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1.
Parasitol Res ; 101(2): 443-52, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17342533

ABSTRACT

In this study, we investigated the effects of Ocimum basilicum essential oil on Giardia lamblia and on the modulation of the interaction of these parasites by peritoneal mouse macrophage. The essential oil (2 mg/ml) and its purified substances demonstrated antigiardial activity. Linalool (300 microg/ml), however, was able to kill 100% parasites after 1 h of incubation, which demonstrates its high antigiardial potential. Pretreatment of peritoneal mouse macrophages with 2 mg/ml essential oil dilution reduced in 79% the association index between these macrophages and G. lamblia, with a concomitant increase by 153% on nitric oxide production by the G. lamblia-ingested macrophages. The protein profiles and proteolitic activity of these parasite trophozoites, previously treated or not with 2 mg/ml essential oil or with the purified fractions, were also determined. After 1 and 2 h of incubation, proteins of lysates and culture supernatants revealed significant differences in bands patterns when compared to controls. Besides, the proteolitic activity, mainly of cysteine proteases, was clearly inhibited by the essential oil (2 mg/ml) and the purified linalool (300 microg/ml). These results suggest that, with G. lamblia, the essential oil from O. basilicum and its purified compounds, specially linalool, have a potent antimicrobial activity.


Subject(s)
Antiprotozoal Agents/pharmacology , Giardia lamblia/drug effects , Ocimum basilicum/chemistry , Oils, Volatile/pharmacology , Plant Extracts/pharmacology , Acyclic Monoterpenes , Animals , Cell Survival , Cells, Cultured , Female , Giardia lamblia/chemistry , Macrophages, Peritoneal/immunology , Macrophages, Peritoneal/parasitology , Mice , Monoterpenes/isolation & purification , Monoterpenes/pharmacology , Nitric Oxide/biosynthesis , Oils, Volatile/isolation & purification , Protozoan Proteins/analysis
2.
Parasitol Int ; 55(2): 99-105, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16343984

ABSTRACT

Leishmaniasis is a group of diseases with a large spectrum of clinical manifestations caused by protozoans of the genus Leishmania. Here we demonstrate the leishmanicidal activity of the essential oil of Ocimum gratissimum as well as its main constituent, eugenol. The eugenol-rich essential oil of O. gratissimum progressively inhibited Leishmania amazonensis growth at concentrations ranging from 100 to 1000 microg/ml. The IC50 (sub-inhibitory concentration) of the essential oil for promastigotes and amastigotes were respectively 135 and 100 microg/ml and the IC50 of eugenol was 80 microg/ml for promastigote forms. L. amazonensis exposed to essential oil at concentrations corresponding to IC50 for promastigotes and for amastigotes underwent considerable ultrastructural alterations, as shown by transmission electron microscopy. Two or more nuclei or flagella were observed in 31% and 23.3% of treated amastigote and promastigote forms, respectively, suggesting interference in cell division. Considerable mitochondrial swelling was observed in essential oil-treated promastigotes and amastigotes, which had the inner mitochondrial membrane altered, with a significant increase in the number of cristae; in some amastigotes the mitochondrial matrix became less electron-dense. The minimum inhibitory concentration for both promastigotes and amastigotes was 150 microg/ml. Pretreatment of mouse peritoneal macrophages with 100 and 150 microg/ml essential oil reduced the indices of association between promastigotes and the macrophages, followed by increased in nitric oxide production by the infected macrophages. The essential oil showed no cytototoxic effects against mammalian cells. This set of results suggests that O. gratissimum essential oil and its compounds could be used as sources for new antileishmanial drugs.


Subject(s)
Antiprotozoal Agents/pharmacology , Eugenol/pharmacology , Leishmania/drug effects , Leishmaniasis/drug therapy , Ocimum/chemistry , Oils, Volatile/chemistry , Animals , Dose-Response Relationship, Drug , Inhibitory Concentration 50 , Leishmania/ultrastructure , Macrophages, Peritoneal/parasitology , Microscopy, Electron, Transmission/methods , Nitric Oxide/biosynthesis , Parasitic Sensitivity Tests
3.
Antimicrob Agents Chemother ; 47(6): 1895-901, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12760864

ABSTRACT

The in vitro leishmanicidal effects of a linalool-rich essential oil from the leaves of Croton cajucara against Leishmania amazonensis were investigated. Morphological changes in L. amazonensis promastigotes treated with 15 ng of essential oil per ml were observed by transmission electron microscopy; leishmanial nuclear and kinetoplast chromatin destruction, followed by cell lysis, was observed within 1 h. Pretreatment of mouse peritoneal macrophages with 15 ng of essential oil per ml reduced by 50% the interaction between these macrophages and L. amazonensis, with a concomitant increase by 220% in the level of nitric oxide production by the infected macrophages. Treatment of preinfected macrophages with 15 ng of essential oil per ml reduced by 50% the interaction between these cells and the parasites, which led to a 60% increase in the amount of nitric oxide produced by the preinfected macrophages. These results provide new perspectives on the development of drugs with activities against Leishmania, as linalool-rich essential oil is a strikingly potent leishmanicidal plant extract (50% lethal doses, 8.3 ng/ml for promastigotes and 8.7 ng/ml for amastigotes) which inhibited the growth of L. amazonensis promastigotes at very low concentrations (MIC, 85.0 pg/ml) and which presented no cytotoxic effects against mammalian cells.


Subject(s)
Antiprotozoal Agents/pharmacology , Croton/chemistry , Leishmania/drug effects , Monoterpenes/pharmacology , Phytotherapy , Plant Oils/pharmacology , Acyclic Monoterpenes , Animals , Female , Leishmaniasis/drug therapy , Macrophages, Peritoneal/drug effects , Macrophages, Peritoneal/metabolism , Macrophages, Peritoneal/parasitology , Mice , Microbial Sensitivity Tests , Microscopy, Electron , Nitric Oxide/biosynthesis
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