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PLANTS-PSYCHOACTIVE

Classification   |    Detailed evidence-based information

Therapeutic Toxic Class

    A) Psychoactive plants are a diverse group of substances that can alter perception (state of consciousness), thought, and mood. In developed countries, these plants are used primarily as drugs of abuse. In some cultures, they are used for traditional healing and in religious ceremonies.
    B) Many different genera of plants may produce alterations in mood and are discussed in individual managements. Some topics described in this management may overlap with plants that act as hallucinogens and can alter perception, emotional state and alterations in time and space.

Specific Substances

    A) BANISTERIOPSIS
    1) Ayahuasca vine
    2) B. caapi
    3) B. inebrians
    4) B. quitensis
    5) Banisteria quitensis
    DESFONTAINIA
    1) Chapico ("chili water")
    2) D. hookeri
    3) D. obovata
    4) D. parvifolia
    DUBOISIA
    1) D. hopwoodii
    2) Emu plant
    3) Pitchiri
    4) Pitcheri
    LACTUCA
    1) L. virosa linnaeus ("wild lettuce")
    LAGOCHILUS
    1) L. inebrians
    LEONOTIS
    1) L. leonurus
    2) Wild dagga (L. leonurus)
    3) L. nepetaefolia
    4) World flower (L. nepetaefolia)
    PEGANUM
    1) P. harmala linnaeus
    2) Harmel
    3) African rue
    4) Turkish rue
    5) Mexican rue
    6) Syrian rue
    SCELETIUM
    1) S. tortuosum
    2) Mesembryanthemum tortusoum L.
    TURBINA
    1) T. corymbosa
    2) Badoh (seeds)
    3) Ololiuqui Vine (seeds)

    1.2.1) MOLECULAR FORMULA
    1) PITURI: C(12)H(16)N(2) suggested formula (Langley & Dickinson, 1890)

