Marine Drugs (Oct 2017)

Marine Algae as Source of Novel Antileishmanial Drugs: A Review

  • Lauve Rachel Tchokouaha Yamthe,
  • Regina Appiah-Opong,
  • Patrick Valere Tsouh Fokou,
  • Nole Tsabang,
  • Fabrice Fekam Boyom,
  • Alexander Kwadwo Nyarko,
  • Michael David Wilson

DOI
https://doi.org/10.3390/md15110323
Journal volume & issue
Vol. 15, no. 11
p. 323

Abstract

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Leishmaniasis is a vector-borne neglected tropical disease caused by protozoan parasites of the Leishmania genus and transmitted by the female Phlebotomus and Lutzomyia sand flies. The currently prescribed therapies still rely on pentavalent antimonials, pentamidine, paromomycin, liposomal amphotericin B, and miltefosine. However, their low efficacy, long-course treatment regimen, high toxicity, adverse side effects, induction of parasite resistance and high cost require the need for better drugs given that antileishmanial vaccines may not be available in the near future. Although most drugs are still derived from terrestrial sources, the interest in marine organisms as a potential source of promising novel bioactive natural agents has increased in recent years. About 28,000 compounds of marine origin have been isolated with hundreds of new chemical entities. Recent trends in drug research from natural resources indicated the high interest of aquatic eukaryotic photosynthetic organisms, marine algae in the search for new chemical entities given their broad spectrum and high bioactivities including antileishmanial potential. This current review describes prepared extracts and compounds from marine macroalgae along with their antileishmanial activity and provides prospective insights for antileishmanial drug discovery.

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