Kratom & Kratom Extract: What Is It?
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Kratom refers to the plant Mitragyna speciosa Korth.,
a tree indigenous to Thailand; it is mostly grown in the central and
southern regions of the country, and only rarely in the north. The Mitragyna
genus, part of the family Rubiaceae, is found in tropical and sub-tropical
regions of Asia and Africa. Asian Mitragynas are often found in rainforests,
while the African species (which are sometimes still classed in a separate
genus, Hallea) are often found in swamps. Most species are arborescent, some
reaching heights of almost 100 feet. The genus was given its name by
Korthals because the stigmas in the first species he examined resembled the
shape of a bishop's mitre. This genus is characterized by a globular
flowering head, bearing up to 120 florets each. During the flower bud stage,
the developing florets are surrounded and completely covered by numerous
overlapping bracteoles. Mitragyna species are used medicinally as well as
for their fine timber through the areas they grow.
Mitragyna speciosa itself reaches heights of 50 feet with a spread of over
15 feet. The stem is erect and branching. Flowers are yellow. Leaves are
evergreen, and are a dark glossy green in color, ovate-acuminate in shape,
and opposite in growth pattern. Kratom is evergreen rather than deciduous,
and leaves are constantly being shed and being replaced, but there is some
quasi-seasonal leaf shedding due to environmental conditions. During the dry
season of the year leaf fall is more abundant, and new growth is more
plentiful during the rainy season. When grown outside their natural tropical
habitat, leaf fall occurs with colder temperatures, around 4 degrees
Celsius.
Kratom prefers wet, humusy soils in a protected position. Being a heavy
feeder, it requires very rich, fertile soil. It is drought sensitive, and if
grown out of its native habitat, sensitive to frost. Propagation is by very
fresh seed or cuttings. There is a low strike rate, due to an endogenous
fungus which attacks xylem tissue.
Over 25 alkaloids have been isolated from kratom. The most abundant
alkaloids consist of three indoles and two oxindoles. The three indoles are
mitragynine, paynanthine, and speciogynine - the first two of which appear
to be unique to this species. The two oxindoles are mitraphylline and
speciofoline. Other alkaloids present include other indoles, and oxindoles
such as ajmalicine, corynanthedine, mitraversine, rhychophylline, and
stipulatine.
Mitragynine is the dominant alkaloid in the plant. It was first isolated in
1907 by D. Hooper, a process repeated in 1921 by E. Field who gave the
alkaloid its name. Its structure was first fully determined in 1964 by D.
Zacharias, R. Rosenstein and E. Jeffrey. It is structurally related to both
the yohimbe alkaloids and voacangine. It is more distantly related to other
tryptamine-based psychedelic drugs such as psilocybin or LSD. Chemically,
mitragynine is 9-methoxy-corynantheidine. It has the molecular formula
C23H30N2O4 and a molecular weight of 398.5. Physically the freebase is a
white, amorphous powder with a melting point of 102-106 degrees and a
boiling point of 230-240 degrees. It is soluble in alcohol, chloroform and
acetic acid. The hydrochloride salt has a melting point of 243 degrees.
The alkaloid content of the leaves of Mitragyna speciosa is about 0.5%,
about half of which is mitragynine. An average leaf weighs about 1.7 grams
fresh or 0.43 grams dried. Twenty leaves contain approximately 17mg of
mitragynine. All leaves appear to contain mitragynine, speciogynine,
paynanthine, and small quantities of speciociliatine. Oxindole alkaloids
usually occur only in small or trace ammounts.
Alkaloid content varies from place to place and at different times. Within
each location, there is a quantitative variation in alkaloid content from
month to month. While indole content seems to be fairly stable, oxindole
content shows tremendous variation.
Kratom is traditionally only used in Thailand, although some use in Malaysia
has been reported. Besides kratom (or krathom), it also goes by the names
ithang, kakuam, and in southern regions, thom. Use dates far enough back
that its beginning can't be determined. In addition to being used as a
narcotic drug in its own right, it is often used as a substitute for opium
when opium is unavailable, or to moderate opium addiction. In folk medicine,
it is often used to tread diarrhea. A small minority of users use kratom to
prolong sexual intercourse.
Users distinguish different types of kratom, two main kinds being
distinguished by the color of veins in the leaf - red or green/white. The
green-veined variety is supposed to have a stronger effect. One study which
surveyed Thai kratom users found that most users preferred a mixture of
both, followed by red-veined alone and then white-veined alone. Growers in
Australia report that both red and white veining occurs at different times
in different plants which were all cloned from the same mother plant. They
have not yet undertaken comparisons between the two.