Available Forms Sources

    A) SOURCES
    1) GENERAL
    a) The following is a list of plants that may produce psychoactive effects (Ratsch, 1998). The content includes common names, a basic description of the plant and typical distribution, along with the predominant constituents of the plant if known, as well as what part or parts of the plant may produce psychoactive effects.
    2) GENUS: BANISTERIOPSIS
    a) SPECIES: CAAPI, INEBRIANS
    1) FAMILY: Malpighiaceae
    2) SYNONYMS/COMMON NAMES: Ayahuasca vine; Banisteria quitensis; B. inebrians; B. quitensis.
    3) DESCRIPTION: A large vine that forms very long and very woody stems that branch repeatedly. It has large round-ovate shaped leaves and contains flowers that are 12 to 14 mm in size and have 5 white or pale pink sepals. The plant flowers rarely. The vine is easily confused with the B. membranifolia and B. muricata vines (Ratsch, 1998).
    4) DISTRIBUTION: Its origins are unknown, but it has been cultivated in Peru, Ecuador, Colombia and Brazil (ie, the entire Amazon region) (Ratsch, 1998).
    5) CONSTITUENTS: This plant is known to contain alkaloids of the beta-carboline type (primary alkaloids include: harmine, harmaline and tetrahydroharmine). The vine is a potent MAO inhibitor. If used alone, the vine can produce mood enhancing and sedative qualities. If taken in higher doses (150 to 200 mg), the effects of the harmine may cause nausea and vomiting (Ratsch, 1998).
    6) PSYCHOACTIVE ELEMENT: Stems (fresh or dried); bark (fresh or dried); and leaves (dried) (Ratsch, 1998).
    7) USES: It has been used in South American for ayahuasca brews to treat various conditions and diseases. These drinks are sometimes referred to as "yage" (Ratsch, 1998).
    8) SEE also HALLUCINOGENIC TRYPTAMINES for further information.
    3) GENUS: DESFONTAINIA
    a) SPECIES: SPINOSA
    1) FAMILY: Desfontainiaceae
    2) SYNONYMS/COMMON NAMES: Michay; Chapico ("chili water"); Taique; D. obovata; D. parvifolia; D. hookeri.
    3) DESCRIPTION: Small evergreen bush or shrub-like tree; grows up to 2 to 3 meters. The leaves are thick and medium to dark green in color (they appear similar to English ivy). The flowers are funnel-shape that are orange to red with yellow margins (Ratsch, 1998).
    4) CONSTITUENTS: At the time of this review, no constituents have been identified (Ratsch, 1998).
    5) DISTRIBUTION: The bush grows in Colombia, Ecuador and the higher regions of Argentina. It also grows in southern Chile (Ratsch, 1998).
    6) PSYCHOACTIVE ELEMENT: Leaves and fruit (Ratsch, 1998).
    7) USES: The leaves can be brewed to produce a hallucinogenic tea. The tea has also been used to treat an upset stomach (Ratsch, 1998).
    4) GENUS: DUBOISIA
    a) PITURI (SPECIES: HOPWOODII)
    1) FAMILY: Solanaceae
    2) SYNONYMS/COMMON NAMES: Pitchiri; Pitcheri; Pituri Bush; Emu plant; poison bush; Anthoceris hopwoodii.
    3) DESCRIPTION: D. hopwoodii is an erect shrub that grows to 3 to 4 meters tall. The plant produces a berry fruit and flowers (Cawte, 1985).
    a) Typically, the D. hopwoodii leaves are combined with alkaline plant ashes and chewed as quid. The chewing of D. hopwoodii has purportedly produced magical and religious effects. Various agents may be added to the dried leaves to produce quid (ie, plant ash, binding agents, plant fibers). The final product is referred to as "Pituri" (Watson et al, 1983; Cawte, 1985).
    4) DISTRIBUTION: Australia. Found in all the arid regions of the mainland states, except Victoria (Cawte, 1985).
    5) PSYCHOACTIVE ELEMENT: Leaves (Ratsch, 1998).
    6) CONSTITUENTS: The seeds reportedly have an antidepressant effect and may stimulate the imagination. Chemical variation has been reported with D. hopwoodii. In west Australia, the D. hopwoodii yielded nicotine, nornicotine, hyoscyamine and metanictoine, while the root contained nornicotine, hyoscyamine, myosmine, and N-formylnornicotine (Watson et al, 1983). The primary alkaloid appears to be nicotine (Rothera, 1911).
    a) There is some confusion presented in the literature that suggests "pituri" refers to Nicotiana spp. or Duboisia hopwoodii, however, the use of pituri by Australian Aborigines differs due to the addition of ash and the continuous administration of nicotine (Ratsch, 1998). More recently pituri may be one of several common terms used by both Aboriginal and Europeans in Central Australia to describe the plant substance being retained in the mouth (Ratsch, 1998).
    b) In certain species of D. hopwoodii found in Australia, d-nornicotine has been found to be the active and toxic constituent of the plant rather than nicotine. In some species, nornicotine content (0.1 and 4.1%) was highly variable, while nicotine (0 and 5.3%) could be absent (Ratsch et al, 2010). This variation may relate to different outcomes reported in the historical literature from elation and rapture (high nicotine concentrations) to catalepsy and death (high nornicotine concentrations; approximately 4 times as strong as nicotine) observed in Aboriginal tribes (Ratsch, 1998).
    c) In the late 1800's, one researcher suggested that piturine, although in some ways similar to nicotine was more closely aligned to the genus D. myoporoides which contained an atropine alkaloid, hyoscine or hyoscyamine and sometimes both. Hyoscyamine was more often found in the older tissues, while scopolamine was found in the younger leaves (Ratsch, 1998).
    7) USES: Pituri has been used by Australian aborigines for its hedonistic and magical effects. Historically, it was used as a stimulant and in larger doses as a narcotic (Watson et al, 1983). It may be used as a substitute for tobacco (Ringer & Murrell, 1878). It may also decrease hunger and thirst, and has an inebriating effect and may produce ardent dreams(Cawte, 1985).
    8) The addition of ash and possible other constituents may produce variable clinical effects (Cawte, 1985; Ratsch, 1998).
    9) SEE also NICOTINE management for further information.
    5) GENUS: LACTUCA
    a) WILD LETTUCE (SPECIES: LACTUCA VIROSA LINNAEUS)
    1) FAMILY: Compositate: Asteraceae
    2) SYNONYMS/COMMON NAMES: Wild lettuce, opium lettuce; bitter lettuce; great lettuce; lactucarium; laitue vireuse.
    3) DESCRIPTION: May grow up to 2 to 4 feet; maximum 6 feet. The stem is smooth and pale green; may be spotted with purple. Leaves can be 6 to 18 inches long. Flowers are pale yellow with large open clusters.
    4) CONSTITUENTS: Lactucarium contains the sedative sesquiterpene lactones (bitter); triterpene alcohols and other guaianolides (Ratsch, 1998).
    5) PSYCHOACTIVE ELEMENT: Thickened juice (latex); lactucarium, lactucarium germanicum; dried leaves that can be smoked alone or blended with other herbs (Ratsch, 1998).
    6) USES: In ancient times it was used as an aphrodisiac and used in rituals. In recent times, it has been used as a sedative and a mild substitute for opium (Ratsch, 1998).
