Artemisia annua

"Sweet annie" redirects here. For the song, see Sweet Annie.
Artemisia annua
Scientific classification
Kingdom: Plantae
(unranked): Angiosperms
(unranked): Eudicots
(unranked): Asterids
Order: Asterales
Family: Asteraceae
Genus: Artemisia
Species: A. annua
Binomial name
Artemisia annua
L.
Synonyms[1]

Artemisia chamomilla C.Winkl.

Artemisia annua, also known as sweet wormwood, sweet annie, sweet sagewort, annual mugwort[2] or annual wormwood (Chinese: 青蒿; pinyin: qīnghāo), is a common type of wormwood native to temperate Asia, but naturalized in many countries including scattered parts of North America.[3][4][5][6]

Characteristics

Artemisia annua belongs to the plant family of Asteraceae and is an annual short-day plant. Its stem is erect brownish or violet brown. The plant itself is hairless and naturally grows from 30 to 100 cm tall, although in cultivation it is possible for plants to reach a height of 200 cm. The leaves of A. annua have a length of 3–5 cm and are divided by deep cuts into two or three small leaflets. The intensive aromatic scent of the leaves is characteristic.[7] The Artemisinin content in dried leaves is in between 0% and 1.5%.[8] New hybrids of Artemisia annua developed in Switzerland can reach a leaf artemisinin content of up to 2%.[9] The small flowers have a diameter of 2-2.5 mm and are arranged in loose panicles. Their color is green-yellowish. The seeds are brown achenes with a diameter of only 0.6-0.8 mm. Their thousand-kernel weight (TKW) averages around 0.03 g (in comparison, wheat has a TKW of approximately 45 g).[7][10]

Agricultural practice

The growing period of Artemisia annua from seeding till harvest is 190–240 days, depending on the climate and altitude of the production area. The plant should be harvested at the beginning of flowering. At that time the artemisinin content is the highest.[8] Dry leave yields of Artemisia annua plantations vary between 0.5 and 3 t/ha.[9]

Growth Phases Days after sowing
Seed germination 4-10
Appearance of 1st pair of leaves 15-30
Appearance of 2nd pair of leaves 21-50
Branching 60-90
Cessation of growth in height 170-200
Flowering 190-240
Full frutition 230-280
Withering 260-310

Source: [8]

In terms of the climate A. annua prefers sunny and warm conditions. Its optimal growth temperature lies within 20 and 25 °C. Annual temperature sums of 3500-5000 °C (sum of temperatures higher 10 °C over one year) are required to guarantee a proper maturing. The rainfall during the growing season should not be less than 600 mm (annual rainfall higher 1150 mm). Especially the seedlings of A. annua. are susceptible to drought or water lodging. The mature plants on the other hand are quite resistance to those climate conditions. Nevertheless, the preferred soil conditions for A. annua are light soils with deep topsoils and good drainage properties.[8] But it is reported, that the plant is adaptable to different soil types. Paired with the relatively low demand on the environment Artemisia annua can have characteristics of a neophytic plant.[11]

Artemisia annua is best sown in rows. That facilitates weeding, which has to be done mechanically or manually since no chemical crop protection agents are admitted. It is recommended to sow 1.4 – 2 seeds per square meter.[9] The fertilizer requirements are on a low level. Potassium should be used as base fertilizer. It is taken up by the plant during the whole growing season.[8] Nitrogen is required during early branching stages, an amount of approximately 70 kg N/ha is sufficient for the plant.[12] Phosphate on the other hand is required during the blooming stages. Phosphate fertilization can lead to a higher artemsinin content in the leaves.[13] The application of salicylic acid on the leaves shortly before harvesting the plant also can raise its artemisinin content.[14] Besides few viral diseases Artemisia a. has no major diseases that need to be controlled.

The harvest of the plant is best done in the state of flower budding. The whole plant is harvested and cut into branches which are dried in the sun or in an oven. The drying temperature should not exceed 40 °C. The dry branches are shaken or beaten to separate the leaves from the stem. The leaves are then packed into fabric bags and shipped to further processing.[8] It is important that the temperatures during transportation and storage never get higher than 40 °C, otherwise artemisinin gets volatile and is lost into the air. The leaves should not be crushed before long time storage (1 year). The optimal storage conditions are either 20 °C with 85% relative humidity (RH) or 30 °C with 30-40% RH.[15]

Medicinal uses

Folk medicine

In traditional Chinese medicine, A. annua is traditionally used to treat fever.[16]

