Remedy/Plants/Asteraceae

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In Asteraceae, although the energy store is generally in the form of inulin rather than starch, they produce iso/chlorogenic acid, sesquiterpene lactones, pentacyclic triterpene alcohols, various alkaloids, acetylenes (cyclic, aromatic, with vinyl end groups), tannins and have terpenoid essential oils which never contain iridoids.[1]

Asteraceae produce secondary metabolites, such as flavonoids and terpenoids, some of which can inhibit protozoan parasites such as Plasmodium, Trypanosoma, Leishmania and parasitic intestinal worms, and thus have potential in medicine.[2]


Achillea millefolium[edit | edit source]

Yarrow (Achillea millefolium) on top of Janče hill (800 m), Slovenia. Credit: Petar Milošević.{{free media}}

Achillea millefolium', commonly known as yarrow (or common yarrow, is a flowering plant in the family Asteraceae, native to temperate regions of the Northern Hemisphere in Asia and Europe and North America.[3] It has been introduced as a feed for livestock in New Zealand[4] and Australia, where it is a common weed of both wet and dry areas, such as roadsides, meadows, fields and coastal places.[4]

Yarrow can be used for dying wool as it contains apigenin and luteolin. Depending on the mordant the color may be green to yellow.[5]

A. millefolium was used as in traditional medicine, possibly due to its astringent effects.[3] Yarrow and its North American varieties were traditionally used by many Native American nations.[6] The Navajo historically considered it a "life medicine" and chewed the plant for toothaches and used its infusions for earaches. The Miwok in California used the plant as an analgesic and head cold remedy.[6] Native American nations used the plant for healing cuts and abrasions, for relief of ear-aches, and throat infections, and for an eye-wash.[7] Common yarrow was used by Plains indigenous peoples to reduce pain or fever and aid sleep.[6]

In the early 20th century, some Ojibwe people used a decoction of yarrow leaves on hot stones and inhaled it to treat headaches,[8] or applied decoctions of the root onto skin for its stimulating effect.[9]

The dark blue essential oil of yarrow contains chemicals called proazulenes.[10]

Chamazulene and δ-Cadinol are chemical compounds found in A. millefolium. The chromophore of azulene was discovered in yarrow and wormwood and named in 1863 by Septimus Piesse.

Yarrow contains isovaleric acid, salicylic acid, asparagine, sterols, and flavonoids.[11]

Ambrosia acanthicarpa[edit | edit source]

Ambrosia acanthicarpa is shown at Santa Monica Mountains National Recreation Area, California, USA. Credit: Anthony Valois and the National Park Service.{{Free media}}

Ambrosia acanthicarpa is common across much of the western United States and in the Prairie Provinces of Canada.[12][13]

Ambrosia ambrosioides[edit | edit source]

Ambrosia ambrosioides is shown at Pima Wash Trail, South Mountain, Phoenix, Arizona. Credit: Miwasatoshi.{{Free media}}

Ambrosia ambrosioides is found in the deserts of northern Mexico (Baja California, Baja California Sur, Chihuahua, Durango, Sonora), Arizona, and California (Ventura County, California + San Diego County, California).[14][15][16][17]

Flowering occurs mainly in February through April.

Ambrosia arborescens[edit | edit source]

A large weed known as Marco in the highlands of Peru is shown. Credit: Dick Culbert from Gibsons, B.C., Canada.{{Free media}}

A. arborescens is used as a medicinal plant with analgesic, antiinflammatory and antiseptic properties.[18]

Ambrosia artemisiifolia[edit | edit source]

Ambrosia artemisiifolia is a native of North America, in bare or disturbed areas, such as roadsides, stockyards and stream banks, occasionally pastures. Credit: Harry Rose from South West Rocks, Australia.{{Free media}}

Its bloom period is July to October in North America.[19] Its pollen is wind-dispersed, and can be a strong allergen to people with Allergic rhinitis (hay fever).[20][21]

Three sesquiterpene lactones isolated from the aerial parts of Ambrosia artemisiifolia were identified as psilostachyin A, psilostachyin B and psilostachyin C. All of them have some molluscicidal activity against the small tropical freshwater snail Oncomelania hupensis.[22]

Ambrosia confertiflora[edit | edit source]

Flowering branches of Ambrosia confertiflora (Weakleaf Bur Ragweed) are shown. Credit: Richard Spellenberg.{{free media}}

Ambrosia confertiflora is native to much of northern Mexico (from Sonora to Tamaulipas) and the southwestern United States from California east as far as Kansas, Oklahoma, and central Texas.[23]

Ambrosia cordifolia[edit | edit source]

Ambrosia cordifolia, called the Tucson bur ragweed,[24] is native to northern Mexico (Sonora, Sinaloa, San Luis Potosí, Guanajuato, Baja California Sur) and the State of Arizona in the United States.[25][26][27]

The reference to the Arizona city of Tucson in the common name refers to the species' first discovery by Cyrus G. Pringle in the mountains near Tucson in 1884.[28]

Ambrosia deltoidea[edit | edit source]

The plant is native to the Sonoran Desert region of North America, where it can be found in Baja California, Baja California Sur, and Sonora in Mexico, with its distribution extending north into Arizona in the United States.[29][30][31]

Ambrosia dumosa[edit | edit source]

Photo shows Ambrosia dumosa (white bur-sage) at the Springs Preserve garden in Las Vegas, Nevada Credit: Stan Shebs.{{free media}}

Ambrosia dumosa is a common constituent of the creosote-bush scrub community throughout the Mojave desert of California, Nevada, and Utah and the Sonoran Desert of Arizona and northwestern Mexico (Baja California, Baja California Sur, Sonora, Chihuahua).[32][33][34][35]