    7) See also PLANTS-SESQUITERPENE LACTONES management.
    6) GENUS: LAGOCHILUS
    a) INTOXICATING MINT (SPECIES: LAGOCHILUS INEBRIANS)
    1) FAMILY: Lamiaceae (formerly known as: Labiatae)
    2) SYNONYMS/COMMON NAMES: Turkish mint; Intoxicating mint.
    3) DESCRIPTION: A bushy mint plant (Ratsch, 1998).
    4) DISTRIBUTION: Turkistan and Uzbekistan; difficult to find (Ratsch, 1998).
    5) PSYCHOACTIVE ELEMENT: The leaves contain up to 17% lagochiline, a diterpene alkaloid, that has been associated with the plants sedative, hypotensive and hemostatic effects (Ratsch, 1998).
    6) USES: The leaves have been dried to make tea. It has also been used in Russian folk medicine to treat allergies and skin conditions, as well as promote blood coagulation (Ratsch, 1998).
    7) GENUS: LEONOTIS (FORMERLY: PHLOMIS)
    a) WILD DAGGA (SPECIES: LEONOTIS LEONURUS)
    1) SYNONYMS/COMMON NAMES: Lion's tail, lion's ear.
    2) DESCRIPTION: A perennial that may grow 2 to 3 meters and produces red, orange, yellow, or white tubular flowers.
    3) PSYCHOACTIVE ELEMENT: Leaves and flowers (dried) (Ratsch, 1998).
    4) USES: The dried flowers when smoked may provide a mild sedative effect, similar to Cannabis. In California, it has been used as a substitute for marijuana. The dried herbage is referred to as "wild dagga" (Ratsch, 1998).
    b) WORLD FLOWER (SPECIES: LEONOTIS NEPETAEFOLIA)
    1) SYNONYMS/COMMON NAMES: This plant is closely related to L. leonurus (Ratsch, 1998).
    2) USES: It has been used in Caribbean folk medicine. In Mexico, the plant is known as "world flower" or mota (usually known as marijuana). It is likely used as a marijuana substitute (Ratsch, 1998).
    3) PSYCHOACTIVE ELEMENT: Leaves and flowers (Ratsch, 1998).
    8) GENUS: PEGANUM
    a) SYRIAN RUE (SPECIES: PEGANUM HARMALA LINNAEUS)
    1) FAMILY: Zygophyllaceae
    2) SYNONYMS/COMMON NAMES: Turkish rue; Mexican rue; African rue; Harmel.
    3) DESCRIPTION: A perennial hemicrytophyte with a strong, offensive odor. It is a glabrous, herbaceous plant that grows up to 50 to 100 cm. The leaves are thong-like with an unpleasant odor. The fruit is a 3 chambered capsule with several angular black seeds (Ratsch, 1998).
    4) DISTRIBUTION: The Middle East and South Africa in semi-arid regions (Ratsch, 1998).
    5) PSYCHOACTIVE ELEMENT: Seeds (Ratsch, 1998).
    6) CONSTITUENTS: The seeds contain beta-carbolines, harmine, harmaline and harmalol and harmidine reportedly have an antidepressant effect and may stimulate the imagination (Ratsch, 1998).
    7) USES: In herbal medicine it has been used as an emmenagogue and abortifacient (Ratsch, 1998).
    8) SEE also HALLUCINOGENIC TRYPTAMINES for further information.
    9) GENUS: SCELETIUM
    a) KANNA (SPECIES: TORTUOSUM)
    1) FAMILY: Mesembryanthemaceae (Iced Plant Family)
    2) SYNONYMS/COMMON NAMES: Mesembryanthemum tortusoum L.; Canna; Canna-root; Channa; Gunua; Kaugoed; Kougoed.
    3) DESCRIPTION: Succulent ground cover that can grow as tall as 30 cm. Fleshy leaves are attached directly to the branches. The flowers are pale yellow (3 to 4 cm) are attached to the ends of the branches. The fruit is angular shaped with small seeds (Ratsch, 1998).
    4) DISTRIBUTION: Grown only in South Africa ("kanna" land). It has become a relatively difficult species to find (Ratsch, 1998).
    5) PSYCHOACTIVE ELEMENTS: Entire plant with root (Ratsch, 1998).
    6) USES: It has purportedly been used since prehistoric times as a mood altering substance (Stafford et al, 2008). It can also reduce anxiety and stress and lessen feelings of inferiority. In contemporary South African society, it has been used as a party drug (Ratsch, 1998).
    a) More recently it has been developed as a commercial product for the treatment of mild depression (Stafford et al, 2008).
    10) GENUS: TURBINA
    a) TURBINA CORYMBOSA (SPECIES: CORYMBOSA)
    1) FAMILY: Convolvulaceae
    2) SYNONYMS/COMMON NAMES: Badoh (seeds); Ololiuqui Vine (seeds); Coaxihuitl.
    3) DESCRIPTION: A large woody vine, that has flowering branches with funnel-shaped flowers. The flowering portion of the plant may contain a significant amount of psychoactive honey. The leaves and stalks (not the roots) contain psychoactive indole alkaloids (Ratsch, 1998).
    4) DISTRIBUTION: Indigenous to tropical Mexico (Ratsch, 1998).
    5) PSYCHOACTIVE ELEMENTS: Seeds (fresh or dried), leaves, and roots (Ratsch, 1998).
    6) USES: Used as a psychedelic ("visionary inebriant"). It has been used in traditional and folk medicine to treat wounds and bruises and as an aid to parturition (Ratsch, 1998).
    11) OTHER PSYCHOACTIVE AGENTS
    a) There are other toxicology plant managements that describe psychoactive activity produced by a plant and include all of the following:
    1) PLANTS-MITRAGYNA
    2) PLANTS-MUCUNA SPECIES
    3) PLANTS-NICOTINIC
    4) PLANTS-PASSIFLORA
    5) PLANTS-SALVIA DIVINORUM
    6) PLANTS-SOLANINE
    7) PLANTS-STIMULANTS
    8) PLANTS-THEOBROMA CACAO
    9) PLANTS-VERATRUM ALKALOIDS
    b) In addition, a genus or species containing a HALLUCINOGENIC TRYPTAMINE is coded to the management HALLUCINOGENIC TRYPTAMINES:
    1) The following GENERA or SPECIES contain a hallucinogenic tryptamine(s):
    1) Banisteriopsis
    2) Mimosa
    3) Peganum
    4) Psychotria
    2) BACKGROUND INFORMATION: Tryptamine and DMT and its derivatives are naturally occurring compounds. All other agents are synthetic. All compounds are available in pure powder forms. DMT (also referred to as the "businessman's high"), AMT, 5-OMe-DMT, beta carbolines, and bufotenine are found in a variety of South American plants including species of Myristicaceae (Virola species), Fabaceae (Anadenanthera or piptadenia peregrina, Mimosa hostilis), Zygophillaceae (Pegonum harmala), Malpighiaceae (Banisteriopsis species, Tetrapteris methystica), Rubiaceae (Psychotria species) Apocyanaceae (Restonia amazonica), and Acanthaceae (Justicia pectoralis) (Halpern, 2004; Long et al, 2003; Lewis & Elvin-Lewis, 1977). They may be smoked or inhaled as snuffs, or used in beverages.
    3) Hallucinogenic derivatives of tryptamine and beta-carboline (eg, harmine, harmoline, and tetrahydroharmine) have structures and properties in common with ergotamine, LSD (lysergic acid diethylamide), and serotonin (5-hydroxytryptamine).
    4) DMT, alpha MT, 5-OMe-DMT, bufotenine, and beta-carbolines are found in a variety of South American plants which are smoked, ingested (as resin or tea), or used as snuff.
    5) Bufotenine, an indole alkaloid, has been obtained from the seeds and leaves of Piptadenia peregrina, from which hallucinogenic snuff cohoba is made, and P. macrocarpa (Mimosaceae).
    B) USES
    1) Psychoactive plants are a diverse group of substances that can alter perception, thought, and mood. In developed countries, these plants are used primarily as drugs of abuse. In some cultures, they are used in religious ceremonies and traditional healing (Ratsch, 1998)

