Jump to content

Atropa belladonna

From Wikipedia, the free encyclopedia
(Redirected from Belladonna alkaloids)
"Deadly nightshade" redirects here. For other uses, see Deadly Nightshade.

Atropa belladonna
Illustration from Köhler's Medicinal Plants 1887
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Asterids
Order: Solanales
Family: Solanaceae
Genus: Atropa
Species:
A. belladonna
Binomial name
Atropa belladonna

Atropa belladonna, commonly known as belladonna or deadly nightshade, is a toxic perennial herbaceous plant in the nightshade family Solanaceae,[1] which also includes tomatoes, potatoes and aubergine (eggplant). It is native to Europe and Western Asia, including Turkey. Its distribution extends from Ireland in the west to western Ukraine and the Iranian province of Gilan in the east. It is also naturalised or introduced in some parts of Canada, North Africa and the United States.

The foliage and berries are extremely toxic when ingested, containing tropane alkaloids.[1][2][3][4] These toxins include atropine, scopolamine, and hyoscyamine, which cause delirium and hallucinations,[1][2][3][5][6] and are also used as pharmaceutical anticholinergics.[1] Tropane alkaloids are of common occurrence not only in the Old World tribes Hyoscyameae (to which the genus Atropa belongs) and Mandragoreae, but also in the New World tribe Datureae—all of which belong to the subfamily Solanoideae of the plant family Solanaceae.[1]

Atropa belladonna has unpredictable effects.[2] The antidote for belladonna poisoning is physostigmine or pilocarpine, the same as for atropine.[7]

The potentially deadly ripe fruit of Atropa belladonna can be distinguished from the similar Solanum nigrum by its larger berry size, its much larger calyx than S. nigrum that extends wider than the fruit (either encasing it or extending flat), and that A. belladonna has singular berries, whilst S. nigrum grows as a cluster of berries located on a descending stem, similar to tomatoes. Solanum nigrum has other potentially toxic look alikes and should be confidently identified before attempts at foraging. This plant's structure looks the same as an egg plant, but its flower looks a little bit different. This plant's flowers are very attractive, looking like a lily flower, and its fruits are ball-shaped. It is very dangerous to consume.

History

[edit]

Atropa belladonna has a long history of use as a medicine, cosmetic, and poison.[8][3][9] Known originally under various folk names (such as "deadly nightshade" in English), the plant was named Atropa belladonna by Carl Linnaeus (1707–1778) when he devised his classification system. Linnaeus chose the genus name Atropa because of the poisonous properties of these plants. Atropos (lit. "unturning one"), one of the Three Fates in Greek mythology, is said to have cut a person's thread of life after her sisters had spun and measured it. Linnaeus chose the species name belladonna ("beautiful woman" in Italian) in reference to [dubious – discuss] the cosmetic use of the plant during the Renaissance, when women were believed to have used the juice of the berries in eyedrops intended to dilate the pupils and make the eyes appear more seductive.[10][3][11][12]

Extracts of plants in the deadly nightshade family have been in use since at least the 4th century BC, when Mandragora (mandrake) was recommended by Theophrastus for treatment of wounds, gout, and sleeplessness, and as a love potion. In the first century BC, Cleopatra used Atropine-rich extracts from the Egyptian henbane plant (another nightshade) for the above-mentioned purpose of dilating the pupils of her eyes. [citation needed]

The use of deadly nightshades as a poison was known in ancient Rome, as attested by the rumour that the Roman empress Livia Drusilla used the juice of Atropa belladonna berries to murder her husband, the emperor Augustus.[13]

In the first century AD, Dioscorides recognized wine of mandrake as an anaesthetic for treatment of pain or sleeplessness, to be given prior to surgery or cautery.[14] The use of nightshade preparations for anaesthesia, often in combination with opium, persisted throughout the Roman and Islamic empires and continued in Europe until superseded in the 19th century by modern anaesthetics.

The modern pharmacological study of Atropa belladonna extracts was begun by the German chemist Friedlieb Ferdinand Runge (1795–1867). In 1831, the German pharmacist Heinrich F. G. Mein (1799–1864)[15] succeeded in preparing a pure crystalline form of the active substance, named atropine.[16] [17]

Description

[edit]
Atropa belladonna

Atropa belladonna is a branching herbaceous perennial rhizomatous hemicryptophyte, often growing as a subshrub from a fleshy rootstock. Plants can reach a height of 2 m (7 ft) (more commonly 1.5 m (5 ft)), and have ovate leaves up to 18 cm (7 in) long. The bell-shaped flowers are dull purple tinged yellow-green toward the base and are faintly scented. The fruits are berries, which are green, ripening to a shiny black, and approximately 1.5 cm (0.6 in) in diameter. The berries are sweet and are consumed by animals that disperse the seeds in their droppings, even though they contain toxic alkaloids (see Toxicity).[18] There is a pale-yellow flowering form called Atropa belladonna var. lutea with pale yellow fruit.

