Antiprotozoal Explained

Antiprotozoal agents (ATC code: ATC P01) is a class of pharmaceuticals used in treatment of protozoan infection.

A paraphyletic group, protozoans have little in common with each other. For example, Entamoeba histolytica, a unikont eukaryotic organism, is more closely related to Homo sapiens (humans), which also belongs to the unikont phylogenetic group, than it is to Naegleria fowleri, a "protozoan" bikont. As a result, agents effective against one pathogen may not be effective against another.

Antiprotozoal agents can be grouped by mechanism[1] or by organism.[2] Recent papers have also proposed the use of viruses to treat infections caused by protozoa.[3] [4]

Overuse or misuse of antiprotozoals can lead to the development of antiprotozoal resistance.[5]

Medical uses

Antiprotozoals are used to treat protozoal infections, which include amebiasis, giardiasis, cryptosporidiosis, microsporidiosis, malaria, babesiosis, trypanosomiasis, Chagas disease, leishmaniasis, and toxoplasmosis.[6] Currently, many of the treatments for these infections are limited by their toxicity.[7]

Outdated terminology

Protists were once considered protozoans, but of late the categorization of unicellar organisms has undergone rapid development, however in literature, including scientific, there tends to persist the usage of the term antiprotozoal when they really mean anti-protist. Protists are a supercategory of eukaryota which includes protozoa.

Mechanism

The mechanisms of antiprotozoal drugs differ significantly drug to drug. For example, it appears that eflornithine, a drug used to treat trypanosomiasis, inhibits ornithine decarboxylase, while the aminoglycoside antibiotic/antiprotozoals used to treat leishmaniasis are thought to inhibit protein synthesis.[8]

Examples

Notes and References

  1. Book: Cynthia R. L. Webster. Clinical pharmacology. 2 May 2010. 15 June 2001. Teton NewMedia. 978-1-893441-37-8. 86–.
  2. Book: Anthony J. Trevor. Bertram G. Katzung. Susan B. Masters. Katzung & Trevor's pharmacology: examination & board review. 2 May 2010. 11 December 2007. McGraw-Hill Professional. 978-0-07-148869-3. 435–.
  3. Keen . E. C. . Beyond phage therapy: Virotherapy of protozoal diseases . 10.2217/FMB.13.48 . Future Microbiology . 8 . 7 . 821–823 . 2013 . 23841627.
  4. Hyman . P. . Atterbury . R. . Barrow . P. . 10.1016/j.tim.2013.02.006 . Fleas and smaller fleas: Virotherapy for parasite infections . Trends in Microbiology . 21 . 5 . 215–220 . 2013 . 23540830.
  5. Ouellette . Marc . November 2001 . Biochemical and molecular mechanisms of drug resistance in parasites . Tropical Medicine and International Health . 6 . 11 . 874–882 . 10.1046/j.1365-3156.2001.00777.x . 1360-2276.
  6. Khaw. M. Panosian. C B. Claire Panosian . Human antiprotozoal therapy: past, present, and future.. Clinical Microbiology Reviews. 1 July 1995. 8. 3. 427–439. 174634. 0893-8512. 7553575. 10.1128/CMR.8.3.427.
  7. Graebin. C.. Uchoa. F.. Bernardes. L.. Campo. V.. Carvalho. I.. Eifler-Lima. V.. Antiprotozoal Agents: An Overview. Anti-Infective Agents in Medicinal Chemistry. 1 October 2009. 8. 4. 345–366. 10.2174/187152109789760199. 1871-5214.
  8. CREEK. DARREN J.. Michael Barrett (parasitologist). BARRETT. MICHAEL P.. Determination of antiprotozoal drug mechanisms by metabolomics approaches. Parasitology. 9 January 2017. 141. 1. 83–92. 10.1017/S0031182013000814. 3884841. 0031-1820. 23734876.