Kanna

Common Name
Kanna
Scientific Name
Sceletium tortuosum
Mechanism of Action
Primarily inhibits the serotonin transporter (acting as an SSRI) and phosphodiesterase-4 (PDE4); also promotes the release of serotonin and other monoamines via VMAT2 modulation.
Route
Oral, Sublingual, Intranasal
Dose Amount
Traditional use involved a small quid of dried, fermented plant (several hundred milligrams of material) chewed for its juice. Modern commercial extracts (e.g. Zembrin®) are used at ~25 mg (standardized to ~0.4% total alkaloids) once daily, and dried herb capsules typically range from 50–200 mg per dose.
Onset
When chewed or taken sublingually, effects begin in ~5–15 minutes; with oral ingestion (capsules/tea) onset is ~30–60 minutes. Insufflated kanna can produce effects within just a few minutes.
Peak
Approximately 1–2 hours after administration (sooner via insufflation)
Duration
Roughly 4–6 hours of noticeable effects when taken orally or sublingually; shorter (2–3 hours) with insufflation.
Dose Notes
Kanna’s effects are dose-dependent: low doses provide subtle anxiolytic and mood-brightening effects, whereas higher doses can have more pronounced euphoria or sedation. Users are advised to start with low doses to gauge sensitivity.

Overview

Kanna is a low-growing succulent plant native to South Africa, renowned for its mood-altering and anxiolytic properties. Scientifically identified as Sceletium tortuosum, this unassuming herb has long been used by indigenous Khoisan peoples as a natural remedy to “take the edge off” – relieving anxiety, lifting mood, and even suppressing hunger and thirst on long huntspubmed.ncbi.nlm.nih.goven.wikipedia.org. Traditionally, tribes would ferment and chew kanna (the dried preparation known as kougoed, meaning “chewable thing”) to experience gentle euphoria, stress relief, and enhanced sociability. Unlike overtly hallucinogenic plants, kanna induces no visions or dissociation; its psychoactive effects are subtle, characterized by calm upliftment and mental clarity. In recent years, kanna has caught the attention of ethnobotanists and neuropharmacologists worldwide for its potential as a novel therapeutic in mental health. The plant’s chief active compounds – mesembrine and related alkaloid molecules – interact with the brain’s serotonin system and other neural targets to produce antidepressant and anxiolytic effectspubmed.ncbi.nlm.nih.goven.wikipedia.org. Preliminary clinical studies in healthy volunteers have shown that a standardized kanna extract can reduce activity in the brain’s fear center (the amygdala) and improve stress reactivitydrugs.compubmed.ncbi.nlm.nih.gov, lending scientific credence to its traditional reputation as a “mood tonic.” Though more research is needed, kanna stands out as a prime example of a neurobotanical – a plant that bridges indigenous wisdom and modern neuroscience. It offers an intriguing, natural avenue for enhancing mood, resilience to stress, and cognitive well-being, all while carrying the rich cultural legacy of southern Africa into contemporary usage.

History & Cultural Context

Kanna’s story begins in the arid plains and karoo of South Africa, where it has been an integral part of San and Khoikhoi (Khoisan) culture for perhaps millenniaen.wikipedia.org. In these communities, Sceletium tortuosum was far more than a casual mood enhancer – it was a sacred ally for survival and spirit. Khoisan healers and hunters would prepare kougoed by fermenting the succulent leaves and stems in closed containers (often burying or bagging the plant matter) and then drying it under the sundrugs.com. This cured product could be chewed slowly, releasing salivary juices that were swallowed to impart a sense of calm euphoria, stamina, and hunger suppression. Oral tradition holds that kanna chewing helped alleviate fear, loneliness, and physical pain during long journeys in the desert, while also quenching thirst and suppressing appetite when game and water were scarcepubmed.ncbi.nlm.nih.goven.wikipedia.org.

Early written accounts of kanna by European colonists date back to the mid-17th century. In 1662, Jan van Riebeeck – founder of the Dutch Cape Colony – recorded trading for a plant called “Kanna” from local Khoi, describing it as a coveted item thought to “cheer the spirits”sceletium.org. Later explorers like Simon van der Stel in 1685 documented Sceletium in the wild and even commissioned illustrations of the plantsceletium.com. By the 18th century, kougoed had become a notable trade commodity in the Cape: colonial writings compared its effects to those of mandrake or ginseng in their ability to revive and comfort the mindsceletium.org. One 18th-century account by German settler Peter Kolben effusively called kanna “the greatest Cheerer of the Spirits, and the noblest Restorative in the World,” noting its similarity to mandrake in its mood-elevating effectssceletium.org. Despite such glowing testimonials, Kanna was not viewed as a hallucinogen by these observers but rather as a narcotic comforter – something to soothe nerves and lift mood without causing intoxication in the dramatic sense.

