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Nuphar lutea: in vitro anti-leishmanial activity against Leishmania major promastigotes and amastigotes.

Phytomedicine : international journal of phytotherapy and phytopharmacology (2009-03-24)
J El-On, L Ozer, J Gopas, R Sneir, A Golan-Goldhirsh
RESUMEN

Several anti-leishmanial drugs of choice are of plant origin. Many of the available drugs against the disease are toxic and in certain cases parasite drug resistance is developed. The development of new compounds is urgently required. To determine the leishmanicidal activity of the Nuphar lutea plant extract against Leishmania major in vitro. The leishmanicidal activity of methanolic plant extract against L. major free living promastigotes and intracellular amastigotes was evaluated, using microscopic examinations and the enzymatic XTT assay. Methanolic extract of N. lutea was highly effective against both Leishmania promastigotes and L. amastigotes (IC(50)=2+/-0.12 microg/ml; ID(50)=0.65+/-0.02 3 microg/ml; LD(50)=2.1+/-0.096 microg/ml, STI=3.23). The extract at 1.25 microg/ml totally eliminated the intracellular parasites within 3 days of treatment. Also, a synergistic anti-leishmanial activity was demonstrated with N. lutea extract combined with the anti-leishmanial drug--paromomycin. The partially purified N. lutea active component was found to be a thermo-stable alkaloid(s) with no electrical charge and is resistant to boiling and to methanol, dichloromethane and xylene treatment. The present study suggests that N. lutea might be a potential source of anti-leishmanial compounds.

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6,6′-Dihydroxythiobinupharidine, ≥95% (HPLC)