ORIGINAL ARTICLES AND REVIEWS
iKem BT, Budapest, Hungary
Natural psychoactive substances have fascinated the curious mind of shamans, artists, scholars and laymen since antiquity. During the twentieth century, the chemical composition of the most important psychoactive drugs, that is opium, cannabis, coca and "magic mushrooms", has been fully elucidated. The mode of action of the principal ingredients has also been deciphered at the molecular level. In the past two decades, the use of herbal drugs, such as kava, kratom and Salvia divinorum, began to spread beyond their traditional geographical and cultural boundaries. The aim of the present paper is to briefly summarize recent findings on the psychopharmacology of the most prominent psychoactive natural products. Current knowledge on a few lesser-known drugs, including bufotenine, glaucine, kava, betel, pituri, lettuce opium and kanna is also reviewed. In addition, selected cases of alleged natural (or semi-natural) products are also mentioned.
Key words: ethnopharmacology, mode of action, natural products, psychopharmacology, toxicology
O, mickle is the powerful grace that lies
In herbs, plants, stones, and their true qualities
William Shakespeare (Romeo and Juliet)
During the past 200 years, there has been major progress in our understanding of the composition and effects of many psychoactive natural products, particularly those that have therapeutic uses. This article reviews the pharmacohistory, the chemistry, the mode of action, and, where pertinent, the toxicology of some globally emerging and some lesser-known psychoactive natural products with emphasis on recent findings. Some of these substances or potions have been known for decades but became popular on the recreational drug scene only recently; the prevalence and extent of their use, however, are not captured by regular epidemiological questionnairs. Others appear to have only marginal use, yet they provide an interesting insight into how new drugs emerge from obscurity. Some of the substances were detected for the first time in Europe and reported to the Early warning system (EWS) of the European Monitoring Centre for Drugs and Drug Addiction as a "new psychoactive substance"1 just recently. Regulatory aspects are only briefly mentioned since drug legislation varies from country to country and is currently undergoing dynamic changes.
Historical background of psychoactive natural products research
The biochemical machinery of an organism generates many structurally related chemicals (Nature's "combinatorial library") of which some have physiological or ecological relevance, aiding survival of the producer in a hostile environment. For mankind, natural2 products also represent an ancient and rich source of bioactive substances .
The unique psychoactivity of these drugs has fascinated shamans, artists, writers, scholars and laymen alike since antiquity. Through a lengthy, and sometimes dangerous, process of trial and error each culture discovered and developed a natural product-based tradition of "mind altering". In modern societies, the most extensively produced and widely consumed psychoactive drugs, that is alcoholic beverages, caffeine-containing drinks and tobacco products are all of natural origin.
Psychoactive natural products display an astonishing structural diversity and may come from three sources: plants, microorganisms or animals. According to estimates, the number of plants with proven or reputed psychoactivity exceeds 300 ; a recent compendium by the European Food Safety Authority lists hundreds of addictive or psychoactive botanical preparations . The hallucinogenic properties of mushrooms have been known for millennia and over 200 fungal species that produce psychotropic substances have been described . However, there are only sporadic reports on psychic effects elicited by deliberate or accidental ingestion of animals [5, 6] (for toads, see later).
The bioactive extracts obtained from an organism by selfexperiments or biochemical and receptor-based screening methods are typically suites of structurally related chemicals interacting with a wide variety of biological targets. Furthermore, any single component of such a "chemical shotgun" may have more than one molecular target. In addition, one constituent may have high receptor affinity but low efficacy to elicit significant pharmacological response, while an other, sometimes minor, component may have low affinity but high efficacy thus the relevant pharmacological effect manifests only at a high dose (see, e.g., ). Therefore, the overall psychosomatic response is complex and dose-dependent and this explains the versatility of many ethnobotanical preparations.
It has often been observed that the psychic and somatic effects of a natural preparation differ from those of the pure main ingredients indicating that minor constituents contribute to or modulate the activity of the major component. Mixtures containing synergistically acting ingredients pose methodological difficulties: bioassays using purified samples might miss the activity observed for the crude extract.
The isolation of the alkaloid morphine from opium by Serturner six generations ago (1805) laid the foundation of phytochemistry and modern pharmacy. Further research on opioids culminated on one hand in the chemical total synthesis of morphine in 1952 and, on the other, in the discovery of endogenous opioid peptides and their receptors in the 1970s. Building on the results of these investigations, many (semi-)synthetic analgesics, cough suppressants, antidiarrheal agents as well as molecular probes for mode of action studies have been developed , Heroin, oxycodone, desomorphine, naloxone, pethidine, methadone, the fentanils, dextromethorphan, loperamide, and ketazocine have become "household names" not only among specialists of medicine but also among those working in the broad field of addiction. Subsequently, the active principles of other natural psychoactive agents were also elucidated and, as shown in Table 1, the "Golden Area" of psychoactive natural products discovery appears to have lasted for almost two centuries.
A note of caution regarding olden literature: several chemicals have been isolated from exotic drugs, Yet, recent phytochemical re-analysis of many such plants detected these substances in trace amounts only (< 0.1%), a concentration unlikely to elicit the reported effects of the preparation. In other instances, the activity of an isolated substance was not verified in bioassays. In these cases the genuine bioactive component awaits identification. Publications solely relying on early literature thus must be assessed critically.
MAJOR EMERGING PSYCHOACTIVE NATURAL PRODUCTS
Khat refers to the evergreen shrub Catha edulis indigenous to East Africa. Khat also refers to the leaves and shoots of the plant chewed to provide mild stimulant effects. Khat has a variety of regional names such as mairungi (Uganda), miraa (Kenya), qat (Yemen), or tschat (Ethiopia and Somalia). The shrub is an intensively cultivated, highincome cash crop in East Africa and the southwestern part of the Arabian Peninsula. In addition to supplying domestic markets, fresh khat bundles, each weighing 250-300 g, are nowadays shipped by airfreight into Europe, Australia and North America to ethnic groups immigrated from countries where khat-chewing is a tradition [9-13]. During the daily 3-6 hour-long afternoon chewing sessions, at least one bundle is consumed, mainly in social setting, to provide euphoric and stimulant affects. The number of regular, predominantly male, khat consumers is at least ten million although epidemiological data are lacking.
Several types of compounds have been isolated from khat, including amino acids, ascorbic acid, flavonoids, phenylalkylamine alkaloids, sesquiterpene polyester alkaloids (cathedulins), steroids, tannins, and terpenoids. The main psychoactive constituent was identified in 1975 and named cathinone (Figure 1) . The cathinone-content of the leaves typically ranges from 0.04 to 0.3 %. Biosynthetically related alkaloids also present in khat are cathine (i.e., norpseudoephedrine) (Figure 1), and norephedrine, though they are only slightly active. Data on the bioactivity of other khat constituents are scarce.
Cathinone is a chemically unstable aminoketone. In the leaves it undergoes enzymatic reduction into cathine (e.g., ), thus the harvested shoots lose psychoactivity within 2-3 days explaining the chewers' preference for fresh khat (see, e.g., ). Interestingly, the chemical synthesis of racemic "cathinone" by Schmidt in 1889 preceded by many decades the identification of the natural product; its tendency to undergo decomposition was also noted a century ago.
Khat and its main ingredients are amphetamine-like dopaminergic psychostimulants with peripheral sympathomimetic effects [17, 18]. In the central nervous system, cathinone inhibits the reuptake of dopamine and norepinephrine into presynaptic nerve terminals without affecting serotonin transport . Several reports indicate that khat use may lead to dependence, induce psychoses and cause cardiovascular diseases [20-23], but robust information on the somatic and mental health problems associated with regular use is lacking. Due to intensive farming of the plant, pesticides may contaminate the bundles  although the health consequences of such contamination have not been investigated. The environmental, socio-economic and health problems associated with the production and use of khat have recently become a focus of scientific and political debates [25, 26]3. While cathinone and cathine are scheduled according to the UN Convention on Psychotropic Substances of 1971, khat leaves do not fall under any international regulatory system. Yet, Australia, several US states and European countries have recently introduced measures to control the trade of Catha edulis [9, 27].
It is interesting to follow the chronology of appearances of such aminoketone stimulants: first, in the late 1970s, the semi-synthetic methcathinone, i.e., the N-methyl derivative of cathinone (also called ephedrone indicating that it is made by oxidizing ephedrine) appeared on the drugs scene in the then-Soviet Union; a decade later, in 1989, methcathinone was introduced into Michigan ; a decade later it reappeared in several countries. Around the same time, in 2003, synthetic cathinone containing capsules ("Hagigat") were beginning to be sold in kiosks in Israel . In retrospect, these appearances seem to have been preludes to the subsequent alarming emergence of synthetic cathinones (commonly referred to as "bath salts").
The psychoactive mint Salvia divinorum, or the diviner's sage, is indigenous to the highlands of the Oaxaca state in Mexico, where Mazatec shamans have been using it for medical purposes, in healing ceremonies and divinatory rituals. Traditionally, the fresh leaves are chewed or pressed to make a drink. Since the late 1990s, the "recreational" use of S. divinorum as an herbal hallucinogen has been spreading globally especially among young adults [30, 31]4. For this purpose, 0.25-0.75 grams of crushed dried leaves are smoked from a pipe or water bong to provide profound hallucinations and unique, "out-of-body" experiences that commence within a minute and last for 15-20 minutes [32, 33].
The psychoactive principle of the leaves is salvinorin A (Figure 1). This non-nitrogenous, neoclerodane diterpene was isolated first by Ortega et al. in 1982. Independently, in 1984, the same compound was isolated and biologically characterized by Valdes et al., who called it "divinorin A". Salvinorin A has not been detected in any other Salvia species examined to date , It is the most potent natural hallucinogen: inhalation of the vapors of doses equivalent to 200-500 microgram pure salvinorin A elicits strong hallucinations with virtually no discernible somatic effects. This dose is comparable to the effective oral dose of the semi-synthetic LSD (lysergic acid diethylamide) (100 microgram) or the synthetic DOB (4-bromo-3,5-dimethoxyphenylisopropylamine) (1000 microgram), although the subjective effects are qualitatively different from those of any other known hallucinogens [32, 35-37]. The short duration of the effects is explained by the rapid, esterasecatalyzed hydrolysis of the 2-O-acetate of salvinorin A to its inactive alcohol (salvinorin B) [38, 39].
Unlike classical hallucinogens that target serotonin (5-HT) receptors, 5-HT2A-type in particular , salvinorin A acts as a selective κ-opioid receptor agonist [41, 42], as corroborated by recent X-ray crystal structure studies . The analgesic and antiinflammatory activities of salvinorin A are of particular interest [44, 45]. There is also intensive research to explore the therapeutic potential of structurally related opioid receptor agonists or antagonists [46, 47]. For example, the hydrolytically stable salvinorin B 2-0 ethoxymethyl ether is several-fold more active as a κ-opioid receptor ligand than the natural product ; users' experience reports indicate that this semi-synthetic ether, named "Symmetry", is at least as potent as salvinorin A5. Interestingly, replacement of the 2-0-acetyl group of salvinorin A with a benzoyl group provides salvinorin B 2-0-benzoate (herkinorin), which is, in turn, a selective µ-opioid receptor agonist with antinociceptive activity in vivo [49, 50].
Preliminary experiments indicated low rodent toxicity  but no other study has examined the acute or chronic physiological adverse effects of Salvia divinorum leaves or extracts.
The vegetatively propagated plant as well as dried leaf preparations, often enriched with extracts from other S. divinorum leaves, are widely available but pure salvinorin A is rarely encountered. Analyses of Salvia leaf samples obtained from various vendors indicated large variations in salvinorin A content (0.13-5.0 mg/g) [52, 53]. The plant and/or salvinorin A are controlled in an increasing number of countries.
The discovery and psychopharmacology of LSD (from the German "Lysergsaure-diathylamid") have been well documented [54, 55]. LSD is a semi-synthetic compound usually prepared from lysergic acid, which is obtained hydrolytically from ergot alkaloids produced for the pharmaceutical industry by fermentation of Claviceps fungi. Lysergamide (LSA, ergine or LA-111; Figure 1) was first obtained as a semi-synthetic product by the degradation of ergotoxin by Smith and Timmis in 1932, In 1960, Hofmann and Tscherter isolated it as a genuine natural product from "ololiuqui", the seeds Rivea corymbosa (syn. Turbina corymbosa), the sacred narcotic-hallucinogen of the Aztecs. Since then LSA has been found in several ornamental morning glory ( Ipomoea) species [56, 57]. The total ergot alkaloid content of the seeds of these plants is less than 0.2% with LSA and its 8-epimer (iso-LSA) being the most abundant.