Within indigenous culture, kanna was often used socially and spiritually. Oral histories suggest that Khoisan communities would chew kanna in group settings to foster relaxation and communal bonding after days of hunting and gathering. It was sometimes taken before ritual dances or trance ceremonies, and intriguingly, anthropologists have noted a symbolic link between kanna and the eland antelope in San spiritualitysceletium.orgsceletium.org. The eland – often depicted in San rock art – is considered a trance animal, symbolizing potency and spiritual power; the Khoi of the Little Karoo used the same word “kanna” for Sceletium and for the eland, hinting at a mystical association between the plant’s effects and the eland’s trance-inducing vitalitysceletium.org. Some early reports even mention that chewing kanna (especially when mixed with cannabis, locally known as dagga) could inspire spontaneous dancing and a joyful, tipsy camaraderie among the Khoisceletium.orgdrugs.com.

As colonial influence expanded, traditional knowledge of kanna declined – often suppressed or forgotten amidst cultural upheaval. Yet the practice never fully died out. In rural South African communities, elders quietly passed down the methods of preparing kougoed. Folk uses of kanna persisted for treating ailments: a bit of kanna would be given to colicky infants to soothe them, or a fresh leaf applied to an aching tooth to numb the paindrugs.com. These uses illustrate the plant’s versatility as both medicine and masticatory. In the late 20th century, interest in kanna experienced a revival. Ethnobotanists and Afrikaner herbalists published accounts of Sceletium, leading to renewed appreciation of its cultural heritage and psychoactive properties. Notably, South African researchers like Dr. Nigel Gericke began cultivating kanna and investigating its chemistry in the 1990s, coinciding with a global resurgence in “herbal highs” and natural therapeutics. By the early 2000s, commercial cultivation programs were established to meet growing demand while protecting wild populationstrugen3.comtrugen3.com. Today, kanna is exported worldwide as an ethnobotanical supplement. There is also an important ethical dimension: modern developers of kanna extracts (such as the patented formula Zembrin®) have engaged in benefit-sharing agreements with the San people, acknowledging the indigenous knowledge at the root of kanna’s popularity. Thus, the cultural journey of kanna—from the firesides of Khoisan camps to international nutraceutical markets—underscores a blend of mystique and medicine. It remains both a cultural treasure of South Africa and a subject of global scientific fascination.

Chemistry & Pharmacology

Phytochemistry: Kanna contains a suite of biologically active alkaloids, collectively termed “mesembrine-type” alkaloidspubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov. Over two dozen alkaloids have been identified in Sceletium tortuosum to date, falling into several structural classes (mesembrine, mesembrenone and related Δ⁷ mesembrine isomers, as well as rarer types like Sceletium A4, joubertiamine, and tortuosamine)pubmed.ncbi.nlm.nih.gov. The mesembrine class is the most abundant and pharmacologically significant. Mesembrine itself is a prominent compound first isolated from kanna in the late 19th century, and it can constitute up to ~0.3% of the plant’s dried leaves (higher concentrations are found in stems, up to ~0.8%)drugs.com. Other major alkaloids include mesembrenone, mesembrenol (mesembrinol), and tortuosamine, among othersdrugs.comdrugs.com. Interestingly, the traditional fermentation process markedly alters kanna’s alkaloid profile. Fresh (unfermented) plant material actually contains higher total alkaloid content than the dried kougoed; during fermentation, a portion of mesembrine is enzymatically converted to Δ⁷-mesembrenonedrugs.com. This transformation reduces mesembrine’s concentration dramatically (one analysis found mesembrine dropping from ~1.3% down to 0.05% after fermentation)drugs.com. Some have hypothesized that indigenous fermenting methods were aimed not at increasing potency, but at degrading potentially harsh compounds – for example, oxalates in the plant that can irritate the stomach and kidneyssceletium.orgsceletium.org. Fermentation may break down oxalates and also produce mesembrenone, which could slightly shift the subjective effects. In any case, both mesembrine and mesembrenone contribute to kanna’s activity profile, and modern chemical analyses confirm that properly cured kougoed retains an abundance of alkaloids, albeit in a somewhat different balance than the raw plantdrugs.comdrugs.com.

Mechanisms of Action: The pharmacology of kanna is unique, acting on multiple neurochemical pathways. Primarily, mesembrine and related alkaloids function as serotonin reuptake inhibitors (in the same general manner as SSRI antidepressants). Mesembrine has extremely high affinity for the serotonin transporter (K<sub>i</sub> ≈ 1.4 nM)en.wikipedia.org, meaning it potently blocks the reuptake of serotonin into neurons, thereby increasing serotonin levels in synapses. This action is believed to underlie much of kanna’s mood-elevating and anxiolytic effect, as enhanced serotonergic signaling can produce feelings of calm and well-being. In fact, S. tortuosum extracts standardized for mesembrine show antidepressant-like properties in animal models, supporting the role of this mechanismen.wikipedia.org. However, kanna’s pharmacology doesn’t stop at serotonin reuptake. It has a dual action on the phosphodiesterase-4 (PDE4) enzymeen.wikipedia.org. Mesembrine itself is a weak PDE4 inhibitor (K<sub>i</sub> ~7.8 µM)en.wikipedia.org, and other alkaloids (like mesembrenone) may contribute to this effect. Inhibiting PDE4 raises cAMP levels inside cells, which in the brain can lead to anti-inflammatory effects and enhancement of cognitive processes (PDE4 is a target for pro-cognitive and anti-depressant drug research)drugs.com. The significance of PDE4 inhibition by kanna is still being studied, but it likely synergizes with serotonin reuptake inhibition to produce a unique therapeutic profile – potentially improving mood and anxiety while also promoting neuroprotection and cognitive flexibilitydrugs.comdrugs.com.

