Biology:Biodiversity and drugs

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Short description: Biodiversity Is helpful

Biodiversity plays a vital role in maintaining human and animal health because numerous plants, animals, and fungi are used in medicine to produce vital vitamins, painkillers, antibiotics, and other medications.[1][2][3] Natural products have been recognized and used as medicines by ancient cultures all around the world.[4] Some animals are also known to self-medicate using plants and other materials available to them.[5]

Plant drugs

Many plant species have been studied thoroughly for their value as a source of medicine.[6][7] They have a wide range of benefits such as anti-fever and anti-inflammatory properties, can treat diseases such as malaria and diabetes, and are used as vitamins and antibiotic and antifungal medications.[7][8][9][10] More than 60% of the world's population relies almost entirely on plant medicine for primary health care,[11] and about 119 pure chemicals such as caffeine, methyl salicylate, and quinine are extracted from less than 90 species of higher plants and used as medicines throughout the world.[4]

In China, Japan, India, and Germany, there is a great deal of interest in and support for the search for new drugs from higher plants.[4]

Sweet Wormwood

Sweet wormwood (Artemisia annua)

Sweet Wormwood (Artemisia annua) grows in all continents besides Antarctica.[12] It is the only known source of artemisinin, a drug that has been used to treat fevers due to malaria, exhaustion, or many other causes, since ancient times.[13] Upon further study, scientists have found that Sweet Wormwood inhibits activity of various bacteria, viruses, and parasites and exhibits anti-cancer and anti-inflammatory properties.[13][14][15]

Animal-derived drugs

Animal-derived drugs are a major source of modern medications used around the world.[2][16] The use of these drugs can cause certain animals to become endangered or threatened; however, it is difficult to identify the animal species used in medicine since animal-derived drugs are often processed, which degrades their DNA.[2]

Medicinal Animal Horns and Shells

Cells from animal horns and shells are included in a group of medications call Medicinal Animal Horns and Shells (MAHS).[2][17] These drugs are often used in dermatology and have been reported to have anti-fever and anti-inflammatory properties and treat some diseases.[17][18]

Drugs derived from animal toxins

The shell of a cone snail (Conus magus).

Certain animals have obtained many adaptations of toxic substances due to a coevolutionary arms race between them and their predators.[19] Some components of these toxins such as enzymes and inorganic salts are used in modern medicine.[20] For example, drugs such as Captopril and Lisinopril are derived from snake venom and inhibit the angiotensin-converting enzyme.[21][20] Another example is Ziconotide, a drug from the cone snail, Conus magus, that is used to reduce pain.[20][22]

Medicinal fungi

Edible fungi can contain important nutrients and biomolecules that can be used for medical applications.[3] For example, medicinal fungi have polysaccharides that can be used to prevent the spread of cancer by activating different types of immune cells (namely T lymphocytes, macrophages, and NK cells), which inhibit cancer cell reproduction and metastasis (the process by which cancer can spread to different parts of the body).[3][23]

Fungi have been used to make many antibiotics since Sir Alexander Flemming discovered Penicillin from the mold, Penicillium notatum.[24][25] Recently, there has been a renewed interest in using fungi to create antibiotics since many bacteria have obtained antibiotic resistance due to the heavy selection pressures that antibiotics cause.[24] The diversity of marine fungi makes them a potential new source of antibiotic compunds; however, most are difficult to cultivate in a laboratory setting.[24][26]

Countries in Asia such as Egypt and China have been using fungi for medical uses for centuries.[3][23]

Turkey Tail Mushrooms

Turkey tail mushrooms found in Georgia, USA.

Toxoplasmosis is a disease caused by an infection by the parasite: Toxoplasma gondii (T. gondii).[27][28] Current drugs used to treat this disease have many side effects and do not inhibit all forms of T. gondii.[29] An in vitro study by Sharma et al. suggests that Turkey Tail mushroom extract could be used to treat Toxoplasmosis since it inhibited T. gondii growth.[27]

Pestalone

Pestalone is an antibiotic created from the marine fungus: Pestalotia sp.[24][30] M. Cueto et al. (2001–11) found that it has antibiotic activity against two bacteria species that have gained resistance to antibiotics: vancomycin-resistant Enterococcus faecium and methicillin-resistant Staphylococcus aureus.[31]

Zoopharmacognosy

Apes and monkeys are an example of animals using plants as medicine rather than food.
Main page: Biology:Zoopharmacognosy