A. belladonna is sometimes confused with the much less poisonous black nightshade, Solanum nigrum, belonging to a different genus within Solanaceae.[19] A comparison of the fruit shows that black nightshade berries are spherical, have a dull lustre and grow in clusters, whereas the berries of deadly nightshade are much glossier, twice as large, somewhat flattened and are borne singly. Another distinction is that black nightshade flowers are not tubular but white and star-shaped, bearing a central cone of yellow anthers.

Distribution

[edit]

Atropa belladonna is native to temperate southern, Central and Eastern Europe, Turkey, Iran and the Caucasus, but has been cultivated and introduced outside its native range. In southern Sweden it was recorded in Flora of Skåne in 1870 as grown in apothecary gardens near Malmö.[20]

In Britain it is native only on calcareous soils, on disturbed ground, field margins, hedgerows and open woodland. More widespread as an alien, it is often a relic of cultivation as a medicinal herb. Seed is spread mainly by birds.[21]

It is naturalised in parts of North America and North Africa, where it is often found in shady, moist locations with limestone-rich soils. It is considered a weed species in parts of the world,[22] where it colonizes areas with disturbed soils.[23]

Cultivation

[edit]
Belladonna cultivation, Eli Lilly and Company, 1919

Atropa belladonna is rarely used in gardens, but, when grown, it is usually for its large upright habit and showy berries.[24] Germination of the small seeds is often difficult, due to hard seed coats that cause seed dormancy. Germination takes several weeks under alternating temperature conditions, but can be sped up with the use of gibberellic acid.[25] The seedlings need sterile soil to prevent damping off and resent root disturbance during transplanting.[citation needed]

Taxonomy

[edit]

Atropa belladonna is in the nightshade family (Solanaceae), which it shares with potatoes, tomatoes, eggplants, jimsonweed, tobacco, wolfberry, and chili peppers. The common names for this species include belladonna, deadly nightshade, divale, dwale,[26] banewort, devil's berries, death cherries, beautiful death, devil's herb, great morel, and dwayberry.[27]

Etymology

[edit]

The name Atropa belladonna was published by Carl Linnaeus in Species Plantarum in 1753.[28] Atropa is derived from the name of the Greek goddess Atropos ('she who may not be turned aside' i.e. 'the inflexible' or 'the implacable')—one of the three Greek fates or destinies who would determine the course of a man's life by the weaving of threads that symbolized his birth, the events in his life, and finally his death, with Atropos cutting these threads to mark the last of these.[29][30] The name "belladonna" comes from the two words bella and donna in the Italian language, meaning 'beautiful' and 'woman', respectively,[26] originating either from its usage as a cosmetic to beautify pallid skin,[31] or more probably, from its usage to increase the pupil size in women.[29][30]

Toxicity

[edit]
Attractively sweet and cherry-like fruit of Atropa belladonna

Belladonna is one of the most toxic plants known,[32][33] and its use by mouth increases risk in numerous clinical conditions, such as complications of pregnancy, cardiovascular diseases, gastrointestinal disorders, and psychiatric disorders, among others.[2][3] All parts of the plant contain tropane alkaloids;[2][34][35] roots have up to 1.3%,[a] leaves 1.2%, stalks 0.65%, flowers 0.6%, ripe berries 0.7%, and seeds 0.4% tropane alkaloids; leaves reach maximal alkaloid content when the plant is budding and flowering, roots are most poisonous in the end of the plant's vegetation period.[36] Belladonna nectar is transformed by bees into honey that also contains tropane alkaloids.[37] The berries pose the greatest danger to children because they look attractive and have a somewhat sweet taste.[27][38][39] The root of the plant is generally the most toxic part, though this can vary from one specimen to another.[27][34]

The active agents in belladonna, atropine, hyoscine (scopolamine), and hyoscyamine, have anticholinergic properties.[3][40][35] The symptoms of belladonna poisoning include dilated pupils, sensitivity to light, blurred vision, tachycardia, loss of balance, staggering, headache, rash, flushing, severely dry mouth and throat, slurred speech, urinary retention, constipation, confusion, hallucinations, delirium, and convulsions.[3][32][41][42][35] In 2009, A. belladonna berries were mistaken for blueberries by an adult woman; the six berries she ate were documented to result in severe anticholinergic syndrome.[43] The plant's deadly symptoms are caused by atropine's disruption of the parasympathetic nervous system's ability to regulate involuntary activities, such as sweating, breathing, and heart rate. The antidote for belladonna poisoning is an anticholinesterase (such as physostigmine) or a cholinomimetic (such as pilocarpine), the same as for atropine.[44]

Atropa belladonna is also toxic to many domestic animals, causing narcosis and paralysis.[45] However, cattle and rabbits eat the plant seemingly without suffering harmful effects.[42] In humans, its anticholinergic properties will cause the disruption of cognitive capacities, such as memory and learning.[40]