Notably, recent research indicates that at least some kanna alkaloids act as releasing agents for monoamine neurotransmitters. A high-mesembrine extract was found to increase the release of serotonin and other monoamines by upregulating the vesicular monoamine transporter (VMAT2), rather than acting purely as a reuptake blockeren.wikipedia.org. In practical terms, this means kanna may boost serotonin availability through two avenues: preventing its reuptake and stimulating its release. This dual action has prompted comparisons to empathogenic substances, though kanna’s effect is far milder (discussed further below). There is also evidence that kanna’s alkaloids have mild inhibitory effects on enzymes like acetylcholinesterase (AChE) and monoamine oxidase-A (MAO-A)en.wikipedia.org. These effects are modest, but they could contribute to kanna’s overall pharmacological profile – for instance, slight AChE inhibition might enhance cognitive function or alertness, and slight MAO-A inhibition could further elevate monoamine levels (though not nearly to the degree of pharmaceutical MAOIs).

Pharmacokinetics: Formal pharmacokinetic data on kanna in humans are limited, but its traditional use and modern anecdotal reports provide insight. The alkaloids in S. tortuosum appear to be readily absorbed via the oral and sublingual/buccal routes. Chewing fermented kanna allows transmucosal absorption in the mouth, leading to a fairly rapid onset of effects (often within minutes). Swallowing the plant matter or taking kanna as a capsule/tea results in absorption through the GI tract, with onset typically in 30–60 minutes as the alkaloids reach systemic circulationhealingherbals.storehealingherbals.store. Users often notice that sublingual or nasal (insufflated) administration produces faster but somewhat shorter-lasting effects than oral ingestionhealingherbals.storehealingherbals.store. A common report is that, after an oral dose, gentle effects begin by the half-hour mark, peak around 1–2 hours post-intakehealingherbals.store, and then gradually taper off over the next few hours, with the primary experience lasting about 4–6 hourshealingherbals.store. By contrast, insufflation of kanna can induce effects almost immediately (within ~5 minutes), but the peak might arrive within 30–60 minutes and fade by 2–3 hourshealingherbals.storehealingherbals.store.

The distribution and metabolism of mesembrine alkaloids in the body are still being studied. Mesembrine is a relatively lipophilic molecule, suggesting it crosses the blood-brain barrier efficiently. Some in vitro work using animal tissues indicates these alkaloids can permeate mucosal membranes welldrugs.com, aligning with the efficacy of sublingual use. In terms of elimination, no severe accumulation has been noted in animal studies; for instance, rats tolerated very high daily doses (several grams per kg) of kanna extract without organ damage or toxic buildupen.wikipedia.org. It is presumed that the liver metabolizes mesembrine-type alkaloids via typical alkaloid pathways (e.g., cytochrome P450 enzymes), but specific metabolites have not been well characterized publicly. Some fraction is likely excreted in urine as transformed metabolites within 24 hours. Kanna’s pharmacokinetic half-life in humans isn’t published, but given the duration of effect and daily dosing in trials, a rough estimate might be on the order of a few hours (perhaps 4–8 hours). This aligns with users feeling back to baseline by the next day with no lingering effects, aside from a subtle afterglow of calm for some. Notably, a 9-week clinical study found no accumulation of adverse effects over time, implying that steady-state levels of kanna’s actives do not dramatically increase with daily usedrugs.comdrugs.com.

Neuropharmacological Effects: The combination of serotonin modulation and PDE4 inhibition makes kanna pharmacologically intriguing. Neuroimaging and neurochemical studies give a glimpse of its impact on the brain. In a placebo-controlled fMRI study, a single 25 mg dose of a kanna extract (Zembrin) significantly dampened amygdala reactivity when participants were exposed to fearful/threatening stimulidrugs.com. The extract also reduced the coupling between the amygdala and hypothalamus – essentially “turning down the volume” on the brain’s fear and stress circuitrydrugs.com. Such effects align with the reported anxiolytic (anxiety-reducing) properties of kanna and suggest a direct serotonergic calming action in limbic regions. Additionally, EEG studies in animals (electropharmacograms) have indicated dose-dependent enhancement of frontal brain wave patterns associated with cognitive arousal and focus when high-mesembrine kanna extracts are administereddrugs.com. There is preliminary evidence that kanna’s alkaloids can protect neurons under stress: in vitro, mesembrine-rich extracts reduced inflammatory damage in astrocyte cells, whereas mesembrenone-rich extracts were less neuroprotective and even cytotoxic at high dosesdrugs.comdrugs.com. This finding suggests that mesembrine (the dominant alkaloid in unfermented material) might be more beneficial for cognitive effects, whereas too much mesembrenone could be counterproductive – a nuance that could explain why traditional preparation opted to lower mesembrine content (to avoid peripheral side effects) but not eliminate it entirelydrugs.comsceletium.org.

