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| Mitragyna speciosa is barely known in the United
States, but one of the most interesting plants we have
ever found... |
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| Kratom grows in the lush rainforests in the South of
Thailand, and has the unique position of being banned in
the country it is indigenous to...true story... |
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Kratom: Nature’s Gift
to the Sick & Fit Alike
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by Victor Lasato
DISCLAIMER: The following article addresses a plant which is a powerful
drug. Just because it’s natural and legal (for now) do not write it off as
herbal-ecstasy crap or take it lightly if you decide to take it at all. I do
not condone the use of this or any drugs by anyone under 18 or anyone under
180lbs for that matter. In fact, drugs are bad, you shouldn’t do drugs,
mmmmmmK?
In mankind’s never-ending quest to gain an edge over genetic limitations,
feelings of discontent, and/or other members of the species, we often turn
to doctors and their prescription pads to fill our medicine cabinets and
ease our minds. Despite the massive pharmaceutical machine dominating modern
medicine, Mother Nature is still a source and inspiration for modern
medicines. Synthetic versions of human hormones are perhaps the best example
for Mind & Muscle readers. Another excellent example is seen in the Opium
Poppy and the dozens of natural and synthetic drugs that have been derived
from it. However, unlike hormones and opiates, one very versatile source of
pharmacologically active alkaloids, capable of producing three distinctly
different effects, has flown under the radar (at least in our neck of the
woods). Native to Thailand and Malaysia (and illegal in both countries as
well as Australia), the leaves of the Kratom tree (Mitragyna speciosa) may
be as close as modern medicine will get to the fabled panacea of
patent-medicine days. The claims made on antique medicine bottles from the
late nineteenth century, once laughable, may soon be laudable, and true.
Though heed this warning before reading on: Kratom is one plant that we do
not want to see go the way of ephedra, GHB, and PH/PS supplements. Myself
and other ethno-botanists envision fears of unethical chemists synthesizing
99% pure Mitragynine (Kratom’s major alkaloid) or other analogues; spawning
a new generation of junkies free-basing and mainlining what could improve
the quality of life for millions of people. Actually, we fear the
pharmaceutical industry using their foot-soldier-senators along with the FDA
will put the above scenario into the minds of millions of Americans. So
please, for the love of mankind, for the love of what freedoms we have left,
let’s not ruin this one too.
Pharmacology
Kratom contains over twenty different active alkaloids, the major one being
the indole-alkaloid Mitragynine.1 Other alkaloids vary depending on the age
and geographic origin of the plant. Specifically, studies of Kratom’s
constituents has led to the isolation of several “9-methoxy-Corynanthe-type
monoterpenoid indole alkaloids.”1 Although the analgesic effects of
Mitragynine resemble that of morphine (Mitragynine is approximately ¼ the
potency of morphine1), structurally the alkaloids are similar to those found
in the yohimbe tree (Corynanthe yohimbe). In fact, over twenty Corynanthe-type
Oxyindole alkaloids have been found in Kratom leaves, explaining its
differing effects at different doses. Yet why would alkaloids with
stimulant, appetite suppressant, and vasodilating properties completely
change their in vivo effects with larger doses, and activate kappa, delta,
and mu opiate receptors?
The answer is pretty involved. Anyone who has experimented with various
opiates knows that some knock you out (morphine, codeine), while others get
you wired (hydrocodone, Buprenex, oxycodone). Even these effects differ from
person to person. The effects of Mitragynine and several of its derivatives
were completely reversed by the opiate antagonist naloxone,1 proving
Mitragynine to be a potent opiate receptor agonist, though it’s not
technically even an opiate.
Bodybuilding Applications & Dosages
For legal reasons, this section will be limited. I am not a doctor, and even
if I were, I cannot claim “if you take X amount of Kratom, Y will happen”
without breaking any laws. That being said, as far as know (and I spent
quite a bit of time looking) there are no laws against purchasing or selling
Kratom for human consumption in the United States (there is conflicting
information on this). However, like many other legal botanicals, it is not
listed on the FDA’s GRAS list. There are currently five basic preparations
of Kratom available on the Internet. The first, and cheapest, is crushed,
dried leaf which contains ~2.5mg/g. of alkaloids. The second, resins, can
vary drastically; not just in alkaloid concentration, but in alkaloid
content as well. The reason being that some alkaloids are water soluble,
while others are soluble in alcohol, and still others in acetic acid (yes,
vinegar).