Ingestion of 50 to 100 seeds is needed to produce observable effects. Phytochemical screening of tropical climbing vines led to the discovery of LSA in the seeds of the Hawaiian baby woodrose (Argyreia nervosa) . Interestingly, it is not the seeds but the leaves A. nervosa that are used in Ayurvedic medicine in India, where the plant is indigenous. The LSA-content of A. nervosa seeds shows high variability between batches and may reach 1% . Five to ten seeds provide intoxication that lasts for 4-8 hours. Recent studies indicate that LSA and related alkaloids are not biosynthesized by the plant but produced by an associated fungus, which can be eliminated by fungicide treatment [60, 61]. Lysergamide and other alkaloid toxins are often present in endophyte-infected grasses and may cause poisoning in grazing animals .
Ergot alkaloids are "dirty drugs": they bind to several receptors thus eliciting a broad range of effects. However, neither the seeds, nor LSA induce classical hallucinations: rather, the (psycho)pharmacological effects are sedativenarcotic with feeling of complete emptiness . The observed vegetative and psychotropic effects can be rationalized by the results of recent in vitro studies revealing that the receptor profile of LSA is different from that of LSD . The unpleasant effects of intoxication include salivation, nausea, diarrhea, tremor as well as psychosis, unpredictable behavior and even suicidal ideation [65-68].
Lysergamide is not listed in the UN Conventions, though it may be controlled either as a psychotropic substance or a precursor in some countries. The trade and sale of Ipomoea and A. nervosa seeds are largely uncontrolled.
Ayahuasca and its constituents
Ayahuasca or ayawaska ("vine of the souls"), also known as hoasca, caapi or yagé, is an ancient hallucinogenic decoction traditionally used in northern South America in ethnomedicine and, since the 1930s, as a sacrament by syncretic religious sects, such as the União do Vegetal or the Santo Daime in Brazil6. The key ingredients in the brew are the pounded bark of the Amazonian woody liana Banisteriopsis caapi and the leaves of either the shrub Psychotria viridis or the vine Diplopterys cabrerana. The drink is usually made by mixing the two key components in boiling water, Admixtures, mostly solanaceous plants containing nicotine or tropane alkaloids, are occasionally added. Drinking the brew often induces vomiting, while the cardiovascular effects (bradycardia and reduced blood pressure) are only mild; mydriasis is typically observed. The psychotropic effects, accompanied by vivid visual imagery, usually last for 4-6 hours [71-73]. The side effects and relative safety of ayahuasca use have been reviewed [74, 75]. The physiological and psychological mechanisms of the promising anti-addiction effects of the brew offered in religious setting have recently been discussed .
The chemicals responsible for the dreamlike, colorful hallucinogen effects elicited by the brew were identified by Rivier and Lindgren in 1972: of the two plants, B. caapi is the source of harmala alkaloids, while P. viridis provides N,N-dimethyltryptamine (DMT) (Figure 1) [77, 78]. The first harmala alkaloid from the seeds of Syrian rue, Peganum harmala, was isolated by Goebel in 1841, while structural determinations were carried out by Manske et al. in 1927. These alkaloids, such as harmine, or 7-methoxy-1-methyl-9H-b-carboline (Figure 1), and its di- or tetrahydro derivatives, are not particularly psychoactive on their own but, mainly in the gastrointestinal tract, inhibit monoamine oxidase (MAO) enzymes involved in the metabolism of monoamine neurotransmitters and certain xenobiotics [79, 80]. Passion flowers (Passiflora spp.) also contain harmala alkaloids but only in trace amounts; the pharmacological effects of preparations made from the plant are probably due to its flavonoid constituents [81, 82].
The primary hallucinogen component of ayahuasca is DMT, a low-melting point solid. The alkaloid was isolated from the seeds of Piptadenia (syn. Anadenanthera) species by Fish et al. in 1955 although it had already been synthesized by Manske two decades earlier. DMT, along with 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT), is also a psychoactive component of South American ceremonial snuffs prepared from Anadenanthera, Mimosa or Virola plants having various local names (cohoba, ebene, parica, yopo, etc.) (see, e.g., ). The psychoactivity and metabolism of DMT in humans were first studied by Szara in injection experiments in Hungary in the mid-1950s, Like all classical hallucinogens, DMT activates 5-HT2 A receptors in vitro. However, due to rapid inactivation by MAO enzymes, DMT is devoid of activity when taken orally explaining why the ritually or "recreationally" used DMT-preparations are administered either nasally or by inhalation to give hallucinations lasting for 15-20 minutes only. Ayahuasca is thus a unique, synergistic ethnobotanical drink in which the MAO-inhibitory action of harmala alkaloids enable the manifestation of the hallucinogen effects of the metabolically labile DMT.
There is no record on how or why these two particular plants were selected from the rich biodiversity of the Amazonian forest for the brew. The present author speculates that the ancient shamans initially experimented with a complex concoction made from several, perhaps dozens of plants, Having discovered activity of such a mixture, they could then proceed by using the leave-one-out technique, that is testing one by one a series of mixtures lacking just a single ingredient. This would then quickly reveal which plants are indispensable for activity. Reconstituting a brew from the key components would then validate the procedure. It should also be pointed out that the brew contains other bioactive substances the contribution of which to the overall psychobiological activity has not been studied. The term "endohuasca" refers to human endogenous alkaloids chemically identical or similar to those present in the brew ; the actual (psycho)pharmacological role, if any, of such trace tryptamine metabolites is unknown . The popular term "pharmahuasca" refers to the concomitant use of a synthetic MAO inhibitor with a tryptamine-type natural or synthetic hallucinogen .
Adopting practices of religious ayahuasca use, a number of follower groups have been established outside the Americas in recent years. While harmala alkaloids are regulated in a few countries only, DMT is an internationally scheduled psychotropic substance. In the USA, the sacramental use of "hoasca" falls under the "Religious Freedom Restoration Act" . Nevertheless, the blooming "ayahuasca tourism" in Amazonia as well as the spread of ayahuasca and related preparations beyond traditional cultural boundaries have raised concerns and elicited debates on their regulation .
Bufotenine, that is 5-hydroxy-N,N-dimethyltryptamine (Figure 1), is an N-alkylated derivative of serotonin and also a structural isomer of the hallucinogenic psilocin, the 4-hydroxy counterpart, The chemical structure of bufotenine7 was established by synthesis by Wieland et al. in 1934. Bufotenine and its ether derivative, 5-MeO-DMT, are the main ingredients of the psychoactive secretion of the American desert toad, Bufo alvarius. In fact, 5-MeO-DMT is one of the few psychoactive substances found in animals, and the hallucinogenic properties of this alkaloid is most likely behind the contemporary myth that "toad licking" elicits psychedelic effects . The psychoactivity of bufotenine, however, is contested [85, 91]. Accompanying congeneric tryptamines, bufotenine also occurs in several hallucinogenic plants (see, e.g., ). Interestingly, 5-MeO-DMT is oxidatively demethylated to bufotenine in the body . The alkaloid binds to 5-HT2A receptors in vitro with an affinity similar to that of DOB: the respective Ki values are 2.7 and 3.7 nM . When taken orally, however, it lacks psychoactivity due to rapid inactivation by MAO enzymes [93-95]. Bufotenine is not listed in the UN Conventions yet it is controlled in a number of countries.
A related substance worth mentioning here is 5-methoxytryptamine, mexamine or 5-MeO-T, This endogenous trace amine is a serotonin receptor agonist and an enigmatic minor metabolite of the multifunctional neurohormone melatonin , It has antioxidant and radioprotective effects in various biological systems but there is no information on its psychoactivity.
The root of the tropical West African shrub Tabernanthe iboga is used in Gabon and Cameroon for its stimulatory and sedative-hallucinogenic properties. On one hand, the bitter roots of the plant, locally called iboga, are chewed to combat fatigue and to keep hunters awake. Based on such ethnopharmacological observations, a root extract (Lambarene®) was available in France (1939-1966) as "neuromuscular stimulant". On the other hand, consumption of massive doses of iboga is part of the initiation ritual of the local Bwiti cult during which the initiate fells in deep coma that may last for a day. Of the structurally related alkaloids isolated from the plant the most important is ibogaine (12-methoxyibogamine) (Figure 1), which is most abundant in the root bark (0.2-0.6%). The isolation of the light- and air-sensitive crystalline ibogaine was reported first in 1901, its structure was determined by Taylor in 1957. A with the root, ibogaine is stimulant at low (< 200 mg), while hallucinogenic at high (500-1000 mg) oral doses. The anti-addictive potential of ibogaine has received attention recently. In preclinical animal studies, acute ibogaine treatment reduced self-administration or symptoms of withdrawal of various addictive drugs, including ethanol, methamphetamine, nicotine and morphine. In humans, single or repeated oral doses of 4-25 mg/kg have been shown to alleviate withdrawal symptoms and craving, confirming anecdotal reports and patent claims originating from the 1960s [97-99]. However, due to serious adverse side effects, such as tremor, ataxia, cardiac toxicity and even fatalities, NIDA-coordinated human clinical trials were halted in 1995 [100-102]. According to recent studies, the alkaloid, at therapeutic concentrations, disrupts the heart's electrophysiology that could lead to life-threatening cardiac arrhythmias [103, 104]. In rodent models of ethanoladdiction, certain synthetic analogues have improved toxicological profile and appear to be as effective as the natural alkaloid . Ibogaine and its demethylated metabolite, namely 12-noribogaine (12-hydroxyibogamine) (see, e.g., ), have complex pharmacology affecting several neurotransmitter and transporter systems [99, 107, 108]. The glial cell line-derived neutrophic factor, which is necessary for the proper functioning of dopaminergic neurons, appears to be also involved in the sustained anti-addictive effects of the alkaloid . In the mouse, ibogaine was more toxic than 12-noribogaine (the respective intragastric LD50 values are 263 and 630 mg/kg) . In spite of the health risks, controversial "ibogaine anti-addiction therapies" continue in private clinics and non-clinical setting in some countries where the substance is not regulated. Ibogaine is seldom used recreationally.
Kratom (Mitragyna speciosa)8, or "krathom" (Thailand) and "biak" or "ketum" (Malaysia), is a tropical tree indigenous to South East Asia, the Philippines and New Guinea. Traditionally, the chopped fresh or dried leaves of the tree are chewed or made into tea. Kratom preparations have been used in local medicine, and also as stimulants or an opium substitute. Of the over 40 structurally related alkaloids isolated from various parts of the tree the most abundant (up to 2% in the leaves and leaf preparations) is mitragynine (9-methoxycorynantheidine) (Figure 1) . The alkaloid was isolated first by Field in 1921, its chemical structure was clarified by Joshi and Zacharias in 1963-1964. A minor though pharmacologically important alkaloid, namely 7-hydroxymitragynine, was discovered in
the leaves by Ponglux et al. in 1994. There are few human clinical studies with kratom or its alkaloid constituents [114- 116]. At a low dose, leaf preparations act as "cocaine-like" stimulants and are traditionally used to combat fatigue during work. At high dosages (10-25 g of dried leaves), however, "morphine-like" sedative-narcotic effects manifest: the initially occurring sweating, dizziness, nausea and dysphoria are superseded with calmness, euphoria and a dreamlike state lasting for several hours. Contracted pupils (miosis) are also noted. Regular kratom use may cause constipation, anorexia and hyperpigmentation of the cheek; dependence may develop . Withdrawal symptoms are relatively mild and typically diminish within a week .
The narcotic and antinociceptive effects of kratom are attributed to mitragynine and 7-hydroxymitragynine acting as μ-opioid receptor agonists . In this respect, 7-hydroxymitragynine is several times more active than morphine both in vitro and in vivo. Recent studies revealed the roles of κ -opioid and dopamine D1 receptors in the various effects of kratom . The serotonergic and adrenergic systems are also involved in the psychological and physiological effects of mitragynine. The pharmacological mechanisms responsible for stimulant activity are yet to be established.
According to animal studies, kratom is only slightly toxic . In rats, for example, oral administration of a kratom leaf-extract (1.6% mitragynine content) at 1000 mg/kg caused transient toxicity (slow movement and rapid breathing) but no mortality, while morphine had depressant activity with 25% mortality at 430 mg/kg; oral mitragynine doses as high as 806 mg/kg were not lethal. Intravenous injection of mitragynine at 9.2 mg/kg to rhesus monkeys produced only transient toxic symptoms. In mice, repeated 7-hydroxymitragynine administrations elicit tolerance, cross-tolerance to morphine, and naloxone-precipitated withdrawal symptoms . There have been few poisoning cases related to kratom consumption [122-124].
According to animal studies, kratom is only slightly toxic . In rats, for example, oral administration of a kratom leaf-extract (1.6% mitragynine content) at 1000 mg/kg caused transient toxicity (slow movement and rapid breathing) but no mortality, while morphine had depressant activity with 25% mortality at 430 mg/kg; oral mitragynine doses as high as 806 mg/kg were not lethal. Intravenous injection of mitragynine at 9.2 mg/kg to rhesus monkeys produced only transient toxic symptoms. In mice, repeated 7-hydroxymitragynine administrations elicit tolerance, cross-tolerance to morphine, and naloxone-precipitated withdrawal symptoms . There have been few poisoning cases related to kratom consumption [122-124].