Overall, from a pharmacological perspective, kanna functions as a sort of natural SSRI with a twist: it boosts serotonin and also tweaks other pathways involved in mood, stress, and cognition. This polypharmacology might underlie the broad array of effects reported, from mood elevation and anxiolysis to improved focus and even libido enhancement (PDE4 inhibition can theoretically aid sexual function, and anecdotal use of kanna as an aphrodisiac has been noted in modern products)drugs.comtabs.co. It’s important to note, however, that kanna is not a hallucinogen or a classical psychostimulant – its pharmacological effects yield a subtler profile (as discussed in the next section), and at typical doses it does not induce dramatic alterations in perception or heart rate/blood pressure. This gentle yet multifaceted mechanism of action is what makes kanna a compelling subject for further neuropsychiatric research, especially as a candidate for managing anxiety and depression in a novel waypubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov. Indeed, some researchers have pointed out that kanna’s mixed mechanism might resemble a mild form of MDMA-like activity (because of monoamine release) combined with an SSRI’s steady support of serotonin – but without the stimulant overload or neurotoxicity concerns of synthetic drugsverywellmind.comverywellmind.com. As one clinician famously quipped, “Comparing kanna to MDMA is like comparing a high dose of caffeine to cocaine” – highlighting that while kanna can elevate mood and reduce inhibitions, its effect is far more subtle than potent entactogensverywellmind.com. This balance between efficacy and gentleness is a key theme in understanding kanna’s pharmacology.

Subjective Profile

Mental and Emotional Effects: Kanna is often described as a gentle mood enhancer and anxiolytic, producing a state that users characterize as calm, content, and clear-headed. After consuming kanna (whether chewing a quid or swallowing a tablet), individuals typically feel a gradual lifting of anxiety and stress. Within the first hour, a subtle euphoria may bloom – not an intense “high,” but a noticeable improvement in mood and outlookverywellmind.comverywellmind.com. One might experience a sense of inner tranquility or emotional resilience: problems seem less pressing, and a quiet optimism or “everything is okay” feeling settles in. In line with its traditional uses, kanna often reduces social inhibitions. Users report feeling more comfortable and talkative in social settings, with increased empathy and ease of connection. This has led some to nickname kanna “Nature’s MDMA,” although, as mentioned, its effects are much milder than the euphoric rush of true MDMAverywellmind.com. A better analogy is that kanna can make one feel like they’ve had a glass of good wine – an anxiety-relieving relaxation – combined with the clear-minded stimulation of a cup of coffeeverywellmind.com. Indeed, many users note a dual effect: simultaneous relaxation and mental activation. Low-to-moderate doses of kanna tend to sharpen cognitive focus slightly (some describe a “mind-clearing” or nootropic effect where thoughts become more organized), likely due to enhanced serotonin and slight PDE4-related alertness. At the same time, there’s a reduction in negative self-talk and rumination, contributing to a calmer mental space.

Physical and Sensory Effects: Kanna’s physical effects are generally subtle and mostly positive or neutral. Unlike stimulants, it does not typically raise heart rate or blood pressure significantly; instead, a mild bodily relaxation is common. Muscular tension may ease, and at higher doses some sedation or drowsiness can occurtabs.cotabs.co. In fact, some people use kanna in the evening to unwind or improve sleep (consistent with traditional use as a sedative tea) – though timing and dosage are key, as taking too much kanna too late might cause grogginess the next morning for some. Kanna has analgesic properties as well: historically it was used to relieve pain from toothaches or abdominal cramps, and modern users occasionally note that minor aches (headaches, muscle soreness) diminish after taking kanna. This analgesia may be partly due to direct effects on opioid or cannabinoid pathways (unconfirmed) or simply a consequence of elevated mood and relaxation threshold for pain. When kanna is chewed or insufflated, one tangible sensation is a slight local numbing or tingling of the gums, tongue, or nasal passages – this is likely due to the presence of oxalic acid crystals and alkaloids acting locally. It’s not unpleasant for most, and indeed the numbing was traditionally valued for dental pain reliefdrugs.com.

Sensory perception is not dramatically altered under kanna, which distinguishes it from psychedelic botanicals. Colors and sounds might gain a gentle richness simply because one is in a better mood, but there are no hallucinations or sensory distortions. If anything, some users feel a light enhancement of tactile sensation and sexual arousal, which ties into kanna’s reputation as an aphrodisiac. The combination of reduced anxiety and increased serotonin can heighten libido and ease, for example, social or performance anxieties that interfere with intimacy. Kanna is an ingredient in certain modern “sensuality” supplements and chocolates for this reasontabs.co, though its effects on libido are secondary to its primary calming action.