Life Support

    A) This overview assumes that basic life support measures have been instituted.

Clinical Effects

    0.2.1) SUMMARY OF EXPOSURE
    A) USES: Psychoactive plants are a diverse group of substances that can alter perception, thought, and mood. In developed countries, these plants are used primarily as drugs of abuse. In some cultures, they are used for traditional healing and in religious ceremonies.
    B) TOXICOLOGY: In many plants, the exact mechanism may be unknown. However, many plants contain various alkaloids (ie, mesembrine, acts as a serotonin reuptake inhibitor isolated from Sceletium tortuosum; ergot alkaloids (ie turbina corymbosa) can produce hypnotic effects) that may produce significant toxicity.
    C) EPIDEMIOLOGY: Poisoning is not common, but may rarely be severe. Exposure may occur via ingestion, transmucosal absorption (usually nasal or buccal), or inhalation, depending on the substance. As with any drug of abuse, other substances may be added to enhance clinical effects.
    D) WITH THERAPEUTIC USE
    1) TRADITIONAL MEDICINE: Psychoactive plants are often used as part of a cultural ritual for their ability to produce a hypnotic or dream-like state, euphoria, sedation, stimulation or as an analgesic in some cases.
    E) WITH POISONING/EXPOSURE
    1) MILD TO MODERATE TOXICITY: Many psychoactive plants have the potential to cause an altered mental state (ie, euphoria, sedation, hallucination in some cases) and may produce unpredictable behavior. Nausea, vomiting, and agitation may occur. Mild alterations in blood pressure and pulse may be observed.
    2) SEVERE TOXICITY: May manifest as severe anxiety and possibly agitation, hypertension, sinus tachycardia and rarely hyperthermia. Severe toxicity may also produce significant CNS depression (ie, unconsciousness, coma) and potentially seizures.

Laboratory Monitoring

    A) Routine laboratory studies (eg, CBC, electrolytes) are generally not indicated, unless otherwise clinically indicated.
    B) A urine drug screen may be a useful adjunct in the altered patient to rule out exposure from other pharmacologic agents, but the active constituents of these plants will NOT be detected on urine drug screens.
    C) Monitor vital signs and neurologic function.
    D) Monitor fluid and electrolytes in patients with prolonged vomiting or diarrhea.
    E) Monitor liver enzymes and renal function following a significant exposure.
    F) Obtain a baseline ECG in symptomatic patients and perform continuous cardiac monitoring as indicated.
    G) Serum testing is not available in the hospital setting for these plants.