Mechanism

Seeds

The proposed mechanism of action of artemisinin involves cleavage of endoperoxide bridges by iron, producing free radicals (hypervalent iron-oxo species, epoxides, aldehydes, and dicarbonyl compounds) which damage biological macromolecules causing oxidative stress in the cells of the parasite.[17] Malaria is caused by apicomplexans, primarily Plasmodium falciparum, which largely reside in red blood cells and itself contains iron-rich heme-groups (in the form of hemozoin).[18] In 2015 artemisinin was shown to bind to a large number targets suggesting that it acts in a promiscuous manner.[19]

Extractions

In 1971, scientists demonstrated the plant extracts had antimalarial activity in primate models, and in 1972, the active ingredient, artemisinin (formerly referred to as arteannuin), was isolated and its chemical structure described. Artemisinin may be extracted using a low boiling point solvent, such as diethylether, and is found in the glandular trichomes of the leaves, stems, and inflorescences, and it is concentrated in the upper portions of plant within new growth.[20] The first isolation of artemisinin from the herb occurred from a military project known as Project 523, following the study of traditional medicine pharmacopoeias performed by Tu Youyou and other researchers within the project.[21]

Antioxidant activity

Apart from the active compound Artemisinin, recent studies show that A. annua is one of the four medical plants with the highest Oxygen radical absorbance capacity (ORAC) level.[22]

Artemisia annua possesses the capacity to produce high phenolic compounds, which result in high antioxidant activity. Five major groups (coumarins, flavones, flavonols, phenolic acids and miscellaneous) containing over 50 different phenolic compounds were identified analyzing A. annua.[23]

Flavonoids are generally known for their redox properties involved in the delay or inhibition of the initiation or propagation in oxidizing chain reactions.[23]

Even though the beneficial effect of these phenolic compounds in association of a great number of diseases is often discussed, different studies show beneficial effects of flavonoids compound produced by A. annua. It has been stated that there is a negative correlation between the presence of the mentioned components and cardiovascular diseases, cancer and parasitic disease such as malaria.[23]

Artemisinin and flavonoids

In the last 20 years researchers focused on the activity of artemisinin against malaria. Therefore, fewer studies have been done about the relationship between flavonoids and cancer. Despite that, recent studies show that the flavonoids present in the A. annua leaf are linked to suppression of CYP450 enzymes responsible for altering the absorption and metabolism of artemisinin in the body.[23] Further researches in the synergistic effect of artemisinin and flavonoids and their biological interaction between malaria and cancer are needed.[23]

Malaria treatment

Artemisia annua

Research to develop antimalarial drugs led to the discovery of artemisinin, a compound which is extracted from Artemisia annua, in the 1970s by Chinese scientist Tu Youyou, for which she shared the 2015 Nobel Prize in Physiology or Medicine.[16][24] While most TCM herbs are boiled at high temperature that can damage the active ingredient in Artemisia annua,[24] one traditional source says that this herb is to be steeped in cold water;[25] knowing this, scientists found that a better extract was obtained by using a low-temperature ether-based extraction method. Purification processes were used to isolate the active molecule. And, clinical trials showed the active ingredient to be an effective drug.[24]

Artemisinin is a sesquiterpene lactone with an endoperoxide bridge and has been produced semisynthetically as an antimalarial drug. The efficacy of tea made from A. annua in the treatment of malaria is dubious. Research has found that artemesinin is not soluble in water and the concentrations in these infusions are considered insufficient to treat malaria.[26][27][28] In 2004, the Ethiopian Ministry of Health changed Ethiopia's first line antimalaria drug from sulfadoxine/pyrimethamine (Fansidar), which has an average 36% treatment failure rate, to artemether/lumefantrine (Coartem), a drug therapy containing artemesinin which is 100% effective when used correctly, despite a worldwide shortage at the time of the needed derivative from A. annua.[29] A 2012 review said that artemisinin-based remedies are the most effective drugs for the treatment of malaria.[30] A 2013 review suggested that although Artemisia annua may not cause hepatotoxicity, haematotoxicity, or hyperlipidemia, it should be used cautiously during pregnancy due to a potential risk of embryotoxicity at a high dose.[31]

