Tropical Protozoan Diseases: Natural Product Drug Discovery and DevelopmentView this Special Issue
Eugenia uniflora L. Essential Oil as a Potential Anti-Leishmania Agent: Effects on Leishmania amazonensis and Possible Mechanisms of Action
Eugenia uniflora L. is a member of the Myrtaceae family and is commonly known as Brazilian cherry tree. In this study, we evaluated the chemical composition of Eugenia uniflora L. essential oil (EuEO) by using gas chromatography-mass spectrometry (GC-MS) and assessed its anti-Leishmania activity. We also explored the potential mechanisms of action and cytotoxicity of EuEO. Thirty-two compounds were identified, which constituted 92.65% of the total oil composition. The most abundant components were sesquiterpenes (91.92%), with curzerene (47.3%), γ-elemene (14.25%), and trans-β-elemenone (10.4%) being the major constituents. The bioactivity shown by EuEO against promastigotes (IC50, 3.04 μg·mL−1) and amastigotes (IC50, 1.92 μg·mL−1) suggested significant anti-Leishmania activity. In the cytotoxicity determination, EuEO was 20 times more toxic to amastigotes than to macrophages. Hemolytic activity was 63.22% at the highest concentration tested (400 μg·mL−1); however, there appeared to be no toxicity at 50 μg·mL−1. While the data show that EuEO activity is not mediated by nitric oxide production, they do suggest that macrophage activation may be involved in EuEO anti-Leishmania activity, as evidenced by increases in both the phagocytic capacity and the lysosomal activity. More studies are needed to determine in vivo activity as well as additional mechanisms of the anti-Leishmania activity.
Protozoan parasites of the genus Leishmania are responsible for a spectrum of diseases collectively known as leishmaniasis, which affects the skin, mucous membranes, and internal organs. Over 12 million cases of leishmaniasis have been reported worldwide, with 1 to 2 million new cases being reported annually [1, 2]. Increase in the incidence of leishmaniasis is associated with urban development, deforestation, environmental changes, and increased migration to areas where the disease is endemic . Despite its epidemiological importance, treatment is still performed with chemotherapeutic drugs that are delivered parenterally, require medical supervision, and have many side effects [4, 5].
The need to identify new anti-Leishmania compounds that are more effective and less toxic than conventional drugs has motivated research of substances derived from plant species. In this context, essential oils containing a group of secondary metabolites consisting mainly of monoterpenes, sesquiterpenes, and phenylpropanoids have demonstrated proven anti-Leishmania activity in vivo and in vitro on promastigote and/or amastigote forms of Leishmania. Included among these are Croton cajucara , Ocimum gratissimum , Copaifera cearensis , Chenopodium ambrosioides , Cymbopogon citratus [10, 11], and Lippia sidoides . These studies have shown that essential oils can be a promising source of new drugs with anti-Leishmania activity.
Eugenia uniflora L., commonly known as “pitangueira” or Brazilian cherry tree, is a species belonging to the family Myrtaceae, which is native to South America and common in regions with tropical and subtropical climate . In Brazil, it is used in the treatment of digestive disorders  and is thought to have anti-inflammatory and antirheumatic activities . It is an aromatic species and its essential oil has pharmacological properties that are well characterized in the literature as antioxidant and antimicrobial . E. uniflora has known antihypertensive , antitumor , and antinociceptive properties , and it shows good performance against microorganisms, demonstrating antiviral, antifungal , anti-Trichomonas gallinae , and anti-Trypanosoma cruzi properties .
Considering the potential pharmacological benefits of E. uniflora and the increasing interest in the discovery of essential oils with anti-Leishmania activity, the aim of this study was to investigate the anti-Leishmania activity of leaf essential oil from this species, the chemical composition of the oil, its cytotoxicity, and possible mechanisms of action.
2. Materials and Methods
Dimethyl sulfoxide (DMSO: 99%), anhydrous sodium sulfate, glacial acetic acid, ethanol, formaldehyde, sodium chloride, calcium acetate, zymosan, and neutral red were purchased from Merck Chemical Company (Germany). The -alkane (C8–C20) homologous series, Schneider’s medium, RPMI 1640 medium, fetal bovine serum (FBS), MTT (3-(4,5-dimethylthiazol-2-yl)2,5-diphenyltetrazolium bromide), Griess reagent (1% sulfanilamide in H3PO4 10% (v/v) in Milli-Q water), and the antibiotics penicillin and streptomycin were purchased from Sigma Chemical (St. Louis, MO, USA). The antibiotic amphotericin B (90%) was purchased from Cristália (São Paulo, SP, Brazil).