Ambrosia eriocentra[edit | edit source]

Woolly bursage is shown on a portion of periodically exposed, dry river bed
(Red Rock Canyon in the Spring Mountains of southern Nevada, elevation about 1300 m). Credit: Stan Shebs.{{free media}}

The plant is native to the Mojave Desert in the southwestern United States, within southern California, southern Nevada, northwestern Arizona, and southwestern Utah.[36]

It grows in the Mojave's plains and mountain ridges up to 1,700 metres (5,600 ft) in elevation.[37][38]

Ambrosia ilicifolia[edit | edit source]

Ambrosia ilicifolia is known by the common names hollyleaf burr ragweed and hollyleaf bursage.[39]

It is native to the deserts and mountains of western Arizona, and the adjacent Sonoran Desert areas of southeastern California, Sonora and Baja California. It grows in dry washes, scrub, and other local habitats.[40][41]

Ambrosia monogyra[edit | edit source]

The plant is native to the southwestern United States (California, Arizona, New Mexico, Texas), and northern Mexico (Baja California, Baja California Sur, Chihuahua, Sinaloa, Sonora).[42][43]

Ambrosia psilostachya[edit | edit source]

Ambrosia psilostachya is widespread across much of North America. Credit: Krzysztof Ziarnek.{{free media}}

Ambrosia psilostachya contains a group of phytochemicals called psilostachyins.[44]

The plant is widespread across much of North America (United States, Canada, and northern Mexico).[45]

Ambrosia salsola[edit | edit source]

Hymenoclea salsola (cheesebush) is shown near Thousand Palms Oasis in Coachella Valley, California. Credit: Stan Shebs.{{Free media}}

Ambrosia salsola is native to the southwestern United States (Arizona, California, Nevada, Utah) and northwestern Mexico (Sonora, Baja California, Baja California Sur), where it is a common plant of the local deserts, where it thrives on sandy soil, alkaline environments, and disturbed sites.[46][47]

Ambrosia trifida[edit | edit source]

Ambrosia trifida, the giant ragweed, is a species of flowering plant native to North America. Credit: Le.Loup.Gris.{{Free media}}

The Cherokee used it as a remedy for insect stings, urticaria (hives), fever, and pneumonia, and the Iroquois used it to treat diarrhea.[48]

Arnica cordifolia[edit | edit source]

Arnica cordifolia is from Wenatchee Mountains, Washington USA. Credit: Walter Siegmund.{{free media}}

The dried leaves can be made into a poultice or tincture to treat strains and bruises.[49]

Arnica montana[edit | edit source]

Arnica is a genus of perennial, herbaceous plants in the sunflower family Asteraceae.

The species Arnica montana, native to Europe, has long been used medicinally, but the effectiveness of this use has not been substantiated.[50]

Arnica montana contains the toxin helenalin, which can be poisonous if large amounts of the plant are eaten, and contact with the plant can also cause skin irritation.[51]

Artemisia abrotanum[edit | edit source]

Image shows a garden plot of Artemisia abrotanum. Credit: Kurt Stüber.{{free media}}

In the traditional medicine of East and North Bosnia and Herzegovina, aerial parts of Artemisia abrotanum are used in jaundice therapy.[52]

Artemisia absinthium[edit | edit source]

Artemisia absinthium leaves and flowers are used in homeopathy as a remedy. Credit: H. Zell.{{free media}}

Wormwood herb contains bitter substances from the group of sesquiterpene lactones; absinthin, at 0.20 to 0.28%, is the main component of these bitter substances. Essential oils make up 0.2 to 0.8% and contain (-) - thujone, (+) - isothujone, thujyl alcohol and its esters, chamazulene and other mono- and sesquiterpenes.[53][54] A chemotype does not produce β-thujone but does contain terpenoids not seen elsewhere.[55]

It is used for dyspepsia, as a bitter to counteract poor appetite, for various infectious diseases, Crohn's disease, and IgA nephropathy.[56][57][58][59]

Artemisia afra[edit | edit source]

Artemisia afra, the African wormwood, is a common species of the genus Artemisia in Africa. Credit: H Brisse.{{free media}}

Artemisia pallens[edit | edit source]

Davana essential oil is shown. Credit: Itineranttrader.{{free media}}
Image shows leaves and flowers of Artemisia pallens. Credit: Yercaud-elango.{{free media}}

Davana oil, from the Artemisia pallens, is used as a perfume ingredient.

Davanone, davan ether, davana furan and linaloo are the major constituents of davana oil, while methyl cinnamate, ethyl cinnamate, bicyclogermacrene, 2-hydroxyisodavanone, farnesol, geranyl acetate, sesquiterpene lactones, and germacranolides also occur.[60] The amount of davanone and linalool decreased while those of (Z)− and (E)−methyl cinnamate, (E)−ethyl cinnamate, bicyclogermacrene, davana ether, 2-hydroxyisodavanone, and farnesol increased from flower heads emergence stage to the initiation of seed set stage. Five compounds, (Z)− and (E)−methyl cinnamates, (Z)− and (E)−ethyl cinnamates, and geranyl acetate, were identified for the first time in davana oil.[61]

Oral administration of high doses aqueous/methanolic extract from the aerial parts of the plants was observed to reduce blood glucose levels in glucose−fed hyperglycemic and alloxan-treated rabbits and rats.[62]

Calendula officinalis[edit | edit source]

Calendula officinalis, the pot marigold, common marigold, ruddles or Scotch marigold,[63] is a flowering plant in the daisy family Asteraceae.