Dose-Dependent Variations: The subjective effects of kanna do depend on the dose and preparation. At low doses (say, 25–50 mg of a standard extract or a small pinch of raw herb), the effects are quite subtle – a slight mellowing of mood, a touch of mental brightness, akin to having done a short meditation. Some first-time users at low doses may even report “I didn’t feel much except maybe a bit more relaxed.” At moderate doses (for instance, 100–200 mg of raw herb or ~50 mg extract), the classic effects emerge: noticeable anxiety reduction, mood elevation, and sociability. One may feel more talkative, more interested in engaging with others, and everyday annoyances seem to slide off one’s back. There is often a gentle energy boost or motivation increase, described as a “positive drive” to do tasks without the edginess of caffeine. Concurrently, there is emotional warmth and empathy, which is why kanna has occasionally been used in group therapy or heart-to-heart social situations. At these moderate doses, many people also experience the flow state type of focus – enhanced concentration and present-mindedness, making it popular among students or professionals seeking a natural aid for work-related stress and attention. At higher doses, the effects can shift. Very large amounts of kanna (especially potent extracts or concentrates) do not infinitely increase euphoria; instead, users report diminishing returns or even reversal of effects. For example, an excessively high dose might lead to overstimulation or jitteriness, probably because too much serotonin in certain brain areas can cause restlessness and because PDE4 inhibition at high levels might lead to nausea or dizziness (a known effect of strong PDE4 inhibitors). Some individuals who have experimented with high doses (>200 mg extract or several grams of herb) report transient headaches, nausea, or agitation, confirming that “more is not always better” with kannatabs.cotabs.co. Intriguingly, experienced users note a “plateau” effect: once the serotonin transporters are fully occupied by mesembrine, additional amounts won’t produce more bliss and could instead trigger irritability or anxiety – a phenomenon also mentioned by therapists familiar with kanna, who observe that raising the dose beyond a point paradoxically increases anxiety rather than relieving itverywellmind.comverywellmind.com. Thus, kanna teaches moderation; its subjective benefits are best at moderate intake.

Aftereffects and Tolerance: One of kanna’s appealing aspects is the gentle comedown and minimal hangover. As the primary effects wane (after 4–6 hours orally), users are typically left with a residual calm for a few more hours. There is no “crash” or rebound anxiety in most cases – rather, people often report sleeping well after an evening dose, or if taken in daytime, they continue about their activities feeling normal, just a bit more serene. Side effects during the experience are usually scarce (more on safety in the next section), and unlike many synthetic anxiolytics or stimulants, kanna does not commonly cause heavy sedation or insomnia at normal doses. The aftereffects, if any, might include a pleasant afterglow of improved mood into the next day, or just a neutral return to baseline. Physically, there’s no hangover except slight dehydration if one forgot to drink fluids (serotonin elevation can increase thirst, as seen in one trial where increased thirst was noted as a mild side effect)drugs.comdrugs.com.

Regular daily use of kanna, however, can lead to tolerance. Repeated dosing over consecutive days tends to dull the subjective effects. Users find that by the third or fourth day of daily use, the mood boost is less pronounced. The traditional practice was not to chew kanna habitually all day every day, but rather as-needed, which likely prevented strong tolerance buildup. Modern clinical observations concur: a psychologist has noted that taking kanna too frequently can reduce its efficacy, and attempting to overcome this by increasing the dose doesn’t work – instead it might reintroduce anxietyverywellmind.comverywellmind.com. For this reason, kanna is often suggested to be used intermittently or on days when extra support is desired, rather than as a continuous daily supplement (unless under guidance for a specific therapy). On the plus side, tolerance to kanna seems to fade after a short break, and there are no significant withdrawal symptoms reported. People do not crave kanna or experience a comedown beyond wanting the continued sense of well-being. This aligns with kanna’s lack of classical addiction potential. In summary, the subjective profile of kanna is one of subtle yet meaningful positive shifts in mood and mindset: it brings about relaxation without fogginess, stimulation without jitters, and social ease without loss of control. It’s a plant that gently opens the door to a brighter mental space, but allows the user to walk through on their own – an effect deeply appreciated by those who seek natural alternatives for anxiety and low mood.

Preparation & Forms

Traditional Preparation: The most time-honored form of kanna is kougoed, the dried fermented plant material. Indigenous preparation of kougoed was an art passed down generations. Typically, harvested Sceletium tortuosum plants (leaves, stems, and sometimes roots) were crushed and bruised between stones or with a mallet to liberate juices, then tightly packed into a closed container (such as a skin bag or clay pot) to fermentdrugs.com. The mash was often left in the sun or a warm place for several days. During this fermentation, naturally occurring bacteria and enzymes break down certain plant components (as discussed, reducing oxalates and converting some alkaloids). The process was sometimes accompanied by ceremonial care – for instance, keeping the ferment out of direct evil spirits, according to lore, or adding a bit of previous batch as a “starter.” After fermentation (ranging from 2 days up to a week depending on custom), the now semi-moist mass was spread out and dried under the sun until it became brown, fibrous, and crumblydrugs.com. This final product, kougoed, could be stored for long periods and was easy to transport wrapped in animal hide or gourds. To administer it, a “plug” of kougoed about the size of a marble or larger was typically chewed slowly. Kanna is quite bitter, but chewers would keep the quid in the cheek, periodically squeezing out the juices and swallowing saliva. The fibrous remains would eventually be spat out. Traditional users might chew kanna for hours in the evening or during social encounters, much like how coca leaves are chewed in the Andes.