Despite global efforts in combating malaria, it remains a large burden for the population, particularly in tropical and subtropical regions.[32] Although WHO recommends artemisinin-based remedies for treating uncomplicated malaria, artemisinin resistance can no longer be ignored.[32] The causes that affected the emergence of artemisinin resistance include, for example, the use of artemisinin-based remedies.[32] Encouraging herbal alternatives are in the pipeline, but the only indelible solution for the eradication of malaria would be for the creation of an effective vaccination.[32] Emergence of artemisinin resistance has been identified in Cambodia and the border of Thailand.[33] It will likely spread to other endemic areas across the world in the impending future.[33] As of 2013, it seems that the pathogenic agent of malaria is slowly becoming resistant to artemisinin-based drugs.[34][35]

Anti-cancer properties

Several studies show that flavonoids assimilation beverages treatments such as tea might prevent, delay or help to cure cancer. Recent investigations linked the influence of flavonoids with different enzymes involved in drug metabolism and in chemical Carcinogenesis process. This induces to a therapeutic potential.[36]

Many studies show anti-cancer results analyzing different flavonoids, such as flavones and flavonols. In general it has been shown that specific flavonoid compounds can inhibit specific cancer cell growth as well as cell proliferation. Furthermore, these flavonoids induce cell Apoptosis.[23]

It is proven, that artemisinin has anti-cancer activity as well, because it contains an endoperoxide group. Artemisinin has a high anti-cancer activity due to its interaction with iron complexes[37] in the blood. This shows that artemisinin derivatives induce apoptosis of cancer cells as well.[38]

Synthetic derivatives of artemisinin are being investigated for their potential use as anticancer drugs.[39]

Asthma

Animal experiments showed that artesunate, a synthetic derivative of artemisinin, has anti-allergic properties, by effecting mast cell degranulation. This makes artesunate a candidate for treatment of allergic asthma.[40] A Metabolomics animal study further strengthens this hope.[41]