The petals and pollen of Calendula officinalis contain triterpenoid esters and the carotenoids flavoxanthin and auroxanthin (antioxidants and the source of the yellow-orange coloration). The leaves and stems contain other carotenoids, mostly lutein (80%), zeaxanthin (5%), and beta-carotene. Plant extracts are also widely used by cosmetics, presumably due to presence of compounds such as saponins, resins, and essential oils.[64]

The flowers of Calendula officinalis contain flavonol glycosides, triterpene oligoglycosides, oleanane-type triterpene glycosides, saponins, and a sesquiterpene glucoside.[65][66] Calendula flowers are a rich source of lutein, containing 29.8 mg/100g.[67]

Plant pharmacological studies have suggested that Calendula extracts may have anti-viral, anti-genotoxic, and anti-inflammatory properties in vitro.[68] In an in vitro assay, the methanol extract of C. officinalis exhibited antibacterial activity and both the methanol and the ethanol extracts showed antifungal activities.[69]

Chamaemelum nobile[edit | edit source]

Chamomile essential oil contains sesquiterpenes, terpene lactones (including the blue compound, chamazulene), acetylene derivatives, and polyphenols, which contribute to the fragrance and may be extracted individually.[70]

Cichorium intybus[edit | edit source]

Common chicory (Cichorium intybus)[71] is a somewhat woody, perennial herbaceous plant of the Asteraceae (daisy) family, usually with bright blue flowers, rarely white or pink. Many varieties are cultivated for salad leaves, chicons (blanched buds), or roots (var. sativum), which are baked, ground, and used as a coffee substitute and food additive. In the 21st century, inulin]], an extract from chicory root, has been used in food manufacturing as a sweetener and source of dietary fiber.[72]

The root contains up to 20% inulin, a polysaccharide similar to starch. Inulin is mainly found in the plant family Asteraceae as a storage carbohydrate (for example Jerusalem artichoke, dahlia, yacon, etc.). It is used as a sweetener in the food industry with a sweetening power 10% that of sucrose[73] and is sometimes added to yogurts as a 'prebiotic'.[74]

Fresh chicory root may contain between 13 and 23% inulin, by total weight.[75]

The bitter substances are primarily the two sesquiterpene lactones, lactucin and lactucopicrin. Other ingredients are aesculetin, aesculin, cichoriin, umbelliferone, scopoletin, 6,7-dihydrocoumarin, and further sesquiterpene lactones and their glycosides.[76]

Cynara cardunculus[edit | edit source]

Matricaria recutita[edit | edit source]

More than 120 chemical constituents have been identified in chamomile flower as secondary metabolites, with most of them found in the blue essential oil of the flowers.[77] Chemical constituents of its essential oil include: the terpenes bisabolol,[78] farnesene, and chamazulene; the flavonoids apigenin, quercetin, patuletin, and luteolin; and coumarin.[78]

Silybum marianum[edit | edit source]

Def. a "mixture of flavonolignans extracted from the blessed milk thistle (Silybum marianum), used as a source of silibinin"[79] is called a silymarin.

Silibinin (International Nonproprietary Name (INN)), also known as silybin (both from Silybum, the generic name of the plant from which it is extracted), is the major active constituent of silymarin, a standardized extract of the Silybum marianum (milk thistle) seeds, containing a mixture of flavonolignans consisting of silibinin, isosilibinin, silychristin, silidianin, and others. Silibinin itself is a mixture of two diastereomers, silybin A and silybin B, in approximately equimolar ratio.[80] The mixture exhibits a number of pharmacological effects, particularly in the fatty liver, non-alcoholic fatty liver, non-alcoholic steatohepatitis, and there is great clinical evidence for the use of silibinin as a supportive element in alcoholic and Child–Pugh grade 'A', liver cirrhosis.[81] However, despite its several beneficial effects on the liver, silibinin and all the other compounds found in silymarin, especially silychristin seem to act as potent disruptors of the thyroid system by blocking the Monocarboxylate transporter 8 (MCT8) transporter.[82] The long term intake of silymarin can lead to some form of thyroid disease and if taken during pregnancy, silymarin can cause the development of the Allan–Herndon–Dudley syndrome.[82] Although this information is unfortunately still not being taken into consideration by all regulatory bodies, several studies now consider silymarin and especially silychristin to be important inhibitors of the MCT8 transporter and a potential disruptor of the thyroid hormone functions.[82]

Silipide (trade name Siliphos, not to be confused with the water treatment compound of the same name, a glass-like polyphosphate containing sodium, calcium magnesium and silicate, formulated for the treatment of water problems), a complex of silymarin and phosphatidylcholine (lecithin), is about 10 times more bioavailable than silymarin.[83] An earlier study had concluded Siliphos to have 4.6 fold higher bioavailability.[84] It has been also reported that silymarin inclusion complex with β-cyclodextrin is much more soluble than silymarin itself.[85] There have also been prepared glycosides of silybin, which show better water solubility and even stronger hepatoprotective effect.[86]

Silymarin, like other flavonoid]]s, has been shown to inhibit P-glycoprotein-mediated cellular efflux.[87] It has been reported that silymarin inhibits cytochrome P450 enzymes and an interaction with drugs primarily cleared by P450s cannot be excluded.[88]