Although still uncommon - and mostly unregulated - outside Asia, kratom has become one of the most widely abused illicit substances in Malaysia and Thailand either as a drug by itself or a substitute for opium or alcohol [117, 127, 128].
Kava, awa, yaqona or "intoxicating pepper" (Piper methysticum) is a large-leaved shrub indigenous to the South Pacific Islands. It is also the name of the mildly narcotic beverage made by extracting the rootstocks of the plant by water at ambient temperature. On many of the Islands, kava drinking is an integral part of social life. The plant was probably first domesticated in Vanuatu and, by now, it has spread throughout the region. The many different cultivars (or chemotypes) grown on the Islands today have been selected over generations; the clones are propagated vegetatively. Kava products, either the dried and powdered roots or root organic solvent extracts, are important agricultural commodities in that region with annual export values exceeding US$ 11 million . Kava preparations have also been used in traditional medicine to cure fever, pain, headache, respiratory problems, insomnia, diarrhea or constipation, skin diseases, convulsion, urogenital and menstrual problems. In the early twentieth century, kava products were sold in Europe for the treatment of various illnesses . The effects of the drink include mild euphoria and sociability, as well as anesthesia and astringency in the tongue and the inner lining of the mouth. Small doses typically produce stimulation while larger ones cause muscle relaxation, incoordination, and somnolescence. Regular and heavy use of kava, either the drink or the extracts, is not without risks: transient dermopathy (dry scaling skin), liver and kidney problems, gastrointestinal distress, as well as impaired vision have been observed [131, 132].
Since the initial studies on the separation of the individual kava-constituents by Cuzent around 1860 and by Lewin in the mid-1880s, the phytochemistry of P. methysticum, has been fully explored [133, 134]. The psychoactive principles of the roots are the so-called kavalactones (kavapyrones), exemplified by kavain (also spelled kawain) and yangonin (Figure 1). The total kavalactone content may vary from 3 to 20% of the dried root. The composition of the aqueous beverage and the organic extracts mainly depends on the type of the cultivar though environmental factors and the extraction method employed also affect the kavalactone content [135, 136].
The mode of action of kava in the central and peripheral nervous system is complex and not fully understood. Each kavalactone has a distinct pharmacological profile involving GABA and benzodiazepine receptor sites, voltage-gated cation channels, monoamine reuptake and metabolism, the arachidonate cascade, and the endocannabinoid system [131, 137]. Accordingly, there can be substantial variations in the effects between various chemotypes; drinkers are said to prefer cultivars with high kavain content . It must also be noted that constituents other than the kavalactones may play a role in the various pharmacological or pathophysiological effects of the aqueous extract though this issue has received scant attention (see, e.g., [138, 139]).
In recent decades, kava root extracts, formulated as capsules or tinctures, became available worldwide as dietary supplements and clinically proven over-the-counter medicines for anxiety, depression and insomnia [131, 140]. Since 2002, however, several European countries restricted the sale of such extracts due to reports about hepatotoxicity of still unresolved etiology [141-143]. Nonetheless, dried and finely ground roots, having a light greyish-brown color resembling sawdust, are offered in herbal shops and on the Internet. Because of the economic importance on one hand and of the uncertainties of the health risk associated with kava products on the other, the developments of regional and FAO-WHO Codex Alimentarius standards for kava have been recommended9. A few countries have, in recent years, regulated kava as a psychotropic drug.
After caffeine-containing beverages and tobacco, betel is the third most widely used stimulant: it is chewed regularly by at least 400 million people throughout east Africa, Asia and the Pacific Islands as well as migrant communities therefrom [144-147]10. Betel or, more accurately, a betel quid is made of three essential ingredients: slices of nuts of the areca palm (Areca catechu), spread with slaked lime and wrapped in the heart-shaped leaf of the betel palm (Piper betle). Tobacco may be a common ingredient and spices, such as aniseed, cardamom, cloves, coconut, ginger, nutmeg or sugar, are frequent flavoring additives. In India, the sale of tobaccocontaining betel products known as "gutka" was restricted in 2011. Freshly prepared quids are usually sold by street vendors or, in Taiwan, by "betel nut beauties" along busy roads. The quids are placed between the cheek and the tongue, pressed against the teeth to remove the juice, which is then swallowed. Due to the coloring ingredients of the nuts, the reddish spittle stains the chewer's gums and lips (as well as the roadside...). Industrially manufactured, tobacco-free areca products called "pan masala" are sold in convenient sachets. Fresh or dried nuts, called "supari" in India, cut into small pieces may also be masticated alone. Areca and betel preparations have been used in traditional, for example Ayurvedic, medicine for centuries. Areca nut is a commodity in Asia with about 650 000 tonnes produced annually . Bulk quantities of synthetic arecoline salts have also appeared recently in on the Internet for sale.
The alkaloid constituents of areca nut were structurally characterized by Jahns in 1888-1891. The principal alkaloid is arecoline, namely the methyl ester of 1-methyl- 1,2,5,6-tetrahydropyridine-3-carboxylic acid (Figure 1), a nicotinic acid derivative. The arecoline content of the nuts may reach 1%. Arecoline, a colorless liquid, can readily be synthesized and its salts are deworming (purgative) agents used in veterinary medicine. There are three other related alkaloids present in the nut: arecaidine, which is the free carboxylic acid derivative of arecoline formed also during mastication and ingestion; guvacine, which is the N-desmethyl derivative of arecaidine; and guvacoline, which is the N-desmethyl derivative of arecoline.
The leaves of the betel palm contain phenylpropanoids, such as chavibetol (Figure 1), eugenol and safrole, as well as terpenes but the contribution of these aroma constituents to the psychoactivity of the quid is not known.
In spite of widespread use, the physiological and psychological profile of betel quid intoxication is just beginning to be delineated . More is known about the pharmacology and toxicology of its alkaloidal constituents . The active ingredients, absorbed into the blood via the mucous membranes of the mouth and the intestine, affect both the central and peripheral nervous systems. Betel, due to its predominant alkaloid, arecoline, which is a known muscarinic acetylcholine receptor agonist, elicits mostly cholinergic (parasympathomimetic) symptoms and elevated adrenaline plasma concentrations. The minor alkaloids are GABA uptake inhibitors and presumably modulate the psychoactivity of the quid.
The typical psychological effects are mild and include relaxation, light euphoria and improved concentration. Somatic symptoms include miosis, intense salivation, facial flushing, sweating, palpitation, bronchoconstriction (risk of asthma!), and increased gastrointestinal motility, though chronic users develop tolerance to many of these effects. Novice users or regular chewers ingesting large amounts may experience tremor, dizziness, diarrhoea, vomiting and acute psychosis.
Excessive use of areca nut and betel quid has been associated with a number of health-related problems: discoloration of teeth and gums, sometimes turning reddish-brown, mouth ulcers and gum disease, oral submucous fibrosis and oral cancers, including squamous cell carcinoma, peptic ulceration, increased risk of cardiovascular disease. The major concern of betel chewing is the risk for the development of oral cancer associated with its alkaloid ingredients and, in particular, their nitroso and N-oxide derivatives [152,153]. The risk of malignant oral disorders increases when tobacco is included in the quid . Recently, however, Rai et al.  have proposed that some non-alkaloidal phytochemicals (polyphenols and terpenoids) present in betel palm leaves may, by various mechanisms, counteract the carcinogenic effects of areca and tobacco alkaloids. Due to its cholinergic effects, arecoline may clinically improve the cognitive performance of Alzheimer's patients . Dependence and withdrawal symptoms have been noted . Few countries regulate the palm or its alkaloids.
LESSER-KNOWN PSYCHOACTIVE NATURAL PRODUCTS
The alkaloid glaucine, also known as boldine dimethyl ether or 1,2,9,10-tetramethoxyaporphine (Figure 1), is found in the yellow horned poppy (Glaucium flavum, formerly G. luteum), indigenous to the Mediterranean region, as well as in other plants, such as Croton lechleri (source of the latex "sangre de grado") or the Chinese medicinal plant Corydalis yanhusuo. The alkaloid was isolated by Fischer in 1901, its structure determined by Gadamer in 1911. Glaucine can also be synthesized either from the readily available boldine or, in racemic form, from papaverine. The therapeutic value of glaucine is similar to that of codeine or dextromethorphan [158, 159] but with lower abuse potential . The plant has been used in folk medicine while glaucine itself is registered in some East European countries as an over-the-counter, non-opioid antitussive and bronchodilatory medicine. The alkaloid was shown to be an effective blocker of calcium ion channels of bronchial smooth muscles, as a week antagonist of dopamine receptors, as an antagonist of peripheral serotonin receptors, as a non-selective a-adrenoreceptor antagonist, as a selective inhibitor of phosphodiesterase type 4 isoenzyme, as an antioxidant and a resensitizer of multidrug resistance of cancer cells (see, for example, ). Glaucine has been reported to cause weakness, sleepiness, nausea, mydriasis and visual or dissociative-hallucinations both with therapeutic and recreational use but the underlying pharmacology responsible for these central effects remains to be determined [162, 163]. Glaucine-containing tablets and herbal mixtures have appeared recently as "herbal highs" in the several European countries [162, 164, 165].
Pituri, pitchery or chewing tobacco (Duboisia hopwoodii), is a solanaceous shrub growing in the arid region of Australia. Its dried and powdered leaves, often mixed with ash obtained from the burning of some other plant, are made into a quid, which is then chewed by Aboriginal groups to alleviate fatigue, hunger and pain; plant preparations are also used to kill game and fish . The identity of one of the alkaloids in the leaves was unequivocally confirmed in 1911 by Rothera as the cholinergic nicotine (Figure 1). The roots of D. hopwoodii are, however, particularly rich in anticholinergic tropane alkaloids, e.g., hyoscyamine, also called duboisine or daturine (Figure 1), and its 6,7-epoxide, scopolamine. Related alkaloids have also been isolated from the leaves and roots of other Australian Duboisia (corkwood) species since the 1870s , and are of ethnopharmacological interest. Such deliriant tropanes are the principal bioactive alkaloids of many solanaceous plants, including the legendary Atropa (belladonna), Brugmansia (angel's trumpet), Datura (jimsonweed, thornapple), Mandragora (mandrake) and Solandra (chalice vines) species. Some Solandra species called "cup of gold" are woody, treelike climbers indigenous to Mexico and tropical America and were once used by the Aztecs as sacred hallucinogen ("tecomaxochitl"); the plants are still revered in Mexico by Huichol Indians who call them "kiéri" . Hyoscyamine is used in medicine in some countries, for example in antiulcer therapy, while scopolamine and its derivatives are employed in veterinary and human medicine; for example, transdermal scopolamine formulations, to prevent nausea and motion sickness . The not uncommon abuse of Datura species to induce hallucinations is often associated with severe complications, although these are rarely fatal (see, e.g., [170, 171]). Pure scopolamine or Datura and Brugmansia preparations ("burundanga"; popularized as Devil's breath) cause transient amnesia and their use to incapacitate crime victims, especially in Colombia, is well documented [172, 173].
Wild lettuce, bitter lettuce or lettuce opium (Lactuca virosa), wildly growing in Eurasia and Northern Africa, is a tall (up to 150 cm high), poisonous and skin irritating relative of the garden lettuce (L. sativa). The analgesic, sedating, hypnotic and cough-suppressing properties of its seed extracts and of the milky latex (lactucarium), released from its stem and leaves upon wounding, have been known for millennia [2, 174]11. Lactucarium is obtained from L. virosa or L. sativa and used like opium in traditional medicine and various preparations form these species were listed in pharmacopoeias of several countries up to the early twentieth century. The smoked dried leaves of the plant can also serve as marijuana substitute. In spite of the long history of its use, not much is known about the pharmacology of L. virosa and of its chemical constituents. The latex contains bitter sesquiterpene lactones thought to be responsible for the characteristic pharmacological properties of the plant . One of the most studied sesquiterpene is lactucin (Figure 1), which is present either in free or esterified form also in other lettuce species as well as in chicory. Crystalline lactucin was isolated in pure form by Schenk and Graf in 1936 and its bicyclic lactone structure, related to that of the bitter principle of absinthe, was established independently in the laboratories of Barton and of Šorm in 1958. Apart from the (user-)reported narcotic-euphoric effects resulting form recreational use, there is scant contemporary information on the (psycho)-pharmacological properties of either the latex or its pure ingredients . The sedative and analgesic activities of lactucin were confirmed in mice though opioid receptors were unaffected in vitro [177, 178]. The symptoms observed in human wild lettuce-poisoning cases differ from those of traditional opiates [179, 180]. The precise molecular targets of the latex and its constituents are yet to be established. Wild lettuce preparations, including fortified extracts, are freely offered on many Internet sites and by herbal (smart) shops.