Treatment Overview

    0.4.2) ORAL/PARENTERAL EXPOSURE
    A) MANAGEMENT OF MILD TO MODERATE TOXICITY
    1) Treatment is symptomatic and supportive; patients may only require observation. Benzodiazepines should be given for agitation as needed. Reassure the patient. Intravenous fluids may be indicated, if the patient develops significant nausea and vomiting.
    B) MANAGEMENT OF SEVERE TOXICITY
    1) Liberal use of benzodiazepines (first-line therapy) are the mainstay of therapy. Goal of therapy is to control agitation and support the paranoid or delirious patient. Provide a supportive environment. Orotracheal intubation is indicated for airway protection in cases of severe agitation, coma or seizure activity.
    C) DECONTAMINATION
    1) GI decontamination is generally not recommended as toxicity is usually self limited, aspiration is a concern and spontaneous vomiting is common.
    D) AIRWAY MANAGEMENT
    1) Airway management should be performed early in a patient with signs of severe poisoning (ie, CNS depression, coma).
    E) ANTIDOTE
    1) There is no specific antidote.
    F) ENHANCED ELIMINATION PROCEDURE
    1) Hemodialysis and hemoperfusion are not likely to be of any value.
    G) SEIZURES
    1) Some plants may produce generalized tremors which may lead to seizure activity. At the times of this review, there have been no reports of seizure with these plants. If seizures occur, administer IV benzodiazepines; barbiturates or propofol may be needed if seizures persist or recur.
    H) PATIENT DISPOSITION
    1) HOME CRITERIA: Adults with mild symptoms may be monitored at home. Asymptomatic children with inadvertent ingestions can be monitored at home if abuse or neglect are not concerns.
    2) OBSERVATION CRITERIA: Patients with deliberate self-harm ingestions, and adults or children who are symptomatic should be sent to a healthcare facility for observation for 6 to 8 hours.
    3) ADMISSION CRITERIA: Patients with significant persistent central nervous system effects (ie, prolonged sedation, agitation), or other persistent clinical symptoms should be admitted. Patients with significant CNS depression or coma should be admitted to an intensive care setting.
    4) CONSULT CRITERIA: Consult a poison center or medical toxicologist for assistance in managing patients with severe toxicity or in whom the diagnosis is not clear. Patients with a history of chronic abuse should be referred for rehabilitation.

Range Of Toxicity

    A) TOXICITY: Varies by species and the constituents (type and amount) that are found in an individual plant. Severe toxicity is exceedingly rare and fatalities have not been reported.
    B) LACTUCA VIROSA LINNAEUS: WILD LETTUCE: A psychoactive dosage of wild lettuce leaves is 28 g.
    C) PEGANUM HARMALA: A woman developed nausea, vomiting, visual hallucinations, diaphoresis, coma, hypertension, tachycardia, elevated liver enzymes, and renal dysfunction after drinking a hot mixture of approximately 100 g of peganum harmala seeds in water (10 to 20 times the recommended dose for "calming one's nerves"). She recovered following supportive care.
    D) SCELETIUM TORTUOSUM (KOUGOED): About 5 g of the powder can relieve anxiety, while higher doses may produce euphoria and visions.

Summary Of Exposure

    A) USES: Psychoactive plants are a diverse group of substances that can alter perception, thought, and mood. In developed countries, these plants are used primarily as drugs of abuse. In some cultures, they are used for traditional healing and in religious ceremonies.
    B) TOXICOLOGY: In many plants, the exact mechanism may be unknown. However, many plants contain various alkaloids (ie, mesembrine, acts as a serotonin reuptake inhibitor isolated from Sceletium tortuosum; ergot alkaloids (ie turbina corymbosa) can produce hypnotic effects) that may produce significant toxicity.
    C) EPIDEMIOLOGY: Poisoning is not common, but may rarely be severe. Exposure may occur via ingestion, transmucosal absorption (usually nasal or buccal), or inhalation, depending on the substance. As with any drug of abuse, other substances may be added to enhance clinical effects.
    D) WITH THERAPEUTIC USE
    1) TRADITIONAL MEDICINE: Psychoactive plants are often used as part of a cultural ritual for their ability to produce a hypnotic or dream-like state, euphoria, sedation, stimulation or as an analgesic in some cases.
    E) WITH POISONING/EXPOSURE
    1) MILD TO MODERATE TOXICITY: Many psychoactive plants have the potential to cause an altered mental state (ie, euphoria, sedation, hallucination in some cases) and may produce unpredictable behavior. Nausea, vomiting, and agitation may occur. Mild alterations in blood pressure and pulse may be observed.
    2) SEVERE TOXICITY: May manifest as severe anxiety and possibly agitation, hypertension, sinus tachycardia and rarely hyperthermia. Severe toxicity may also produce significant CNS depression (ie, unconsciousness, coma) and potentially seizures.

Monitoring Parameters Levels

    4.1.1) SUMMARY
    A) Routine laboratory studies (eg, CBC, electrolytes) are generally not indicated, unless otherwise clinically indicated.
    B) A urine drug screen may be a useful adjunct in the altered patient to rule out exposure from other pharmacologic agents, but the active constituents of these plants will NOT be detected on urine drug screens.
    C) Monitor vital signs and neurologic function.
    D) Monitor fluid and electrolytes in patients with prolonged vomiting or diarrhea.
    E) Monitor liver enzymes and renal function following a significant exposure.
    F) Obtain a baseline ECG in symptomatic patients and perform continuous cardiac monitoring as indicated.
    G) Serum testing is not available in the hospital setting for these plants.
    4.1.2) SERUM/BLOOD
    A) BLOOD/SERUM CHEMISTRY
    1) Monitor serum electrolyte levels, particularly in symptomatic patients with prolonged vomiting or diarrhea.
    B) MONITORING
    1) Monitor vital signs and neurologic function.
    4.1.4) OTHER
    A) OTHER
    1) ECG MONITORING
    a) Obtain a baseline ECG in symptomatic patients and perform continuous cardiac monitoring as indicated.