2.2. Plant Material
E. uniflora leaves were collected (January 2010) from a mature tree in the flowering stage in São Luís (2°30′45.3′′S and 44°18′1.1′′W) in the state of Maranhão in northeast Brazil. The samples were collected from a cultivated plant and its fruits have red color. A voucher specimen (no. 0998/SLS017213) was deposited at the Herbarium “Ático Seabra” of the Federal University of Maranhão, and plant identification was confirmed by botanists of the Herbarium “Murça Pires” from Museu Paraense Emílio Goeldi, Belém, PA, Brazil.
2.3. Extraction of the Essential Oil
The plant material was air-dried for 7 days, cut into small pieces, and subjected to hydrodistillation using a Clevenger-type apparatus (300 g, 3 h) to obtain a sesquiterpene-rich essential oil. Once collected, the essential oil was dried over anhydrous sodium sulfate, filtered, and weighed, and then the oil yield was calculated in terms of % (w/w). Its percentage content was estimated based on the plant dry weight by calculating the water content by using a moisture analyzer prior to distillation. EuEO was then stored in a dark flask and refrigerated (at +5°C) until use.
2.4. Gas Chromatography-Mass Spectrometry Analysis of the Essential Oil
EuEO was analyzed using a THERMO DSQ II GC-MS instrument (Thermo Fisher Scientific, Austin, TX, USA), under the following conditions: DB-5 ms ( i.d.; 0.25 μm film thickness) fused silica capillary column, with the following temperature program: 60°C, subsequently increased by 3°C/min up to 240°C; injector temperature: 250°C; carrier gas: helium (high purity), adjusted to a linear velocity of 32 cm/s (measured at 100°C). The injection type was splitless. The oil sample was diluted 1 : 100 in hexane solution, and the volume injected was 0.1 μL. The split flow was adjusted to yield a 2 : 1000 ratio, and the septum sweep was constant at 10 mL/min. All mass spectra were acquired in electron impact (EI) mode with an ionization voltage of 70 eV over a mass scan range of 35–450 amu. The temperature of the ion source and connection parts was 200°C.
2.5. Identification and Quantification of Constituents
The quantitative data regarding the volatile constituents were obtained by peak-area normalization using a FOCUS GC/FID operated under conditions similar to those used in the GC-MS assay, except for the carrier gas, which was nitrogen. The retention index was calculated for all the volatile constituents by using an -alkane (C8–C20) homologous series. When possible, individual components were identified by coinjection with authentic standards. Otherwise, the peak assignment was performed by comparison of both mass spectrum and GC retention data by using authentic compounds previously analyzed and stored in our private library, as well as with the aid of commercial libraries containing retention indices and mass spectra of volatile compounds commonly found in essential oils [23, 24]. Percentage (relative) of the identified compounds was computed from the GC peak area.
2.6. Parasites and Mice
Leishmania (Leishmania) amazonensis (IFLA/BR/67/PH8) was used for the determination of the anti-Leishmania activity. Parasites were grown in supplemented Schneider’s medium (10% heat-inactivated fetal bovine serum (FBS), 100 U·mL−1 penicillin, and 100 μg/mL streptomycin at 26°C). Murine macrophages were collected from the peritoneal cavities of male and female BALB/c mice (4-5 weeks old) from Medicinal Plants Research Center (NPPM/CCS/UFPI), located at Teresina, PI, Brazil. The macrophages were maintained at a controlled temperature (°C) and light conditions (12 h light/dark cycle). All protocols were approved by the Animal Research Ethics Committee (CEEAPI no. 001/2012).
2.7. Anti-Leishmania Activity Assay
Promastigotes in the logarithmic growth phase were seeded in 96-well cell culture plates at Leishmania per well. Then, essential oil was added to the wells in serial dilutions of 400, 200, 100, 50, 25, 12.5, 6.25, and 3.12 μg·mL−1. The plate was kept at 26°C in a biological oxygen demand (BOD) incubator, and Leishmania was observed and counted by using a Neubauer hemocytometer after 24, 48, and 72 h to monitor growth and viability . Assays were performed in triplicate and were repeated 3 times on different days.