References

  1. ↑ The Plant List Artemisia annua L.
  2. ↑ "BSBI List 2007" (xls). Botanical Society of Britain and Ireland. Retrieved 2014-10-17.
  3. ↑ Flora of China Vol. 19, 20 and 21 Page 523 Sweet Annie, sweet sagewort, armoise annuelle Artemisia annua Linnaeus, Sp. Pl. 2: 847. 1753.
  4. ↑ Flora of China Vol. 20-21 Page 691 黄花蒿 huang hua hao Artemisia annua Linnaeus, Sp. Pl. 2: 847. 1753
  5. ↑ Flora of Pakistan
  6. ↑ Altervista Flora Italiana, Assenzio annuale Artemisia annua L.
  7. 1 2 Anonymus. "Artemisia annua (sweet wormwood)". Royal Botanic Gardens. Retrieved November 25, 2015.
  8. 1 2 3 4 5 6 World Health Organisation (2006). WHO monograph on good agricultural and collection practices (GACP) for Artemisia annua L.
  9. 1 2 3 Simonnet, X.; Quennoz, M.; Carlen, C. (2006). "New Artemisia annua hybrids with high artemisinin content". XXVII International Horticultural Congress-IHC2006: International Symposium on Asian Plants with Unique Horticultural 769: 371–373.
  10. ↑ Forestry, Government of Alberta, Alberta Agriculture and (1993-09-01). "Using 1,000 Kernel Weight for Calculating Seeding Rates and Harvest Losses". www1.agric.gov.ab.ca. Retrieved 2015-11-15.
  11. ↑ Müller, Meike; Brandes, Dietmar (1997). "Growth and development of Artemisia annua L. on different soil types". Verhandlungen-Gesellschaft Fur Okologie. 27: 453–460.
  12. ↑ Simon, James E; et al. (1990). "Artemisia annua L.: A promising aromatic and medicinal". Advances in New Crops: 522–526.
  13. ↑ Kapoor, Rupam; Chaudhary, Vidhi; Bhatnagar, AK (2007). "Effects of arbuscular mycorrhiza and phosphorus application on artemisinin concentration in Artemisia annua L" (PDF). Mycorrhiza. 17 (7): 581–587. doi:10.1007/s00572-007-0135-4. PMID 17578608.
  14. ↑ Pu, Gao-Bin; et. al (2009). "Salicylic acid activates artemisinin biosynthesis in Artemisia annua L" (PDF). Plant cell reports. 28 (7): 1127–1135. doi:10.1007/s00299-009-0713-3. PMID 19521701.
  15. ↑ Carlen, Christophe (2015). "Medicinal and Aromatic plants". Powerpoint Presentation in Lecture "Alternative Crops" at ETH Zürich.
  16. 1 2 "Hard to swallow". Nature. 448 (7150): 105–6. 2007. doi:10.1038/448106a. PMID 17625521.
  17. ↑ Cumming JN; Ploypradith P; Posner GH (1997). "Antimalarial activity of artemisinin (qinghaosu) and related trioxanes: mechanism(s) of action". Adv. Pharmacol. Advances in Pharmacology. 37: 253–97. doi:10.1016/S1054-3589(08)60952-7. ISBN 9780120329380. PMID 8891104.
  18. ↑ Gary H. Posner & Paul M. O’Neil (2004). "Knowledge of the Proposed Chemical Mechanism of Action and Cytochrome P450 Metabolism of Antimalarial Trioxanes Like Artemisinin Allows Rational Design of New Antimalarial Peroxides". Acc. Chem. Res. 37 (6): 397–404. doi:10.1021/ar020227u. PMID 15196049.
  19. ↑ Wang J, Zhang CJ, Chia WN, Loh CC, Li Z, Lee YM, He Y, Yuan LX, Lim TK, Liu M, Liew CX, Lee YQ, Zhang J, Lu N, Lim CT, Hua ZC, Liu B, Shen HM, Tan KS, Lin Q (2015). "Haem-activated promiscuous targeting of artemisinin in Plasmodium falciparum". Nature Communications. 6: 10111. doi:10.1038/ncomms10111. PMC 4703832Freely accessible. PMID 26694030.
  20. ↑ Duke SO, Paul RN (1993). "Development and Fine Structure of the Glandular Trichomes of Artemisia annua L.". Int. J Plant Sci. 154 (1): 107–18. doi:10.1086/297096. JSTOR 2995610.
    Ferreira JF, Janick J (1995). "Floral Morphology of Artemisia annua with Special Reference to Trichomes". Int. J Plant Sci. 156 (6): 807. doi:10.1086/297304.
  21. ↑ Tom Phillips (October 6, 2015). "Tu Youyou: how Mao's challenge to malaria pioneer led to Nobel prize". The Guardian.
  22. ↑ Brisibe, Ebiamadon Andi; Umoren, Umoren E.; Brisibe, Fraideh; Magalhäes, Pedro M.; Ferreira, Jorge F. S.; Luthria, Devanand; Wu, Xianli; Prior, Ronald L. (2009-08-15). "Nutritional characterisation and antioxidant capacity of different tissues of Artemisia annua L.". Food Chemistry. 115 (4): 1240–1246. doi:10.1016/j.foodchem.2009.01.033.
  23. 1 2 3 4 5 6 Ferreira, Jorge F. S.; Luthria, Devanand L.; Sasaki, Tomikazu; Heyerick, Arne (2010-04-29). "Flavonoids from Artemisia annua L. as Antioxidants and Their Potential Synergism with Artemisinin against Malaria and Cancer". Molecules. 15 (5): 3135–3170. doi:10.3390/molecules15053135. PMID 20657468.
  24. 1 2 3 Miller, Louis H.; Su, Xinzhuan (2011). "Artemisinin: Discovery from the Chinese Herbal Garden". Cell. 146 (6): 855–8. doi:10.1016/j.cell.2011.08.024. PMC 3414217Freely accessible. PMID 21907397.