Kanna, channa or sceletium (Mesembryanthemum -formerly Sceletium -tortuosum) is a creeping perennial plant with succulent leaves. It is indigenous to southern Africa where it has traditionally been used (mainly chewed as quid) by the Khoe-San people to elevate mood, relieve hunger and thirst. The psychoactivity of this relatively little studied plant and its "fermentation" product ("kougoed" in Afrikaans) is attributed to a structurally related group of alkaloids of which the most abundant is mesembrine (Figure 1). Mesembrine was isolated by Zwicky in 1914 and its structure identified in 1960 (see [181, 182]). Laboratory experiments with various plant preparations have revealed anti-stress, antidepressant, narcotic, anxiolytic and anti-addictive but not hallucinogenic effects [182, 183]. Screening in vitro a range of potential pharmacological targets revealed that mesembrine was an effective inhibitor of 5-HT reuptake, while its unsaturated derivative( i.e., mesembrenone) inhibited both 5-HT reuptake and phosphodiesterase type 4 isoenzyme [184, 185]. These results, at least partly, support the observed psychoactive properties of the plant.
Many Internet sites and herbal shops offer powdery kanna preparations, including fortified extracts, that vary in their mesembrine-type alkaloid-content and, consequently, in their psychoactivity , In 2013, a standardized extract (Zembrin®) became available as a mood-enhancer and anxiolytic botanical supplement ,
OBSCURE OR FALSE "NATURAL" PSYCHOACTIVE SUBSTANCES
There has been a resurgence of interest in natural products in general, and suppliers of dietary supplement and unregulated psychoactive substances try to profit from it. In recent years, however, chemical scrutiny have revealed that some herbal mixtures advertised as "natural" or "herbal high" contain undisclosed synthetic additives as bioactive constituents. Fake kratom products adulterated with synthetic opioids have already been mentioned. A most dramatic development was the appearance on the drug market, in around 2004, of smokable herbal mixtures under the brand name "Spice", mimicking the effect of marijuana . Since then, the number of herbal preparations laced with structurally diverse synthetic cannabinoid receptor agonists, originally invented by academic or industrial research laboratories, has been growing incessantly . There have been, however, other cases for which the origin of psychoactive ingredients in the natural products was or still is enigmatic. A few selected but representative examples are mentioned below.
Clement et al.  reported the detection of psychoactive phenethylamines, including mescaline as well as amphetamine and p-methoxyamphetamine, in Acacia species growing in southwest Texas and northern Mexico, No other analyses have substantiated these intriguing findings. Since drugs have been found to be ubiquitous in our environment, including air (see, e.g., ), it is suspected that the isolated compounds, the amphetamines in particular, were artifacts due atmospheric transport from the site of their production or use. A similar case concerns the sub-Saharan Nauclea latifolia (or N. esculentus), commonly known as pin cushion tree, African peach or Guinea peach, which has been used in local ethnomedicine for the treatment various ailments. Recently, the synthetic opioid analgesic tramadol has been isolated from the root bark of the plant . Although the structure of the compound was unequivocally proven by multiple analytical methods, the true origin of this substance with a structure unprecedented in nature remains to be established. In the author's opinion these two cases are most likely further examples of the so-called "semi-natural products", defined recently as man-made substances that are (re)isolated from natural sources .
Another widely occurring natural phenethylamine is also worth mentioning here. Hordenine or N,N-dimethyltyramine ( p-hydroxy-N, N-dimethylphenethylamine; also known as anhaline) is a minor alkaloid not only of peyotl ( Lophophora williamsii) and other cacti, but Acacia, Sceletium and Phalaris plants . Since germinating barley (Hordeum spp.) produces hordenine, the alkaloid is present in beer  and is readily identifiable in the urine of beer drinkers. Thus, its presence in urine should not be considered an indicator of synthetic drug use, as proposed , but rather as an indicator of beer consumption . The human psychoactivity of hordenine is not known. It is of note, however, that this phenolic alkaloid could cause false positives in morphine immunoassays of beer drinkers' urine .
The final case concerns a stimulant substance, namely 1,3-dimethylamylamine or DMAA in short (systematic name is 4-methylhexan-2-amine; four stereoisomers exist) (Figure 1). It is often advertised as "geranamine" alluding to an obscure report on its detection in geranium essential oil (see: ). Recent studies, unable to identify this volatile amine in commercial geranium oil samples and food supplements, refuted the claims that "geranamine" is natural product [201-203]. In fact, DMAA is one of the branched aliphatic amines synthesized by pharmaceutical companies in search for novel amphetamine analogues . It was marketed as a nasal decongestant (Forthran®) until the 1970s. The mild stimulant effect of DMAA is comparable to caffeine , but its use is not without health risk . Though a prohibited doping agent, DMAA is a frequent ingredient of dietary supplements sold for athletes. Immunoassays developed for amphetamine-type drugs may show cross-reactivity with DMAA .
Tourism, migration, international trade as well as the boundless flow of information via the Internet all contribute to the global spread of many once exotic psychoactive drugs [208, 209]. Between January 2005 and December 2012, some 230 new psychoactive substances have been reported to the EWS of EMCDDA but only less than twenty of these can be considered as natural products. For practical reasons, many of them (e.g., bufotenine, harmaline, 5-MeO-DMT, phenethylamine) are certainly obtained by synthesis rather than isolated from a natural source. Acknowledging that the numbers reported by the EMCDDA indicate only the mere presence (actually the detection) of a substance and not the amount of sales or the extent of use, it appears that the new drugs market is now dominated by synthetic substances. Apparently, the importance of natural products and the role of traditional ethnopharmacological research, oriented mainly towards plants, have diminished over the past two decades. In spite of extensive screening campaigns (e.g., [210-213]), hardly any novel natural psychoactive substance has been discovered since the identification of salvinorin A in 1982. Could the natural sources of new drugs be exhausted? Although there are dozens of exotic herbal drugs that are sold and used for their proven or alleged "psychoactivity", neither their psychopharmacology nor their key ingredients have been characterized and it is unlikely that they contain hitherto unknown but potent ingredients. Perhaps marine organisms, a largely untapped source of psychoactive compounds, will provide novel substances with interesting structure and activity [214, 215]. One thing is certain, however: the molecular scaffolds created and used by Nature will continue to serve as key design elements in future generations of (semi-)synthetic substances that could become valuable research tools or even therapeutic agents. It also seems to be inevitable that some of such potent synthetic analogues will be diverted into the recreational scene.
Conflict of interest statement
There are no potential conflicts of interest or any financial or personal relationships with other people or organizations that could inappropriately bias conduct and findings of this study.
1. Koehn FE, Carter GT. The evolving role of natural products in drug discovery. Nat Rev Drug Discov 2005;4(3):206-20. DOI: 10.1038/nrd1657
2. Ratsch C. The encyclopedia of psychoactive plants. Ethnopharmacology and its applications. Rochester, Vermont: Park Street Press; 2005.
3. EFSA (European Food Safety Authority). EFSA Compendium of botanicals that have been reported to contain toxic, addictive, psychotropic or other substances of concern on request of EFSA. EFSA Journal 2009;7(9):1-100.
4. Guzman G, Allen JW, Gartz J. A worldwide geographical distribution of the neurotropic fungi, an analysis and discussion. Annali del Museo Civico di Rovereto, Sezione: Archeologia- Storia-Scienze Naturali 1998;14:189-280. Available from: www.museocivico.rovereto.tn.it/UploadDocs/104_art09_ Guzman___C.pdf.
5. de Haro L, Pommier P. Hallucinatory fish poisoning (ichthyoallyeinotoxism): two case reports from the Western Mediterranean and literature review. Clin Toxicol 2006;44(2):185- 58. DOI: 10.1080/15563650500514590
6. Groark KP. Taxonomic identity of "hallucinogenic" harvester ant (Pogonomyrmex californicus) confirmed. J Ethnobiol 2001;21(2):133-44.
7. Roth BL, Choudhary MS, Khan N, Uluer AZ. High-affinity agonist binding is not sufficient for agonist efficacy at 5-hydroxytryptamine2A receptors: evidence in favor of a modified ternary complex model. J Pharmacol Exp Ther 1997;280(2):576-83.
8. Prisinzano TE. Natural products as tools for neuroscience: discovery and development of novel agents to treat drug abuse. J Nat Prod 2009;72(3):581-7. DOI: 10.1021/ np8005748
9. Advisory Council on the Misuse of Drugs. Khat: A review of its potential harms to the individual and communities in the UK. London: ACMD; 2013. Available from: www.gov.uk/government/publications/khat-report-2013.
10. Douglas H, Boyle M, Lintzeris N. The health impacts of khat: a qualitative study among Somali-Australians. Med J Aust 2011;195(11/12):666-9. DOI: 10.5694/mja11.10166
11. European Monitoring Centre for Drugs and Drug Addiction. Khat use in Europe: implications for European policy. Lisbon, Portugal: EMCDDA; 2011. Available from: www.emcdda.europa.eu/publications/drugs-in-focus/khat.
12. Griffiths P, Lopez D, Sedefov R, Gallegos A, Hughes B, Noor A, Royuela L. Khat use and monitoring drug use in Europe: The current situation and issues for the future. J Ethnopharmacol 2010;132(3):578-83. DOI: 10.1016/j. jep.2010.04.046
13. Odenwald M, Klein A, Warfa N. Introduction to the special issue: The changing use and misuse of khat (Catha edulis)-Tradition, trade and tragedy. J Ethnopharmacol 2010;132(3):537-9. DOI: 10.1016/j.jep.2010.11.012.
14. Szendrei K. The chemistry of khat. Bull Narc 1980;32(3):5-36.
15. Chappell JS, Lee MM. Cathinone preservation in khat evidence via drying. Forensic Sci Int 2010;195(1-3):108-20. DOI: 10.1016/j.forsciint.2009.12.002
16. Geisshusler S, Brenneisen R. The content of psychoactive phenylpropyl and phenylpentenyl khatamines in Catha edulis Forsk. of different origin. J Ethnopharmacol 1987;19(3):269- 77. DOI: 10.1016/0378-8741(87)90004-3
17. Feyissa AM, Kelly JP. A review of the neuropharmacological properties of khat. Prog Neuro-Psychopharmacol Biol Psychiatry 2008;32(5):1147-66. DOI: 10.1016/j.pnpbp.2007.12.033
18. Graziani M, Milella MS, Nencini P. Khat chewing from the pharmacological point of view: an update. Subst Use Misuse 2008;43(6):762-83. DOI: 10.1080/10826080701738992.
19. Rothman RB, Vu N, Partilla JS, Roth BL, Hufesein SJ, Compton-Toth BA, Birkes J, Young R, Glennon RA. In vitro characterization of ephedrine-related stereoisomers at biogenic amine transporters and the receptorome reveals selective actions as norepinephrine transporter substrates. J Pharmacol Exp Ther 2003;307(1):138-45. DOI: 10.1124/ jpet.103.053975
20. Odenwald M. Chronischer Khatkonsum und psychotische Storungen: ein Literaturuberblick und Ausblick. Sucht 2007;53(1):9-22.
21. Al Suwaidi J, Ali WM, Aleryani SL. Cardiovascular complications of Khat. Clin Chim Acta 2013;419(April):11-14. DOI: 10.1016/j.cca.2013.01.007
22. Corkery JM, Schifano F, Oyefeso A, Ghodse AH, Tonia T, Naidoo V, Button J. Overview of literature and information on "khat related" mortality: a call for recognition of the issue and further research. Ann Ist Super Sanità 2011;47(4):445- 64. DOI: 10.4415/ANN_11_04_17
23. Al-Motarreb A, Al-Habori M, Broadley KJ. Khat chewing, cardiovascular diseases and other internal medical problems: The current situation and directions for future research. Journal of Ethnopharmacology 2010;132(3):540-8. DOI: 10.1016/j.jep.2010.07.001
24. Daba D, Hymete A, Bekhit AA, Mohamed AMI, Bekhit AE-DA. Multi residue analysis of pesticides in wheat and khat collected from different regions of Ethiopia. Bull Environ Contam Toxicol 2011;86(3):336-41. DOI: 10.1007/ s00128-011-0207-1
