www.SCELETIUM.org
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Sceletium – Kougoed – Kanna – A natural mood elevator
Sceletium tortuosum is a small groundcover plant native to Southern Africa. For hundreds of years the Hottentots of Southern Africa used Sceletium tortuosum as a mood enhancer, relaxant and empathogen. It is also known as Kanna or Kauwgoed, Kougoed and Canna.
Historically Sceletium tortuosum (Kanna) was chewed, smoked or used as snuff producing euphoria and alertness which gently fade into relaxation. If chewed in sufficient quantity Sceletium has a mild aneastheticeffect in the mouth, much like kava, and is used by the San tribes if you are about to have a tooth extracted, or in minute doses, for children with colic. A tea made from Sceletium/Kanna is sometimes used to wean alcoholics off alcohol.
Sceletium tortuosum has a long history of use in South African. In fact it is in it’s 4th century of recorded use there. With written records dating back to 1662, Sceletium was a bartering currency. Traditionally, the prepared dried plant material (called Kanna or Kougoed) was chewed and the saliva swallowed, but it has also been made into teas and tinctures. Less commonly, it has been reported that it used to be inhaled as a snuff, or smoked, usually with the addition of other herbs.
Kanna was used in rural areas in very small doses as a treatment for colic in infants, added to a teaspoon of breast milk, and this use still survives in some local communities.
Chemistry and Pharmacologyof Kanna
The mood-elevating action of sceletium is caused by a number of alkaloids including mesembrine, mesembrenol and tortuosamine which interact with the brain’s dopamine and serotonin receptors. Mesembrine is a major alkaloid present in Sceletium. Mesembrine has been demonstrated to be a potent serotonin-uptake inhibitoand serotonin releasing agent.
This receptor-specific activity, and receptor activities also found on nicotinic, dopamine and nor-adrenaline sites certainly validate the traditional mood-elevating uses, and suggest additional therapeutic and wellness potential.
By isolating this and other bio-chemically active compounds, researchers are now confirming what many people have known for many hundreds of years, that Sceletium has a remarkable ability to effectively treat symptoms of anxiety.
Mesembrine is an alkaloid which is derived from the Sceletium Tortuosum plant and is now being acknowledged as a key active component in the ability of the plant to produce beneficial effects which are closely related to it are the alkaloids mesembrenone, mesembrenol and tortuosamine, which are also present and produce very similar effects to mesembrine.
Fermenting Kanna increases mesembrenone and decreases mesembrine.
It is a confirmed serotonin (re)-uptake inhibitor, as understood by the US Patent office, which means that it regulates the effects of one of the brain’s most important neurotransmitters.
Tablets and capsules of Sceletium / Kanna are being used successfully by a number of psychiatrists, psychologists and doctors with excellent results for anxiety states and mild to moderate depression; and they can also be used by the lay public as supplements to elevate mood and for stress and tension.
In addition to Sceletium’s common use for the stress and mental fatigue of modern industrial living, Sceletium has been used as a natural supplement in:
- uplifts the mood
- decrease anxiety, stress and tension
- gives you energy
Sceletium elevates mood and decreases anxiety, stress and tension. Kanna has also been used as an appetite suppressant by shepherds walking long distances in arid areas. In intoxicating doses it can cause euphoria, initially with stimulation and later with sedation. Long-term use in the local context followed by abstinence has not been reported to result in a withdrawal state. Kanna is not hallucinogenic, and no severe adverse effects have been documented.
Sceletium is also being used as a natural anti-depressant that is said to be safer than many pharmaceutical alternatives.
Individuals suffering from depression and anxiety can benefit from Sceletium.
Mesembrine works thus:
The brain is made up of countless neurons, which transmit signals to each other only by jumping the gap (synapse) to neighboring neurons. The signal cannot however jump the synapse without assistance.
The message can only travel when the neuron releases a neurotransmitter to fill this gap and allow the signal to transient via it.
The receiving neuron has many points on its surface that which act as potential locks, each of which is known as a receptor and is effected by a particular type of neurotransmitter. When sufficient amounts of the neurotransmitter are received by the relevant receptor, a nerve impulse is started and the message continues to its ultimate destination. To permit recovery of the neuron to receive new messages, the brain takes away the neurotransmitter from the neuron receptors and permitting it to be sent back to the originating nerves, a process known as re-uptake.
In individuals suffering from depression, the neurotransmitter serotonin (also known as 5-hydroxytryptamine) is lacking. Mesembrine slows down the re-uptake process, making it more probable there will be more serotonin in the relevant receptors, greatly increasing the possibility that there will be sufficient levels to set up the signal transfer in all neighboring neurons.
Mesembrine allows the brain to function with reduced levels of serotonin, allowing time for natural levels to build up, whereupon the mesembrine dosage can be reduced or eliminated.
Very few people experience side-effects. The reported side-effects include occasional episodes of:
- Mild headache
- Slight nausea, no vomiting
- Soft stool or loose stool with no cramping
- Transient increase in anxiety or irritability an hour after initiating
treatment, which resolves after an hour or so - Insomnia: corrected by lowering the dose or taking the product not later than midday
- A feeling of sedation: corrected by taking the product as a single 50mg dose at night
NO severe adverse effects have been documented from using Kanna.
There have been no confirmed reports of drug interactions, However, because of the neuro-receptor activities of Sceletium there may be interactions with other pharmacokinetic drugs. People taking any psychiatric drug (including all anti-anxiety drugs, sedatives, hypnotics, antidepressants and anti-psychotics and so-called designer or recreational drugs) or any cardiac medications, are advised not to take Sceletium-containing products.