Nearly all kratom use is by chewing fresh leaves. Other ways it is taken
include grinding up and eating fresh, dried, or reconstituted dried leaves.
Some villagers use the leaves in cooking. When preparing fresh leaf, the
vein is extracted and sometimes salt is added to try and prevent
constipation. Consumption of the leaf is usually followed by drinking
something hot, such as warm water or coffee. Leaves can also be smoked, made
into a tea, or a crude resin extraction can be made. This resin extract is
made by preparing a water extract of the leaves, boiling it down, and then
shaping it into small balls which are rolled in a material such as flour,
then stored until use. This is apparently a quite popular method of
consumption.
Users of kratom tend to be peasants, laborers, and farmers who use the plant
to overcome the burdens of their hard work and meager existences. Female
users are apparently quite rare. Age of usage onset seems to be higher than
for other drugs. Some studies have found no addiction problems in villagers
using kratom, while others apparently have. It seems likely that if used in
doses high enough for mu receptor crossover (discussed below), addiction is
a strong possibility. Heavy users may chew kratom between 3 and 10 times a
day. While new users may only need a few leaves to obtain the desired
effects, some users find with time they need to increase doses to 10-30
leaves or even more per day.
In some parts of the country, it was said that parents would choose to give
their daughters in marriage to men who used kratom rather than men who used
marijuana. The belief is that kratom users are hard working, while marijuana
users are lazy. This belief is also maintained by many of the users
themselves, who report beginning use because of a desire to work more
efficiently, and who say using the drug gives them a strong desire to do
work.
The Thai government passed the Kratom Act 2486 which went into effect on
August 3, 1943. This law makes planting the tree illegal and requires
existing trees to be cut down. This law was not found effective, since the
tree is indigenous to the country. Today, kratom is classed in the same
enforcement group as cocaine and heroin by Thai law, and has the same
penalties. One ounce of extract is punishable by death. As with prohibition
laws elsewhere in the world, this has succeeded only at increasing black
market prices. A related species, Mitragyna javanica, is often used as a
substitute to get around the law, but it is not considered as effective. The
dominant alkaloid in this species is mitrajavine, which has not yet been
pharmacologically tested.
While the main alkaloids in kratom are structurally related to psychedelics,
there appears to be no psychedelic activity. The dominant effects seem to be
similar to opiate drugs, and include analgesia and cough suppression. These
effects are roughly comparable in strength to codeine. Mitragynine
suppresses opiate withdrawal, but its effects are not reversed by the opiate
antagonist nalorphine. These opiate-like effects appear to be mediated
mostly by delta and mu opioid receptors. In lower dosages, mitragynine
exhibits a yohimbine-like binding to alpha-adrenergic receptors, as well as
some binding to the delta opioid receptors. As doses increase, binding to
delta receptors increases, and in yet higher doses, crossover to mu
receptors occurs. Interestingly, mu crossover is increased by the presence
of opiate drugs. While delta receptor selective opiate drugs have little
abuse potential, it seems that they could be used as a primer which would
allow mitragynine to more effectively bind to the mu receptor, which
mediates the euphoric high produced by narcotics such as morphine.
Other effects of mitragynine are a reduction in smooth muscle tone, local
anesthesia, and central nervous system depression. Acute side effects
include dry mouth, increased urination, loss of appetite, and constipation
coupled with small, blackish stools. Unlike opiates, mitragynine does not
appear to cause nausea or vomiting. Heavy use can result in a prolonged
sleep.
Side effects from long term use include anorexia and weight loss, insomnia,
and a darkening of the skin, particularly on the cheeks, giving an
appearance similar to a hepatic face. Among addicts, 30% report limited
sexual desire and the need to use a combination of kratom and alcohol to
become sexually stimulated. One study found 5 people who had psychotic
conditions which may or may not have been revealed by very heavy kratom use.
As discussed earlier, addiction seems to be a possibility if high doses are
used. Some withdrawal symptoms reported by addicts include hostility,
aggression, wet nose, inability to work, flow of tears, muscle and bone
aches, and jerky limb movement.
While one study of Thai users reported that it is sedative in low doses
changing over to stimulation in higher doses, this seems to be incorrect.