[edit]

Belladonna cultivation is legal in Southern and Eastern Europe, Pakistan, North America, and Brazil.[36] Belladonna leaves and roots can be bought with a medical prescription in pharmacies throughout Germany.[46] In the United States, drugs containing tropane alkaloids such as atropine are prescription-only, and the FDA regards any over-the-counter products claiming efficacy and safety as an anticholinergic drug, to be illegal.[47]

Uses

[edit]

Cosmetics

[edit]

The common name belladonna originates from its historic use by women, as bella donna is Italian for "beautiful woman". Drops prepared from the belladonna plant were used to dilate women's pupils, an effect considered to be attractive and seductive.[11][12][9] Belladonna drops act as a muscarinic antagonist, blocking receptors in the muscles of the eye that constrict pupil size.[48] Belladonna is currently rarely used cosmetically, as it carries the adverse effects of causing minor visual distortions, inability to focus on near objects, and increased heart rate. Prolonged usage was reputed to cause blindness.[49]

Dietary supplements

[edit]

In the United States, belladonna is marketed as a dietary supplement, typically as an atropine ingredient in over-the-counter cold medicine products.[32][47] Although such cold medicine products are probably safe for oral use at typical atropine dosages (0.2 milligram), there is inadequate scientific evidence to assure their effectiveness.[47] By FDA guidelines for supplements, there are no regulated manufacturing standards for cold medicines containing atropine, with some belladona supplements found to contain contaminants.[32]

Medicinal uses

[edit]
A belladonna plaster, Hunterian Museum, Glasgow

Scientific evidence to recommend the use of A. belladonna in its natural form for any condition is insufficient,[2][3][32] although some of its components, in particular l-atropine, which was purified from belladonna in the 1830s, have accepted medical uses.[42] Donnatal is a prescription pharmaceutical, that combines natural belladonna alkaloids in a specific, fixed ratio with phenobarbital to provide peripheral anticholinergic or antispasmodic action and mild sedation.[50] Donnatal contains 0.0194 mg of atropine.[50] According to the FDA and Donnatal labeling, it is possibly effective for use as adjunctive therapy in the treatment of irritable bowel syndrome (irritable colon, spastic colon, mucous colitis) and acute enterocolitis.[50][51] Donnatal is not approved by the FDA as being either safe or effective.[50] According to the FDA, Donnatal use has significant risks: it can cause harm to a fetus if administered to a pregnant woman, can lead to heat prostration if used in hot climates, may cause constipation, and may produce drowsiness or blurred vision.[50]

The Towns-Lambert or Bella Donna Cure was a regimen for treating alcoholism in the early 20th century.[52]

Alternative medicine and toxicity risk

[edit]
A homeopathic preparation of belladonna

Belladonna has been used in herbal medicine for centuries as a pain reliever, muscle relaxer, and anti-inflammatory, and to treat menstrual problems, peptic ulcer disease, histaminic reaction, and motion sickness.[2][3][53][54][9]

At least one 19th-century eclectic medicine journal explained how to prepare a belladonna tincture for direct administration.[55] In homeopathic practices, belladonna was prescribed by German physician Samuel Hahnemann as a topical medication for inflammation and pain diluted to such an extent that none of the plant was actually present in the preparation.[2] In the form of Doktor Koster's Antigaspills, belladonna was a homeopathic medication for upset stomach and excessive flatulence, again with no actual belladonna present in the medication.[56] There is insufficient scientific evidence justifying the use of belladonna for these or any other clinical disorders.[2]

In 2010 and 2016, the US Food and Drug Administration warned consumers against the use of homeopathic teething tablets and gels containing belladonna as used for infants and children, stating that the products may be toxic, causing "seizures, difficulty breathing, lethargy, excessive sleepiness, muscle weakness, skin flushing, constipation, difficulty urinating, or agitation" especially for the lower potencies which are, counterintuitively, the ones that are more likely to include belladonna since they are less diluted.[57][58]

Recreational drug

[edit]

Atropa belladonna and related plants, such as Datura stramonium (commonly known as jimson weed), have occasionally been used as recreational drugs because of the vivid hallucinations and delirium they produce.[59] These hallucinations are most commonly described as very unpleasant, and recreational use is considered extremely dangerous because of the high risk of unintentional fatal overdose.[60][61][62][63][9] The main psychoactive ingredients are the alkaloids scopolamine and, to a lesser extent, hyoscyamine.[64] The effects of atropine on the central nervous system include memory disruption, which may lead to severe confusion.[65] The major effects of belladonna consumption last for three to four hours; visual hallucinations can last for three to four days, and some negative aftereffects are preserved for several days.[36]

Poison

[edit]