2.8. Cytotoxicity Determination
Cytotoxicity of EuEO was assessed using the MTT test. In a 96-well plate, 100 μL of supplemented RPMI 1640 medium and about macrophages were added per well. They were then incubated at 37°C in 5% of CO2 for 2 h to allow cell adhesion. After this time, 2 washes with supplemented RPMI 1640 medium were performed to remove cells that did not adhere. Subsequently, EuEO was added, in triplicate, after being previously diluted in supplemented RPMI 1640 medium to a final volume of 100 μL for each well at the tested concentrations (100, 50, 25, 12.5, 6.25, and 3.12 μg·mL−1). Cells were then incubated for 48 h. At the end of the incubation, 10 μL of MTT diluted in PBS was added at a final concentration of 5 mg·mL−1 (10% of volume, i.e., 10 μL for each 100 μL well) and was incubated for an additional 4 h at 37°C in 5% CO2. The supernatant was then discarded, and 100 μL of DMSO was added to all wells. The plate was then stirred for about 30 min at room temperature to complete formazan dissolution. Finally, spectrophotometric reading was conducted at 550 nm in an ELISA plate reader .
2.9. Hemolytic Activity
The hemolytic activity was investigated by incubating 20 μL of serially diluted essential oil in phosphate-buffered saline (PBS; 400, 200, 100, 50, 25, 12.5, 6.25, and 3.12 μg·mL−1) with 80 μL of a suspension of 5% red blood cells (human O+) for 1 h at 37°C in assay tubes. The reaction was slowed by adding 200 μL of PBS, and then the suspension was centrifuged at 1000 g for 10 min. Cell lysis was then measured spectrophotometrically (540 nm). The absence of hemolysis (blank control) or total hemolysis (positive control) was determined by replacing the essential oil solution with an equal volume of PBS or Milli-Q sterile water, respectively. The results were determined by the percentage of hemolysis compared to the positive control (100% hemolysis), and the experiments were performed in triplicate .
2.10. Treatment of Infected Macrophages
Macrophages were collected in 24-well culture plates at a concentration of cells/500 μL in RPMI 1640, containing sterile 13 mm round coverslips. They were then incubated at 37°C in 5% of CO2 for 2 h to allow cell adhesion. After this time, the medium was replaced with 500 μL of supplemented RPMI 1640 and incubated for 4 h. The medium was then aspirated, and a new medium containing promastigotes (in the stationary phase) at a ratio of 10 promastigotes to 1 macrophage was added to each well. After 4 h of incubation in 5% CO2 at 37°C, the medium was aspirated to remove free promastigotes, and the test samples were added at nontoxic concentrations to the macrophages (3.12, 1.56, and 0.78 μg·mL−1). This preparation was then incubated for 48 h, after which the coverslips were removed, fixed in methanol, and stained with Giemsa. For each coverslip, 100 cells were evaluated and both the number of infected macrophages and the amount of parasites per macrophage were counted .
2.11. Lysosomal Activity
Measurement of the lysosomal activity was carried out according to the method of Grando et al. . Peritoneal macrophages were plated and incubated with EuEO in serial dilutions of 100, 50, 25, 12.5, 6.25, and 3.12 μg·mL−1. After 4 h of incubation at 37°C in 5% CO2, 10 μL of neutral red solution was added and incubated for 30 min. Once this time had elapsed, the supernatant was discarded, the wells were washed with 0.9% saline at 37°C, and 100 mL of extraction solution was added (glacial acetic acid 1% v/v and ethanol 50% v/v dissolved in bidistilled water) to solubilize the neutral red inside the lysosomal secretion vesicles. After 30 min on a Kline shaker (model AK 0506), the plate was read at 550 nm by using an ELISA plate reader.