25. Gatter P. Politics of Qat. The role of a drug in Ruling Yemen. Wiesbaden: Dr. Ludwig Reichert Verlag; 2012.
26. Gebissa E. Khat in the Horn of Africa: Historical perspectives and current trends. J Ethnopharmacol 2010;132(3):607- 14. DOI: 10.1016/j.jep.2010.01.063
27. Klein A, Beckerleg S, Hailu D. Regulating khat - Dilemmas and opportunities for the international drug control system. Int J Drug Policy 2009;20(6):509-13. DOI: 10.1016/j.drugpo. 2009.05.002
28. Calkins RF, Aktan GB, Hussain KL. Methcathinone: The next illicit stimulant epidemic? J Psychoactive Drugs 1995;27(3):277-85. DOI: 10.1080/02791072.1995.10472472
29. Bentur Y, Bloom-Krasik A, Raikhlin-Eisenkraft B. Illicit cathinone ("Hagigat") poisoning. Clin Toxicol 2008;46(3):206-10. DOI: 10.1080/15563650701517574
30. Perron BE, Ahmedani BK, Vaughn MG, Glass JE, Abdon A, Wu L-T. Use of Salvia divinorum in a nationally representative sample. Am J Drug Alcohol Abuse 2012;38(1):108-13. DOI: 10.3109/00952990.2011.600397
31. Prisinzano TE, Rothman RB. Salvinorin A analogs as probes in opioid pharmacology. Chem Rev 2008;108(5):1732-43. DOI: 10.1021/cr0782269
32. Ranganathan M, Schnakenberg A, Skosnik PD, Cohen BM, Pittman B, Sewell RA, D'Souza DC. Dose-related behavioral, subjective, endocrine, and psychophysiological effects of the κ opioid agonist salvinorin A in humans. Biol Psychiatry 2012;72(10):871-9. DOI: 10.1016/j.biopsych.2012.06.012
33. Johnson MP, MacLean KA, Reissig CR, Prisinzano TE, Griffiths RR. Human psychopharmacology and dose-effects of salvinorin A, a kappa opioid agonist hallucinogen present in the plant Salvia divinorum. Drug Alcohol Depend 2011;115(1- 2):150-5. DOI: 10.1016/j.drugalcdep.2010.11.005
34. Topcu G. Bioactive triterpenoids from Salvia species. J Nat Prod 2006;69(3):482-7. DOI: 10.1021/np0600402
35. MacLean KA, Johnson MW, Reissig CJ, Prisinzano TE, Griffiths RR. Dose-related effects of salvinorin A in humans: dissociative, hallucinogenic, and memory effects. Psychopharmacology 2013;226(2):381-92. DOI: 10.1007/s00213- 012-2912-9
36. Sumnall HR, Measham F, Brandt SD, Cole JC. Salvia divinorum use and phenomenology: results from an online survey. J Psychopharmacol 2011;2(11):1496-507. DOI: 10.1177/0269881110385596
37. Albertson DN, Grubbs LE. Subjective effects of Salvia divinorum: LSD- or marijuana-like? J Psychoactive Drugs 2009;41(3):213-7.
38. Hooker JM, Xu Y, Schiffer W, Shea C, Carter P, Fowler JS. Pharmacokinetics of the potent hallucinogen, salvinorin A in primates parallels the rapid onset and short duration of effects in humans. NeuroImage 2008;41(3):1044-50. DOI: 10.1016/j.neuroimage.2008.03.003
39. Schmidt MD, Schmidt MS, Butelman ER, Harding WW, Tidgewell K, Murry DJ, Kreek MJ, Prisinzano TE. Pharmacokinetics of the plant-derived κ-opioid hallucinogen salvinorin A in nonhuman primates. Synapse 2005;58(3):208-10.
40. Nichols DE. Hallucinogens. Pharmacol Ther 2004;101(2):131-81.
41. Roth BL, Baner K, Westkaemper R, Siebert D, Rice KC, Steinberg S, Ernsberger P, Rothman RB. Salvinorin A: A potent naturally occurring nonnitrogenous κ-opioid selective agonist. Proc Natl Acad Sci U S A 2002;99(18):11934- 11939. DOI: 10.1073/pnas.182234399
42. Cunningham CW, Rothman RB, Prisinzano TE. Neuropharmacology of the naturally occurring κ-opioid hallucinogen salvinorin A. Pharmacol Rev 2011;63(2):316-47. DOI: 10.1124/pr.110.003244
43. Wu H, Wacker D, Mileni M, Katritch V, Han GW, Vardy E, Liu W, Thompson AA, Huang X-P, Carroll FI, Mascarella SW, Westkaemper RB, Mosier PD, Roth BL, Cherezov V, Stevens RC. Structure of the human κ-opioid receptor in complex with JDTic. Nature 2012;485(7398):327-32. DOI: 10.1038/nature10939
44. Aviello G, Borrelli F, Guida F, Romano B, Lewellyn K, De Chiaro M, Luongo L, Zjawiony JK, Maione S, Izzo AA, Capasso R. Ultrapotent effects of salvinorin A, a hallucinogenic compound from Salvia divinorum, on LPS-stimulated macrophages and its anti-inflammatory action in vivo. J Mol Med 2011;89(9):891-902. DOI: 10.1007/s00109-011-0752-4
45. McCurdy CR, Sufka KJ, Smith GH, Warnick JE, Nieto MJ. Antinociceptive profile of salvinorin A, a structurally unique kappa opioid receptor agonist. Pharmacol Biochem Behav 2005;83(1):109-13. DOI: 10.1016/j.pbb.2005.12.011
46. Carlezon WA Jr, Beguin C, Knoll AT, Cohen BM. Kappaopioid ligands in the study and treatment of mood disorders. Pharmacol Ther 2009;123(3):334-43. DOI: 10.1016/j. pharmthera.2009.05.008
47. Vortherms TA, Roth BL. Salvinorin A. From natural product to human therapeutics. Mol Interv 2006;6(5):257-65. DOI: 10.1124/mi.6.5.7
48. Munro TA, Duncan KK, Xu W, Wang Y, Liu-Chen L-Y, Carlezon WA, Jr, Cohen BM, Beguin C. Standard protecting groups create potent and selective κ opioids: Salvinorin B alkoxymethyl ethers. Bioorg Med Chem 2008;16(3):1279-86. DOI: 10.1016/j.bmc.2007.10.06
49. Lamb K, Tidgewell K, Simpson DS, Bohn LM, Prisinzano TE. Antinociceptive effects of herkinorin, a MOP receptor agonist derived from salvinorin A in the formalin test in rats: New concepts in mu-opioid receptor pharmacology. Drug Alcohol Depend 2012;121(3):181-8. DOI: 10.1016/j.drugalcdep. 2011.10.026
50. Butelman ER, Rus S, Simpson DS, Wolf A, Prisinzano TE, Kreek MJ. The effects of herkinorin, the first μ-selective ligand from a salvinorin A-derived scaffold, in a neuroendocrine biomarker assay in nonhuman primates. J Pharmacol Exp Ther 2008;327(1):154-160. DOI: 10.1124/ jpet.108.140079
51. Mowry M, Mosher M, Briner W. Acute physiologic and chronic histologic changes in rats and mice exposed to the unique hallucinogen salvinorin A. J Psychoactive Drugs 2003;35(3):379- 82. DOI: 10.1080/02791072.2003.10400021
52. Tsujikawa K, Kuwayama K, Miyaguchi H, Kanamori T, Iwata YT, Yoshida T, Inoue H. Determination of salvinorin A and salvinorin B in Salvia divinorum-related products circulated in Japan. Forensic Sci Int 2008;180(2-3):105-9. DOI: 10.1016/j. forsciint.2008.07.008
53. Wolowich WR, Perkins AM, Cienki JJ. Analysis of the psychoactive terpenoid salvinorin A content in five Salvia divinorum herbal products. Pharmacotherapy 2006;26(9):1268-72. DOI: 10.1592/phco.26.9.1268
54. Hintzen A, Passie T. The pharmacology of LSD. A critical review. Oxford: Oxford University Press; 2010.
55. Hofmann A. LSD - Mein Sorgenkind. Die Entdeckung einer "Wunderdroge". Stuttgart: Klett-Cotta; 1979.
56. Schultes RE, Hofmann A. The botany and chemistry of hallucinogens, 2nd ed. Springfield: Charles C Thomas Publisher; 1980.
57. Genest K, Sahasrabudhe MR. Alkaloids and lipids in Ipomoea, Rivea and Convolvulus and their application to chemotaxonomy. Econ Bot 1966;20(4):416-28. DOI: 10.1007/BF02904064
58. Hylin JW, Watson DP. Ergoline alkaloids in tropical wood roses. Science 1965;148(3669):499-500. DOI: 10.1126/science. 148.3669.499
59. Kremer C, Paulke A, Wunder C, Toennes SW. Variable adverse effects in subjects after ingestion of equal doses of Argyreia nervosa seeds. Forensic Sci Int 2012;214(1-3):e6-e8. DOI: 10.1016/j.forsciint.2011.06.025
60. Markert A, Steffan N, Ploss K, Hellwig S, Steiner U, Drewke C, Li S-M, Boland W, Leistner E. Biosynthesis and accumulation of ergoline alkaloids in a mutualistic association between Ipomoea asarifolia (Convolvulaceae) and a clavicipitalean fungus. Plant Physiol 2008;147(1):296-305. DOI: 10.1104/pp.108.116699
61. Kucht S, Groß J, Hussein Y, Grothe T, Keller U, Basar S, Konig WA, Steiner U, Leistner E. Elimination of ergoline alkaloids following treatment of Ipomoea asarifolia (Convolvulaceae) with fungicides. Planta 2004;219(4):619-25. DOI: 10.1007/s00425-004-1261-2
62. Powell RG, Petroski RJ. Alkaloid toxins in endophyte-infected grasses. Nat Toxins 1992;1(3):163-70. DOI: 10.1002/ nt.2620010304
63. Isbell H, Gorodetzky CW. Effect of alkaloids of ololiuqui in man. Psychopharmacologia (Berl) 1966;8(5):331-9. DOI: 10.1007/BF00453511
64. Paulke A, Kremer C, Wunder C, Achenbach J, Djahanschiri B, Elias A, Schwed JS, Hubner H, Gmeiner P, Proschak E, Toennes SW, Stark H. Argyreia nervosa (Burm. f.): Receptor profiling of lysergic acid amide and other potential psychedelic LSD-like compounds by computational and binding assay approaches. J Ethnopharmacol 2013;148(2):492-7. DOI: 10.1016/j.jep.2013.04.044
65. Juszczak GR, Swiergiel AH. Recreational use of Dlysergamide from the seeds of Argyreia nervosa, Ipomoea tricolor, Ipomoea violacea, and Ipomoea purpurea in Poland. J Psychoactive Drugs 2013;45(1):79-93. DOI: 10.1080/02791072.2013.763570
66. Paulke A, Kremer C, Wunder C, Toennes SW. Analysis of lysergic acid amide in human serum and urine after ingestion of Argyreia nervose seeds. Anal Bioanal Chem 2012;404(2):531- 8. DOI: 10.1007/s00216-012-6121-5
67. Klinke HB, Muller IB, Steffenrud S, Dahl-Sorensen R. Two cases of lysergamide intoxication by ingestion of seeds from Hawaiian Baby Woodrose. Forensic Sci Intl 2010;197(1- 3):e1-e5. DOI: 10.1016/j.forsciint.2009.11.017
68. Borsutzky M, Passie T, Paetzold W, Emrich HM, Schneider U. Hawaiianische Holzrose: (Psycho-)Pharmakologische Wirkungen der Samen der Argyreia nervosa. Nervenartz 2002;73(9):892-6. DOI: 10.1007/s00115-002-1374-4
69. dos Santos RG. The ethnopharmacology of ayahuasca. Trivandrum: Transworld Research Network; 2011. Available from: www.trnres.com/ebookcontents.php?id=93.
70. Metzner R (Ed). Sacred vine of spirits: Ayahuasca. Rochester, Vermont: Park Street Press; 2006.
71. dos Santos RG, Grasa E, Valle M, Ballester MR, Bouso JC, Nomdedeu JF, Homs R, Barbanoj MJ, Riba, J. Pharmacology of ayahuasca administered in two repeated doses. Psychopharmacology (Berl) 2012;219(4):1039-53. DOI: 10.1007/ s00213-011-2434-x
72. de Araujo DB, Riberio S, Cecchi GA, Carvalho FM, Sanchez TA, Pinto JP, de Martinis BS, Crippa JA, Hallak JEC, Santos AC. Seeing with the eyes shut: neural basis of enhanced imagery following ayahuasca ingestion. Human Brain Mapp 2011;33(11):2550-60. DOI: 10.1002/hbm.21381
73. Riba J, Valle M, Urbano G, Yritia M, Morte A, Barbanoj MJ. Human pharmacology of ayahuasca: subjective and cardiovascular effects, monoamine metabolite excretion, and pharmacokinetics. J Pharmacol ExpTher 2003;306(1):73-83. DOI: 10.1124/jpet.103.049882
74. dos Santos RG. Safety and side effects of ayahuasca in humans - An overview focusing on developmental toxicology. J Psychoactive Drugs 2013;45(1):68-78.
75. Bouso JC, Gonzalez D, Fondevila S, Cutchet M, Fernandez X, Riberio Barbosa PC, Alcazar-Corcoles MA, Araujo WS, Barbanoj MJ, Fabregas JM, Riba J. Personality, psychopathology, life attitudes and neuropsychological performance among ritual users of ayahuasca: a longitudinal study. PLoS One 2012;7(8):e42421. DOI: 10.1371/journal. pone.0042421
76. Liester MB, Prickett JI. Hypotheses regarding the mechanisms of ayahuasca in the treatment of addictions. J Psychoactive Drugs 2012;44(3):200-8. DOI: 10.1080/02791072.2012.704590
77. Herraiz T, Gonzalez D, Ancin-Azpilicueta C, Aran VJ, Guillen H. s-Carboline alkaloids in Peganum harmala and inhibition of human monoamine oxidase (MAO). Food Chem Toxicol 2010;48(3):839-45. DOI: 10.1016/j.fct.2009.12.019
78. Callaway JC, Brito GS, Neves ES. Phytochemical analyses of Banisteriopsis caapi and Psychotria viridis. J Psychoactive Drugs 2005;37(2):145-50.