Zoopharmacognosy is the study of how animals select certain plants as self-medication to treat or prevent disease.[5] Usually, this behavior is a result of coevolution between the animal and the plant that it uses for self-medication.[5] For example, apes have been observed selecting a particular part of a medicinal plant by taking off leaves and breaking the stem to suck out the juice.[32] In an interview with the late Neil Campbell, Eloy Rodriguez describes the importance of biodiversity:

"Some of the compounds we've identified by zoopharmacognosy kill parasitic worms, and some of these chemicals may be useful against tumors. There is no question that the templates for most drugs are in the natural world."[32]

References

  1. ↑ Fajinmi, Olufunke O.; Olarewaju, Olaoluwa O.; Van Staden, Johannes (2023-03-03). "Propagation of Medicinal Plants for Sustainable Livelihoods, Economic Development, and Biodiversity Conservation in South Africa". Plants 12 (5): 1174. doi:10.3390/plants12051174. ISSN 2223-7747. 
  2. ↑ 2.0 2.1 2.2 2.3 Luo, Jiaoyang; Yan, Dan; Zhang, Da; Han, Yumei; Dong, Xiaoping; Yang, Yong; Deng, Kejun; Xiao, Xiaohe (2011-09-09). "Application of 12S rRNA Barcodes for the Identification of Animal-Derived Drugs". Journal of Pharmacy & Pharmaceutical Sciences 14 (3): 358. doi:10.18433/j3n017. ISSN 1482-1826. 
  3. ↑ 3.0 3.1 3.2 3.3 Xu, Jing; Shen, Rui; Jiao, Zhuoya; Chen, Weidong; Peng, Daiyin; Wang, Lei; Yu, Nianjun; Peng, Can et al. (2022-06-24). "Current Advancements in Antitumor Properties and Mechanisms of Medicinal Components in Edible Mushrooms". Nutrients 14 (13): 2622. doi:10.3390/nu14132622. ISSN 2072-6643. PMID 35807802. 
  4. ↑ 4.0 4.1 4.2 N.R. Farnsworth. Screening Plants for New Medicine. IN: E.O Wilson, editor. 1988. Biodiversity, Natrional Academy. ISBN:0-309-03783-2(pbk.)
  5. ↑ 5.0 5.1 5.2 Robles, Mario; Aregullin, Manuel; West, Jan; Rodriguez, Eloy (June 1995). "Recent Studies on the Zoopharmacognosy, Pharmacology and Neurotoxicology of Sesquiterpene Lactones*". Planta Medica 61 (3): 199–203. doi:10.1055/s-2006-958055. ISSN 0032-0943. 
  6. ↑ Alaribe, Franca Nneka; Motaung, Keolebogile Shirley Caroline Mamotswere (June 2019). "Medicinal Plants in Tissue Engineering and Regenerative Medicine in the African Continent". Tissue Engineering. Part A 25 (11–12): 827–829. doi:10.1089/ten.TEA.2019.0060. ISSN 1937-335X. PMID 30838937. https://pubmed.ncbi.nlm.nih.gov/30838937. 
  7. ↑ 7.0 7.1 Nayim, Paul; Mbaveng, Armelle T.; Wamba, Brice E. N.; Fankam, Aimé G.; Dzotam, Joachim K.; Kuete, Victor (2018). "Antibacterial and Antibiotic-Potentiating Activities of Thirteen Cameroonian Edible Plants against Gram-Negative Resistant Phenotypes". TheScientificWorldJournal 2018: 4020294. doi:10.1155/2018/4020294. ISSN 1537-744X. PMID 30275799. 
  8. ↑ Alaribe, Franca Nneka; Motaung, Keolebogile Shirley Caroline Mamots (June 2019). "Medicinal Plants in Tissue Engineering and Regenerative Medicine in the African Continent". Tissue Engineering Part A 25 (11–12): 827–829. doi:10.1089/ten.tea.2019.0060. ISSN 1937-3341. http://dx.doi.org/10.1089/ten.tea.2019.0060. 
  9. ↑ Zarayneh, Simin; Sepahi, Abbas Akhavan; Jonoobi, Mehdi; Rasouli, Hassan (2018-10-15). "Comparative antibacterial effects of cellulose nanofiber, chitosan nanofiber, chitosan/cellulose combination and chitosan alone against bacterial contamination of Iranian banknotes". International Journal of Biological Macromolecules 118 (Pt A): 1045–1054. doi:10.1016/j.ijbiomac.2018.06.160. ISSN 1879-0003. PMID 29966671. https://pubmed.ncbi.nlm.nih.gov/29966671. 