Methods

    A) GENUS: DUBOISIA
    1) GAS CHROMATOGRAPHY/MASS SPECTROMETRY: Chemical variation has been detected with D. hopwoodii (the plant used to create pituri) analysis of the plant including the leaves and root material. Historically, the chemicals isolated have included: nicotine, cotinine, hyoscyamine, myosmine, nornicotine, and n-formylnornicotine and the variation appeared to be based on geographic differences (found in several regions of Australia) (Watson et al, 1983).
    B) GENUS: PEGANUM HARMALA
    1) GAS CHROMATOGRAPHY/MASS SPECTROMETRY: Harmala alkaloids were identified by using gas-chromatography-mass spectrometry in both the seed extract and urine of an adult who made a preparation with P. harmala seeds that were purchased over the Internet. Three major beta-caroline alkaloids were identified: harmine, harmaline and tetrahydroharmaline in both samples, along with 2 quinazoline alkaloids (ie, peganine and deoxypeganine). No trace of hallucinogenic compounds were detected (Frison et al, 2008).

Life Support

    A) Support respiratory and cardiovascular function.

Patient Disposition

    6.3.1) DISPOSITION/ORAL EXPOSURE
    6.3.1.1) ADMISSION CRITERIA/ORAL
    A) Patients with significant persistent central nervous system effects (ie, prolonged sedation, agitation), or other persistent clinical symptoms should be admitted. Patients with significant CNS depression or coma should be admitted to an intensive care setting.
    6.3.1.2) HOME CRITERIA/ORAL
    A) Adults with mild symptoms may be monitored at home. Asymptomatic children with inadvertent ingestions can be monitored at home if abuse or neglect are not concerns.
    6.3.1.3) CONSULT CRITERIA/ORAL
    A) Consult a poison center or medical toxicologist for assistance in managing patients with severe toxicity or in whom the diagnosis is not clear. Patients with a history of chronic abuse should be referred for rehabilitation.
    6.3.1.5) OBSERVATION CRITERIA/ORAL
    A) Patients with deliberate self-harm ingestions, and adults or children who are symptomatic should be sent to a healthcare facility for observation for 6 to 8 hours.

Monitoring

    A) Routine laboratory studies (eg, CBC, electrolytes) are generally not indicated, unless otherwise clinically indicated.
    B) A urine drug screen may be a useful adjunct in the altered patient to rule out exposure from other pharmacologic agents, but the active constituents of these plants will NOT be detected on urine drug screens.
    C) Monitor vital signs and neurologic function.
    D) Monitor fluid and electrolytes in patients with prolonged vomiting or diarrhea.
    E) Monitor liver enzymes and renal function following a significant exposure.
    F) Obtain a baseline ECG in symptomatic patients and perform continuous cardiac monitoring as indicated.
    G) Serum testing is not available in the hospital setting for these plants.

