Chelidonium majus explained

Chelidonium majus, the greater celandine, is a perennial herbaceous flowering plant in the poppy family Papaveraceae. One of two species in the genus Chelidonium, it is native to Europe and western Asia and introduced widely in North America.

The plant known as lesser celandine (Ficaria verna) is not closely related, as it belongs to the buttercup family Ranunculaceae.

Description

Greater celandine is a perennial herbaceous plant with an erect habit, and reaches 30cm-120cmcm (10inches-50inchescm) high. The blue-green leaves are pinnate with lobed and wavy margins, up to 30cm (10inches) long. When injured, the plant exudes a yellow to orange latex.[1]

The flowers consist of four yellow petals, each about 18mm long, with two sepals. A double-flowered variety occurs naturally. The flowers appear from late spring to summer, May to September (in the UK),[2] in umbelliform cymes of about four flowers.

The seeds are small and black, borne in a long, cylindrical capsule. Each has an elaiosome, which attracts ants to disperse the seeds (myrmecochory).

Taxonomy and naming

Chelidonium majus is one of the many species described by the father of taxonomy, Carl Linnaeus, in volume one of his Species Plantarum in 1753.[3]

According to the Oxford English Dictionary, the name celandine comes from Late Latin celidonia, from earlier Latin chelidonia or chelidonium, and ultimately from Ancient Greek Greek, Ancient (to 1453);: χελιδόνιον, from Greek, Ancient (to 1453);: χελιδών (chelidṓn) "swallow", hence the common name "swallowwort". Ancient writers said that the flower bloomed when the swallows returned and faded when they left.[4] [5] Chelidonium majus has also been called great celandine,, nipplewort, tetterwort,[6] or simply "celandine". The common name tetterwort also refers to Sanguinaria canadensis.[7]

Distribution and habitat

Chelidonium majus is native in most regions of Europe. It is also found in North Africa in Macaronesia, Algeria and Morocco. In Western Asia it is found in the Caucasus, Armenia, Azerbaijan, Georgia, Kazakhstan, Mongolia, Siberia, Iran and Turkey. Its habitats include rocky slopes, woodlands, waste areas, and roadsides.[8]

Ecology

It is considered an aggressive invasive plant in parts of North America, and an invasive plant in other areas. In Wisconsin, for example, it is a restricted plant.[9] [10] Control is obtained mainly via pulling or spraying the plant before seed dispersal.

Constituents and pharmacology

The whole plant is toxic in moderate doses as it contains a range of isoquinoline alkaloids; use in herbal medicine requires the correct dose.[11] The main alkaloid present in the herb and root is coptisine. Other alkaloids present include methyl 2'-(7,8-dihydrosanguinarine-8-yl)acetate, allocryptopine,[12] stylopine, protopine, cryptopine, hemochelidonine, homochelidonine, norchelidonine, berberine, chelidonine, sanguinarine, chelerythrine,[13] and 8-hydroxydihydrosanguinarine.[14] Sanguinarine is particularly toxic with an of 18 mg per kg body weight (IP in rats).[15] Caffeic acid derivatives, such as caffeoylmalic acid, are also present.[16]

The characteristic latex also contains proteolytic enzymes and the phytocystatin chelidostatin, a cysteine protease inhibitor.[17] It is a traditional folk remedy against warts in France[18] and the UK. It is used in the preparation of a range of off-the-shelf treatments for warts and skin conditions.[19]

Chelidonium is used to make Ukrain, a drug that has been promoted for, but is not known to be effective for, the treatment of cancer and viral infections.[20] [21]

The fresh herb is no longer used officially. No dose-finding studies exist and the reported clinical studies are characterised by a considerable heterogeneity.[22]

Except for homeopathic medicines, the drug is no longer used in most English-speaking countries. In Germany and Switzerland, extracts of Chelidoni herba are a controversial component of the gastric remedy "Iberogast". The OTC-preparation is a top-selling product for the company Bayer, which is now under investigation for not warning consumers from possible hepatotoxic side-effects when taking the drug. Elevated liver-enzymes and toxic hepatitis with a documented fatality have been reported.[23] [24]

The plant is poisonous to chickens.[25]

Herbalism

The aerial parts and roots of greater celandine are used in herbalism. The above-ground parts are gathered during the flowering season and dried at high temperatures. The root is harvested in autumn between August and October and dried. The fresh rhizome is also used. Celandine has a hot and bitter taste. Preparations are made from alcoholic and hot aqueous extractions. The related plant bloodroot has similar chemical composition and uses as greater celandine.