The tropane alkaloids of A. belladonna were used as poisons, and early humans made poisonous arrows from the plant.[66][9] In Ancient Rome, it was used as a poison by Agrippina the Younger, wife of Emperor Claudius, on the advice of Locusta, a woman who specialized in poisons, and Livia, who is rumored to have used it to kill her husband Emperor Augustus.[66][67]

The Scots used it during a truce to poison the troops of the invading Harold Harefoot, King of England, to the point that the English troops were unable to stand their ground and had to retreat to their ships.[30][9]

Medical historians also suspect that Solomon Northup, a free black man who was kidnapped and sold into slavery in 1841, was poisoned using a combination of Atropa belladonna and laudanum.[68]

Folklore

[edit]
Main articles: European witchcraft and shamanism
Leaves of belladonna

Flying ointment

[edit]
Main article: Flying ointment

In the past, witches were believed to use a mixture of belladonna, opium poppy and other plants, typically poisonous (such as monkshood and hemlock), in flying ointment, which they allegedly applied to help them fly to gatherings with other witches or to experience bacchanalian carousal.[69][9] Carlo Ginzburg and others have argued that flying ointments were preparations meant to encourage hallucinatory dreaming; a possible explanation for the inclusion of belladonna and opium poppy in flying ointments concerns the known antagonism between tropane alkaloids of belladonna (scopolamine) and opiate alkaloids in the opium poppy, Papaver somniferum (to be specific, morphine), which produces a dream-like waking state (hypnagogia) or potentiated dreams while the user is asleep. This antagonism was known in folk medicine and discussed in traditional medicine formularies.[70][71] Belladonna is also notable for the unpredictability of its toxic effects.[72][73]

Female attractiveness

[edit]

Among the ancient folk traditions of the Romanian (Moldavian) / Ukrainian region of Bukovina in the Carpathians is the ritual for a Bukovinian girl to enhance her attractiveness by making an offering to deadly nightshade. She entered the fields on a Sunday in Shrovetide, clad in her Sunday best, accompanied by her mother and bringing a bag of bread, salt, and brandy. She would dig up a deadly nightshade root and leave the three offerings in its place. As she returned home, she carried the root on the top of her head. On the way both to and from home, she avoided all quarrels and arguments. If asked by anyone on the way back what she was taking home, she would not divulge the truth or the spell would break.[74]

[edit]
  • Specimen with abundant flowers and green, immature berries
    Specimen with abundant flowers and green, immature berries
  • Single flower, showing long pedicel springing from leaf axil.
    Single flower, showing long pedicel springing from leaf axil.
  • Atropa belladonna L. Corolla and calyx of single flower in profile.
    Atropa belladonna L. Corolla and calyx of single flower in profile.
  • Atropa belladonna L. Single flower angled to show both exterior and interior.
    Atropa belladonna L. Single flower angled to show both exterior and interior.
  • Atropa belladonna L. Single flower, full face, showing reticulated corolla base and insertion of (characteristically curled) stamens, and pistil.
    Atropa belladonna L. Single flower, full face, showing reticulated corolla base and insertion of (characteristically curled) stamens, and pistil.
  • Single flower, three-quarter face, showing fine detail of puberulent stigma
    Single flower, three-quarter face, showing fine detail of puberulent stigma
  • Atropa belladonna L. single flower back-lit by bright sunlight to reveal purple reticulation of yellowish-green corolla tube.
    Atropa belladonna L. single flower back-lit by bright sunlight to reveal purple reticulation of yellowish-green corolla tube.
  • Back-lit corolla, showing contrast between pubescent, ribbed exterior and more glabrous interior
    Back-lit corolla, showing contrast between pubescent, ribbed exterior and more glabrous interior
  • Cross-section of corolla, showing ripe anthers with flocculent, cream pollen
    Cross-section of corolla, showing ripe anthers with flocculent, cream pollen
  • Atropa belladonna L. Reverse of fruiting calyx, showing concave backs of calyx lobes with dirt from air pollution coating sticky trichomes.
    Atropa belladonna L. Reverse of fruiting calyx, showing concave backs of calyx lobes with dirt from air pollution coating sticky trichomes.
  • The translucent yellow berries of Atropa belladonna lutea.
    The translucent yellow berries of Atropa belladonna lutea.

See also

[edit]

Notes

[edit]
  1. ^ Fresh weight percentages. Dry weight percentages would cut these figures roughly in half.