Oral Exposure

    6.5.1) PREVENTION OF ABSORPTION/PREHOSPITAL
    A) EMESIS/NOT RECOMMENDED
    1) Prehospital GI decontamination is generally not recommended as toxicity is usually self limited, aspiration is a concern and spontaneous vomiting is common.
    6.5.2) PREVENTION OF ABSORPTION
    A) SUMMARY
    1) GI decontamination is generally not recommended as toxicity is usually self limited, aspiration is a concern and spontaneous vomiting is common.
    6.5.3) TREATMENT
    A) SUPPORT
    1) Treatment is SYMPTOMATIC and SUPPORTIVE. Patients may only require observation. Monitor CNS function. Benzodiazepines should be given for agitation as needed. Reassure the patient. Intravenous fluids may be indicated, if the patient develops significant nausea and vomiting.
    B) MONITORING OF PATIENT
    1) Routine laboratory studies (eg, CBC, electrolytes) are generally not indicated, unless otherwise clinically indicated.
    2) A urine drug screen may be a useful adjunct in the altered patient to rule out exposure from other pharmacologic agents, however the active constituents of these plants will NOT be detected on urine drug screens.
    3) Monitor vital signs and neurologic function.
    4) Monitor fluid and electrolytes in patients with prolonged vomiting or diarrhea.
    5) Monitor liver enzymes and renal function following a significant exposure.
    6) Obtain a baseline ECG in symptomatic patients and perform continuous cardiac monitoring as indicated.
    7) Serum testing is not available in the hospital setting for these plants.
    C) PSYCHOMOTOR AGITATION
    1) Psychomotor agitation may develop after ingestion or inhalation of these plants (Frison et al, 2008).
    2) Sedate patient with benzodiazepines as necessary; large doses may be required.
    3) INDICATION
    a) If patient is severely agitated, sedate with IV benzodiazepines.
    4) DIAZEPAM DOSE
    a) ADULT: 5 to 10 mg IV initially, repeat every 5 to 20 minutes as needed (Brophy et al, 2012; Prod Info diazepam IM, IV injection, 2008; Manno, 2003).
    b) CHILD: 0.1 to 0.5 mg/kg IV over 2 to 5 minutes; up to a maximum of 10 mg/dose. May repeat dose every 5 to 10 minutes as needed (Loddenkemper & Goodkin, 2011; Hegenbarth & American Academy of Pediatrics Committee on Drugs, 2008).
    5) LORAZEPAM DOSE
    a) ADULT: 2 to 4 mg IV initially; repeat every 5 to 10 minutes as needed (Manno, 2003).
    b) CHILD: 0.05 to 0.1 mg/kg IV over 2 to 5 minutes, up to a maximum of 4 mg/dose; may repeat in 5 to 15 minutes as needed (Brophy et al, 2012; Loddenkemper & Goodkin, 2011; Hegenbarth & American Academy of Pediatrics Committee on Drugs, 2008).
    6) Extremely large doses of benzodiazepines may be required in patients with severe intoxication in order to obtain adequate sedation. Titrate dose to clinical response and monitor for hypotension, CNS and respiratory depression, and the need for endotracheal intubation.
    D) SEIZURE
    1) Some plants may produce generalized tremors which may lead to seizure activity. At the times of this review there have been no reports of seizure with these plants.
    2) SUMMARY
    a) Attempt initial control with a benzodiazepine (eg, diazepam, lorazepam). If seizures persist or recur, administer phenobarbital or propofol.
    b) Monitor for respiratory depression, hypotension, and dysrhythmias. Endotracheal intubation should be performed in patients with persistent seizures.
    c) Evaluate for hypoxia, electrolyte disturbances, and hypoglycemia (or, if immediate bedside glucose testing is not available, treat with intravenous dextrose).
    3) DIAZEPAM
    a) ADULT DOSE: Initially 5 to 10 mg IV, OR 0.15 mg/kg IV up to 10 mg per dose up to a rate of 5 mg/minute; may be repeated every 5 to 20 minutes as needed (Brophy et al, 2012; Prod Info diazepam IM, IV injection, 2008; Manno, 2003).
    b) PEDIATRIC DOSE: 0.1 to 0.5 mg/kg IV over 2 to 5 minutes; up to a maximum of 10 mg/dose. May repeat dose every 5 to 10 minutes as needed (Loddenkemper & Goodkin, 2011; Hegenbarth & American Academy of Pediatrics Committee on Drugs, 2008).
    c) Monitor for hypotension, respiratory depression, and the need for endotracheal intubation. Consider a second agent if seizures persist or recur after repeated doses of diazepam .
    4) NO INTRAVENOUS ACCESS
    a) DIAZEPAM may be given rectally or intramuscularly (Manno, 2003). RECTAL DOSE: CHILD: Greater than 12 years: 0.2 mg/kg; 6 to 11 years: 0.3 mg/kg; 2 to 5 years: 0.5 mg/kg (Brophy et al, 2012).
    b) MIDAZOLAM has been used intramuscularly and intranasally, particularly in children when intravenous access has not been established. ADULT DOSE: 0.2 mg/kg IM, up to a maximum dose of 10 mg (Brophy et al, 2012). PEDIATRIC DOSE: INTRAMUSCULAR: 0.2 mg/kg IM, up to a maximum dose of 7 mg (Chamberlain et al, 1997) OR 10 mg IM (weight greater than 40 kg); 5 mg IM (weight 13 to 40 kg); INTRANASAL: 0.2 to 0.5 mg/kg up to a maximum of 10 mg/dose (Loddenkemper & Goodkin, 2011; Brophy et al, 2012). BUCCAL midazolam, 10 mg, has been used in adolescents and older children (5-years-old or more) to control seizures when intravenous access was not established (Scott et al, 1999).
    5) LORAZEPAM
    a) MAXIMUM RATE: The rate of intravenous administration of lorazepam should not exceed 2 mg/min (Brophy et al, 2012; Prod Info lorazepam IM, IV injection, 2008).
    b) ADULT DOSE: 2 to 4 mg IV initially; repeat every 5 to 10 minutes as needed, if seizures persist (Manno, 2003; Brophy et al, 2012).
    c) PEDIATRIC DOSE: 0.05 to 0.1 mg/kg IV over 2 to 5 minutes, up to a maximum of 4 mg/dose; may repeat in 5 to 15 minutes as needed, if seizures continue (Brophy et al, 2012; Loddenkemper & Goodkin, 2011; Hegenbarth & American Academy of Pediatrics Committee on Drugs, 2008; Sreenath et al, 2009; Chin et al, 2008).
    6) PHENOBARBITAL
    a) ADULT LOADING DOSE: 20 mg/kg IV at an infusion rate of 50 to 100 mg/minute IV. An additional 5 to 10 mg/kg dose may be given 10 minutes after loading infusion if seizures persist or recur (Brophy et al, 2012).
    b) Patients receiving high doses will require endotracheal intubation and may require vasopressor support (Brophy et al, 2012).
    c) PEDIATRIC LOADING DOSE: 20 mg/kg may be given as single or divided application (2 mg/kg/minute in children weighing less than 40 kg up to 100 mg/min in children weighing greater than 40 kg). A plasma concentration of about 20 mg/L will be achieved by this dose (Loddenkemper & Goodkin, 2011).
    d) REPEAT PEDIATRIC DOSE: Repeat doses of 5 to 20 mg/kg may be given every 15 to 20 minutes if seizures persist, with cardiorespiratory monitoring (Loddenkemper & Goodkin, 2011).
    e) MONITOR: For hypotension, respiratory depression, and the need for endotracheal intubation (Loddenkemper & Goodkin, 2011; Manno, 2003).
    f) SERUM CONCENTRATION MONITORING: Monitor serum concentrations over the next 12 to 24 hours. Therapeutic serum concentrations of phenobarbital range from 10 to 40 mcg/mL, although the optimal plasma concentration for some individuals may vary outside this range (Hvidberg & Dam, 1976; Choonara & Rane, 1990; AMA Department of Drugs, 1992).
    7) OTHER AGENTS
    a) If seizures persist after phenobarbital, propofol or pentobarbital infusion, or neuromuscular paralysis with general anesthesia (isoflurane) and continuous EEG monitoring should be considered (Manno, 2003). Other anticonvulsants can be considered (eg, valproate sodium, levetiracetam, lacosamide, topiramate) if seizures persist or recur; however, there is very little data regarding their use in toxin induced seizures, controlled trials are not available to define the optimal dosage ranges for these agents in status epilepticus (Brophy et al, 2012):
    1) VALPROATE SODIUM: ADULT DOSE: An initial dose of 20 to 40 mg/kg IV, at a rate of 3 to 6 mg/kg/minute; may give an additional dose of 20 mg/kg 10 minutes after loading infusion. PEDIATRIC DOSE: 1.5 to 3 mg/kg/minute (Brophy et al, 2012).
    2) LEVETIRACETAM: ADULT DOSE: 1000 to 3000 mg IV, at a rate of 2 to 5 mg/kg/min IV. PEDIATRIC DOSE: 20 to 60 mg/kg IV (Brophy et al, 2012; Loddenkemper & Goodkin, 2011).
    3) LACOSAMIDE: ADULT DOSE: 200 to 400 mg IV; 200 mg IV over 15 minutes (Brophy et al, 2012). PEDIATRIC DOSE: In one study, median starting doses of 1.3 mg/kg/day and maintenance doses of 4.7 mg/kg/day were used in children 8 years and older (Loddenkemper & Goodkin, 2011).
    4) TOPIRAMATE: ADULT DOSE: 200 to 400 mg nasogastric/orally OR 300 to 1600 mg/day orally divided in 2 to 4 times daily (Brophy et al, 2012).