Resins are by far the easiest way to consume the herb, as they can be
heated, rolled into different size balls, and swallowed. However, caution
must be used as resins vary drastically between suppliers and even batches.
Different vendors use different techniques to extract the resin. Some
unscrupulous vendors even combine other plants into their resins to bring
the prices down. Ironically though, the resin I found to be the most potent
is also the least expensive.
Different retailers refer to different strength preparations by various
names, so to maintain objectivity rather than advocate one retailer, I will
refer to the different grades of powdered Kratom as: premium (~7mg/g.),
enhanced premium (~12mg/g.) and super-enhanced, which can range from
~15-20mg/g. of Mitragynine. The latter two simply infuse Kratom Resin over
the leaf to jack-up the alkaloid content. For safety’s sake, your best bet
is to find one retailer you like and stick to them. And, the biggest
retailer is not necessarily the best when it comes to Kratom.
There are three distinct dosing levels for Kratom: a light dose acts as a
stimulant, both mentally and physically and also suppresses the appetite.
The light dose by far has the most potential bodybuilding applications,
especially if some of the industry’s great minds start formulating their
“proprietary blends.” This dosage ranges from 1-5 g. of dried leaf,
depending on the grade and supplier. For more in-depth dosing guidelines,
click here to read what Erowid.org has to say. Myself and others have found
this dose to put one in a very focused state. It makes manual labor somewhat
enjoyable and, combined with certain stimulant amino-acids such as
L-tyrosine or ALCAR (NOT DLPA- we’ll discuss that later), is great for a
workout.
The second dosing threshold is more suited for coming home after a hard
day’s work and a grueling workout at the gym, and consists of approximately
twice the “light” dose. At this higher dose, Kratom has some crossover to
the mu-opiate receptors, possibly responsible for its addictive properties.
With the second and third dosing threshold, the addition of 200-500 mg. D,L-Phenylalanine
significantly increases the analgesia and euphoria; it can also cause nausea
and a bit of a crash afterwards. A higher dose can ease the mind, numb the
pain of DOMS without the drawbacks of anti-inflammatory medications, and
provide a legal alternative to people who like to catch a buzz, but don’t
enjoy alcohol. A word of advice for those of you who are “on”: there is
really no information regarding hepatic or renal impairment from Kratom.
At the third and highest dosing threshold Kratom takes on disassociative
effects, not unlike GHB or ketamine. Be warned though, there is no valid
reason for using Kratom at such doses. No one knows how toxic it may or may
not be. In addition, many people have reported severe tachycardia, paranoid
delusions, and other effects that may bring about a trip to the emergency
room. Never assume that just because you ate 5 grams of resin from supplier
X, that you can eat five grams from supplier Y, or even the same dose from a
different batch. If you’re going to go high dose with Kratom, resin is the
obvious choice, along with some ginger for the nausea. And NEVER go at it
alone.
Besides giving you an extra boost, or relieving the minor aches and pains of
daily life, Kratom has stepped up to the plate and cleared the bases where
even the strongest narcotics have struck out. Steven A. is a
life-long fitness enthusiast who has been using dietary supplements since
the industry first started expanding in the mid 90s. When his wife was
diagnosed with Multiple Sclerosis in 2001, he redirected his efforts to find
a natural way to help ease her pain and increase her quality of life. After
much research and frustration with bogus and/or overpriced product as well
as customs hassles Abrahamson added Kratom to his wife’s daily supplement
regimen. He noted that it, “seems to have a much better effect on her
overall pain and is less harsh on her system while also simultaneously
boosting energy levels. This has been a godsend as M.S. brings on the most
intense fatigue I have ever seen.” Abrahmson added that, “Kratom has allowed
her to again live life with much less synthetic pain killers and a
considerable amount more energy and overall quality [of life]. Kratom really
has been a gift.” Abrahamson, like many others, emphasizes that although
Kratom is a miracle plant for many people, retailers have a responsibility
to keep government regulation out of the picture.
