Venoms in medicine

Venom in medicine is the medicinal use of venoms for therapeutic benefit in treating diseases.

Venom is any poisonous compound secreted by an animal intended to harm or disable another. When an organism produces a venom, its final form may contain hundreds of different bioactive elements that interact with each other inevitably producing its toxic effects.[1] This mixture of ingredients includes various proteins, peptides, and non-peptidic small molecules.[2] The active components of these venoms are isolated, purified, and screened in assays. These may be either phenotypic assays to identify component that may have desirable therapeutic properties (forward pharmacology) or target directed assays to identify their biological target and mechanism of action (reverse pharmacology).[3] In this way, toxic venomous poisons may be a starting point for a therapeutic drug.

Background

Venoms are naturally occurring substances that organisms evolved to deploy against other organisms, in defense or attack.[2] They are often mixtures of proteins that act together or singly to attack their specific targets within the organism against which they are used, generally with high specificity and generally easily accessible through the vascular system.[2] This has made venoms a subject of study for people who work in drug discovery.[2] With developments in omic technologies (proteomics, genomics, etc.), researchers in this field became able to identify genes that produce certain elements in an animal's venom, as well as protein domains that have been used as building blocks across many species.[2] In conjunction with methods of separation and purification of compounds, scientists are able to study each individual compound that exists within a venom "concoction", looking for compounds to serve as drug leads or other use.[2] Each venomous organism produces thousands of different proteins giving access to millions of different molecules that still have potential uses. In addition, nature is continuously evolving; as prey develop resistance to these venoms, the predators also evolve as well, creating novel toxins that can continue to act upon its respective prey.[4]

History

The earliest known use of venom is medicine dates back to 380 B.C. in ancient Greece.[5] Aristotle's "Historia Animalium", describes how venom can be used in the production of antidotes for the venom.[5] During the height of the Roman empire, there is evidence of venom being added into medicine used to treat smallpox, leprosy, fever, and wounds.[5] Despite this, early uses of venom were primarily involved in the process of making antidotes. This use of venom continued into the Middle Ages and well into the 19th century. The first modern study of venom in a medical light occurred in the late 19th century. A scientist, Albert Calmatte, injected animals with small amounts of venom, using their blood as the antidote.[5]

Marketed drugs

Captopril

Captopril emulates the function of the toxin found in Brazilian pit viper venom and is generally accepted as the first venom "success" story. Captopril is an ACE inhibitor (angiotensin converting enzyme) that was approved by the FDA approved in April 1981. It lowers blood pressure by inhibiting the production of angiotensin II which acts in a pathway that leads to vasoconstriction which raises blood pressure. After the creation of this drug, many analogues (enalapril, lisinopril, perindopril, ramipril, etc.) were produced.[6]

Ziconotide

Ziconotide is a synthetically made version of the ω-conotoxin made by the cone snail,[7] that is used to treat severe pain and is delivered as an infusion into the cerebrospinal fluid using an intrathecal pump system.[8] Ziconitide acts presynaptically on N-type calcium channels, blocking the receptors of this channel with high selectivity and affinity,[7]

Eptifibatide

Eptifibatide was modeled after a component in southeastern pygmy rattlesnake venom and is used in anticoagulation therapies in an effort to reduce the risk of heart attacks; it is used in only severe cases because of the possible side effect of thrombocytopenia, a condition where platelets are unable to aggregate at all.[9][10][11] Eptifibatide binds reversibly to platelets reducing the risk of thrombosis. It is an antagonist of glycoprotein IIb/IIIa.[9]

Exenatide

Exenatide is a 39-amino-acid peptide that is a synthetic version of exendin-4, a hormone found in the saliva of the Gila monster.[12] It is used to treat Type II Diabetes as an adjunct to insulin and other drugs.[13][14] It is GLP-1 receptor agonist that was first isolated by John Eng in 1992 while working at the Veterans Administration Medical Center in the Bronx, New York.[12]

Batroxobin

Batroxobin, is a serine protease found in snake venom produced by Bothrops atrox and Bothrops moojeni, venomous species of pit viper found east of the Andes in South America. It cleaves fibrinogen, similarly to thrombin. Batroxobin from B atrox is used as a drug called "Reptilase" that is used to stop bleeding, while batroxobin from B moojeni is a drug called "Defibrase", used to break up blood clots. It is also used in a system called "Vivostat", where a person's blood is taken just before surgery and exposed to batroxobin; the resulting clots are then harvested, and then dissolved, forming a fibrin glue that is then used on the person during the surgery.[15]

gollark: If you want a tablet comparable to your actual computer thing™, you'll pay more for it.
gollark: Tablets are generally worse in various ways because people are used to that (and use it more for media consumption than anything heavier).
gollark: Oh, I guess that's maybe also a thing.
gollark: Yes, the light laptop needs to use more specialized materials and optimize for weight over cost in other ways.
gollark: What? We use deep neural networks. Shallow ones are so last decade.