79. Cao R, Peng W, Wang Z, Xu A. s-Carboline alkaloids: biochemical and pharmacological functions. Curr Med Chem 2007;14(4):479-500. DOI: 10.2174/092986707779940998
80. Grella B, Dukat M, Young R, Teitler M, Herrick-Davis K, Gauthier CB, Glennon RA. Investigation of hallucinogenic and related s-carbolines. Drug Alcohol Depend 1998;50(2):99-107. DOI: 10.1016/S0376-8716(97)00163-4
81. Ingale AG, Hivrale AU. Pharmacological studies of Passiflora sp. and their bioactive compounds. Afr J Plant Sci 2010;41(10):417-26.
82. European Medicines Agency. Assessment report on Passiflora incarnata L., herba. London, UK: EMA; 2008.
83. Rodd R, Sumabila A. Yopo, ethnicity and social change: a comparative analysis of Piaroa and Cuiva yopo use. J Psychoactive Drugs 2011;43(1):36-45. DOI: 10.1080/02791072.2011.566499
84. Ott J. Ayahuasca analogues. Pangæan entheogens. Kennewick, WA: Natural Products Co; 1994.
85. Barker SA, McIlhenny EH, Strassman R. A critical review of reports of endogenous psychedelic N,N-dimethyltryptamines in humans: 1955-2010. Drug Test Anal 2012;4(7- 8):617-35. DOI: 10.1002/dta.422
86. Ott J. Pharmahuasca: human pharmacology of oral DMT plus harmine. J Psychoactive Drugs 1999;31(2):171-7. DOI: 10.1080/02791072.1999.10471741
87. Gonzales v. O Centro Espirita Beneficiente Uniao do Vegetal. 2006. 546 U.S. 418. Available from: www.supremecourt.gov/opinions/05pdf/04-1084.pdf.
88. Anderson BT, Labate BC, Meyer M, Tupper KW, Barbosa PCR, Grob CS, Dawson A, McKenna D. Statement on ayahuasca. Int J Drug Policy 2012;23(3):173-5. DOI: 10.1016/j. drugpo.2012.02.007
89. Kostakis C, Byard RW. Sudden death associated with intravenous injection of toad extract. Forensic Sci Int 2009;188(1- 3):e1-e5. DOI: 10.1016/j.forsciint.2009.02.006
90. Weil AT, Davis W. Bufo alvarius: a potent hallucinogen of animal origin. J Ethnopharmacol 1994;41(1):1-8. DOI: 10.1016/0378-8741(94)90051-5
91. Lyttle T, Goldstein D, Gartz J. Bufo toads and bufotenine: Fact and fiction surrounding an alleged psychedelic. J Psychoactive Drugs 1996;28(3):267-90. DOI: 10.1080/02791072.1996.10472488
92. Moretti C, Gaillard Y, Grenand P, Bévalot FP, Prévosto J-M. Identification of 5-hydroxytryptamine (bufotenine) in takini (Brosimum acutifolium Huber subsp. acutifolium C.C. Berg, Moraceae), a shamanic potion used in the Guiana Plateau. J Ethnopharmacol 2006;106(2):198-202. DOI: 10.1016/j. jep.2005.12.022. ISSN: 0378-8741
93. Shen H-W, Jiang X-L, Winter JC, Yu A-M. Psychedelic 5-methoxy-N,N-tryptamine: Metabolism, pharmacokinetics, drug interactions, and pharmacological actions. Curr Drug Metab 2010;11(8):659-66. DOI: 10.2174/138920010794233495
94. Karkkainen J, Forsstrom T, Tornaeus J, Wahala K, Kiuru P, Honkanen A, Stenman U-H, Turpeinen U, Hesso A. Potentially hallucinogenic 5-hydroxytryptamine receptor ligands bufotenine and dimethyltryptamine in blood and tissues. Scand J Clin Lab Invest 2005;65(3):189-99.
95. Fuller RW, Snoddy HD, Perry KW. Tissue distribution, metabolism and effects of bufotenine administered to rats. Neuropharmacology 1995;34(7):799-804. DOI: 10.1016/0028- 3908(95)00049-C
96. Hardeland R. Melatonin metabolism in the central nervous system. Curr Neuropharmacol 2010;8(3):168-81. DOI: 10.2174/157015910792246164
97. Alper KR, Lotsof HS, Kaplan CD. The ibogaine medical subculture. J Ethnopharmacol 2008;115(1):9-24. DOI: 10.1016/j.jep.2007.08.034
98. Lotsof HS, Wachtel B. Manual for ibogaine therapy. Screening, safety, monitoring & aftercare. 2003. Available from: www.ibogaine.org/manual.html.
99. Alper KR, Glick SD (Eds). The Alkaloids. Vol. 56, Ibogaine: Proceedings of the first international conference. San Diego: Academic Press; 2001.
100. Alper KR, Stajić M, Gill JR. Fatalities temporally associated with the ingestion of ibogaine. J Forensic Sci 2012;57(2):398- 412. DOI: 10.1111/j.1556-4029.2011.02008.x
101. Paling FP, Andrews LM, Valk GD, Blom HJ. Life-threatening complications of ibogaine: three case reports. Neth J Med 2012;70(9):422-4.
102. Maas U, Strubelt S. Fatalities after taking ibogaine in addiction treatment could be related to sudden cardiac death caused by autonomic dysfunction. Med Hypotheses 2006;67(4):960-4. DOI: 10.1016/j.mehy.2006.02.050
103. Koenig X, Kovar M, Boehm S, Sandtner W, Hilber K. Anti-addiction drug ibogaine inhibits hERG channels: a cardiac arrhythmia risk. 2013; Addict Biol (in press) DOI: 10.1111/j.1369-1600.2012.00447x
104. Vlaanderen L, Martial LC, van der Voort PHJ, Oosterwerff E, Somsen GA, Franssen EJF. Cardiac arrest after ibogaine ingestion. J Clin Toxicol 2013;S12:005; DOI: 10.4172/2161- 0495.S12-005
105. Carnicella S, He D-Y, Yowell QV, Glick SD, Ron D. Noribogaine, but not 18-MC, exhibits similar actions as ibogaine on GDNF expression and ethanol self-administration. Addict Biol 2010;15(4):424-33. DOI: 10.1111/j.1369- 1600.2010.00251.x
106. Kontrimavičiūtė V, Mathieu O, Balas L, Escale R, Blayac JP, Bressolle FMM. Ibogaine and noribogaine: structural analysis and stability studies. Use of LC-MS to determine alkaloid contents of the root bark of Tabernanthe iboga. J Liq Chromatogr Related Technol 2007;30(8):1077-92. DOI: 10.1080/10826070601128451
107. Maisonneuve IM, Glick SD. Anti-addictive actions of an iboga alkaloid congener: a novel mechanism for a novel treatment. Pharmacol Biochem Behav 2003;75(3):607-18. DOI: 10.1016/S0091-3057(03)00119-9
108. Popik P, Skolnick P. Pharmacology of ibogaine and ibogainerelated alkaloids. In: Cordell GA (Ed). The Alkaloids, Vol. 52. San Diego: Academic Press; 1999. DOI: 10.1016/S0099- 9598(08)60027-9
109. He D-Y, McGough NNH, Ravindranathan A, Jeanblanc J, Logrip ML, Phamluong K, Janak PH, Ron D. Glial cell linederived neurotrophic factor mediates the desirable actions of the anti-addiction drug ibogaine against alcohol consumption. J Neurosci 2005;25(3):619-28. DOI: 10.1523/JNEUROSCI. 3959-04.2005
110. Kubilienė A, Marksienė R, Kazlauskas S, Sadauskienė I, Ražukas A, Ivanov L. Acute toxicity of ibogaine and noribogaine. Medicina (Kaunas) 2008;44(12):984-8.
111. Adkins JE, Boyer EW, McCurdy CR. Mitragyna speciosa, a psychoactive tree from Southeast Asia with opioid activity. Curr Top Med Chem 2011;11(9):1165-75.
112. Kikura-Hanajiri R, Kawamura M, Maruyama T, Kitajima M, Takayama H, Goda Y. Simultaneous analysis of mitragynine, 7-hydroxymitragynine, and other alkaloids in the psychotropic plant "kratom" (Mitragyna speciosa) by LC-ESI-MS. Forensic Toxicol 2009;27(2):67-74. DOI: 10.1007/s11419- 009-0070-5
113. Takayama H. Chemistry and pharmacology of analgesic indole alkaloids from the rubiaceous plant, Mitragyna speciosa. Chem Pharm Bull 2004;52(8):916-28. DOI: 10.1002/ chin.200452220
114. Vicknasingam B, Narayanan S, Beng GT, Mansor SM. The informal use of ketum (Mitragyna speciosa) for opioid withdrawal in the northern states of peninsular Malaysia and implications for drug substitution therapy. Int J Drug Policy 2010;21(4):283-8. DOI: 10.1016/j.drugpo.2009.12.003
115. Boyer EW, Babu KM, Adkins JE, McCurdy CR, Halpern JH. Self-treatment of opioid withdrawal using kratom (Mitragyna speciosa korth). Addiction 2008;103(6):1048-50. DOI: 10.1111/j.1360-0443.2008.02209.x
116. Grewal KS. The effect of mitragynine on man. Br J Med Psychol 1932;12(1):41-58. DOI: 10.1111/j.2044-8341.1932. tb01062.x
117. Saingam D, Assanangkornchai S, Geater AF, Balthip Q. Pattern and consequences of krathom (Mitragyna speciosa Korth.) use among male villagers in southern Thailand: a qualitative study. Int J Drug Policy 2013;24(4):351-8. DOI: 10.1016/j.drugpo.2012.09.004
118. McWhirter L, Morris S. A case report of inpatient detoxification after kratom (Mitragyna speciosa) dependence. Eur Addict Res 2010;16(4):229-31. DOI: 10.1159/000320288
119. Stolt A-C, Schroder H, Neurath H, Grecksch G, Hollt V, Meyer MR, Maurer HH, Ziebolz N, Havemann-Reinecke U, Becker A. Behavioral and neurochemical characterization of kratom (Mitragyna speciosa) extract. Psychopharmacology 2014;231(1):13-25. DOI: 10.1007/s00213-013-3201-y.
120. Macko E, Weisbach JA, Douglas B. Some observations on the pharmacology of mitragynine. Arch Int Pharmacodyn Ther 1972;198(1):145-61.
121. Matsumoto K, Horie S, Takayama H, Ishikawa H, Aimi N, Ponglux D, Murayama T, Watanabe K. Antinociception, tolerance and withdrawal symptoms induced by 7-hydroxymitragynine, an alkaloid from the Thai medicinal herb Mitragyna speciosa. Life Sci 2005;78(1):2-7. DOI: 10.1016/j. lfs.2004.10.086
122. Neerman MF, Frost RE, Deking J. A drug fatality involving kratom. J Forensic Sci 2012;58(S1):S278-S279. DOI: 10.1111/1556-4029.12009
123. Kapp FG, Maurer HH, Auwarter V, Winkelman M, Hermanns- Clausen M. Intrahepatic cholestasis following abuse of powdered kratom (Mitragyna speciosa). J Med Toxicol 2011;7(3):227-31. DOI: 10.1007/s13181-011-0155-5
124. Tungtananuwat W, Lawanprasert S. Fatal 4x100: Homemade kratom juice cocktail. J Health Res 2010;24(1):43-7.
125. Kronstrand R, Roman M, Thelander G, Eriksson A. Unintentional fatal intoxications with mitragynine and O-desmethyltramadol from the herbal blend Krypton. J Anal Toxicol 2011;35(4):242-7. DOI: 10.1093/anatox/35.4.242
126. US DoJ (Unites States Department of Justice). Anchorage man sentenced to 160 months for conspiracy to distribute synthetic heroin. 2012. Available at: www.justice.gov/usao/ak/news/2012/March_2012/BrackstonMoores.html.
127. Chittrakarn S, Penjamras P, Keawpradub N. Quantitative analysis of mitragynine, codeine, caffeine, chlorpheniramine and phenylephrine in a kratom (Mitragyna speciosa Korth.) coctail using high-performance liquid chromatography. Forensic Sci Int 2012;217(1-3):81-6. DOI: 10.1016/j.forsciint. 2011.10.027
128. Assanangkornchai S, Aramrattana A, Perngparn U, Kanato M, Kanika N, Sirivongs Na Ayudhaya A. Current situation of substance-related problems in Thailand. J Psychiatr Assoc Thai 2008;53(Suppl. 1):24S-36S.