  10. ↑ Benedik, Evgen (March 2022). "Sources of vitamin D for humans". International Journal for Vitamin and Nutrition Research 92 (2): 118–125. doi:10.1024/0300-9831/a000733. ISSN 0300-9831. PMID 34658250. https://pubmed.ncbi.nlm.nih.gov/34658250. 
  11. ↑ Kevin J. Gaston & John I. Spicer. 2004. Biodiversity: an introduction, Blackwell Publishing. 2nd Ed. ISBN:1-4051-1857-1(pbk.)
  12. ↑ Septembre-Malaterre, Axelle; Lalarizo Rakoto, Mahary; Marodon, Claude; Bedoui, Yosra; Nakab, Jessica; Simon, Elisabeth; Hoarau, Ludovic; Savriama, Stephane et al. (2020-07-15). "Artemisia annua, a Traditional Plant Brought to Light". International Journal of Molecular Sciences 21 (14): 4986. doi:10.3390/ijms21144986. ISSN 1422-0067. 
  13. ↑ 13.0 13.1 Feng, Xinchi; Cao, Shijie; Qiu, Feng; Zhang, Boli (2020). "Traditional application and modern pharmacological research of Artemisia annua L". Pharmacology & Therapeutics 216: 107650. doi:10.1016/j.pharmthera.2020.107650. ISSN 1879-016X. PMID 32758647. https://pubmed.ncbi.nlm.nih.gov/32758647. 
  14. ↑ Wojtkowiak-Giera, Agnieszka; Derda, Monika; Kosik-Bogacka, Danuta; Kolasa-Wołosiuk, Agnieszka; Wandurska-Nowak, Elżbieta; Jagodziński, Paweł P.; Hadaś, Edward (2019). "The modulatory effect of Artemisia annua L. on toll-like receptor expression in Acanthamoeba infected mouse lungs". Experimental Parasitology 199: 24–29. doi:10.1016/j.exppara.2019.02.011. ISSN 0014-4894. http://dx.doi.org/10.1016/j.exppara.2019.02.011. 
  15. ↑ Efferth, Thomas (2018). "Beyond malaria: The inhibition of viruses by artemisinin-type compounds". Biotechnology Advances 36 (6): 1730–1737. doi:10.1016/j.biotechadv.2018.01.001. ISSN 0734-9750. http://dx.doi.org/10.1016/j.biotechadv.2018.01.001. 
  16. ↑ Wragge-Morley, Alexander (December 2022). "Medicine, connoisseurship, and the animal body". History of Science 60 (4): 481–499. doi:10.1177/0073275320949001. ISSN 1753-8564. PMID 32847416. https://pubmed.ncbi.nlm.nih.gov/32847416. 
  17. ↑ 17.0 17.1 Luo, Jiaoyang; Yan, Dan; Zhang, Da; Feng, Xue; Yan, Yan; Dong, Xiaoping; Xiao, Xiaohe (2011-06-14). "Substitutes for endangered medicinal animal horns and shells exposed by antithrombotic and anticoagulation effects". Journal of Ethnopharmacology 136 (1): 210–216. doi:10.1016/j.jep.2011.04.053. ISSN 1872-7573. PMID 21549826. https://pubmed.ncbi.nlm.nih.gov/21549826. 
  18. ↑ Paul Pui-Hay But; Lai-Ching, Lung; Yan-Kit, Tam (September 1990). "Ethnopharmacology of rhinoceros horn. I: Antipyretic effects of rhinoceros horn and other animal horns". Journal of Ethnopharmacology 30 (2): 157–168. doi:10.1016/0378-8741(90)90005-e. ISSN 0378-8741. http://dx.doi.org/10.1016/0378-8741(90)90005-e. 
  19. ↑ King, Glenn F (2011-09-23). "Venoms as a platform for human drugs: translating toxins into therapeutics". Expert Opinion on Biological Therapy 11 (11): 1469–1484. doi:10.1517/14712598.2011.621940. ISSN 1471-2598. http://dx.doi.org/10.1517/14712598.2011.621940. 
  20. ↑ 20.0 20.1 20.2 Fischer, Thomas; Riedl, Rainer (February 2022). "Paracelsus' legacy in the faunal realm: Drugs deriving from animal toxins". Drug Discovery Today 27 (2): 567–575. doi:10.1016/j.drudis.2021.10.003. ISSN 1359-6446. 