Aside from chewing, other folk methods existed. Dried kanna could be ground into a powder and used as a snuff (insufflated through the nose)drugs.comen.wikipedia.org. Some Khoisan groups practiced this, claiming it cleared the head and acted faster – though it could sting the nostrils due to the plant’s coarse particles. Kanna was also smoked or blended with other smoking herbs. Historical accounts describe the Khoi occasionally mixing kanna with cannabis (dagga) in their pipes to potentiate the effects of bothdrugs.com. Smoking pure kanna was less common but known; the smoke was said to produce a quick, euphoric calm that didn’t last as long as chewing. Additionally, kanna could be made into a tea or decoction. Early Cape settlers and indigenous people alike sometimes brewed kanna into a medicinal tisane, drinking it as a relaxant or soporific (for instance, to lull children to sleep)drugs.com. Another interesting traditional use was topical or sublingual application of the fresh plant: a fresh kanna leaf might be placed directly on a painful tooth or a few drops of juice squeezed under the tongue as a quick remedydrugs.com. These methods hint at kanna’s local anesthetic and rapid absorption properties.

Modern Forms: Today, kanna is available in a variety of preparations, bridging traditional practices and contemporary convenience. The whole dried herb (fermented) can still be purchased from ethnobotanical suppliers – often shredded or powdered kougoed, to be chewed or brewed by the end user. For those who chew, some vendors provide pressed “kanna chew tabs” or simply advise rolling the dried plant into a quid with chewing gum. Capsules and tablets are a very popular form: these typically contain milled S. tortuosum herb or extracts thereof, in doses usually ranging 50 mg to 200 mg per capsuledrugs.comdrugs.com. The advantage is precise dosing and ease of ingestion, though the onset is slower (since one usually swallows the capsule). Standardized extracts have been developed to ensure consistent alkaloid content. Zembrin®, the most well-known proprietary extract, is standardized to about 0.4% total alkaloids (mesembrine, mesembrenone, etc.) and is often sold in 25 mg tablets – a dose used in clinical studies for daily stress reliefdrugs.com. Other extracts (with brand names like Trimesemine) emphasize a high-mesembrine profile. Extracts may be made via alcohol or water extraction from the plant, yielding a concentrated powder sometimes labeled by “X” strength (e.g. a 10× extract means 10 grams of plant per gram of extract). Users of raw kanna should be mindful of these extracts’ potency, as a small amount can equal a much larger dose of plain herb.

Additionally, kanna is increasingly found in herbal blends and functional products. For instance, some nootropic or mood-enhancing supplements combine kanna with other ingredients (like L-theanine or Rhodiola) to create a synergistic formula. There are also teas that mix kanna with calming herbs like chamomile or peppermint to mask its bitterness and add to relaxation. An emerging trend is kanna chocolates and edibles – niche companies infuse dark chocolate with kanna extract, capitalizing on chocolate’s own mild psychoactive effects (via theobromine and flavonoids) to complement kanna. These “mood chocolates” or “aphrodisiac chocolates” aim to deliver a pleasant social buzz and are marketed for date nights or stress relief snackstabs.co.

For those looking for immediacy, kanna can be vaporized or insufflated in its pure form. Insufflation (snorting) of kanna powder has gained some popularity among experimenters because of the rapid onset. Finely sifted kanna (or an isolate of mesembrine) is insufflated in small amounts (say 50 mg), yielding a quick mood lift. However, many users find the nasal irritation unpleasant and the duration short, so this is not mainstream. Sublingual use without chewing is another method: placing a pinch of powdered kanna under the tongue and holding it there for ~15 minutes can allow absorption without the need to actually chew the fibrous material. Tinctures of kanna (alcohol-based liquid extracts) are also available – a dropperful under the tongue provides a fast route for those who don’t like capsules.

It’s worth noting that fresh kanna plant is seldom used in modern practice (most prefer the fermented dried material as it’s considered “activated” and safer due to lower oxalates). Nonetheless, some growers of Sceletium may experiment with juicing the fresh plant or making their own kougoed at home following traditional guidelines. Seeds and live plants of S. tortuosum can be purchased by enthusiasts, as the plant is relatively easy to grow in arid climates or indoors as a succulent. Home preparation requires caution to avoid mold during fermentation, but it allows a hands-on appreciation of the traditional craft.

In summary, whether one chooses to chew it like the ancients or pop a modern capsule, kanna is accessible in many forms. Traditionalists might argue there is something special about the slow mastication ritual and the full-spectrum crude plant, whereas pharmacologists point to standardized extracts as the future for precise dosing and therapeutic use. Both perspectives co-exist in today’s use of kanna – reflecting a blend of old and new. What remains constant is that the fundamental experience of kanna is tied to the plant’s alkaloids, which survive through these various preparations to deliver the characteristic calming uplift.