References
  1. Gottlieb Z (3 November 2010). "These 5 Poisons May Save Your Life". Popular Mechanics. Retrieved 2018-02-22.
  2. Casewell NR, Wüster W, Vonk FJ, Harrison RA, Fry BG (April 2013). "Complex cocktails: the evolutionary novelty of venoms". Trends in Ecology & Evolution. 28 (4): 219–29. doi:10.1016/j.tree.2012.10.020. PMID 23219381.
  3. Harvey AL (December 2014). "Toxins and drug discovery". Toxicon. 92: 193–200. doi:10.1016/j.toxicon.2014.10.020. PMID 25448391.
  4. "On The Origin of Venom". Phenomena. 2013-01-09. Retrieved 2018-04-21.
  5. Utkin YN (May 2015). "Animal venom studies: Current benefits and future developments". World Journal of Biological Chemistry. 6 (2): 28–33. doi:10.4331/wjbc.v6.i2.28. PMC 4436903. PMID 26009701.
  6. Slagboom J, Kool J, Harrison RA, Casewell NR (June 2017). "Haemotoxic snake venoms: their functional activity, impact on snakebite victims and pharmaceutical promise". British Journal of Haematology. 177 (6): 947–959. doi:10.1111/bjh.14591. PMC 5484289. PMID 28233897.
  7. McGivern JG (February 2007). "Ziconotide: a review of its pharmacology and use in the treatment of pain". Neuropsychiatric Disease and Treatment. 3 (1): 69–85. doi:10.2147/nedt.2007.3.1.69. PMC 2654521. PMID 19300539.
  8. "Prialt solution for infusion - Summary of Product Characteristics (SmPC) - (eMC)". Electronic Medicines Compendium. January 2017. Retrieved 21 April 2018.
  9. Saab F, Ionescu C, Schweiger MJ (March 2012). "Bleeding risk and safety profile related to the use of eptifibatide: a current review". Expert Opinion on Drug Safety. 11 (2): 315–24. doi:10.1517/14740338.2012.650164. PMID 22233272.
  10. Pothineni NV, Watts TE, Ding Z, Dai Y, Deshmukh AJ (2016). "Eptifibatide-Induced Thrombocytopenia--When Inhibitor Turns Killer". American Journal of Therapeutics. 23 (1): e298–9. doi:10.1097/01.mjt.0000438283.01797.1a. PMID 24368608.
  11. Shah I, Khan SO, Malhotra S, Fischell T (June 2010). "Eptifibatide: The evidence for its role in the management of acute coronary syndromes". Core Evidence. 4: 49–65. doi:10.2147/ce.s6008. PMC 2899786. PMID 20694065.
  12. Raufman, JP (16 January 1996). "Bioactive peptides from lizard venoms". Regulatory Peptides. 61 (1): 1–18. doi:10.1016/0167-0115(96)00135-8. PMID 8701022.
  13. "Byetta 10 micrograms solution for injection, prefilled pen - Summary of Product Characteristics". Electronic Medicines Compendium. 30 March 2017. Retrieved 21 April 2018.
  14. "Bydureon 2 mg powder and solvent for prolonged-release suspension for injection in pre-filled pen - Summary of Product Characteristics". Electronic Medicines Compendium. 10 November 2017. Retrieved 21 April 2018.
  15. Serrano, SM (February 2013). "The long road of research on snake venom serine proteinases". Toxicon. 62: 19–26. doi:10.1016/j.toxicon.2012.09.003. PMID 23010164.

Further reading
  • King GF, ed. (2015). Venoms to Drugs: Venom as a Source for the Development of Human Therapeutics. RCS Drug Discovery Series. 42. Cambridge, UK: Royal Society of Chemistry. ISBN 978-1-84973-787-6.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.