As far back as Pliny the Elder and Dioscorides (1st century CE) this herb has been recognized as a useful detoxifying agent. The root has been chewed to relieve toothache.[26] John Gerard's Herball (1597) states that "the juice of the herbe is good to sharpen the sight, for it cleanseth and consumeth away slimie things that cleave about the ball of the eye and hinder the sight and especially being boiled with honey in a brasen vessell."[27]

It was formerly used by some Romani people as a foot refresher; modern herbalists use its purgative properties.[28] The modern herbalist Juliette de Baïracli Levy recommended greater celandine diluted with milk for the eyes and the latex for getting rid of warts.[29] Chelidonium was a favourite herb of the French herbalist Maurice Mességué.Chelidonium majus has traditionally been used for treatment of various inflammatory diseases including atopic dermatitis.[30] It is also traditionally used in the treatment of gallstones and dyspepsia.[31]

The Iroquois give an infusion of whole plant, another plant and milk to pigs that drool and have sudden movements.[32]

It was also once used to treat liver disorders, owing to the juice's resemblance to bile.[25]

Notes and References

  1. Book: Stace, C. A.. Stace, C. A.. 2019. New Flora of the British Isles. Fourth. C & M Floristics. Middlewood Green, Suffolk, U.K.. 978-1-5272-2630-2.
  2. Book: 1981 . Reader's Digest Field Guide to the Wild Flowers of Britain . 30 . . 978-0-276-00217-5.
  3. Book: Linnaeus C . Species Plantarum. Laurentii Salvii . Stockholm . 1753. Tomus I . 1. 505. https://www.biodiversitylibrary.org/page/358524 . la.
  4. Web site: Swallow . Oxford English Dictionary, Second Edition . 1989 . Oxford University Press, Oxford.
  5. Hanzlik, P.J. . 1920 . The pharmacology of chelidonin, a neglected alkaloid of chelidonium, or tetterwort . Journal of the American Medical Association . 75 . 20 . 1324–1325 . 10.1001/jama.1920.02620460022007.
  6. Book: Xu, J.P. . Cancer Inhibitors from Chinese Natural Medicines . CRC Press . 2016 . 978-1-4987-8766-6 . 2023-08-23 . 441.
  7. Book: Predny . M.L. . Chamberlain . J.L. . United States. National Park Service . Bloodroot (Sanguinaria Canadensis): An Annotated Bibliography . U.S. Department of Agriculture, Forest Service, Southern Research Station . General technical report SRS . 2005 . 2023-08-23 .
  8. Web site: Chelidonium majus - Plant Finder . 2024-03-30 . www.missouribotanicalgarden.org.
  9. Web site: Chapter NR 40 INVASIVE SPECIES IDENTIFICATION, CLASSIFICATION AND CONTROL. wisconsin.gov. 3 November 2017.
  10. Web site: Invasive Plant Atlas of New England . 2015-06-03 . https://web.archive.org/web/20150730220930/http://www.eddmaps.org/ipane/ipanespecies/herbs/Chelidonium_majus.htm . 2015-07-30 . dead .
  11. Book: Gruenwald, Joerg . PDR for Herbal Medicines . Thomson PDR . 2000 . 978-1-56363-361-4 .
  12. Cahlikova L., Opletal L., Kurfurst M., Macakova K., Kulhankova A., Host'alkova A.,"Acetylcholinesterase and butyrylcholinesterase inhibitory compounds from Chelidonium majus (Papaveraceae)." Natural Product Communications. 5 (11) (pp 1751–1754), 2010. Date of Publication: 2010.
  13. Li X.-L., Yao J.-Y., Zhou Z.-M., Shen J.-Y., Ru H.-S., Liu X.-L.,"Activity of the chelerythrine, a quaternary benzo[c]phenanthridine alkaloid from Chelidonium majus L. on Dactylogyrus intermedius." Parasitology Research. 109 (1) (pp 247-252), July 2011