All of the flavonolignan compounds found in the silymarin mixture seem to block the uptake of thyroid hormones into the cells by selectively blocking the Monocarboxylate transporter 8 (MCT8) transmembrane transporter.[82] The author of this study noted that especially silychristin, one of the compounds of the silymarin mixture seems to be perhaps the most powerful and selective inhibitor for the (MCT8) transporter.[82] Due to the essential role played by the thyroid hormone in human metabolism in general it is believed that the intake of silymarin can lead to thyroid disease (disruptions of the thyroid system).[82] Because the thyroid hormones and the MCT8 as well are known to play a critical role during early and fetal development, the administration of silymarin during pregnancy is especially thought to be dangerous, potentially leading to the Allan–Herndon–Dudley syndrome, a brain development disorder that causes both moderate to severe intellectual disability and problems with speech and movement.[89]

A phase I clinical trial in humans with prostate cancer designed to study the effects of high dose silibinin found 13 grams daily to be well tolerated in patients with advanced prostate cancer with asymptomatic liver toxicity (hyperbilirubinemia and elevation of alanine aminotransferase) being the most commonly seen adverse event.[90]

Silymarin is also devoid of embryotoxic potential in animal models.[91] [92]

For approved drug preparations and parenteral applications in the treatment of Amanita mushroom poisoning, the water-soluble silibinin-C-2',3-dihyrogensuccinate disodium salt is used and in 2011, it also received Orphan Medicinal Product Designation for the prevention of recurrent hepatitis C in liver transplant recipients by the European Commission.[93]

Silibinin is under investigation to see whether it may have a role in cancer treatment (e.g. due to its inhibition of STAT3 signalling).[94]

Silibinin has a number of potential mechanisms that could benefit the skin: chemoprotective effects from environmental toxins, anti-inflammatory effects, protection from UV induced photocarcinogenesis, protection from sunburn, protection from Ultraviolet (UVB)-induced epidermal hyperplasia, and DNA repair for UV induced DNA damage (double strand breaks).[95] Studies on mice demonstrate a significant protection on chronic unpredictable mild stress (CUMS) induced depressive-like behavior on mice[96] and increased cognition in aged rats as a result of consuming silymarin.[97]

Due to its immunomodulatory,[98] iron chelating and antioxidant properties, this herb has the potential to be used in beta-thalassemia patients who receive regular blood transfusions and suffer from iron overload.[99]

Silymarin can be produced in callus and cells suspensions of Silybum marianum and substituted pyrazinecarboxamides can be used as abiotic elicitors of flavolignan production.[100]

The biosynthesis of silibinin A and silibinin B is composed of two major parts, taxifolin and coniferyl alcohol.[101][102] Coniferyl alcohol is synthesized in milk thistle seed coat, starting with the transformation of phenylalanine into cinnamic acid mediated by phenylalanine ammonia-lyase (PAL).[103]

See also[edit | edit source]

References[edit | edit source]