References

[edit]
  1. ^ a b c d e Kennedy, David O. (2014). "The Deliriants - The Nightshade (Solanaceae) Family". Plants and the Human Brain. New York: Oxford University Press. pp. 131–137. ISBN 9780199914012. LCCN 2013031617. Archived from the original on 2023-04-22. Retrieved 2021-09-17.
  2. ^ a b c d e f g h i Ulbricht, C; Basch, E; Hammerness, P; Vora, M; Wylie Jr, J; Woods, J (2004). "An evidence-based systematic review of belladonna by the natural standard research collaboration" (PDF). Journal of Herbal Pharmacotherapy. 4 (4): 61–90. doi:10.1080/J157v04n04_06. PMID 15927926. S2CID 218876043. Archived (PDF) from the original on 2018-07-12. Retrieved 2017-10-17.
  3. ^ a b c d e f g h i "Belladonna". MedlinePlus, US National Institutes of Health. 23 February 2015. Archived from the original on 20 December 2010. Retrieved 17 October 2017.
  4. ^ Fatur, Karsten; Kreft, Samo (April 2020). "Common anticholinergic solanaceaous plants of temperate Europe - A review of intoxications from the literature (1966–2018)". Toxicon. 177: 52–88. Bibcode:2020Txcn..177...52F. doi:10.1016/j.toxicon.2020.02.005. PMID 32217234. S2CID 213559151. Archived from the original on 2022-05-24. Retrieved 2021-05-19.
  5. ^ Kuhn, Cynthia; Swartzwelder, Scott; Wilson, Wilkie; Wilson, Leigh Heather; Foster, Jeremy (2008). Buzzed. The Straight Facts about the Most Used and Abused Drugs from Alcohol to Ecstasy. New York: W. W. Norton & Company. p. 107. ISBN 978-0-393-32985-8.
  6. ^ Fatur, Karsten; Kreft, Samo (April 2020). "Common anticholinergic solanaceaous plants of temperate Europe - A review of intoxications from the literature (1966–2018)". Toxicon. 177: 52–88. Bibcode:2020Txcn..177...52F. doi:10.1016/j.toxicon.2020.02.005. PMID 32217234. S2CID 213559151. Archived from the original on 2022-05-24. Retrieved 2021-05-19.
  7. ^ Potter, Samuel O.L. (1893). A Handbook of Materia Medica Pharmacy and Therapeutics. London: P. Blakiston's. pp. 53. the antidote for belladonna is physostigmine or pilocarpine the same as for atropine.
  8. ^ "Cult Presents: Sherlock Holmes – Bert Coules Interview". BBC. Archived from the original on 2023-05-28. Retrieved 2023-06-08.
  9. ^ a b c d e f g Fatur, Karsten (June 2020). ""Headless Her still in ICU at A time" in Ethnobotanical Perspective: A Historical Review of the Uses of Anticholinergic Solanaceae Plants in Europe". Economic Botany. 74 (2): 140–158. Bibcode:2020EcBot..74..140F. doi:10.1007/s12231-020-09498-w. ISSN 0013-0001. S2CID 220844064.
  10. ^ Brunton, Laurence; Knollmann, Bjorn. Goodman and Gilman's Pharmacological Basis of Therapeutics "Muscarinic receptor antagonists – History" (2001 ed.). p. 163.
  11. ^ a b Hofmann, Albert; Schultes, Richard Evans (1987). Plants of the Gods: Origins of Hallucinogenic Use. New York: Van der Marck Editions. pp. 88. ISBN 0-912383-37-2.
  12. ^ a b Tombs S, Silverman I (2004). "Pupillometry: A sexual selection approach". Evolution and Human Behavior. 25 (4): 211–228. Bibcode:2004EHumB..25..221T. doi:10.1016/j.evolhumbehav.2004.05.001.
  13. ^ According to the historian Tacitus, Livia was rumored to have squeezed the juice of the berries into a plate of figs which she fed to Augustus. (Tacitus, Annals 1.5. See also John Emsley, Molecules of Murder: Criminal Molecules and Classic Cases, ch. 3.6, "History of Atropine as a poison".
  14. ^ Robert S. Holzman, MD (July 1998). "The Legacy of Atropos". Anesthesiology. 89 (1): 241–249. doi:10.1097/00000542-199807000-00030. PMID 9667313. S2CID 28327277. Retrieved 2007-05-21. citing J. Arena, Poisoning: Toxicology-Symptoms-Treatments, 3rd edition. Springfield, Charles C. Thomas, 1974, p 345
  15. ^ "Heinrich Friedrich Georg Mein". ostfriesischelandschaft.de (in German). Archived from the original on 2013-05-11. Retrieved 2019-10-20.{{cite web}}: CS1 maint: unfit URL (link)
  16. ^ Heinrich Friedrich Georg Mein (1833). "Ueber die Darstellung des Atropins in weissen Kristallen" [On the preparation of atropine as white crystals]. Annalen der Pharmacie (in German). Vol. 6 (1 ed.). pp. 67–72. Archived from the original on 2023-01-12. Retrieved 2020-01-15.
