidase (GGT) levels in the blood. Research is clear that “while elevated GGT and white blood cells [lymphocytes] were abnormal [to those unfamiliar with kava’s effects on the liver], this does not mean that this abnormality is of concern”. Additionally, high kava use over a prolonged period can cause kava dermopathy, or a drying and flaking of the skin. However, this subsides a week or so after use is slowed or ceased, without residual effects.


Kava’s level of safety is recognised in 2000+ years of traditional knowledge and use, and a 2016 World Health Organisation’s (WHO) kava risk assessment report: "On balance, the weight-of-evidence from both a long history of use of kava beverage and from the more recent research findings indicates that it is possible for kava beverage [made with noble cultivars] to be consumed with an acceptably low level of health risk." That same report also cited research showing kava as statistically safer than Paracetamol. Additionally, the 2019 Drug Harms Ranking Study assessed kava as the least-most harmful drug of the 22 assessed substances, with the harm to the user scored at 2, and harm to others 1 (total 3 harm-points). The harm to user score includes the GGT level rise and kava dermopathy (as discussed above) which are reversable. Kava’s safety is reflected in its regulation as a ‘food’ in some countries. However, the WHO (including the UN/WHO Kava CODEX Alimentarius) ‘food’ classification and harm ranking is caveated on kava beverage made only from noble drinking cultivars of Piper methysticum and prepared using a traditionally influenced water-based method. This ‘food’ safety recognition does not extend to contemporary products, extracts and pop-culture products made from, and including, Piper methysticum.


Kava wash-down

Coinciding with kava’s move away from its traditional use environment is the growing practice of washdown in which alcohol is consumed together with, or following, kava consumption. Alcohol, even at very small quantities following, or with, kava use, is known to potentiate the effects of kava. There is concern that the use of ethanol by the pharmaceutical/nutraceutical industry to extract kavalactones potentially caused a chemotype disruption and was a contributing factor in European Kava Ban hepatoxicity cases. It is suspected that kava wash-down increases the likelihood of in-vivo chemotype disruption and liver complication. Kava wash-down is potentially dangerous, as are Piper methysticum products that contain alcohol or used it in processing.


Kava, Piper methysticum preparations and Kratom

Research shows that over 60% of ‘kava bars’ in the USA either mix kratom (Mitragyna speciosa), or have it available to mix, with their kava or pop-culture Piper methysticum drinks. Kratom is a Southeast Asian leaf with addictive, opioid-like effects, and is said to give kava a ‘euphoric hit’. Although the practice of mixing addictive kratom with safe kava is frequently denied, a large collection of kava bar ‘menus’ and social media posts provide a plethora of evidence of this practice. More concerning are reports in online addiction support groups from kava bar patrons who believed they had been drinking kava, only later to learn this had been adulterated with kratom and had led to dependency. The FDA advises that “kratom is not lawfully marketed in the U.S. as a drug product, a dietary supplement, or a food additive.” Kava bar attendees are advised to seek clarification on kava / Piper methysticum preparation ingredients. Customers are strongly advised not to consume ‘kava shots’ or kratom Piper methysticum drinks. These are marketed under names including Phlex, Feel Free, Flayvorz, etc. and are potentially dangerous.


General kava safety comments

Research warns, "[i]t is important to keep in mind that not all … [Piper methysticum preparations are] equal in efficacy and safety and therefore it is critical to characterize a … [Piper methysticum] product with detailed knowledge of its preparation method and chemical composition. Many factors, ranging from cultivars, parts of the plant used, preparation methods, and solvents employed for extraction, affect the composition of the final kava products." Additionally, kava misinformation (see section under), practices such as Kava wash-down, kava drug interactions and unethical behaviour including adulterating Piper methysticum with kratom has led to regulatory confusion.

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How might the drug make you feel?

Even at high consumption volumes (3.6 litres over 6 hours), kava’s effects are subtle, not causing marked euphoria or vestibular disturbance, hallucinations or ‘intoxication’. Kava’s effect subtlety has been likened to an ‘anti-Red Bull’, inducing feelings of relaxation that facilitate clear-headed discussion and promote wellbeing.