  1. ↑ Stevens, Peter F. (2001). "Angiosperm Phylogeny Website: Asterales". Angiosperm Phylogeny Website.
  2. ↑ Panda, Sujogya Kumar; Luyten, Walter (2018). "Antiparasitic activity in Asteraceae with special attention to ethnobotanical use by the tribes of Odisha, India". Parasite 25: 10. doi:10.1051/parasite/2018008. ISSN 1776-1042. PMID 29528842. 
  3. ↑ 3.0 3.1 "Missouri Botanical Gardens".
  4. ↑ 4.0 4.1 "RNZIH – Horticulture Pages – Weeds – Achillea millefolium – yarrow". www.rnzih.org.nz. Retrieved 2 September 2015.
  5. ↑ Kiumarsi; Abomahboub; Rashedi; Parvinzadeh (2009). "Achillea Millefolium, a New Source of Natural Dye for Wool Dyeing". Progress in Color, Colorants and Coatings 2 (2): 87–93. https://www.sid.ir/en/journal/ViewPaper.aspx?ID=226555. 
  6. ↑ 6.0 6.1 6.2 University of Michigan – Dearborn: Native American Ethnobotany; Achillea millefolium . accessed 31 January 2013
  7. ↑ Faran, Mina; Tcherni, Anna (1997). Medicinal herbs in Modern Medicine (ṣimḥei marpé bir'fū'ah ha-modernīt) (in he). 1. Jerusalem: Akademon (Hebrew University of Jerusalem). p. 242. ISBN 965-350-068-6. OCLC 233179155. , s.v. Achillea millefolium
  8. ↑ Densmore, Frances, 1928, Uses of Plants by the Chippewa Indians, SI-BAE Annual Report #44:273–379, page 336
  9. ↑ Densmore, Frances, 1928, Uses of Plants by the Chippewa Indians, SI-BAE Annual Report #44:273–379, page 350
  10. ↑ Michler, Barbara; Arnold, Carl-Gerold (1999). "Predicting Presence of Proazulenes in the Achillea millefolium Group". Folia Geobotanica 34 (1): 143–161. doi:10.1007/BF02803081. 
  11. ↑ Home Herbal: Cook, Brew & Blend Your Own Herbs. DK Pub.. 2011. ISBN 978-0-7566-7183-9. 
  12. ↑ Biota of North America Program 2013 county distribution map
  13. ↑ Great Plains Flora Association. 1986. Flora of the Great Plains i–vii, 1–1392. University Press of Kansas, Lawrence.
  14. ↑ Flora of North America Vol. 21 Page 12 Ambrosia ambrosioides (Delpino) W. W. Payne, J. Arnold Arbor. 45: 410. 1964.
  15. ↑ Raymond M. Turner, Janice E. Bowers, and Tony L. Burgess, Sonoran desert plants: an ecological atlas (Tucson: The University of Arizona Press, 1995) pp. 75–76
  16. ↑ Biota of North America Program 2014 county distribution map
  17. ↑ Calflora taxon report, University of California, Ambrosia ambrosioides (Cav.) Payne, ambrosia bursage, ambrosia leaved burbush
  18. ↑ Duke, James A. (2008). Duke's Handbook of Medicinal Plants of Latin America (in en). CRC Press. pp. 33. ISBN 9781420043174. 
  19. ↑ Jepson eFlora (TJM2): Ambrosia artemisiifolia . accessed 26 August 2016.
  20. ↑ NPIN−Lady Bird Johnson Wildflower Center Native Plant Information Network: Ambrosia artemisiifolia
  21. ↑ Newscientist.com: "North American ragweed to bring autumn allergy misery to Europe."
  22. ↑ Wang, P. H.; Xu, J.; Wu, M. Y. (1993). "Chemical constituents of ragweed (Ambrosia artemisiifolia L.)". Zhongguo Zhong Yao Za Zhi 18 (3): 164–166, 191. PMID 8352903. 
  23. ↑ Biota of North America Program 2014 county distribution map
  24. ↑ Southeastern Arizona Wildflowers and Plants, Ambrosia cordifolia – Tucson Bur Ragweed
  25. ↑ Biota of North America Program 2014 county distribution map
  26. ↑ Tropicos, specimen listing for Ambrosia cordifolia (A. Gray) W.W. Payne
  27. ↑ Payne, Willard William 1964. Journal of the Arnold Arboretum 45(4): 421
  28. ↑ Gray, Asa 1884. Synoptical Flora of North America 1(2): 445 as Franseria cordifolia
  29. ↑ Marshall, K. Anna. 1994. Ambrosia deltoidea. In: Fire Effects Information System, [Online]. U.S. Department of Agriculture, Forest Service, Rocky Mountain Research Station, Fire Sciences Laboratory.
  30. ↑ Tropicos, specimen listing for Ambrosia deltoidea (Torr.) W.W. Payne
  31. ↑ Biota of North America Program 2014 county distribution map
  32. ↑ Flora of North America Vol. 21 Page 13 Bursage Ambrosia dumosa (A. Gray) W. W. Payne, J. Arnold Arbor. 45: 422. 1964.
  33. ↑ Biota of North America Program 2014 county distribution map
  34. ↑ Calflora taxon report, University of California, Ambrosia dumosa (A. Gray) Payne Burrobush, burro weed, white bursage
  35. ↑ Tropicos, specimen listing for Ambrosia dumosa (A. Gray) W.W. Payne
  36. ↑ Calflora taxon report, University of California, Ambrosia eriocentra (A. Gray) Payne woolly bur sage, wooly bursage
  37. ↑ Jepson eFlora: Ambrosia eriocentra
  38. ↑ Biota of North America Program 2013 county distribution map
  39. ↑ Calflora taxon report, University of California, Ambrosia ilicifolia (A. Gray) Payne holly leaved burbush, hollyleaf bursage
  40. ↑ Flora of North America Vol. 21 Page 12 Ambrosia ilicifolia (A. Gray) W. W. Payne
  41. ↑ Biota of North America Program 2014 county distribution map
  42. ↑ Flora of North America Vol. 21 Page 12 Ambrosia monogyra (Torrey & A. Gray) Strother & B. G. Baldwin, Madroño. 49: 143. 2002