  17. ^ Atropine was also independently isolated in 1833 by Geiger and Hesse:
    • Geiger; Hesse (1833). "Darstellung des Atropins" [Preparation of atropine]. Annalen der Pharmacie (in German). Vol. 5. pp. 43–81. Archived from the original on 2023-01-12. Retrieved 2020-01-15.
    • Geiger; Hesse (1833). "Fortgesetzte Versuche über Atropin" [Continued experiments on atropine]. Annalen der Pharmacie (in German). Vol. 6. pp. 44–65. Archived from the original on 2023-01-12. Retrieved 2020-01-15.
  18. ^ Kay QON (2008). Marshall, C.; Grace, J. (eds.). "Edible fruits in a cool climate: the evolution and ecology of endozoochory in the European flora". Fruit and Seed Production: Aspects of Development, Environmental Physiology and Ecology (Society for Experimental Biology Seminar Series). Cambridge, UK: Cambridge University Press: 240. ISBN 978-0-521-05045-6.
  19. ^ Fatur, Karsten; Kreft, Samo (2021-02-22). Mehanathan, Muthamilarasan (ed.). "Nixing the nightshades: Traditional knowledge of intoxicating members of the Solanaceae among hallucinogenic plant and mushroom users in Slovenia". PLOS ONE. 16 (2): e0247688. Bibcode:2021PLoSO..1647688F. doi:10.1371/journal.pone.0247688. ISSN 1932-6203. PMC 7899348. PMID 33617573.
  20. ^ Hylander, N. (1971). "Prima loca plantarum vascularium Sueciae. Första litteraturuppgift för Sveriges vildväxande kärlväxter jämte uppgifter om första svenska fynd. Förvildade eller i senare tid inkomna växter". Svensk Botanisk Tidskrift. 64: 332.
  21. ^ "Online Atlas of the British and Irish Flora: Atropa belladonna (Deadly nightshade)". Botanical Society of Britain and Ireland (BSBI). Archived from the original on 2016-03-11. Retrieved 2016-03-11.
  22. ^ "PLANTS Profile for Atropa bella-donna (belladonna) | USDA PLANTS". Archived from the original on 2013-04-30. Retrieved 2008-07-08.
  23. ^ Stepp JR (June 2004). "The role of weeds as sources of pharmaceuticals". J Ethnopharmacol. 92 (2–3): 163–6. doi:10.1016/j.jep.2004.03.002. PMID 15137997.
  24. ^ Stuart, David (2004). Dangerous garden: the quest for plants to change our lives. Cambridge: Harvard University Press. p. 49. ISBN 0-674-01104-X.
  25. ^ Genova E, Komitska G, Beeva Y (1997). "Study on the germination of Atropa belladonna L. seeds" (PDF). Bulgarian Journal of Plant Physiology. 23 (1–2): 61–66. Archived (PDF) from the original on 2008-12-17. Retrieved 2008-07-08.
  26. ^ a b Spiegl, Fritz (1996). Fritz Spiegl's Sick Notes: An Alphabetical Browsing-Book of Derivatives, Abbreviations, Mnemonics and Slang for Amusement and Edification of Medics, Nurses, Patients and Hypochondriacs. Washington, DC: Taylor & Francis. pp. 21–22. ISBN 1-85070-627-1.
  27. ^ a b c Grieve, Margaret; Leyel, C. F. (1971). Modern Herbal. Courier Dover Publications. p. 584. ISBN 0-486-22799-5. Retrieved 2008-07-08.
  28. ^ "Solanaceae Atropa belladonna L." Plant Name Details. IPNI. 2003-07-02. Archived from the original on 2008-06-07. Retrieved 2008-03-01. Solanaceae Atropa belladonna L. Species Plantarum 2 1753 "Habitat in Austriae, Angliae montibus sylvosis."
  29. ^ a b Edward Harris Ruddock (1867). The Homoeopathic Vade Mecum of Modern Medicine and Surgery: For the Use of Junior Practitioners, Students, Clergymen, Missionaries, Heads of Families, Etc (2 ed.). Jarrold and Sons. pp. 503–508.
  30. ^ a b c R. Groombridge, ed. (1839). The Naturalist: Illustrative of the Animal, Vegetable, and Mineral Kingdoms. R. Groombridge. p. 193. Notes: v.4–5 (1838–1839)
  31. ^ Gledhill, David (2008). The Names of Plants. Cambridge University Press. ISBN 9780521866453 (hardback), ISBN 9780521685535 (paperback). pp. 61, 68.
  32. ^ a b c d e "Belladonna". Drugs.com. 18 April 2019. Archived from the original on 28 August 2019. Retrieved 28 August 2019.
  33. ^ "Herbarium of toxic plants". herbarium.freehostia.com. Archived from the original on August 17, 2011. Retrieved May 31, 2020.
