In vitro antiplasmodial activity and toxicity assessment of some plants from Nigerian ethnomedicine.

نویسندگان

  • Oyindamola Abiodun
  • Grace Gbotosho
  • Edith Ajaiyeoba
  • Tientcha Happi
  • Mofolusho Falade
  • Sergio Wittlin
  • Akintunde Sowunmi
  • Reto Brun
  • Ayoade Oduola
چکیده

CONTEXT The emergence and spread of Plasmodium falciparum-resistant parasites to nearly all available antimalarial drugs pose a threat to malaria control and necessitates the need to continue the search for new effective and affordable drugs. Ethnomedicine has been shown to be a potential source of antimalarial compounds or source of template for the synthesis of novel antimalarial molecules. OBJECTIVE The antiplasmodial activity and toxicity assessment of 30 plant extracts from eight medicinal plants identified in Nigerian ethnomedicine for the treatment of febrile illnesses were evaluated. MATERIALS AND METHODS In vitro antimalarial activity was evaluated using Plasmodium falciparum NF54 (sensitive to all antimalarial drugs) and K1 (chloroquine/pyrimethamine resistant) strains in the [(3)H]-hypoxanthine incorporation assay. Toxicity was determined against mammalian L6 cells using Alamar blue assay. RESULTS The ethyl acetate extract of leaves of Ocimum gratissimum Linn. (Labiatae) and hexane extract of stem bark of Trema orientalis (L.) Blume (Ulmaceae) showed the highest antiplasmodial activity (IC(50) 1.8-1.93 µg/mL) against P. falciparum K1 strain but elicited low cytotoxicity (selective index >10). However, hexane, ethyl acetate or methanol extracts of leaves of Terminalia catappa Linn. (Combretaceae), Jatropha curcas Linn. (Euphorbiaceae), Vitex doniana Sweet. (Verbenaceae) and stem bark of Vitex doniana displayed antiplasmodial activity (IC(50) 2.3-16.9 µg/mL) with good selectivity (21-120) for malaria parasites. DISCUSSION AND CONCLUSION The antiplasmodial activity of Terminalia catappa and Vitex doniana against P. falciparum K1 is being reported for the first time in Nigerian ethnomedicine and these plants could be potential source of antimalarial agents.

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عنوان ژورنال:
  • Pharmaceutical biology

دوره 49 1  شماره 

صفحات  -

تاریخ انتشار 2011