  21. ↑ da Costa Marques, Maria Elizabeth; de Araújo Tenório, Humberto; Dos Santos, Claudio Wilian Victor; Dos Santos, Daniel Moreira; de Lima, Maria Elena; Pereira, Hugo Juarez Vieira (October 2016). "Angiotensin converting enzyme of Thalassophryne nattereri venom". International Journal of Biological Macromolecules 91: 980–986. doi:10.1016/j.ijbiomac.2016.06.051. ISSN 1879-0003. PMID 27327905. https://pubmed.ncbi.nlm.nih.gov/27327905. 
  22. ↑ András, Csaba D.; Albert, Csilla; Salamon, Szidónia; Gálicza, Judit; András, Réka; András, Emil (2011-10-10). "Conus magus vs. Irukandji syndrome: a computational approach of a possible new therapy". Brain Research Bulletin 86 (3–4): 195–202. doi:10.1016/j.brainresbull.2011.07.003. ISSN 1873-2747. PMID 21777663. https://pubmed.ncbi.nlm.nih.gov/21777663. 
  23. ↑ 23.0 23.1 Jayachandran, Muthukumaran; Xiao, Jianbo; Xu, Baojun (2017-09-08). "A Critical Review on Health Promoting Benefits of Edible Mushrooms through Gut Microbiota". International Journal of Molecular Sciences 18 (9): 1934. doi:10.3390/ijms18091934. ISSN 1422-0067. PMID 28885559. 
  24. ↑ 24.0 24.1 24.2 24.3 Silber, Johanna; Kramer, Annemarie; Labes, Antje; Tasdemir, Deniz (2016-07-21). "From Discovery to Production: Biotechnology of Marine Fungi for the Production of New Antibiotics". Marine Drugs 14 (7): 137. doi:10.3390/md14070137. ISSN 1660-3397. PMID 27455283. 
  25. ↑ Fleming, Alexander (1941-09-13). "Penicillin". British Medical Journal 2 (4210): 386. ISSN 0007-1447. 
  26. ↑ Verma, Vijay (2013). Advances in endophytic research. Springer Science & Business Media. doi:10.1007/978-81-322-1575-2. ISBN 978-81-322-1574-5. 
  27. ↑ 27.0 27.1 Sharma, Homa Nath; Catrett, Jonathan; Nwokeocha, Ogechi Destiny; Boersma, Melissa; Miller, Michael E.; Napier, Audrey; Robertson, Boakai K.; Abugri, Daniel A. (2023-05-29). "Anti-Toxoplasma gondii activity of Trametes versicolor (Turkey tail) mushroom extract". Scientific Reports 13 (1): 8667. doi:10.1038/s41598-023-35676-6. ISSN 2045-2322. PMID 37248277. PMC 10225767. Bibcode: 2023NatSR..13.8667S. http://dx.doi.org/10.1038/s41598-023-35676-6. 
  28. ↑ Desmettre, T. (March 2020). "Toxoplasmosis and behavioural changes". Journal Francais d'Ophtalmologie 43 (3): e89–e93. doi:10.1016/j.jfo.2020.01.001. ISSN 1773-0597. PMID 31980266. https://pubmed.ncbi.nlm.nih.gov/31980266. 
  29. ↑ Shiojiri, Daisuke; Kinai, Ei; Teruya, Katsuji; Kikuchi, Yoshimi; Oka, Shinichi (2019). "Combination of Clindamycin and Azithromycin as Alternative Treatment for Toxoplasma gondii Encephalitis". Emerging Infectious Diseases 25 (4): 841–843. doi:10.3201/eid2504.181689. ISSN 1080-6059. PMID 30882331. 
  30. ↑ Slavov, Nikolay; Cvengroš, Ján; Neudörfl, Jörg‐Martin; Schmalz, Hans‐Günther (2010-08-31). "Total Synthesis of the Marine Antibiotic Pestalone and its Surprisingly Facile Conversion into Pestalalactone and Pestalachloride A". Angewandte Chemie International Edition 49 (41): 7588–7591. doi:10.1002/anie.201003755. ISSN 1433-7851. PMID 21038453. http://dx.doi.org/10.1002/anie.201003755. 
  31. ↑ Cueto, M.; Jensen, P. R.; Kauffman, C.; Fenical, W.; Lobkovsky, E.; Clardy, J. (November 2001). "Pestalone, a new antibiotic produced by a marine fungus in response to bacterial challenge". Journal of Natural Products 64 (11): 1444–1446. doi:10.1021/np0102713. ISSN 0163-3864. PMID 11720529. https://pubmed.ncbi.nlm.nih.gov/11720529. 
  32. ↑ 32.0 32.1 Biology (4th edition) N.A.Campbell, p.23 'An Interview with Eloy Rodriguez' (Benjamin Cummings NY, 1996) ISBN:0-8053-1957-3



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