  34. ^ a b "Committee for Veterinary Medicinal Products, Atropa Belladonna, Summary Report" (PDF). emea.europa.eu. The European Agency for the Evaluation of Medicinal Products. 1998. Archived from the original (PDF) on 2006-07-18. Retrieved 2008-07-08.
  35. ^ a b c Fatur, Karsten; Kreft, Samo (April 2020). "Common anticholinergic solanaceaous plants of temperate Europe - A review of intoxications from the literature (1966–2018)". Toxicon. 177: 52–88. Bibcode:2020Txcn..177...52F. doi:10.1016/j.toxicon.2020.02.005. PMID 32217234. S2CID 213559151. Archived from the original on 2022-05-24. Retrieved 2021-05-19.
  36. ^ a b c Raetsch, Ch. (2005). The encyclopedia of psychoactive plants: ethnopharmacology and its applications. US: Park Street Press. pp. 80–85.
  37. ^ Hazlinsky, B. (1956). "Poisonous honey from deadly nightshade". Zeitschrift für Bienenforschung (3): 93–96.
  38. ^ "Atropa belladonna". thepoisongarden.co.uk. Archived from the original on 2019-04-06. Retrieved 2011-10-15.
  39. ^ "Belladonna (Atropa belladonna L. or its variety acuminata Royle ex Lindl)". Wellness.com. 2014-06-14. Archived from the original on 2019-02-15. Retrieved 2011-10-15.
  40. ^ a b Pepeu, Giancarlo; Giovannini, Maria Grazia (2004). "Acetylcholine: I. Muscarinic Receptors". In Gernot Riedel; Bettina Platt (eds.). From messengers to molecules: memories are made of these. Springer. ISBN 978-0-306-47862-8.
  41. ^ Mallinson T (2010). "Deadly Nightshade: Atropa Belladonna". Focus on First Aid (15): 5. Archived from the original on 2010-05-21.
  42. ^ a b c Lee MR (March 2007). "Solanaceae IV: Atropa belladonna, deadly nightshade" (PDF). J R Coll Physicians Edinb. 37 (1): 77–84. PMID 17575737. Archived (PDF) from the original on 2007-10-17. Retrieved 2008-07-07.
  43. ^ Mateo Montoya A, Mavrakanas N, Schutz JS (2009). "Acute anticholinergic syndrome from Atropa belladonna mistaken for blueberries". Eur J Ophthalmol. 19 (1): 170–2. doi:10.1177/112067210901900130. PMID 19123171. S2CID 9387171.
  44. ^ Potter, Samuel O. L. (1893). A Handbook of Materia Medica Pharmacy and Therapeutics. London: P. Blakiston's. pp. 53. the antidote for belladonna is physostigmine or pilocarpine the same as for atropine.
  45. ^ "Poisonous Vascular Plants". cals.ncsu.edu. North Carolina State University Department of Plant Biology. 2000. Archived from the original on 6 July 2008. Retrieved 2008-07-07.
  46. ^ Lindequist, U. (1992). "Atropa". Haegers Handbuch der pharmazeutischen Praxis (in German) (5th ed.). Berlin: Springer. p. 429.
  47. ^ a b c "Sec. 310.533 Drug products containing active ingredients offered over-the-counter (OTC) for human use as an anticholinergic in cough-cold drug products". Code of Federal Regulations, Title 21, US Food and Drug Administration. 1 April 2018. Archived from the original on 14 August 2020. Retrieved 28 August 2019.
  48. ^ "Atropine Eye Drops". Archived from the original on 8 July 2008. Retrieved 2008-07-08.
  49. ^ Wood, George Bacon (1867). A Treatise on Therapeutics, and Pharmacology or Materia Medica. Vol. 1. Philadelphia: J.B. Lippincott & Co. pp. 792–795.
  50. ^ a b c d e "Donnatal tablets". Drugs.com. 1 March 2018. Archived from the original on 28 August 2019. Retrieved 28 August 2019.
  51. ^ "Donnatal Extentabs Prescribing Information". PBM Pharmaceuticals. 2009. Archived from the original on 2008-12-27. Retrieved 2009-03-04.
  52. ^ Markel, Howard; M.d (2010-04-19). "An Alcoholic's Savior: God, Belladonna or Both?". The New York Times. ISSN 0362-4331. Archived from the original on 2022-01-26. Retrieved 2022-01-26.
  53. ^ Ebadi, Manuchair (2007). Pharmacodynamic Basis of Herbal Medicine. CRC Press. p. 203. ISBN 9780849370502.
  54. ^ Vaughan, John Griffith; Patricia Ann Judd; David Bellamy (2003). The Oxford Book of Health Foods. Oxford University Press. pp. 59. ISBN 0-19-850459-4. deadly nightshade homeopathic.
  55. ^ Joseph R. Buchanan; R.S. Newton (1854). Wm. Phillips and co. (ed.). "Officinal preparations". The Eclectic Medical Journal. Wm. Phillips and co.
  56. ^ Lambert, Angela (September 3, 2014). The Lost Life of Eva Braun. St. Martin's Press. p. 262. ISBN 978-1466879966.