Most other sources say that it is a stimulant in lower doses, becoming
sedative in higher doses, which is consistent with mitragynine's receptor
binding profile. Effects come on within five to ten minutes after use, and
last for several hours. The feeling has been described as happy, strong, and
active, with a strong desire to do work. The mind is described as calm. The
Swiss biologist Claude Rifat experimented with a low dose of three smoked
leaves and reported the effects reminded him somewhat of SSRIs, in that it
blocked motivation, induced indifference, made doing everything boring, and
brought on a strong laziness. It seems likely that these two almost opposite
results may be influenced by cultural expectations.
Inspired by traditional use, H. Ridley reported In 1897 that the leaves of
Mitragyna speciosa were a cure for opium addiction. In more recent times,
mitragynine has been used in New Zealand for methadone addiction detox.
Kratom was smoked whenever the patient experienced withdrawal symptoms, over
a 6 week treatment period. Patients reported a visualization effect taking
place at night in the form of vivid hypnagogic dreams. While working on
plans for ibogaine experiments in the USA, Cures Not Wars activist Dana Beal
suggested that mitragynine could be used as an active placebo for comparison
in the study. Acting Deputy Director of the NIDA Charles Grudzinskas
rejected the proposal, however, saying that even less was known about
mitragynine than ibogaine.
Although chemically similar, ibogaine and mitragynine work by different
pathways, and have different applications in treatment of narcotic
addiction. While ibogaine is intended as a one time treatment to cure
addiction, mitragynine used to gradual wean the user off narcotics. The fact
that mitragynine's mu crossover is increased by the presence of opiate drugs
may be exploitable in the treatment of narcotics addiction, because it
directs binding to where it is needed, automatically regulating the
attachment ratio and modulating it towards the delta receptors over a short
time. Within a few days, the addict would stop use of the narcotic they are
addicted to, and the cravings and withdrawal will be moderated by the
binding of mitragynine to the delta receptors. Mitragynine could also
perhaps be used as a maintenance drug for addicts not wishing to quit but
trying to moderate an out of hand addiction.
In 1999, Pennapa Sapcharoen, director of the National Institute of Thai
Traditional Medicine in Bangkok said that kratom could be prescribed both to
opiate addicts and to patients suffering from depression, but stressed that
further research is needed. Chulalongkorn University chemists have isolated
mitragynine which researchers can obtain for study.
In conclusion, there seems to be much more research done into this plant and
its active constituents. Although kratom has been used since time immemorial
by Thai natives, Western science hasn't paid it that much attention. What
research does exist contains some apparent conflicts. Knowledge even of the
plant's existence outside of Thailand has been limited to ethnobotanists and
a handful of pharmacology researchers. Availability of live plants and dried
leaves has been practically non-existent until very recently.
There is much to learn.
Credits
Atthakor P. "Role Seen For Traditional Herbal Stimulant": Bangkok Post
November 27, 1999
De Rienzo P, Beal D, The Statten Island Project. "The
Ibogaine Story"
Idid S Z, Saad L B, Yaacob H, Shahimi M M. "Evaluation Of Analgesia Induced
By Mitragynine, Morphine And Paracetamol On Mice": ASEAN Review of
Biodiversity and Environmental Conservation, Nov-Dec 1999
Merck & Co., Inc. "The
Merck Index": 12th edition, 1996.
Oxford University Press. "Dictionary of Organic Compounds": Volume 4, 4th
edition, 1965.
Rifat, Claude. "Mitragynine": http://www.lycaeum.org/drugs/SSRI/mitragy.html
Shaman Australis. Mitragyna speciosa catalog entry: http://www.shaman-australis.com/Website/Mitragynaspeciosa.htm
Shaman Australis. Personal email from owner: shaman@shaman-australis.com
Shellard E J. "The alkaloids of Mitragyna with special reference to those of
Mitragyna speciosa, Korth": Bulletin On Narcotics, 1974 issue 2
Suwanlert M D Sangun. "A study of kratom eaters in Thailand": Bulletin on
Narcotics, 1975 issue 3
Thongpradichote S, Matsumoto K, Tohda M, Takayama H, Aimi N, Sakai S,
Watanabe H. "Identification of opioid receptor subtypes in antinociceptive
actions of supraspinally-administered mitragynine in mice": Life Sci
1998;62(16):1371-8
Yamada R. "Re: Is Mitragynine anti-addictive?": Usenet post
199702031505.KAA21187@interport.net |