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1.
Phytomedicine ; 21(12): 1689-94, 2014 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-25442278

RESUMO

Protozoan diseases, such as leishmaniasis, are a cause of considerable morbidity throughout the world, affecting millions every year. In this study, two triterpenic acids (maslinic and oleanolic acids) were isolated from Tunisian olive leaf extracts and their in vitro activity against the promastigotes stage of Leishmania (L.) infantum and Leishmania (L.) amazonensis was investigated. Maslinic acid showed the highest activity with an IC50 of 9.32 ± 1.654 and 12.460 ± 1.25 µg/ml against L. infantum and L. amazonensis, respectively. The mechanism of action of these drugs was investigated by detecting changes in the phosphatidylserine (PS) exposure, the plasma membrane permeability, the mitochondrial membrane potential and the ATP level production in the treated parasites. By using the fluorescent probe SYTOX® Green, both triterpenic acids showed that they produce a time-dependent plasma membrane permeabilization in the treated Leishmania species. In addition, spectrofluorimeteric data revealed the surface exposure of PS in promastigotes. Both molecules reduced the mitochondrial membrane potential and decreased the ATP levels to 15% in parasites treated with IC90 for 24h. We conclude that the triterpenic acids tested in this study, show potential as future therapeutic alternative against leishmaniasis. Further studies are needed to confirm this.


Assuntos
Leishmania/efeitos dos fármacos , Potencial da Membrana Mitocondrial/efeitos dos fármacos , Olea/química , Ácido Oleanólico/farmacologia , Extratos Vegetais/farmacologia , Trifosfato de Adenosina/metabolismo , Antiprotozoários/farmacologia , Permeabilidade da Membrana Celular , Estrutura Molecular , Folhas de Planta/química , Triterpenos/farmacologia
2.
Exp Parasitol ; 145 Suppl: S111-4, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-24726697

RESUMO

Pathogenic Acanthamoeba strains are causative agents of Granulomatous Amoebic Encephalitis (GAE) and Acanthamoeba keratitis (AK) worldwide. The existence of the cyst stage complicates Acanthamoeba therapy as it is highly resistant to antibiotics and physical agents. The aim of this study was to investigate the activity of Limouni olive leaf cultivar against the trophozoite stage of Acanthamoeba. The ethyl acetate and methanol extracts of this variety were tested against Acanthamoeba castellanii Neff. The ethyl acetate extract of olive leaf was the most active showing an IC50 of 5.11±0.71µg/ml of dry extract. Bio-guided fractionation of this extract was conducted and led to the identification of three active compounds namely oleanolic and maslinic acids and oleuropein which could be used for the development of novel therapeutic approaches against Acanthamoeba infections.


Assuntos
Acanthamoeba castellanii/efeitos dos fármacos , Olea/química , Extratos Vegetais/farmacologia , Acanthamoeba castellanii/crescimento & desenvolvimento , Bioensaio , Cromatografia em Gel , Concentração Inibidora 50 , Testes de Sensibilidade Parasitária , Extratos Vegetais/isolamento & purificação , Folhas de Planta/química , Trofozoítos/efeitos dos fármacos , Trofozoítos/crescimento & desenvolvimento , Tunísia
3.
Biochem Biophys Res Commun ; 329(2): 502-7, 2005 Apr 08.
Artigo em Inglês | MEDLINE | ID: mdl-15737615

RESUMO

P-glycoprotein (Pgp) transporters play an important role in multidrug resistance in eukaryotic cells and in protozoan parasites such as Leishmania. To search for new reversal agents of the Leishmania tropica Pgp, we developed a screening assay using the Baculovirus-insect cell expression system. We demonstrated a MgATP-dependent, vanadate-sensitive transport of Hoechst 33342 in membrane preparations of Sf9 insect cells expressing Pgp. We have found that dihydro-beta-agarofuran sesquiterpenes from Maytenus cuzcoina inhibited Hoechst 33342 transport that correlates with their reversal effect in a multidrug-resistant L. tropica line overexpressing Pgp. The results suggest that Sf9 cell membrane Hoechst 33342 transport system represents an efficient tool for examining the interactions of Leishmania Pgp with pharmacological agents.


Assuntos
Membro 1 da Subfamília B de Cassetes de Ligação de ATP/metabolismo , Benzimidazóis/farmacocinética , Membrana Celular/metabolismo , Resistência a Múltiplos Medicamentos/fisiologia , Leishmania/metabolismo , Engenharia de Proteínas/métodos , Spodoptera/metabolismo , Membro 1 da Subfamília B de Cassetes de Ligação de ATP/genética , Animais , Linhagem Celular , Membrana Celular/efeitos dos fármacos , Leishmania/efeitos dos fármacos , Sesquiterpenos/farmacologia , Spodoptera/efeitos dos fármacos , Spodoptera/genética , Transfecção/métodos
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