  57. ^ "Consumer Updates – Hyland's Homeopathic Teething Tablets: Questions and Answers". US Food and Drug Administration. 23 October 2010. Archived from the original on 24 April 2018. Retrieved 17 April 2018.
  58. ^ "FDA warns against the use of homeopathic teething tablets and gels". US Food and Drug Administration. 30 September 2016. Archived from the original on 24 April 2018. Retrieved 17 April 2018.
  59. ^ Fatur, Karsten (2021-01-07). Bussmann, Rainer W. (ed.). "Peculiar plants and fantastic fungi: An ethnobotanical study of the use of hallucinogenic plants and mushrooms in Slovenia". PLOS ONE. 16 (1): e0245022. Bibcode:2021PLoSO..1645022F. doi:10.1371/journal.pone.0245022. ISSN 1932-6203. PMC 7790546. PMID 33412556.
  60. ^ Dewitt MS, Swain R, Gibson LB (1997). "The dangers of jimson weed and its abuse by teenagers in the Kanawha Valley of West Virginia". West Virginia Medical Journal. 93 (4): 182–5. PMID 9274142.
  61. ^ Micke MM (October 1996). "The case of hallucinogenic plants and the Internet". J Sch Health. 66 (8): 277–80. doi:10.1111/j.1746-1561.1996.tb03397.x. PMID 8899584.
  62. ^ Cummins BM, Obetz SW, Wilson MR (June 1968). "Belladonna poisoning as a facet of pschyodelia". JAMA. 204 (11): 1011. doi:10.1001/jama.204.11.1011. PMID 5694682.
  63. ^ Fatur, Karsten; Kreft, Samo (April 2020). "Common anticholinergic solanaceaous plants of temperate Europe - A review of intoxications from the literature (1966–2018)". Toxicon. 177: 52–88. Bibcode:2020Txcn..177...52F. doi:10.1016/j.toxicon.2020.02.005. PMID 32217234. S2CID 213559151. Archived from the original on 2022-05-24. Retrieved 2021-05-19.
  64. ^ Schultes, Richard Evans (1976). Hallucinogenic Plants. Illustrated by Elmer W. Smith. New York: Golden Press. p. 46. ISBN 978-0-307-24362-1.
  65. ^ Hardy TK, Wakely D (1962). "The amnesic properties of hyoscine and atropine in pre-anæsthetic medication". Anaesthesia. 17 (3): 331–336. doi:10.1111/j.1365-2044.1962.tb13473.x. PMID 13904669. S2CID 46569975.
  66. ^ a b Michael (1998). Alkaloids : biochemistry, ecology, and medicinal applications. New York: Plenum Press. p. 20. ISBN 0-306-45465-3.
  67. ^ Timbrell, John (2005). The poison paradox : chemicals as friends and foes. Oxford: Oxford Univ. Pr. pp. 2. ISBN 0-19-280495-2. poisons used by the wife of Claudius.
  68. ^ Northup, Solomon (1975). Twelve years a slave (Louisiana pbk. ed.). Baton Rouge: Louisiana State University Press. ISBN 9780807101506. OCLC 804847817.
  69. ^ Hansen, Harold A. The Witch's Garden pub. Unity Press 1978 ISBN 978-0913300473
  70. ^ "Belladonna.—Belladonna". Henrietta's Herbal. Archived from the original on 2008-05-14. Retrieved 2008-07-08.
  71. ^ Kuklin, Alexander (February 1999). How Do Witches Fly?. DNA Press. ISBN 0-9664027-0-7.
  72. ^ Kowalchik, Claire; Carr A Hylton W (1987). Herb gardening. Rodale. pp. 1 and 158. ISBN 0-87596-964-X.
  73. ^ Harner, Michael J. (1973). Hallucinogens and Shamanism. Oxford [Oxfordshire]: Oxford University Press. pp. 123–150. ISBN 0-19-501649-1.
  74. ^ Schenk, Gustav Das Buch der Gifte translated by Michael Bullock as The Book of Poisons pub. Weidenfeld and Nicolson 1956 page 28, quoting Hovorka, Oskar von and Kronfeld, Adolf : Vergleichende Volksmedizin Zweiter Band. Eine Darstellung volksmedizinische Sitten und Gebräuche, Anschauungen und Heilfaktoren des Aberglaubens und der Zaubermedizin [Translation : Comparative Folk Medicine, a study in two volumes: an account of the ethnomedical practices, habits of thought and healing practices to be found in Superstition and Magical Medicine] 2 vols., pub. Strecker und Schröder Stuttgart 1908-9
[edit]
Wikispecies has information related to Atropa belladonna.
Wikimedia Commons has media related to Atropa belladonna.
  • "Compounds in deadly nightshade". Phytochemical and Ethnobotanical Databases. Beltsville, Maryland: National Germplasm Resources Laboratory; USDA, ARS, National Genetic Resources Program. Archived from the original on 2004-11-10. Retrieved 2005-07-28.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Atropa_belladonna&oldid=1257227971"