Safety & Cautions

Kanna has a long history of indigenous use and appears to be well-tolerated in healthy individuals, but like any bioactive substance it comes with precautions. Overall, Sceletium tortuosum is considered to have low toxicity. In animal studies, even very high doses did not produce organ damage or lethal effectsen.wikipedia.org. Indigenous peoples administered it to infants (in tiny quantities for colic) and the elderly alike, which attests to its general safety when used responsiblydrugs.com. Modern clinical trials in adults using standardized extracts (e.g. 25 mg Zembrin daily for several weeks) reported no serious adverse events and only mild side effects with similar frequency to placebodrugs.comdrugs.com. Nonetheless, users should approach kanna with due caution and awareness:

Common Side Effects: The most frequently reported side effects of kanna are quite mild. Some users experience digestive discomfort – this can manifest as a slight stomach ache, nausea, or soft stools, especially if kanna is taken on an empty stomach or in higher dosestabs.cotabs.co. This is possibly due to tannins or other compounds in the herb irritating the gut. Taking kanna with food or in capsule form mitigates this for most people. Headache is another occasionally noted effecttabs.co. Because kanna influences serotonin (a vasoconstrictor in the brain), it might provoke mild headaches in those sensitive to serotonergic changes, similar to how some SSRIs initially cause head tension. Staying hydrated and keeping the dose moderate usually prevents thistabs.cotabs.co. Some individuals report drowsiness or fatigue, particularly if kanna is taken in a large dose or combined with other sedativestabs.co. In essence, if the calming effect overshoots, one might feel inclined to nap. Conversely, a few users (especially first-timers or with low anxiety to begin with) could feel a bit stimulated or jittery if the dose is a bit high – this is less common but speaks to individual variability. It underscores the recommendation to start with low doses to see how one reacts.

Mood and Cognitive Effects: While kanna is generally mood-positive, improper use can cause mood disturbances. For example, taking kanna too often or in excessive amounts might lead to irritability, impatience, or an emotional blunting in some peopletabs.co. This could be due to serotonin overload or simply the body’s down-regulation of its own neurotransmitter production in response to constant supplementation. It’s advisable to monitor one’s emotional state over repeated use – if unusual mood swings or depressive feelings emerge, it may be a sign to take a break from kanna. Importantly, kanna should not be seen as a substitute for a prescribed antidepressant without medical guidance.

Interactions – Serotonin Syndrome Risk: One of the most important cautions with kanna is its interaction with other serotonergic substances. Because kanna acts as an SSRI and also releases serotonin, it can theoretically contribute to serotonin syndrome if combined with other drugs that boost serotonin. In practical terms, this means do NOT combine kanna with pharmaceutical antidepressants, particularly SSRIs, SNRIs, or MAOIstabs.cotabs.co. Doing so could lead to dangerously high serotonin levels, with symptoms like agitation, elevated heart rate, sweating, tremor, or in severe cases seizures and fevertabs.co. While documented cases are scarce (likely because people heed this warning), the risk is real enough that medical professionals explicitly advise against concurrent use. Likewise, combining kanna with other serotonergic recreational drugs (MDMA, LSD, tryptamines, etc.) or even high doses of supplements like 5-HTP or St. John’s Wort is not recommended. Aside from serotonin, kanna’s inhibition of PDE4 might theoretically interact with other PDE inhibitors (for example, it’s remotely possible it could slightly potentiate caffeine or ephedrine since PDE inhibition can increase cAMP, but this is speculative). The main known interaction of concern remains the serotonin-based ones. If someone is switching from an SSRI antidepressant to kanna or vice versa, a safe washout period should be observed (consult a healthcare provider for guidance, typically 2–4 weeks depending on the antidepressant half-life).

Addiction and Dependency: Kanna is not habit-forming in the way opioids, stimulants, or even alcohol can be. It does not induce drug-seeking behavior or physical dependence. In fact, some preliminary investigations have looked at kanna as a tool to help with addiction – for example, to reduce withdrawal symptoms or cravings in people trying to quit alcohol or opioidsdrugs.com. While those studies are very limited, they suggest kanna has low abuse potential. That said, psychological dependency is always possible with any substance that makes one feel good. A person prone to substance abuse might misuse kanna as a crutch, and even though kanna won’t create a chemical hook, the behavior could trigger old patterns. Clinicians like Dr. Vincenzo Sinisi note that individuals in recovery or with addictive tendencies should be cautious – using kanna to cope could potentially lead them to relapse into seeking stronger highsverywellmind.comverywellmind.com. The good news is, if one stops using kanna after regular use, there is no withdrawal syndrome to fear – at worst, they may notice a return of anxiety or low mood that was being managed by kanna. It’s always best to use kanna (and any mood-altering herb) intentionally, not habitually out of unconscious need.

Physiological Effects: Kanna’s impact on blood pressure and heart rate is minimal for most users, but anyone with cardiovascular issues should still be mindful. In one clinical study, kanna extract actually showed a slight reduction in resting heart rate (possibly due to anxiolysis) and no significant change in blood pressurepubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov. There have been no reports of kanna causing arrhythmias or serious cardiovascular strain. Nonetheless, if taken in combination with other stimulants or if one has an underlying heart condition, caution is warranted – mostly because intense serotonin or norepinephrine increases (if someone misuses a very high dose or mixes substances) could affect the cardiovascular system.

Contraindications: Formal contraindications haven’t been established through regulatory bodies, but commonly advised ones include: pregnancy and breastfeeding (due to lack of safety data, and the possibility that alkaloids could cross to the baby)drugs.com; history of severe psychiatric disorders (e.g. bipolar mania or schizophrenia – any substance that alters serotonin could theoretically worsen mania or precipitate psychosis in vulnerable individuals, though there’s no direct evidence of kanna doing so, it’s a general precaution). If someone is on any medication – not just antidepressants, but also things like blood thinners, seizure meds, etc. – it’s wise to consult a doctor before trying kanna, simply because research on drug-herb interactions is scant.