  43. ↑ Calflora taxon report, University of California, Ambrosia monogyra Torr. & Gray singlewhorl burrobrush
  44. ↑ Wan, Shiqiang; Yuan, Tong; Bowdish, Sarah; Wallace, Linda; Russell, Scott D.; Luo, Yiqi (2002). "Response of an allergenic species, Ambrosia psilostachya (Asteraceae), to experimental warming and clipping: Implications for public health". American Journal of Botany 89 (11): 1843–6. doi:10.3732/ajb.89.11.1843. PMID 21665612. 
  45. ↑ Biota of North America Program 2104 county distribution map
  46. ↑ Flora of North America Vol. 21 Page 12, Burrobush, Ambrosia salsola (Torrey & A. Gray) Strother & B. G. Baldwin, Madroño. 49: 143. 2002.
  47. ↑ Biota of North America Program 2013 county distribution map
  48. ↑ Ambrosia trifida. Native American Ethnobotany. University of Michigan, Dearborn.
  49. ↑ Fagan, Damian (2019). Wildflowers of Oregon: A Field Guide to Over 400 Wildflowers, Trees, and Shrubs of the Coast, Cascades, and High Desert. Guilford, CT: FalconGuides. pp. 101. ISBN 1-4930-3633-5. https://www.worldcat.org/oclc/1073035766. 
  50. ↑ E. Ernst; M. H. Pittler (November 1998). "Efficacy of Homeopathic Arnica A Systematic Review of Placebo-Controlled Clinical Trials". JAMA Surgery 133 (11): 1187–1190. doi:10.1001/archsurg.133.11.1187. PMID 9820349. 
  51. ↑ "Poisonous Plants: Arnica montana". Ces.ncsu.edu. Retrieved 2009-12-22. {{cite web}}: |archive-date= requires |archive-url= (help)
  52. ↑ Tewari D, Mocan A, Parvanov ED, Sah AN, Nabavi SM, Huminiecki L, Ma ZF, Lee YY, Horbańczuk JO, Atanasov AG. Ethnopharmacological Approaches for Therapy of Jaundice: Part I. Front Pharmacol. 2017, Aug 15;8:518. doi: 10.3389/fphar.2017.00518.
  53. ↑ Wichtl, Max, ed. (1984). Teedrogen. Ein Handbuch für Apotheker und Ärzte. Wissenschaftliche Verlagsgesellschaft, Stuttgart, ISBN 3-8047-0792-0, pp. 363–365
  54. ↑ European Medicines Agency, Committee on Herbal Medicinal Products (HMPC) (30 May 2017). Assessment report on Artemisia absinthium L., herba, final, London, p. 4
  55. ↑ Isman, Murray B. (2020-01-07). "Botanical Insecticides in the Twenty-First Century—Fulfilling Their Promise?". Annual Review of Entomology (Annual Reviews) 65 (1): 233–249. doi:10.1146/annurev-ento-011019-025010. ISSN 0066-4170. 
  56. ↑ European Scientific Cooperative on Phytotherapy (2009) "Absinthii herba (wormwood)" In: ESCOP Monographs: The Scientific Foundation for Herbal Medicinal Products, 2nd ed, Thieme.
  57. ↑ Abad MJ, Bedoya LM, Apaza L, Bermejo P (2012). "The Artemisia L genus: A review of bioactive essential oils" . Molecules 17: 2542-2566. PMID 22388966. doi:10.3390/molecules17032542.
  58. ↑ Algieri F, Rodriguez-Nogales A, Rodriguez-Cabezas ME, et al. (2015). "Botanical drugs as an emerging strategy in inflammatory bowel disease: a review" . Mediators Inflamm. 2015: 179616. PMID 26576073.PMC 4630406. doi:10.1155/2015/179616.
  59. ↑ Krebs S, Omer B, Omer TN, Fliser D (2010). "Wormwood (Artemisia absinthium) for poorly responsive early-stage IgA nephropathy: a pilot uncontrolled trial" Am. J. Kidney Dis. 56 (6): 1095-9. PMID 20843592.doi:10.1053/j.ajkd.2010.06.025.
  60. ↑ Pujar, PP; Sawaikar, DD; Rojatkar, SR; Nagasampagi, BA (2000). "A new germacranolide from Artemisia pallens". Fitoterapia 71 (5): 590–2. doi:10.1016/S0367-326X(00)00168-4. PMID 11449517. 
  61. ↑ "Artemisia pallens - Davana". Retrieved 2009-01-25. {{cite web}}: |archive-date= requires |archive-url= (help)
  62. ↑ Subramoniam, A; Pushpangadan, P; Rajasekharan, S; Evans, DA; Latha, PG; Valsaraj, R (1996). "Effects of Artemisia pallens Wall. On blood glucose levels in normal and alloxan-induced diabetic rats". Journal of Ethnopharmacology 50 (1): 13–7. doi:10.1016/0378-8741(95)01329-6. PMID 8778502. 
  63. ↑ Germplasm Resources Information Network (GRIN). Agricultural Research Service (ARS), United States Department of Agriculture (USDA).
  64. ↑ National Institutes of Health. "Calendula". Herbs and Supplements. U.S. National Library of Medicine. Retrieved 2007-12-19.
  65. ↑ Ukiya M; Akihisa; Yasukawa; Tokuda; Suzuki; Kimura (2006). "Anti-inflammatory, anti-tumor-promoting, and cytotoxic activities of constituents of pot marigold (Calendula officinalis) flowers". J Nat Prod 69 (12): 1692–1696. doi:10.1021/np068016b. PMID 17190444. 
  66. ↑ Yoshikawa M; Murakami; Kishi; Kageura; Matsuda (2001). "Medicinal flowers. III. Marigold.(1): hypoglycemic, gastric emptying inhibitory, and gastroprotective principles and new oleanane-type triterpene oligolycosides, calendasaponins A, B, C, and D, from Egyptian Calendula officinalis". Chem Pharm Bull 49 (7): 863–70. doi:10.1248/cpb.49.863. PMID 11456093. 
  67. ↑ Manke Natchigal, A.; Oliveira Stringheta, A.C.; Corrêa Bertoldi, M.; Stringheta, P.C. (2012). "QUANTIFICATION AND CHARACTERIZATION OF LUTEIN FROM TAGETES (TAGETES PATULA L.) AND CALENDULA (CALENDULA OFFICINALIS L.) FLOWERS.". Acta Hortic. 939, 309-314. https://www.actahort.org/books/939/939_40.htm. Retrieved 3 July 2019. 