129. FAO-WHO. Discussion paper on the development of a standard for kava. CX/NASWP 10/11/8. Codex Alimentarius Comission. Rome: Joint Office of the Food and Agriculture Organization of the United Nations and the World Health Organization; 2010.
130. Lebot V, Merlin M, Lindstrom L. Kava - the Pacific elixir: the definitive guide to its ethnobotany, history, and chemistry. Rochester, Vermont: Healing Art Press; 1997.
131. Sarris J, LaPorte E, Schweitzer I. Kava: a comprehensive review of efficacy, safety, and psychopharmacology. Aust N Z J Psychiatry 2011;45(1):27-35. DOI: 10.3109/00048674.2010.522554
132. Singh YN. Pharmacology and toxicology of kava and kavalactones. In: Singh YN (Ed). Kava: from ethnology to pharmacology. Boca Raton: CRC Press; 2004.
133. Ramzan I, Tran VH. Chemistry of kava and kavalactones. In: Singh YN (Ed). Kava: from ethnology to pharmacology. Boca Raton: CRC Press; 2004.
134. Parmar VS, Jain SC, Bisht KS, Jain R, Taneja P, Jha A, Tyagi OD, Prasad AK, Wengel J, Olsen CE, Boll PM. Phytochemistry of the genus Piper. Phytochemistry 1997;46(4):597-673. DOI: 10.1016/S0031-9422(97)00328-2
135. Lasme P, Davrieux F, Montet D, Lebot V. Quantification of kavalactones and determination of kava (Piper methysticum) chemotypes using near-infrared reflectance spectroscopy for quality control in Vanuatu. J Agric Food Chem 2008;56(13):4976-81. DOI: 10.1021/jf800439g.
136. Simeoni P, Lebot V. Identification of factors determining kavalactone content and chemotype in Kava (Piper methysticum Forst. f.). Biochem Syst Ecol 2002;30(5):413-24. DOI: 10.1016/S0305-1978(01)00093-X
137. Ligresti A, Villano R, Allara M, Ujvary I, Di Marzo V. Kavalactones and the endocannabinoid system: the plant-derived yangonin is a novel CB1 receptor ligand. Pharmacol Res 2012;66(2):163-9. DOI: 10.1016/j.phrs.2012.04.003
138. Ji T, Lin C, Krill LS, Eskander R, Guo Y, Zi X, Hoang BH. Flavokawain B, a kava chalcone, inhibits growth of human osteosarcoma cells through G2/M cell cycle arrest and apoptosis. Mol Cancer 2013;21:55. DOI: 10.1186/1476-4598- 12-55.
139. Shimoda LMN, Park C, Stokes AJ, Gomes HH, Turner H. Pacific island 'Awa (kava) extracts, but not isolated kavalactones, promote proinflammatory responses in model mast cells. Phytother Res 2012;26(12):1934-41. DOI: 10.1002/ ptr.4652
140. Sarris J, Stough C, Bousman CA, Wahid ZT, Murray G, Teschke R, Savage KM, Dowell A, Ng C, Schweitzer I. Kava in the treatment of generalized anxiety disorder: A double-blind, randomized, placebo-controlled study. J Clin Psychopharmacol 2013;33(5):643-8. DOI: 10.1097/ JCP.0b013e318291be67
141. Teschke R, Sarris J, Schweitzer I. Kava hepatotoxicity in traditional and modern use: The presumed Pacific kava paradox hypothesis revisited. Br J Clin Pharmacol 2012;73(2):170-4. DOI: 10.1111/j.1365-2125.2011.04070.x
142. Rychetnik L, Madronio CM. The health and social effects of drinking water-based infusions of kava: A review of the evidence. Drug Alcohol Rev 2011;30(1):74-83. DOI: 10.1111/j.1465-3362.2010.00184.x
143. Teschke R, Lebot V. Proposal for a Kava Quality Standardization Code. Food Chem Toxicol 2011;49(10):2503-16. DOI: 10.1016/j.fct.2011.06.075
144. Furber S, Jackson J, Johnson K, Sukara R, Franco L. A qualitative study on tobacco smoking and betel quid use among Burmese refugees in Australia. J Immigr Minor Health 2013;15(6):1133-6. DOI: 10.1007/s10903-013-9881-x
145. Auluck A, Hislop G, Pogh C, Zhang L, Rosin MP. Areca nut and betel quid chewing among South Asian immigrants to Western countries and its implications for oral cancer screening. Rural Remote Health 2009;9(2):1118. Available from: http://www.rrh.org.au/publishedarticles/article_print_1118.pdf.
146. Blank M, Deshpande L, Balster RL. Availability and characteristics of betel products in the U.S. J Psychoactive Drugs 2008;40(3):309-13. DOI: 10.1080/02791072.2008.10400646
147. Gupta PC, Warnakulasuriya S. Global epidemiology of areca nut usage. Addict Biol 2002;7(1):77-83. DOI: 10.1080/13556210020091437
148. Rooney DF. Betel chewing traditions in South-East Asia. Oxford: Oxford University Press; 1993.
149. CRNIndia. Areca nut. 2012; Available from: http://crnindia.com/commodity/arecanut.html.
150. Osborne PG, Chou T-S, Shen T-W. Characterization of the psychological, physiological and EEG profile of acute betel quid intoxication in naïve subjects. PLoS One 2011;6(8):e23874. DOI: 10.1371/journal.pone.0023874
151. International Agency for Research on Cancer. Betel-quid and areca-nut chewing and some areca-nut-derived nitrosamines / IARC Working Group on the Evaluation of Carcinogenic Risks to Humans. IARC Monographs on the Evaluation of Carcinogenic Risks to Humans. Vol. 85. Lyon: IARC; 2004.
152. Sharan RN, Mehrotra R, Choudhury Y, Asotra K. Association of betel nut with carcinogenesis: Revisit with a clinical perspective. PLoS ONE 2012;7(8):e42759. DOI: 10.1371/ journal.pone.0042759
153. Lin K-H, Lin C-Y, Liu C-C, Chou M-Y, Lin J-K. Arecoline N-oxide: Its mutagenicity and possible role as ultimate carcinogen in areca oral carcinogenesis. J Agric Food Chem 2011;59(7):3420-8. DOI: 10.1021/jf104831n
154. Sarode SC, Mahuli A, Sarode GS, Mahuli S. Why only areca nut chewing cannot cause oral submucous fibrosis? Med Hypotheses 2013;81(1):47-9. DOI: 10.1016/j.mehy.2013.02.025
155. Rai MP, Thilakchand KR, Palatty PL, Rao P, Rao S, Bhat HP, Baliga MS. Piper betel Linn (betel vine), the maligned Southeast Asian medicinal plant possesses cancer preventive effects: Time to reconsider the wronged opinion. Asian Pac J Cancer Prev 2011;12(9):2149-56.
156. Raffaele KC, Asthana S, Berardi A, Haxby JV, Morris PP, Schapiro MB, Soncrant TT. Differential response to cholinergic agonist arecoline among different cognitive modalities in Alzheimer's disease. Neuropsychopharmacology 1996;15(2):163-70. DOI: 10.1016/0893-133X(95)00179-H
157. Lee C-H, Ko AM-S, Yen C-F, Chu K-S, Gao Y-J, Warnakulasuriya S, Sunarjo Ibrahim SO, Zain RB, Patrick WK, Ko Y-C. Betel-quid dependence and oral potentially malignant disorders in six Asian countries. Br J Psychiatry 2012;201(5):383-91. DOI: 10.1192/bjp.bp.111.107961
158. Ruhle KH, Criscuolo D, Dieterich HA, Kohler D, Riedel G. Objective evaluation of dextromethorphan and glaucine as antitussive agents. Br J Clin Pharmacol 1984;17(5):521-4.
159. Kasé Y, Kawaguchi M, Takahama K, Miyata T, Hirotsu I, Hitoshi T, Okano Y. Pharmacological studies on dlglaucine phosphate as an antitussive. Arzneimittelforschung 1983;33(7):936-46.
160. Schuster CR, Aigner T, Johanson CE, Gieske TH. Experimental studies of the abuse potential of d,l-glaucine·1.5- phosphate in rhesus monkeys. Pharmacol Biochem Behav 1982;16(5):851-4. DOI: 10.1016/0091-3057(82)90248-9
161. Lei Y, Tan J, Wink M, Ma Y, Li N, Su G. An isoquinoline alkaloid from the Chinese herbal plant Corydalis yanhusuo W.T. Wang inhibits P-glycoproptein and multidrug resistance-associate protein 1. Food Chem 2013;136(3-4):1117-21. DOI: 10.1016/j.foodchem.2012.09.059
162. Dargan PI, Button J, Hawkins L, Archer JRH, Ovaska H, Lidder S, Ramsey J, Holt DW, Wood DM. Detection of the pharmaceutical agent glaucine as a recreational drug. Eur J Clin Pharmacol 2008;64(5):553-4. DOI: 10.1007/s00228-007-0451-9
163. Rovinskii VI. [Acute glaucine syndrome in the physician's practice: the clinical picture and potential danger]. Klin Med (Mosk) 2006;84(11):68-70. (in Russian).
164. Geppert B, Wachowiak R, żaba C. Glaucine as a non-declared active component of "legal highs". Problems of Forensic Sciences 2011;84:401-8.
165. Kavanagh P, Spiers P, O'Brien J, McNamara S, Angelov D, Mullan D. Talbot B, Ryder S. Head shop 'legal highs' active constituents identification chart (July - August 2010. 714'- '823'). 2010. Available from: www.medicine.tcd.ie/bulletin/oct-nov-2010/HSID Poster714-823.pdf.
166. Ratsch A, Steadman KJ, Bogossian F. The pituri story: a review of the historical literature surrounding traditional Australian Aborigin use of nicotine in Central Australia. J Ethnobiol Ethnomed 2010;6:26. DOI: 10.1186/1746-4269-6-26.
167. Luanratana O, Griffin WJ. Alkaloids of Duboisia hopwoodii. Phytochemistry 1982;21(2):449-51. DOI: 10.1016/S0031- 9422(00)95286-5
168. Yasumoto M. The psychotropic Kiéri in Huichol culture. In: Schaefer SB, Furst PT (Eds). People of the peyote: Huichol indian history, religion, & survival. Albuquerque: University of New Mexico Press; 1996.
169. White PF, Tang J, Song D, Coleman JE, Wender RH, Ogunnaike B, Sloninsky A, Kapu R, Shah M, Webb T. Transdermal scopolamine: an alternative to ondansetron and droperidol for the prevention of postoperative and postdischarge emetic symptoms. Anest Analg 2007;104(1):92-6. DOI: 10.1213/01. ane.0000250364.91567.72
170. Stella L, Vitelli MR, Palazzo E, Oliva P, De Novellis V, Capuano V, Scafuro MA, Berrino L, Rossi F, Maione S. Datura stramonium intake: A report on three cases. J Psychoactive Drugs 2010;42(4):507-12.
171. Vearrier D, Greenberg MI. Anticholinergic delirium following Datura stramonium ingestion: Implications for the Internet age. J Emerg Trauma Shock 2010;3(3):303. DOI: 10.4103/0974-2700.66565
172. Ardila-Ardila A, Moreno CB, Ardila-Gómez SE. Intoxicacion por escopolamina ("burundanga"): perdida de la capacidad de tomar decisiones. Rev Neurol 2006;42(2):125-8.
173. Uribe-Granja MG, Moreno-Lopez CL, Zamora-Suarez A, Acosta PL. Perfil epidemiológico de la intoxicación con burundanga en la clinica Uribe Cualla S. A. de Bogota, D. C. Acta Neurológica Colombiana 2005;21(3):197-201.
174. Festi F, Samorini G. Scheda Psicoattiva XVI - Psychoactive Card XVI: Lactuca L. (lattuga, lettuce). Eleusis 2004;(8):85-112.
175. Amorim MHR, Gil da Costa RM, Lopes C, Bastos MMSM. Sesquiterpene lactones: Adverse health effects and toxicity mechanisms. Crit Rev Toxicology 2013;43(7):559-79. DOI: 10.3109/10408444.2013.813905
176. Sessa RA, Bennett MH, Lewis MJ, Mansfield JW, Beale MH. Metabolite profiling of sesquiterpene lactones from Lactuca species. Major latex components are novel oxalate and sulfate conjugates of lactucin and its derivatives. J Biol Chem 2000;275(35):26877-84. DOI: 10.1074/jbc. M000244200
177. Wesołowska A, Nikiforuk A, Michalska K, Kisiel W, Chojnacka- Wojcik E. Analgesic and sedative activities of lactucin and some lactucin-like guaianolides in mice. J Ethnopharmacol 2006;107(2):254-8. DOI: 10.1016/j.jep.2006.03.003
178. Funke I, Siems W-E, Schenk R, Melzig MF. Lactuca virosa L. und Lactucarium: Molekularpharmakologische Untersuchungen zur Erklarung der analgetischen Potenz. Z Phytother 2002;23(1):40-5.