2.12. Phagocytosis Test
Peritoneal macrophages were plated and incubated with EuEO in serial dilutions of 100, 50, 25, 12.5, 6.25, and 3.12 μg·mL−1. After 48 h of incubation at 37°C in 5% CO2, 10 μL of zymosan color solution was added and incubated for 30 min at 37°C. After this, 100 mL of Baker’s fixative (formaldehyde 4% v/v, sodium chloride 2% w/v, and calcium acetate 1% w/v in distilled water) was added to stop the phagocytosis process. Thirty minutes later, the plate was washed with 0.9% saline in order to remove zymosan that was not phagocytosed by macrophages. The supernatant was removed and added to 100 mL of extraction solution. After solubilization in a Kline shaker, the absorbances were measured at 550 nm by using an ELISA plate reader .
2.13. Nitric Oxide (NO) Production
In 96-well plates, macrophages were added per well and incubated at 37°C in 5% CO2 for 4 h to allow cell adhesion. A new medium containing promastigotes (in the stationary phase) at a ratio of 10 promastigotes per macrophage was added to half of the wells. The essential oil was added after being previously diluted in a culture medium containing different concentrations (100, 50, 25, 12.5, 6.25, and 3.12 μg·mL−1) in the absence or presence of L. amazonensis, and was then incubated again at 37°C in 5% CO2 for 24 h. After this period, the cell culture supernatant was collected and transferred to another plate for measurement of nitrite. A standard curve was prepared with 150 μM sodium nitrite in Milli-Q water at varying concentrations of 1, 5, 10, 25, 50, 75, 100, and 150 μM diluted in a culture medium. At the time of dosing, 100 μL of either the samples or the solutions prepared for obtaining the standard curve was mixed with an equal volume of Griess reagent. The analysis was performed using an ELISA plate reader at 550 nm .
2.14. Statistical Analysis
All assays were performed in triplicate and in 3 independent experiments. The half-maximal inhibitory concentration (IC50) values and 50% cytotoxicity concentration (CC50) values, with 95% confidence intervals, were calculated using a probit regression model and Student’s -test. Analysis of variance (ANOVA) followed by a Bonferroni test were performed, taking a value of <0.05 as the minimum level required for statistical significance.
3.1. Analysis of the Essential Oil
The yield of EuEO was 0.3%. Thirty-two components were identified in this oil by GC-MS, constituting 92.65% of the total mixture. EuEO was shown to be rich in oxygenated sesquiterpenes (62.55%) and sesquiterpene hydrocarbons (29.37%). Curzerene was the major constituent (47.3%), followed by γ-elemene (14.25%) and trans-β-elemenone (10.4%). The chemical constituents are listed in Table 1.
3.2. Anti-Leishmania Activity Assay
The inhibitory profile of EuEO on L. amazonensis promastigotes showed a significant concentration-dependent decrease () in parasite viability, with 100% inhibition of promastigote growth at concentrations of 400, 200, and 100 μg·mL−1 (Figure 1). The IC50 was 1.75 μg·mL−1 at 72 h of exposure (Table 2). In cultures treated with EuEO, we used an optical microscope to observe morphological changes in the promastigotes, such as cells with rounded or completely spherical shapes, as well as cellular debris, in contrast to the spindle forms present in the control (data not shown). Amphotericin B was used as a positive control and was tested at a concentration of 2 μg·mL−1. The highest inhibitory effect of amphotericin B was observed after 24 h.
3.3. Cytotoxicity and Hemolysis Assay
The cytotoxicity of EuEO for murine peritoneal macrophages and erythrocytes is shown in Figures 2 and 3, respectively, and in Table 2. The EO from E. uniflora significantly altered () macrophage viability at a concentration of 6.25 μg·mL−1 and was able to reduce 50% of the macrophage viability (CC50) at 45.3 μg·mL−1. The cytotoxicity of EO from E. uniflora for human blood type O+ erythrocytes was 63.22% at the highest concentration tested (400 μg·mL−1); however, it appeared to be nontoxic at concentrations less than 50 μg·mL−1 (Figure 3).
3.4. Treatment of Infected Macrophages
Figures 4 and 5 show the results of EuEO treatment of macrophages infected with L. amazonensis. The values obtained revealed a significant and concentration-dependent reduction in macrophage infection at 48 h with all the 3 EuEO concentrations studied. The reduction of infection was 27%, 44.67%, and 50.67% at 0.78, 1.56, and 3.12 μg·mL−1, respectively. EuEO also decreased the number of amastigotes per infected cell in a concentration-dependent manner (Figure 5). The IC50 at 48 h of exposure to EuEO was 1.92 μg·mL−1 (Table 2). These values and the CC50 values for macrophages were used to calculate the selectivity index that is useful for assessing the safety level of EuEO in mammalian cells (Table 2). This index represents the relationship between CC50 and IC50 for amastigotes.