  25. ↑ "Lasker Award Rekindles Debate Over Artemisinin's Discovery | Science/AAAS | News". News.sciencemag.org. Retrieved 2014-01-07.
  26. ↑ Mueller, Markus S; Runyambo, Nyabuhanga; Wagner, Irmela; Borrmann, Steffen; Dietz, Klaus; Heide, Lutz (2004). "Randomized controlled trial of a traditional preparation of Artemisia annua L. (Annual Wormwood) in the treatment of malaria". Trans R Soc Trop Med Hyg. 98 (5): 318–21. doi:10.1016/j.trstmh.2003.09.001. PMID 15109558.
  27. ↑ Räth, K; Taxis, K; Walz, G; Gleiter, CH; Li, SM; Heide, L (1 February 2004). "Pharmacokinetic study of artemisinin after oral intake of a traditional preparation of Artemisia annua L. (annual wormwood)". Am J Trop Med Hyg. 70 (2): 128–32. PMID 14993622.
  28. ↑ Jansen FH (2006). "The herbal tea approach for artemesinin as a therapy for malaria?". Trans R Soc Trop Med Hyg. 100 (3): 285–6. doi:10.1016/j.trstmh.2005.08.004. PMID 16274712.
  29. ↑ "Malaria Update", Focus on Ethiopia, April 2005, UN-OCHA website (accessed 12 March 2009)
  30. ↑ Fairhurst, RM; Nayyar, GM; Breman, JG; Hallett, R; Vennerstrom, JL; Duong, S; Ringwald, P; Wellems, TE; Plowe, CV; Dondorp, AM (2012). "Artemisinin-resistant malaria: Research challenges, opportunities, and public health implications". The American journal of tropical medicine and hygiene. 87 (2): 231–41. doi:10.4269/ajtmh.2012.12-0025. PMC 3414557Freely accessible. PMID 22855752.
  31. ↑ Abolaji, AO; Eteng, MU; Ebong, PE; Brisibe, EA; Dar, A; Kabir, N; Choudhary, MI (2013). "A safety assessment of the antimalarial herb Artemisia annua during pregnancy in Wistar rats". Phytotherapy research : PTR. 27 (5): 647–54. doi:10.1002/ptr.4760. PMID 22736625.
  32. 1 2 3 4 Chrubasik, C; Jacobson, RL (2010). "The development of artemisinin resistance in malaria: Reasons and solutions". Phytotherapy research : PTR. 24 (7): 1104–6. doi:10.1002/ptr.3133. PMID 20578122.
  33. 1 2 Na-Bangchang, K; Karbwang, J (2013). "Emerging artemisinin resistance in the border areas of Thailand". Expert review of clinical pharmacology. 6 (3): 307–22. doi:10.1586/ecp.13.17. PMID 23656342.
  34. ↑ News published on the Center for Strategic and International Studies website (Nov. 7, 2013)
  35. ↑ Tulloch, Jim; David, Benedict; Newman, Robert D; Meek, Sylvia (2013). "Artemisinin-resistant malaria in the Asia-Pacific region". The Lancet. 381 (9881): e16. doi:10.1016/S0140-6736(12)61820-0.
  36. ↑ Kale, Anup; Gawande, Sonia; Kotwal, Swati (2008-05-01). "Cancer phytotherapeutics: role for flavonoids at the cellular level". Phytotherapy Research. 22 (5): 567–577. doi:10.1002/ptr.2283. ISSN 1099-1573. PMID 18398903.
  37. ↑ Efferth, Thomas; Benakis, Achille; Romero, Marta R.; Tomicic, Maja; Rauh, Rolf; Steinbach, Daniel; Häfer, Ralf; Stamminger, Thomas; Oesch, Franz (2004-10-01). "Enhancement of cytotoxicity of artemisinins toward cancer cells by ferrous iron". Free Radical Biology and Medicine. 37 (7): 998–1009. doi:10.1016/j.freeradbiomed.2004.06.023. PMID 15336316.
  38. ↑ Nakase, Ikuhiko; Gallis, Byron; Takatani-Nakase, Tomoka; Oh, Steve; Lacoste, Eric; Singh, Narendra P.; Goodlett, David R.; Tanaka, Seigo; Futaki, Shiroh (2009). "Transferrin receptor-dependent cytotoxicity of artemisinin–transferrin conjugates on prostate cancer cells and induction of apoptosis". Cancer Letters. 274 (2): 290–298. doi:10.1016/j.canlet.2008.09.023. PMID 19006645.
  39. ↑ Lai HC, Singh NP, Sasaki T (February 2013). "Development of artemisinin compounds for cancer treatment". Invest New Drugs. 31 (1): 230–46. doi:10.1007/s10637-012-9873-z. PMID 22935909.
  40. ↑ Cheng, C.; Ng, D. S. W.; Chan, T. K.; Guan, S. P.; Ho, W. E.; Koh, A. H. M.; Bian, J. S.; Lau, H. Y. A.; Wong, W. S. F. (2013). "Anti-allergic action of anti-malarial drug artesunate in experimental mast cell-mediated anaphylactic models". Allergy. 68 (2): 195–203. doi:10.1111/all.12077. PMID 23253152.
  41. ↑ Ho, Wanxing Eugene; Xu, Yong-Jiang; Xu, Fengguo; Cheng, Chang; Peh, Hong Yong; Huang, Shao-Min; Tannenbaum, Steven R.; Ong, Choon Nam; Wong, W. S. Fred (July 2014). "Anti-malarial drug artesunate restores metabolic changes in experimental allergic asthma". Metabolomics. 1 (11): 380. doi:10.1007/s11306-014-0699-x.

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