Enhanced Elimination

    A) SUMMARY
    1) Hemodialysis and hemoperfusion are not likely to be of any value.

Summary

    A) TOXICITY: Varies by species and the constituents (type and amount) that are found in an individual plant. Severe toxicity is exceedingly rare and fatalities have not been reported.
    B) LACTUCA VIROSA LINNAEUS: WILD LETTUCE: A psychoactive dosage of wild lettuce leaves is 28 g.
    C) PEGANUM HARMALA: A woman developed nausea, vomiting, visual hallucinations, diaphoresis, coma, hypertension, tachycardia, elevated liver enzymes, and renal dysfunction after drinking a hot mixture of approximately 100 g of peganum harmala seeds in water (10 to 20 times the recommended dose for "calming one's nerves"). She recovered following supportive care.
    D) SCELETIUM TORTUOSUM (KOUGOED): About 5 g of the powder can relieve anxiety, while higher doses may produce euphoria and visions.

Minimum Lethal Exposure

    A) Fatalities have not been reported in the medical literature.

Maximum Tolerated Exposure

    A) LACTUCA VIROSA LINNAEUS
    1) WILD LETTUCE: A psychoactive dosage of wild lettuce leaves is 28 g (Ratsch, 1998).
    B) PEGANUM HARMALA
    1) SUMMARY
    a) All parts of the plant are thought to be poisonous (el Bahri & Chemli, 1991).
    2) CASE REPORTS
    a) An 18-year-old man created an infusion from peganum harmala seeds which he ingested and subsequently developed agitation, visual hallucinations, tremors, vomiting, and ataxia. Laboratory analysis via liquid chromatography of the seed infusion brought in by the patient identified the presence of harmine and harmaline alkaloids. Those same alkaloids were identified in the patient's urine via gas chromatography-mass spectrometry. The patient completely recovered following supportive care (Frison et al, 2008).
    b) A 41-year-old woman developed nausea and vomiting, visual hallucinations, and diaphoresis approximately 3 hours after drinking a hot mixture of approximately 100 g of peganum harmala seeds in water (10 to 20 times the recommended dose for "calming one's nerves"). She became unconscious and presented 18 hours after ingestion with hypertension, tachycardia, tachypnea, elevated liver enzymes, and renal dysfunction. Following supportive care, she improved gradually over the next 5 days (Yuruktumen et al, 2008).
    3) ANIMAL DATA
    a) CATTLE: Intravenous injection of harmine and harmaline (9 mg/kg) in cattle produced tachypnea, tachycardia, and clonic muscle spasms (el Bahri & Chemli, 1991).
    C) SCELETIUM TORTUOSUM
    1) KOUGOED (a powder that is produced by fermenting and allowing the plant to dry): About 5 g of the powder can relieve anxiety, while higher doses may produce euphoria and visions (Ratsch, 1998).

Molecular Weight

    A) No data to report for the various species.

General Bibliography

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