3.5. Lysosomal Activity and Phagocytosis Assay
Lysosomal activity was assessed based on the retention of neutral red in macrophage lysosomes and was determined colorimetrically. The lysosomal activity of macrophages treated with EuEO showed significant reduction at concentrations of 100 and 50 μg·mL−1 (Figure 6(a)) due to cytotoxicity (CC50 45.3 μg·mL−1). However, we observed a statistically significant increase in lysosomal activity at concentrations from 12.5 to 3.12 μg·mL−1 compared to control. Another parameter reflecting macrophage activation was the phagocytosis of stained zymosan when the cells were exposed to an external stimulus. The phagocytic ability of macrophages incubated with EuEO is shown in Figure 6(b). There was a significant increase in phagocytosis of zymosan particles in the wells treated with EuEO at concentrations ranging from 25 to 3.12 μg·mL−1.
3.6. NO Production
NO production was determined indirectly by measuring nitrite produced by macrophages treated with EuEO and stimulated (or not stimulated) by L. amazonensis promastigotes. Macrophages treated with EuEO, but not stimulated by Leishmania, showed significant reduction in NO production at concentrations of 100 and 50 μg·mL−1 (Figure 7(a)), while macrophages stimulated by the parasite showed increased NO at a concentration of 3.12 μg·mL−1, albeit without statistical significance () (Figure 7(b)).
The need to identify new compounds with anti-Leishmania properties that are more effective and less toxic than conventional drugs has motivated research on natural products isolated from plant species. These substances predominantly consist of alkaloids, terpenes, flavonoids, benzopyrans, phenolics, and sesquiterpene lactones and have been identified in plant species with documented anti-Leishmania activity [29, 30]. The chemical composition of EuEO obtained in this study revealed sesquiterpenes to be the dominant chemical class, corroborating the findings of many previous studies [16, 31–33]. Despite the prevalence of sesquiterpenes, the species has different chemotypes, with different major constituents being observed in different studies. The specimen analyzed in this study had curzerene as the major constituent, which again corroborated previous reported findings [32, 34]. According to Adio , germacrone is a heat-sensitive compound that may degrade to trans-β-elemenone during GC analysis. This may be the explanation of the presence of trans-β-elemenone among the major compounds of EuEO. Some germacrone products have shown pharmacological activity, as antitumor .
According to Costa et al.  the composition of the essential oil from E. uniflora leaves might be influenced by fruit colors. The plants with red fruit colors have curzerene as the major component as in our studied plant. In Maranhão, where the samples were collected, the majority of plants of E. uniflora have red fruit color . Selina-1,3,7(11)-trien-8-one , germacrene B [16, 33], and α- and β-selinene  have been found to be the major constituents of other E. uniflora chemotypes. Genetic variability, geographical and environmental conditions, and the method of environmental management directly influence the yield and composition of essential oils . It is the first report of essential oil analyzed from E. uniflora collected in São Luís, MA, Brazil and this could be an excellent source of natural product with interest for pharmaceutical industry.
The present study was conducted to evaluate the anti-Leishmania activity of EuEO on promastigotes and amastigotes of L. amazonensis, its potential mechanisms of macrophage activation, and its cytotoxicity in mammalian cells. The EuEO showed significant concentration-dependent activity against promastigotes of L. amazonensis, with an IC50 of 1.75 μg·mL−1. Previous studies have suggested that these classes of natural products may have potential anti-Leishmania activity. β-Caryophyllene (a sesquiterpene hydrocarbon) and nerolidol (an oxygenated sesquiterpene) are examples of terpenic substances with well-characterized anti-Leishmania activity, possibly associated with inhibition of cellular isoprenoid biosynthesis [8, 39].
It has been shown that the lipophilic components of essential oils may affect layers of polysaccharides, fatty acids, and phospholipids in plasma membranes of promastigotes of Leishmania spp. This then leads to cell lysis and release of macromolecules . In the cytoplasm, these substances can disrupt the specific metabolic pathways of lipids and proteins or stimulate depolarization of mitochondrial membranes, which can lead to cell necrosis or apoptosis [41, 42].