  68. ↑ Jimenez-Medina E; Garcia-Lora; Paco; Algarra; Collado; Garrido (2006). "A new extract of the plant Calendula officinalis produces a dual in vitro effect: cytotoxic anti-tumor activity and lymphocyte activation". BMC Cancer 6: 119. doi:10.1186/1471-2407-6-119. PMID 16677386. PMC 1513589. //www.ncbi.nlm.nih.gov/pmc/articles/PMC1513589/. 
  69. ↑ Efstratiou E; Hussain; Nigam; Moore; Ayub; Rao (2012). "Antimicrobial activity of Calendula officinalis petal extracts against fungi, as well as Gram-negative and Gram-positive clinical pathogens". Complement Ther Clin Pract 18 (3): 173–176. doi:10.1016/j.ctcp.2012.02.003. PMID 22789794. 
  70. ↑ "Chamomile". Drugs.com. 10 December 2020. Retrieved 7 February 2021.
  71. ↑ "Cichorium intybus". FAO - Food and Agriculture Organization of the UN. Retrieved 2013-12-16. {{cite web}}: |archive-date= requires |archive-url= (help)
  72. ↑ Raninen, K; Lappi, J; Mykkänen, H; Poutanen, K (2011). "Dietary fiber type reflects physiological functionality: Comparison of grain fiber, inulin, and polydextrose". Nutrition Reviews 69 (1): 9–21. doi:10.1111/j.1753-4887.2010.00358.x. PMID 21198631. 
  73. ↑ Joseph O'Neill (2008-06-01). "Using inulin and oligofructose with high-intensity sweeteners". New Hope 360. Penton. Retrieved 2013-12-16. {{cite web}}: |archive-date= requires |archive-url= (help)
  74. ↑ Madrigal L. Sangronis E. "Inulin and derivates as key ingredients in functional foods. [Review]" [Spanish] Archivos Latinoamericanos de Nutricion. 57(4):387-96, 2007 Dec.
  75. ↑ Wilson, Robert; S; Y (2004). "Chicory Root Yield and Carbohydrate Composition is Influenced by Cultivar Selection, Planting, and Harvest Date". Crop Sci. 44 (3): 748–752. doi:10.2135/cropsci2004.0748. Archived on 2008-10-13. Error: If you specify |archivedate=, you must also specify |archiveurl=. https://web.archive.org/web/20081013213941/http://crop.scijournals.org/cgi/content/abstract/44/3/748. Retrieved 2008-08-20. 
  76. ↑ Harsh Pal Bais, GA Ravishankar (2001) Cichorium intybus L – cultivation, processing, utility, value addition and biotechnology, with an emphasis on current status and future prospects. Journal of the Science of Food and Agriculture, 81, 467-484 (online)|date=November 2016 |bot=InternetArchiveBot }}
  77. ↑ Singh, Ompal; Khanam, Zakia; Misra, Neelam; Srivastava, Manoj Kumar (2011). "Chamomile (Matricaria chamomilla L.): An overview". Pharmacognosy Reviews 5 (9): 82–95. doi:10.4103/0973-7847.79103. ISSN 0973-7847. PMID 22096322. 
  78. ↑ 78.0 78.1 McKay DL, Blumberg JB (2006). "A review of the bioactivity and potential health benefits of chamomile tea (Matricaria recutita L". Phytother Res 20 (7): 519–530. doi:10.1002/ptr.1900. PMID 16628544. 
  79. ↑ Equinox (27 March 2009). "silymarin". San Francisco, California: Wikimedia Foundation, Inc. Retrieved 26 June 2021. {{cite web}}: |author= has generic name (help)
  80. ↑ Davis-Searles P, Nakanishi Y, Nam-Cheol K, etal (2005). "Milk Thistle and Prostate Cancer: Differential Effects of Pure Flavonolignans from Silybum marianum on Antiproliferative End Points in Human Prostate Carcinoma Cells". Cancer Research 65 (10): 4448–57. doi:10.1158/0008-5472.CAN-04-4662. PMID 15899838. http://cancerres.aacrjournals.org/content/canres/65/10/4448.full.pdf. 
  81. ↑ Saller R, Brignoli R, Melzer J, Meier R (2008). "An updated systematic review with meta-analysis for the clinical evidence of silymarin". Forschende Komplementärmedizin 15 (1): 9–20. doi:10.1159/000113648. PMID 18334810. https://www.karger.com/Article/PDF/000113648. Retrieved 2010-12-14. 
  82. ↑ 82.0 82.1 82.2 82.3 82.4 82.5 Johannes J, Jayarama-Naidu R, Meyer F, Wirth EK, Schweizer U, Schomburg L, Köhrle J, Renko K (2016). "Silychristin, a Flavonolignan Derived From the Milk Thistle, Is a Potent Inhibitor of the Thyroid Hormone Transporter MCT8". Endocrinology 157 (4): 1694–2301. doi:10.1210/en.2015-1933. PMID 26910310. 
  83. ↑ Kidd P, Head K (2005). "A review of the bioavailability and clinical efficacy of milk thistle phytosome: a silybin-phosphatidylcholine complex (Siliphos)". Alternative Medicine Review 10 (3): 193–203. PMID 16164374. https://web.archive.org/web/20110728045923/http://www.thorne.com/altmedrev/.fulltext/10/3/193.pdf. Retrieved 2010-12-14. 
  84. ↑ Barzaghi N, Crema F, Gatti G, Pifferi G, Perucca E (1990). "Pharmacokinetic studies on IdB 1016, a silybin-phosphatidylcholine complex, in healthy human subjects". Eur J Drug Metab Pharmacokinet 15 (4): 333–8. doi:10.1007/bf03190223. PMID 2088770. 
  85. ↑ Voinovich D, Perissutti B, Grassi M, Passerini N, Bigotto A (2009). "Solid state mechanochemical activation of Silybum marianum dry extract with betacyclodextrins: Characterization and bioavailability of the coground systems". Journal of Pharmaceutical Sciences 98 (11): 4119–29. doi:10.1002/jps.21704. PMID 19226635. 
