Kava: Difference between revisions

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= Dosage =
= Dosage =


== Oral ==
Dried Kava root contains approximately 3-20% kavalactones, depending on the strain. Doses are given for kavalactone.


Dried Kava root contains approximately 3-20% kavalactones, depending on the strain.
{| class="wikitable"
 
|+ Oral
Kavalactone dosage:
|-
 
| Light || 50-70mg
Light: 50-70mg
|-
 
| Common || 70-150mg
Common: 70-150mg
|-
 
| Strong || 150-200mg
Strong: 150-200mg
|-
 
| Heavy || 300mg+
Heavy: 300mg +
|}


= Duration =
= Duration =


== Oral ==
Note: Onset is faster with an increased dose.
 
Onset: 20-30 minutes (onset is faster depending on the dose)
 
Peak: 3 hours
 
Total Duration: 3-6 hours


After-effects: 9-18 hours
{| class="wikitable"
|+ Oral
|-
| Onset || 20-30 minutes
|-
| Peak || 3 hours
|-
| Total || 3-6 hours
|-
| After-effects || 9-18 hours
|}


= Effects =
= Effects =

Revision as of 08:26, 16 July 2014

General Information

Kava (Piper methysticum) is a tropical evergreen shrub with large heart-shaped leaves and woody stems. Its thick roots are mashed or ground and made into a cold and bitter-tasting beverage used similarly to alcohol. It has a long history of ritual and recreational use in Pacific Polynesia and is now a common herbal product, used widely by those in certain societies as part of a 'Kava Culture.'

History

Kava is used for medicinal, religious, political, cultural and social purposes throughout the Pacific, and have been for many years. Though the exact geographical origin and the date of the initial discovery of Kava as a psychoactive plant are unknown, there are several legends as to its discovery in the various ancient Pacific communities.

Kava cultures are the religious and cultural traditions of western Oceania which consume kava. There are similarities in the use of kava between the different cultures, but each one also has its own traditions.

These cultures have a great respect for the plant and place a high importance on it. In Fiji, for example, a formal yaqona (kava) ceremony will often accompany important social, political, religious, etc. functions, usually involving a ritual presentation of the bundled roots as a sevusevu (gift), and drinking of the yaqona itself.

Western interest in the plant started as early as 1778, upon Captain Cook's voyages to the Pacific islands - though it was at the time seen as inferior to alcohol. However, through medium of the Internet, the plant has in recent times become available worldwide to end users - and use is now more widespread either through alternative preperations of the traditional beverage (usually involving additional flavourings such as sugar or coconut milk) or taking a powdered form of the substance in capsules. This has led to regulation in some countries such as the United Kingdom and Switzerland.

Dosage

Dried Kava root contains approximately 3-20% kavalactones, depending on the strain. Doses are given for kavalactone.

Oral
Light 50-70mg
Common 70-150mg
Strong 150-200mg
Heavy 300mg+

Duration

Note: Onset is faster with an increased dose.

Oral
Onset 20-30 minutes
Peak 3 hours
Total 3-6 hours
After-effects 9-18 hours

Effects

Postive

  • Mild euphoria
  • Relaxation

Neutral

  • Eyes become more sensitive
  • High doses cause somnolence (a state of near-sleep) that leads to a deep, dreamless sleep often described as restful

Negative

  • Lazy days after consumption of kava
  • Possible hepatotoxicity (liver damage)

Harm Reduction

  • Avoid driving and operating heavy machinery.
  • Pregnant women and people with endogenous psychoses should avoid Kava.
  • Various components of the plant have been shown to cause hepatotoxicity, though usually issues arise from contaminants due to poor quality control or conditions of growing. Ensure the product is acquired from a reputable source.

Interactions

Check out our Drug Combinations page and chart for interactions and combinations of common drugs.

Chemistry and Pharmacology

Research has suggested that kavalactones potentiate GABAA activity, but do not alter levels of dopamine and serotonin in the CNS. It is thought to do this via modulating GABA activity via altering the lipid membrane structure and sodium channel function.

Heavy, long-term kava use does not cause any reduction of ability in saccade and cognitive tests, but is associated with elevated liver enzymes.

Desmethoxyyangonin, one of the six major kavalactones, is a reversible MAO-B inhibitor (Ki 280 nM) and is able to increase dopamine levels in the nucleus accumbens. This finding might correspond to the slightly euphoric action of kava.

Kavain, in both enantiomeric forms, inhibits the reuptake of norepinephrine at the transporter (NAT), but not of serotonin (SERT). An elevated extracellular norepinephrine level in the brain may account for the reported enhancement of attention and focus.

Yangonin, another major kavalactone, has been demonstrated to act as a CB1 agonist. This mechanism is also responsible for the effects of THC and likely contributes to the psychoactive effects of kava.

Legal status

For a breakdown of the legal status of Kava click here.

Links

https://www.erowid.org/plants/kava/