Amphotericin B is a drug of choice for the treatment of different forms of leishmaniasis. Because of this it was used as a positive control. We observed a significant inhibitory effect on promastigote growth after 24 h of exposure to amphotericin B, but leading to an increase in viable promastigote forms at 48 and 72 h. Similar results were observed in previous studies . Some Leishmania strains have shown mechanisms of resistance to amphotericin B. This may has happened with the strain used in this study. The reproduction of resistant parasites may have led to a higher cell viability after 48 and 72 h [44, 45].
Experimental models using amastigotes internalized into macrophages can produce results that more closely approximate those obtained using animal models, since these forms are responsible for the clinical manifestations of leishmaniasis . Amastigotes can be found in parasitophorous vacuoles of infected macrophages; therefore, a therapeutic drug will only be effective against Leishmania spp. if it can cross the host cell membrane and act on the amastigotes inside the vacuole. Thus, assays of activity against intracellular amastigotes are the most effective way to relate the in vitro activity of a possible substance with its in vivo effectiveness . The inhibition of amastigote growth was even greater at 48 h after exposure to oil, with an IC50 of 1.92 μg/mL, whereas the IC50 for promastigotes was 3.04 μg·mL−1 for the same duration of exposure. Previous studies demonstrated greater activity against amastigotes versus promastigotes of essential oils of Artemisia absinthium and Satureja punctata .
Mechanisms of anti-Leishmania action on Leishmania spp. amastigotes have also been described for essential oils and their terpene compounds. Monoterpenes such as linalool, isolated from leaves of Croton cajucara (Euphorbiaceae), significantly increased NO production in macrophages infected with L. amazonensis and acts directly on the parasite, as evidenced by mitochondrial swelling and changes in the kinetoplast and the organization of nuclear chromatin . In this study, the production of NO was determined by measuring nitrite. The results from macrophages treated with EuEO revealed that EuEO does not induce NO production, which demonstrates that its promising anti-Leishmania activity does not occur by this route.
Natural products that are able to activate macrophages, and are thus biological response modifiers, have been extensively studied [49, 50]. In this context, the EuEO demonstrated potential in the activation of macrophages by increasing phagocytic capacity and lysosomal activity, immunomodulatory activities possibly involved in its anti-Leishmania activity. Phagocytosis and the lysosomal system are critical to macrophage function, because of their roles in internalization, degradation, and eventually presentation of peptides derived from antigens required for host defense. In addition, antigen presentation occurs through phagocytosis and endosomal/lysosomal targeting systems [51–53].
Due to the need for anti-Leishmania substances that are more selective for the parasite and less toxic to host cells and since EuEO showed low IC50 values, it was important to investigate the cytotoxic activity of EuEO against mammalian cells. EuEO showed significant toxicity in macrophages, with a CC50 of 45.3 μg·mL−1, but when compared with its IC50 value in amastigotes, this indicates a secure selectivity index above 20. The literature recommends that for amastigotes internalized in macrophages, this index must be demonstrated as near to or greater than 20 . The investigation of the toxic action of new substances with anti-Leishmania activity on macrophages is important, since they are the main cells of the vertebrate host parasitized by Leishmania spp. [55, 56]. Furthermore, various other cytotoxic assays can be conducted using animal and human cells to determine the safety of a test substance, leading to a future treatment in vivo. Tests performed with erythrocytes enable assessment of a drug’s potential to cause injury to the plasma membrane of a cell, either by forming pores or by total rupture, leading to cellular damage or changes in membrane permeability . This is a model used for the preliminary study of the protective and toxic effects of substances, being a possible indicator of this type of damage to cells in vivo [58–60]. The results obtained in this test with EuEO revealed low toxicity to erythrocytes, since EuEO showed 0% hemolysis at concentrations of 50 μg·mL−1 and lower.
In conclusion, the data in this study show that the essential oil of leaves from E. uniflora (EuEO), characterized by sesquiterpenes, has anti-Leishmania activity in both stages of L. amazonensis. This study also demonstrated that EuEO activity is not mediated by NO production. On the other hand, activation of macrophages may be involved in the mechanisms of EuEO anti-Leishmania activity, as evidenced by increases in both phagocytic capacity and the lysosomal compartment. Further investigation is needed to determine additional mechanisms involved in the anti-Leishmania activity of this plant species, as well as in vivo studies in models of leishmaniasis.