Abrahamson, and his partner Stan Leavy, frown on retail sites that make wide
generalizations about Kratom. In effect, as Abrahamson puts it some sites
are, “slapping the FDA in the face by making wide medical claims on a retail
site which may or may not be true about Kratom's use as a pharmaceutical
replacement.” He adds that despite what many retailers are claiming about
Kratom’s safety, he himself almost overdosed, and urges people to use the
herb responsibly.
Is It Addicting?
Chronic use of Kratom, at any dose, is without a doubt habit forming.
Whether Kratom is actually physically addicting is still up for debate,
however Kratom chewers in Thailand tend to start in their mid to late
thirties and stay addicted for an average of twenty years.3 With daily use
comes tolerance and increased dosages, which correlate to more binding with
the mu opiate receptors and a higher chance of addiction. Going back to
pharmacology briefly, kappa and delta opiate receptors remain unchanged by
chronic administration of opiate agonists, while mu receptors become
drastically down-regulated causing tolerance and addiction4. This may
explain why Kratom is believed to be addicting after years of use and
constantly increasing dosages. The take-home lesson here, as with everything
in life, is moderation; not just in consumption of Kratom but in how we
discuss it, who we share it with, and exactly what we use it for. Another
proprietor of Kratom, Mike Mills, is a daily Kratom user by his own
admission, and has the following to say regarding its addictive potential “I
am not recommending that others should take it every day – it is a personal
choice. My own experience has been that Kratom is not highly physically
addictive, but it can certainly be habit forming, and can cause mild
discomfort if you stop taking it after continuous use for a while.”
Future Applications
Over the past thirty years, several derivatives of Mitragynine have been
developed for various applications. 7-hydroxymitragynine, was found to act
as an opioid agonist with higher potency than that of morphine.2,5 Another
derivative, Mitragynine Pseudoindoxyl, first synthesized in 1974, has a
higher affinity to bind to opiate receptors than morphine, and a ten-fold
greater binding affinity than Mitragynine.2 Only time will tell whether or
not these interesting compounds find their way into our medicine cabinets,
become demonized street drugs, or merely remain in the annals of medical
literature. One thing is certain though: with commercially available Kratom
becoming increasingly potent, Kratom will inevitably gain unwanted
attention.
While some retailers will no doubt play a large role in the downfall of
Mitragyna speciosa, it will be the individual who is truly responsible for
this marvelous plant’s future. That’s right, it’s up to the American (or any
country where it’s still legal) public to show some responsibility. If you
look at our track record, it would appear that Kratom is doomed. But do not
loose all hope—remember prohibition? We did it once and we can do it again
if need be.
For now though, get it while the getting’s good. Finally, I’d like to thank
Stan L., Steven A., Mike & Beth M., and
Bodhi for all your useful
information. As you’ve probably noticed, I did not plug any retail sites
that sell Kratom as I have a journalistic responsibility to remain
objective. However, we do have a forum for such discussion and I will be
glad to answer any questions on said forum in an honest and subjective
manner.
Check out this and other articles by Victor Lasato at
Mind & Muscle.
References
1. Takayama, Hiromitsu. “Chemistry and Pharmacology of Analgesic Indole
Alkaloids from the Rubiaceous Plant, Mitragyna speciosa.” Chemical &
Pharmaceutical Bulletin. 52(8) 916—928 (2004).
2. Leonardo T. Yamamoto, et. al. “Opioid receptor agonistic
characteristics of mitragynine pseudoindoxyl in comparison with mitragynine
derived from Thai medicinal plant Mitragyna speciosa.” General Pharmacology
33 (1999) 73–81
3. Suwanlert, Sangun. “A Study of Kratom Eaters in Thailand.” Bulletin
on Narcotics. 1975 v.27(3): 21-27. Online: 24 September 2005. Available:
www.erowid.org/plants/kratom/kratom_journal3.shtml
4. Bhargava, H.N. “Multiple opiate receptors of brain and spinal cord
in opiate addiction.” General Pharmacology. 1991;22(5):767-72.
5. Hiromitsu Takayma, et. al. “Formation of an Unusual Dimeric Compound
by Lead Tetraacetate Oxidation of a Corynanthe-Type Indole Alkaloid,
Mitragynine.” Chemical & Pharmaceutical Bulletin. 50(7) 960—963 (2002).
Specific to Mitragyna speciosa
(Kratom):
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