  14. Park J.E., Cuong T.D., Hung T.M., Lee I., Na M., Kim J.C., Ryoo S., Lee J.H., Choi J.S., Woo M.H., Min B.S.,"Alkaloids from Chelidonium majus and their inhibitory effects on LPS-induced NO production in RAW264.7 cells". Bioorganic & Medicinal Chemistry Letters. 21 (23) (pp 6960-6963), 2011. Date of Publication: 01 Dec 2011.
  15. Book: Golob, Peter . Caroline Moss . Melanie Dales . Alex Fidgen . Jenny Evans . Irene Gudrups . The use of spices and medicinals as bioactive protectants for grains . 2008-07-17 . FAO Agricultural Services Bulletin . 137 . 1999 . . . 978-92-5-104294-6.
  16. 17230338. 1993. Hahn. R.. Hydroxycinnamic Acid Derivatives, Caffeoylmalic and New Caffeoylaldonic Acid Esters, from Chelidonium majus*,1. Planta Medica. 59. 1. 71–5. Nahrstedt. A.. 10.1055/s-2006-959608. 21131585 .
  17. Rogelj . B. . 1998 . Chelidocystatin, a novel phytocystatin from Chelidonium majus. Phytochemistry . 49 . 6. 1645–9 . 9862139 . 10.1016/s0031-9422(98)00281-7. 1998PChem..49.1645R . etal.
  18. https://www.sciencesetavenir.fr/sante/video-la-chelidoine-une-plante-contre-la-verrue_30991 La chélidoine, une plante contre la verrue dans Science et avenir 2016
  19. Web site: Celandine (Greater) / Greater Celandine - Wild Flower Finder.
  20. Web site: Celandine. American Cancer Society. August 2011. 5 September 2013. 23 April 2015. https://web.archive.org/web/20150423221233/http://www.cancer.org/treatment/treatmentsandsideeffects/complementaryandalternativemedicine/herbsvitaminsandminerals/celandine. dead.
  21. Web site: A telling story about "alternative" cancer cures and their purveyors . 14 October 2012 . December 4, 2012 . Edzard Ernst . Edzard Ernst .
  22. Web site: European Medicines Agency . Assessment report on Chelidonium majus L., herba . January 20, 2012 .
  23. F. Pantano, G. Mannocchi, E. Marinelli, S. Gentili, S. Graziano, F.P. Busardò, N.M. di Luca"Hepatotoxicity induced by greater celandine (Chelidonium majus L.): a review of the literature." Eur Rev Med Pharmacol Sci 2017; 21 (1 Suppl): 46-52. Retrieved 21 July 2019
  24. Aiolfi S (July 2019). Bayer-Medikament im Fokus der Staatsanwaltschaft(in German). Neue Zürcher Zeitung. Retrieved 21 July 2019.
  25. Book: Niering . William A. . William Niering. Olmstead . Nancy C. . The Audubon Society Field Guide to North American Wildflowers, Eastern Region . 1985 . 1979. Knopf . 0-394-50432-1 . 671.
  26. Book: Chevallier, Andrew . The encyclopedia of medicinal plants . DK Publishing . New York . 1996 . 978-0-7894-1067-2 . 185 .
  27. Book: A Modern Herbal: The Medicinal, Culinary, Cosmetic and Economic Properties, Cultivation and Folk-lore of Herbs, Grasses, Fungi, Shrubs, & Trees with All Their Modern Scientific Uses, Volume 1. Grieve, Maud. 1971.
  28. Book: Howard, Michael . Traditional Folk Remedies . Century Paperbacks . 1987-05-21 . Ebury Press . 978-0-7126-1731-4 . 146–147.
  29. Bailes M., "The Healing Garden",
  30. Gabsik Yang . Kyungjin Lee . Mi-Hwa Lee . So-Hyung Kim . In-Hye Ham . Ho-Young Choi . 2011 . Inhibitory effects of Chelidonium majus extract on atopic dermatitis-like skin lesions in NC/Nga mice . . 138 . 2 . 398–403 . 10.1016/j.jep.2011.09.028 . 21963561.
  31. Gabriela Mazzanti . Antonella di Sotto . Antonio Franchitto . Caterina Loredana Mammola . Paola Mariani . Sabina Mastrangelo . Francesca Menniti-Ippolito . Annabella Vitalone . 2009 . Chelidonium majus is not hepatotoxic in Wistar rats, in a 4 weeks feeding experiment . . 126 . 3 . 518–524 . 19761826 . 10.1016/j.jep.2009.09.004.
  32. Rousseau, Jacques 1945 Le Folklore Botanique De Caughnawaga. Contributions de l'Institut botanique l'Universite de Montreal 55:7-72 (p. 45)