A recent study highlights kava's minimal cognitive interference. This research used a validated somatosensory neuro-diagnostic tool to evaluate six specific neurological functions—Focus, Accuracy, Temporal Order Judgement (TOJ), Timing Perception, Plasticity, and Fatigue—before, during, and after six hours of traditional kava consumption. Results were compared with a control group not consuming kava and applied to driver safety. The study found a statistically significant but minor negative impact on TOJ (p=0.007301, BF=6.193058), which relates to the brain's ability to sequence events. Importantly, this impairment was shown to be very different to the effects of alcohol, cannabis, and other recreational substances. These findings align with ethnographic observations suggesting that kava, when consumed traditionally, has a small effect primarily through TOJ disruption. Moreover, this work corroborates traditional knowledge that reports kava does not hinder reasoned thinking or interpersonal connection, which are essential aspects of kava use in communities.


The effects described here do not include those experienced when using contemporary Piper methysticum products.

Is Kava addictive, and what are the long-term effects?

Kava is not physically addictive. As discussed earlier, typical kava consumption is reported as 3.6 litres (6.33 pints) over six hours. In some parts of the Pacific, it is common to consume this amount on a daily basis for weeks. Despite early European colonial assumptions that prolonged kava use led to addiction, research shows that even at high use volumes, kava is not physically addictive. Research reports that “if the label ‘addiction’ is to be applied to yaqona [kava], I would hesitantly use ‘socially addictive’ in the sense that it has been habituated to most aspects of Fijian [Vanuatu, Tongan and Samoa] socialization.”

Harm Reduction and Drug-Drug Interactions

People who have hepatitis or liver problems are encouraged to avoid kava and not to use Piper methysticum pharmaceuticals / nutraceuticals or pop-culture products. Additionally, kava should not be mixed with alcohol or alcohol consumed within 12 hours of drinking kava or consuming Piper methysticum products. Further, people taking antidepressants (selective serotonin reuptake inhibitor [SSRI]), benzodiazepines, antipsychotics, St. John’s Wort (Hypericum perforatum), the Chinese herb Aristolochia, Warfarin, the Parkinsons drug Levodopa and Alprazolam are advised not to consume kava or Piper methysticum products.

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Medical Uses

Traditional knowledge reports kava as having a variety of medicinal uses including antifungal and antibacterial action, mild anesthetic and analgesic effects, and stress relieving and sleep promoting properties. Kava users describe its anxiolytic properties as manifesting “a pleasant, warm, and cheerful, but lazy feeling”, effects that in some cases can be felt for several days. Further, ethnographic research with combat veterans and first responders (police, fire and ambulance) reports the efficacy of kava with talanoa to reducing PTSD symptomology, work that is currently being validated in clinical trials.


Research utilizing contemporary pills, capsules and extracts of Piper methysticum have shown positive mild anesthetic and analgesic effect, and antifungal and antibacterial action, including its use as “as a treatment for gonorrhea in the German Pharmacopoeia prior to the discovery of penicillin." Piper methysticum nutraceuticals have also been shown to improve sleep quality inclusive of “rapid onset of effect … [with] minimal morning after-effects,” and anxiolytic efficacy, particularly in the treatment of generalized anxiety disorder. These Piper methysticum preparation also show viability as a natural hormone replacement therapy (HRT) for women, and more recently anti-cancer action, specifically ovarian, bladder, colon, lung cancer and leukemia.

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Myths and Misconceptions

Regardless of kava’s subtle effects and lack of safety concern as reflected in risk assessment reports and regulation, kava continues to be misunderstood, misrepresented and linked with more potent substances and their adverse social and health consequences, with this perpetuating a harmful anti-Pacific narrative about the drink and its associated culture. Common kava misinformation includes kava being an alcohol, having addictive properties and causing liver problems. These myths and reasoning behind them are discussed at length in the Journal of Drug Science, Policy and Law, 2019, Volume 5, p. 1-13.


​A few of the lesser myths not covered in the Drug Science paper can be found here.

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