179. Besharat S, Besharat M, Jabbari A. Wild lettuce (Lactuca virosa) toxicity. BMJ Case Rep 2009; DOI: 10.1136/ bcr.06.2008.0134
180. Mullins ME, Horowitz BZ. The case of the salad shooters: intravenous injection of wild lettuce extract. Vet Hum Toxicol 1998;40(5):290-1.
181. Patnala S, Kanfer I. Investigations of the phytochemical content of Sceletium tortuosum following the preparation of "Kougoed" by fermentation of plant material. J Ethnopharmacol 2009;121(1):86-91. DOI: 10.1016/j.jep.2008.10.008
182. Gericke N, Viljoen AM. Sceletium-A review update. J Ethnopharmacol 2008;119(3):653-63. DOI: 10.1016/j. jep.2008.07.043
183. Smith MT, Crouch NR, Gericke N, Hirst M. Psychoactive constituents of the genus Sceletium N.E.Br. and other Mesembryanthemaceae: a review. J Ethnopharmacol 1996;50(3):119-30. DOI: 10.1016/0378-8741(95)01342-3
184. Harvey AL, Young LC, Viljoen AM, Gericke NP. Pharmacological actions of the South African medicinal and functional food plant Sceletium tortuosum and its principal alkaloids. J Ethnopharmacol 2011;137(3):1124-9. DOI: 10.1016/j. jep.2011.07.035
185. Terburg D, Syal S, Rosenberg LA, Heany S, Phillips N, Gericke N, Stein DJ, van Honk J. Acute effects of Sceletium tortuosum (Zembrin), a dual 5-HT reuptake and PDE4 inhibitor, in the human amygdala and its connection to the hypothalamus. Neuropsychopharmacology 2013;38(13):2708- 16. DOI: 10.1038/npp.2013.183
186. Shikanga EA, Viljoen AM, Combrinck S, Marston A, Gericke N. The chemotypic variation of Sceletium tortuosum alkaloids and commercial product formulations. Biochem Syst Ecol 2012;44(October):364-73. DOI: 10.1016/j. bse.2012.06.025
187. European Monitoring Centre for Drugs and Drug Addiction. Understanding the 'Spice' phenomenon. Lisbon, Portugal: EMCDDA; 2009. Available from: hwww.emcdda.europa.eu/publications/thematic-papers/spice.
188. European Monitoring Centre for Drugs and Drug Addiction. Synthetic cannabinoids in Europe. Lisbon, Portugal: EMCDDA.; 2013. Available from: www.emcdda.europa.eu/topics/pods/synthetic-cannabinoids.
189. Ogata J, Uchiyama N, Kikura-Hanajiri R, Goda Y. DNA sequence analyses of blended herbal products including synthetic cannabinoids as designer drugs. Forensic Sci Int 2013;227(1-3):33-41. DOI: 10.1016/j.forsciint.2012.09.006
190. Logan BK, Reinhold LE, Xu A, Diamond FX. Identification of synthetic cannabinoids in herbal incense blends in the United States. J Forensic Sci 2012;57(5):1168-80. DOI: 10.1111/j.1556-4029.2012.02207.x
191. Clement BA, Goff CM, Forbes TDA. Toxic amines and alkaloids from Acacia rigidula. Phytochemistry 1998;49(5):1377- 80. DOI: 10.1016/S0031-9422(97)01022-4
192. Viana M, Querol X, Postigo C, López de Alda MJ, Barceló D, Artiňano B. Drugs of abuse in airborne particulates in urban environments. Environ Int 2010;36(6):527-34. DOI: 10.1016/j.envint.2010.04.004
193. Boumendjel A, Sotong Taïwe G, Ngo Bum E, Chabrol T, Beney C, Sinniger V, Haudecoeur R, Marcourt L, Challal S, Ferreira Queiroz E, Souard F, Le Borgne M, Lomberget T, Depaulis A, Lavaud C, Robins R, WolfenderJ-L, Bonaz B, de Waard M. Occurrence of the synthetic analgesic tramadol in an African medicinal plant. Angew Chem 2013;52(45):11780- 4. DOI: 10.1002/anie.201305697.
194. Ujvary I. Semi-natural products and related substances as alleged botanical pesticides. Pest Manag Sci 2000;56(8):703- 5. DOI: 10.1002/1526-4998(200008)56:8<703::aidps190> 3.0.co;2-2
195. Shulgin AT, Manning T, Daley PF. The Shulgin index, Vol. 1. Berkeley, CA: Transform Press; 2011. p. 147-52.
196. Hashitani Y. On the chemical constituents of malt-rootlets with special reference to hordenine. Journal of the College of Agriculture, Hokkaido Imperial University 1925;14(1)1-56. Available from: http://hdl.handle.net/2115/12573.
197. Archer JR, Dargan PI, Hudson S, Wood DM. Analysis of anonymous pooled urine from portable urinals in central London confirms the significant use of novel psychoactive substances. QJM 2013;106(2):147-52. DOI: 10.1093/ qjmed/hcs219
198. Thevis M, Geyer H, Sigmund G, Schanzer W. Sports drug testing: Analytical aspects of selected cases of suspected, purported, and proven urine manipulation. J Pharm Biomed Anal 2012;57:26-32. DOI: 10.1016/j.jpba.2011.09.002
199. Singh AK, Granley K, Misrha U, Naeem K, White T, Jiang Y. Screening and confirmation of drugs in urine: Interference of hordenine with the immunoassays and thin layer chromatography methods. Forensic Sci Int 1992;54(1):9-22. DOI: 10.1016/0379-0738(92)90076-9
200. Fleming HL, Ranaivo PL, Simone PS. Analysis and confirmation of 1,3-DMAA and 1,4-DMAA in geranium plants using high performance liquid chromatography with tandem mass spectrometry at ng/g concentrations. Anal Chem Insights 2012;7:59-78. Available from: http://la-press.com/t.php?i=10455
201. Di Lorenzo C, Moro E, Dos Santos A, Uberti F, Restani P. Could 1,3-dimethylamylamine (DMAA) in food supplements have a natural origin? Drug Test Anal 2013;5(2):116- 21. DOI: 10.1002/dta.1391
202. Zhang Y, Woods RM, Breitbach ZS, Armstrong DW. 1,3-Dimethylamylamine (DMAA) in supplements and geranium products: natural or synthetic? Drug Test Anal 2012;4(12):986-90. DOI: 10.1002/dta.1368
203. Lisi A, Hasick N, Kazlauskas S, Goebel C. Studies of methylhexaneamine in supplements and geranium oil. Drug Test Anal 2011;3(11-12):873-6. DOI: 10.1002/dta.392
204. Rohrmann E, Shonle HA. Aminoalkanes as pressor substances. J Am Chem Soc 1944;66(9):1516-20. DOI: 10.1021/ ja01237a032
205. Bloomer RJ, Farney TM, Harvey IC, Alleman RJ. Safety profile of caffeine and 1,3-dimethylamylamine supplementation in healthy men. Hum Exp Toxicol 2013;32(11):1126-36. DOI: 10.1177/0960327113475680.
206. Gee P, Jackson S, Easton J. Another bitter pill: a case of toxicity from DMAA party pills. N Z Med J 2010;123(1327):124- 7.
207. Vorce SP, Holler JM, Cawrse BM, Magluilo J, Jr. Dimethylamylamine: A drug causing positive immunoassay results for amphetamines. J Anal Toxicol 2011;35(3):183-7. DOI: 10.1093/anatox/35.3.183
208. Walsh C. Drugs, Internet and change. J Psychoactive Drugs 2011;43(1):55-63. DOI: 10.1080/02791072.2011.566501
209. Hillebrand J, Olszewski D, Sedefov R. Legal highs on the Internet. Subst Use Misuse 2010;45(3):330-40. DOI: 10.3109/10826080903443628
210. McKenna DJ, Ruiz JM, Hoye TR, Roth BL, Shoemaker AP. Receptor screening technologies in the evaluation of Amazonian ethnomedicines with potential applications to cognitive deficits. J Ethnopharmacol 2011;134(2):475-92. DOI: 10.1016/j.jep.2010.12.037
211. Bruhn JG, El-Seedi HR, Stephanson N, Beck O, Shulgin AT. Ecstasy analogues found in cacti. J Psychoactive Drugs 2008;40(2):219-22. DOI: 10.1080/02791072.2008.10400635
212. O'Connor KA, Roth BL. Screening the receptorome for plantbased psychoactive compounds. Life Sci 2005;78(5):506-11. DOI: 10.1016/j.lfs.2005.09.002
213. Rothman RB, Baumann MH. Targeted screening for biogenic amine transporters: Potential applications for natural products. Life Sci 2005;78(5):512-8.
214. Elsebai MF, Rempel V, Schnakenburg G, Kehraus S, Muller CE, Konig GM. Identification of a potent and selective cannabinoid CB1 receptor antagonist from Auxanthron reticulatum. ACS Med Chem Lett 2011;2(11):866-9.
215. Kochanowska-Karamyan AJ, Hamann MT. Marine indole alkaloids: potential new drug leads for the control of depression and anxiety. Chem Rev 2010;110(8):4489-97. DOI: 10.1021/cr900211p
Address for correspondence:
iKem BT, Buza u. 32
H-1033 Budapest, Hungary
Received on 30 September 2013
Accepted on 13 November 2013.
István Ujváry (1953) is Hungarian national. He graduated (1977) as a chemical engineer at the Technical University of Budapest where he also obtained (1995) a PhD degree in organic chemistry. For three decades, he enjoyed doing synthetic organic chemistry first in an industrial research laboratory then at the Plant Protection Institute and later at the Chemical Research Centre, both of the Hungarian Academy of Sciences, Budapest. As a visiting scientist, he spent years in academic and government research laboratories in the USA. He has been interested in the chemistry and pharmaco-toxicology of a broad range of natural and synthetic biologically active substances, including pest control agents and psychoactive substances. He received research grants from the Hungarian Academy of Sciences, Hungarian Scientific Research Fund, Hungarian National Office of Technology and Development, American-Hungarian Joint Research Fund and the International Atomic Energy Agency. For two decades, he has been lecturing on psychoactive substances at various universities including the popular one-semester course on the subject at the Budapest University of Technology and Economics, where he is an honorary associate professor. Since 1991, he has also been developing a computer database (Bioster) used globally for bioactive compound design. In recent years, national and international drug agencies, including EMCDDA, often turn to him for expert advice. He has (co)authored over 100 research papers and book chapters and is a (co)inventor of 21 patents. In 2011, he received the prestigious "Elige Vitam" award from the Hungarian Ministry of National Resources for his educational and other professional activities related to psychoactive substances. Homepage (in Hungarian):http://members.iif.hu/ujvary.
1. European Council Decision 2005/387/JHA stipulates a "new psychoactive substance" as a new narcotic or psychotropic drug, in pure form or in preparation, that is not controlled by the relevant 1961 or 1971 United Nations Conventions. However, a new mode of use of a known "traditional" drug is often brought to the attention of the EWS of EMCDD A and relevant data are deposited in a new drugs database.
2. According to the Oxford Dictionary, the adjective "natural" refers to something that exists in or is derived from nature; not made or caused by humankind. The word "natural" is often, but erroneously, thought to be equivalent to "good" or "pure" as if many poisons, including nicotine, strychnine and botulinum toxin, were not products of nature.
3. See also presentations of a conference organized by the European Science Foundation in Linköping, 5-9 October, 2009. Available from: www.esf.org/serving-science/conferences/details/2009/confdetail274/presentations.html.
4. For further details, see: www.emcdda.europa.eu/publications/drug profiles/salvia.
5. Information available from www.erowid.org/chemicals/salvinorin_b_ethoxymethyl_ether.
6. Ayahuasca has been the subject of several scholarly edited books (see, e.g., [69, 70]). The renewed global interest in ayahuasca, as made and used in South America, and ayahuasca-like preparations based on other plants indigenous to other continents, as well as the plethora of studies published recently on its use and effects justify a brief historical description as well as an update on studies not only of the brew but also its key ingredients.
7. Bufotenine is an alkaloid and should not be confused with bufotoxins, or bufadienolides, which are cardiotonic steroids also present in toad skin and are the main bioactive ingredients of "Love Stone", an alleged aphrodisiac sold in some countries .
8. For further details, see: www.emcdda.europa.eu/publications/drug profiles/kratom.
9. See: http://acp-mts-programme.org/en/contents/pacific-high-levelmeeting-on-kava-12-15-march-2012 and ftp://ftp.fao.org/codex/meetings/CCNASWP/CCNASWP12/na12_08e.pdf.
10. For the historical and cultural aspects of as well as artistic utensils associated with betel chewing, see the lavishly illustrated book by Rooney .
11. The sesquiterpene lactones present in the latex have ecological importance: these bitter and chemically reactive substances are part of the defense mechanism against predators (for a recent review covering human health related adverse effects, see ).