  86. ↑ Kosina P, Kren V, Gebhardt R, Grambal F, Ulrichová J, Walterová D (2002). "Antioxidant properties of silybin glycosides". Phytotherapy Research 16 Suppl 1: S33–9. doi:10.1002/ptr.796. PMID 11933137. 
  87. ↑ Zhou S, Lim LY, Chowbay B (2004). "Herbal modulation of P-glycoprotein". Drug Metabolism Reviews 36 (1): 57–104. doi:10.1081/DMR-120028427. PMID 15072439. 
  88. ↑ Wu JW, Lin LC, Tsai TH (2009). "Drug-drug interactions of silymarin on the perspective of pharmacokinetics". Journal of Ethnopharmacology 121 (2): 185–93. doi:10.1016/j.jep.2008.10.036. PMID 19041708. 
  89. ↑ "Allan-Herndon-Dudley syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 2021-05-06.
  90. ↑ Thomas W. Flaig; Daniel L. Gustafson; Lih-Jen Su; Joseph A. Zirrolli; Frances Crighton; Gail S. Harrison; A. Scott Pierson; Rajesh Agarwal et al. (2007). "A phase I and pharmacokinetic study of silybin-phytosome in prostate cancer patients". Investigational New Drugs 25 (2): 139–146. doi:10.1007/s10637-006-9019-2. PMID 17077998. 
  91. ↑ Fraschini F, Demartini G, Esposti D (2002). "Pharmacology of Silymarin". Clinical Drug Investigation 22 (1): 51–65. doi:10.2165/00044011-200222010-00007. https://web.archive.org/web/20121027121930/http://adisonline.com/druginvestigation/Abstract/2002/22010/Pharmacology_of_Silymarin.7.aspx. 
  92. ↑ Hahn G, Lehmann HD, Kürten M, Uebel H, Vogel G (1968). "On the pharmacology and toxicology of silymarin, an antihepatotoxic active principle from Silybum marianum (L.) gaertn". Arzneimittelforschung 18 (6): 698–704. PMID 5755807. 
  93. ↑ Rottapharm|Madaus. Media Communications Legalon®. Retrieved March 6, 2017.
  94. ↑ Bosch-Barrera, Joaquim; Sais, Elia; Cañete, Noemí; Marruecos, Jordi; Cuyàs, Elisabet; Izquierdo, Angel; Porta, Rut; Haro, Manel et al. (2016). "Response of brain metastasis from lung cancer patients to an oral nutraceutical product containing silibinin". Oncotarget 7 (22): 32006–32014. doi:10.18632/oncotarget.7900. PMID 26959886. PMC 5077992. //www.ncbi.nlm.nih.gov/pmc/articles/PMC5077992/. 
  95. ↑ Singh, Rana P.; Agarwal, Rajesh (September 2009). "Cosmeceuticals and silibinin". Clinics in Dermatology 27 (5): 479–484date. doi:10.1016/j.clindermatol.2009.05.012. PMID 19695480. 
  96. ↑ Thakare, Vishnu N; Patil, Rajesh R; Oswal, Rajesh J; Dhakane, Valmik D; Aswar, Manoj K; Patel, Bhoomika M (February 2018). "Therapeutic potential of silymarin in chronic unpredictable mild stress induced depressive-like behavior in mice". Journal of Psychopharmacology 32 (2): 223–235. doi:10.1177/0269881117742666. PMID 29215318. 
  97. ↑ Sarubbo, F.; Ramis, M. R.; Kienzer, C.; Aparicio, S.; Esteban, S.; Miralles, A.; Moranta, D. (March 2018). "Chronic Silymarin, Quercetin and Naringenin Treatments Increase Monoamines Synthesis and Hippocampal Sirt1 Levels Improving Cognition in Aged Rats". Journal of Neuroimmune Pharmacology 13 (1): 24–38. doi:10.1007/s11481-017-9759-0. PMID 28808887. 
  98. ↑ Balouchi, Sima; Gharagozloo, Marjan; Esmaeil, Nafiseh; Mirmoghtadaei, Milad; Moayedi, Behjat (2014-08-01). "Serum levels of TGFβ, IL-10, IL-17, and IL-23 cytokines in β-thalassemia major patients: the impact of silymarin therapy". Immunopharmacology and Immunotoxicology 36 (4): 271–274. doi:10.3109/08923973.2014.926916. PMID 24945737. 
  99. ↑ Esfahani, Behjat Al-Sadat Moayedi; Reisi, Nahid; Mirmoghtadaei, Milad (2015-03-04). "Evaluating the Safety and Efficacy of Silymarin in β-Thalassemia Patients: A Review". Hemoglobin 39 (2): 75–80. doi:10.3109/03630269.2014.1003224. PMID 25643967. 
  100. ↑ Tůmová L, Tůma J, Megušar K, Doleža M (2010). "Substituted Pyrazinecarboxamides as Abiotic Elicitors of Flavolignan Production in Silybum marianum (L.) Gaertn Cultures in Vitro". Molecules 15 (1): 331–340. doi:10.3390/molecules15010331. PMID 20110894. 
  101. ↑ Lv, Yongkun; Gao, Song; Xu, Sha; Du, Guocheng; Zhou, Jingwen; Chen, Jian (2017-11-11). "Spatial organization of silybin biosynthesis in milk thistle [Silybum marianum (L.) Gaertn"]. The Plant Journal 92 (6): 995–1004. doi:10.1111/tpj.13736. PMID 28990236. http://dx.doi.org/10.1111/tpj.13736. 
  102. ↑ Prasad, Ram Raj; Paudel, Sandeep; Raina, Komal; Agarwal, Rajesh (May 2020). "Silibinin and non-melanoma skin cancers". Journal of Traditional and Complementary Medicine 10 (3): 236–244. doi:10.1016/j.jtcme.2020.02.003. PMID 32670818. http://dx.doi.org/10.1016/j.jtcme.2020.02.003. 
  103. ↑ Barros, Jaime; Escamilla-Trevino, Luis; Song, Luhua; Rao, Xiaolan; Serrani-Yarce, Juan Carlos; Palacios, Maite Docampo; Engle, Nancy; Choudhury, Feroza K. et al. (2019-04-30). "4-Coumarate 3-hydroxylase in the lignin biosynthesis pathway is a cytosolic ascorbate peroxidase". Nature Communications 10 (1): 1994. doi:10.1038/s41467-019-10082-7. PMID 31040279. http://dx.doi.org/10.1038/s41467-019-10082-7. 

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