Legal Status: In the United States, kanna is not a controlled substance. It can be legally bought, sold, and possessed as an herbal supplement or incense. The FDA has not approved kanna for any medical indication, but it is generally regarded as a dietary supplement under the DSHEA act. This means quality and purity can vary between products, so consumers should seek reputable brands (standardized extracts, if possible, and those who test for contaminants). Kanna is also legal in most other countries, with a few exceptions or stipulations. For example, in Canada and parts of the EU, it is available but sometimes falls in a grey area (not explicitly scheduled, but not officially approved either). South Africa, the plant’s homeland, permits its use and sale, and in fact encourages benefit-sharing agreements for its commercialization as a way to support indigenous communities. There have been isolated reports of customs seizing kanna imports under the misinterpretation that it’s related to khat (which it is not), but in general kanna does not show up on drug-sniffing radar. One should still verify local laws if unsure, as herbal product regulations differ.

Current Research & Medical Advice: The scientific community is actively studying kanna’s safety and efficacy. A systematic review in 2023 concluded that, so far, evidence is insufficient to definitively say kanna helps clinical anxiety (results have been mixed or modest), but it also noted that adverse effects in trials were mild and not significantly different from placeboverywellmind.comverywellmind.com. This suggests that while kanna may not be a miracle cure, it also doesn’t pose major risks at studied doses. As always, individuals with serious mental health conditions should not replace their prescribed treatments with kanna without medical supervision. But for the general adult population facing everyday stress or low mood, kanna offers a promising natural option. Doctors and pharmacists may not all be familiar with it, so it falls on the user to be educated. A sensible approach is to treat kanna with the same respect as a pharmaceutical: adhere to recommended doses, monitor your body’s responses, and avoid poly-substance use unless you’re sure of the interactions.

In summary, kanna’s safety profile is favorable – when used alone and in moderation, it is gentle on the system, with a very low incidence of troublesome side effects. Most people who try kanna experience either no side effects or only mild ones like a bit of nausea or a headache that quickly passestabs.cotabs.co. By respecting its potency (despite being an herb, it does have real psychoactive power) and avoiding combinations with contraindicated drugs, one can enjoy kanna’s benefits with minimal risk. It’s a testament to the plant that the Khoisan could use it across generations for wellness; modern science, while still catching up, has thus far affirmed that kanna is neither toxic nor addictive. The biggest caution perhaps is managing expectations – kanna isn’t a euphoric high or a cure-all, and those seeking extreme experiences might be tempted to push the dose inappropriately. But for those looking for a natural, nuanced lift, kanna can be a safe companion. Always start low, listen to your body, and consult healthcare professionals if you have any conditions or medications of concern. With those precautions in mind, kanna stands as a shining example of a botanical remedy that offers relief in a relatively safe package, when treated with the respect and knowledge it deserves.

References

  1. Olatunji, T.L., et al. (2022). Sceletium tortuosum: A review on its phytochemistry, pharmacokinetics, biological, pre-clinical and clinical activities. Journal of Ethnopharmacology, 287:114711. DOI: 10.1016/j.jep.2021.114711.
  2. Gericke, N. & Viljoen, A.M. (2008). Sceletium – An overview of a remarkable South African botanical. Journal of Ethnopharmacology, 119(3): 653–663. DOI: 10.1016/j.jep.2008.08.021.
  3. Sceletium Tortuosum (Kanna) – Uses, Benefits & Dosage. (2024). Drugs.com Herbal Database. (Medically reviewed Oct 22, 2024). Online.
  4. Smith, M.T., et al. (1998). The distribution of mesembrine alkaloids in Mesembryanthemaceae species and the preparation of “kougoed” (Sceletium). Pharmaceutical Biology, 36(3): 173–179. DOI: 10.1076/phbi.36.3.173.5926.
  5. Terburg, D., et al. (2013). Acute effects of Sceletium tortuosum (Zembrin®), a dual 5-HT reuptake inhibitor and PDE4 inhibitor, on the human brain. Neuropsychopharmacology, 38(13): 2708–2716. PMID: 23903032.
  6. Chiu, S., et al. (2014). Proof-of-Concept Randomized Controlled Study of Cognition Effects of Sceletium tortuosum (Zembrin) in Healthy Subjects. Evidence-Based Complementary and Alternative Medicine, 2014:682014. DOI: 10.1155/2014/682014.
  7. Reay, J.L., et al. (2020). Sceletium tortuosum (Zembrin®) ameliorates experimentally induced anxiety in healthy volunteers. Human Psychopharmacology: Clin Exp, 35(6): e2753. DOI: 10.1002/hup.2753.
  8. Gouhie, F.A., et al. (2023). Sceletium tortuosum effects on anxiety: A systematic review and meta-analysis of randomized trials. Brain Disorders, 11:100092. DOI: 10.1016/j.dscb.2023.100092.
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