As with most supplements and modern drugs, safety in pregnancy for Kanna has not been established.
Sceletium is used to rebalance the brain and nervous system and thereby relieve symptoms of depression. Combined with other well known herbs, this formulation has been proven to be extremely effective and safe.
Sceletium and Mesembrine
Pharmaceutical Biology
1998, Vol.36, No.3, pp. 173-179
© Swets & Zeitlinger
The Distribution of Mesembrine Alkaloids in Selected Taxa of Kanna and their Modification in the Sceletium Derived `Kougoed’
Michael T. Smith , Courtney R. Field , Neil R. Crouch and Manton Hirst
Univ. Natal, Botany Dept., Pietermaritzburg, South Africa Natal Herbarium, Ethnobotany Programme, National Botanical Institute, Kaffrarian Museum, Kingwilliam’s Town, South AfricaTwenty species from nine genera of the Mesembryanthemaceae (Aptenia, Bergeranthus, Delosperma, Drosanthemum, Glottiphyllum, Lampranthus, Oscularia, Ruschia, and Sceletium) as well as the reportedly psychoactive preparation `kougoed’, prepared from `fermenting’ Sceletium tortuosum, were screened for the presence of the mesembrine alkaloids. Using gas chromatography (GC) with a nitrogen-phosphorous detector (NPD) three putative alkaloids were detected in Sceletium tortuosum whose mass spectra corresponded to those of 4′-O-demethylmesembrenol, mesembrine and mesembrenone. All the Mesembryanthemaceae plants investigated were shown to have Dragendorff-positive compounds on thin layer chromatograms (TLC); those containing mesembrine alkloids, as shown by later GC MS analysis, exhibited similar Rf values to the Sceletium alkaloids. Howev! er, using the technique employed in this study which encompassed the use of column and gas chromatography, the only genus containing mesembrine alkaloids to any significant extent was Aptenia. Alkaloid levels were found to be extremely low in all other taxa investigated. When a `modern’ technique for the preparation of a fermented Sceletium product, `kougoed’, was carried out it was found that levels, as well as the ratios, of the three alkaloids changed markedly. Substantial increases in total alkaloid levels were observed when the Sceletium material was crushed and bruised prior to drying for alkaloid extraction whereas no such changes occured when intact plants were oven dried at 80°C prior to alkaloid extraction. It is speculated that of the many potentially usable Mesembryanthemaceae plants available to the indigenous peoples, Sceletium was selected because it is the only genus with alkaloid levels high enough to! eli cit a psychoactive response. The traditional preparation technique also appears to have evolved as a method of producing a dry, stable, and relatively palatable preparation of increased pharmacological activity.
Keywords: 4′-O-demethylmesembrenol, ethnopharmacology, `kougoed’, mesembrenone, mesembrine, Mesembryanthemaceae, pharmacological activity, psychoactive, Sceletium
The Distribution of Mesembrine Alkaloids in Selected Taxa of Kanna and their Modification in the Sceletium Derived `Kougoed’
by Smith MT, Field CR, Crouch NR, Hirst M
Originally published in Pharmaceutical Biology 1998; 36(3): 173-179.
Michael T. Smith , Courtney R. Field , Neil R. Crouch and Manton Hirst
Univ. Natal, Botany Dept., Pietermaritzburg, South Africa
Natal Herbarium, Ethnobotany Programme, National Botanical Institute
Kaffrarian Museum, Kingwilliam’s Town, South Africa
ABSTRACT
Twenty species from nine genera of the Mesembryanthemaceae (Aptenia, Bergeranthus, Delosperma, Drosanthemum, Glottiphyllum, Lampranthus, Oscularia, Ruschia, and Sceletium) as well as the reportedly psychoactive preparation `kougoed’, prepared from `fermenting’ Sceletium tortuosum, were screened for the presence of the mesembrine alkaloids. Using gas chromatography (GC) with a nitrogen-phosphorous detector (NPD) three putative alkaloids were detected in Sceletium tortuosum whose mass spectra corresponded to those of 4′-O-demethylmesembrenol, mesembrine and mesembrenone. All the Mesembryanthemaceae plants investigated were shown to have Dragendorff-positive compounds on thin layer chromatograms (TLC); those containing mesembrine alkloids, as shown by later GC MS analysis, exhibited similar Rf values to the Sceletium alkaloids. Howev! er, using the technique employed in this study which encompassed the use of column and gas chromatography, the only genus containing mesembrine alkaloids to any significant extent was Aptenia. Alkaloid levels were found to be extremely low in all other taxa investigated. When a `modern’ technique for the preparation of a fermented Sceletium product, `kougoed’, was carried out it was found that levels, as well as the ratios, of the three alkaloids changed markedly. Substantial increases in total alkaloid levels were observed when the Sceletium material was crushed and bruised prior to drying for alkaloid extraction whereas no such changes occured when intact plants were oven dried at 80°C prior to alkaloid extraction. It is speculated that of the many potentially usable Mesembryanthemaceae plants available to the indigenous peoples, Sceletium was selected because it is the only genus with alkaloid levels high enough to! eli cit a psychoactive response. The traditional preparation technique also appears to have evolved as a method of producing a dry, stable, and relatively palatable preparation of increased pharmacological activity.
Source: www.sceletium.org
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