Conflict of Interests
The authors declare no conflict of interests.
The authors are grateful to the CAPES and FAPEMA for financial grants through the concession of scholarships and financial support.
S. Kaur, H. Sachdeva, S. Dhuria, M. Sharma, and T. Kaur, “Antileishmanial effect of cisplatin against murine visceral leishmaniasis,” Parasitology International, vol. 59, no. 1, pp. 62–69, 2010.View at: Publisher Site | Google Scholar
S. Azzouz, M. Maache, R. G. Garcia, and A. Osuna, “Leishmanicidal activity of edelfosine, miltefosine and ilmofosine,” Basic and Clinical Pharmacology and Toxicology, vol. 96, no. 1, pp. 60–65, 2005.View at: Publisher Site | Google Scholar
J. A. Patza, T. K. Graczykb, N. Gellera, and A. Y. Vittorc, “Effects of environmental change on emerging parasitic diseases,” International Journal of Parasitology, vol. 30, no. 12-13, pp. 1295–1304, 2000.View at: Publisher Site | Google Scholar
B. H. Alizadeh, A. Foroumadi, S. K. Ardestani, F. Poorrajab, and A. Shafiee, “Leishmanicidal evaluation of novel synthetic chromenes,” Archiv der Pharmazie, vol. 341, no. 12, pp. 787–793, 2008.View at: Publisher Site | Google Scholar
R. W. Ashford, “The leishmaniases as emerging and reemerging zoonoses,” International Journal for Parasitology, vol. 30, no. 12-13, pp. 1269–1281, 2000.View at: Publisher Site | Google Scholar
M. S. S. Rosa, R. R. Mendonça-Filho, H. R. Bizzo et al., “Antileishmanial activity of a linalool-rich essential oil from Croton cajucara,” Antimicrobial Agents Chemotherapy, vol. 47, no. 6, pp. 1895–1901, 2003.View at: Google Scholar
T. Ueda-Nakamura, R. R. Mendonça-Filho, J. A. Morgado-Díaz et al., “Antileishmanial activity of eugenol-rich essential oil from Ocimum gratissimum,” Parasitology International, vol. 55, no. 2, pp. 55–59, 2006.View at: Google Scholar
A. O. Santos, T. Ueda-Nakamura, B. P. Dias Filho, V. F. Veiga Junior, A. C. Pinto, and C. V. Nakamura, “Effect of Brazilian copaiba oils on Leishmania amazonensis,” Journal of Ethnopharmacology, vol. 120, no. 2, pp. 204–208, 2008.View at: Publisher Site | Google Scholar
L. Monzote, A. M. Montalvo, S. Almanonni, R. Scull, M. Miranda, and J. Abreu, “Activity of the essential oil from Chenopodium ambrosioides grown in Cuba against Leishmania amazonensis,” Chemotherapy, vol. 52, no. 3, pp. 130–136, 2006.View at: Publisher Site | Google Scholar
M. Machado, P. Pires, A. M. Dinis et al., “Monoterpenic aldehydes as potential anti-Leishmania agents: activity of Cymbopogon citratus and citral on L. infantum, L. tropica and L. major,” Experimental Parasitology, vol. 130, no. 3, pp. 223–231, 2012.View at: Publisher Site | Google Scholar
M. R. Santin, A. O. Dos Santos, C. V. Nakamura, B. P. Dias Filho, I. C. P. Ferreira, and T. Ueda-Nakamura, “In vitro activity of the essential oil of Cymbopogon citratus and its major component (citral) on Leishmania amazonensis,” Parasitology Research, vol. 105, no. 6, pp. 1489–1496, 2009.View at: Publisher Site | Google Scholar
V. C. S. Oliveira, D. M. S. Moura, J. A. D. Lopes, P. P. De Andrade, N. H. Da Silva, and R. C. B. Q. Figueiredo, “Effects of essential oils from Cymbopogon citratus (DC) Stapf., Lippia sidoides Cham., and Ocimum gratissimum L. on growth and ultrastructure of Leishmania chagasi promastigotes,” Parasitology Research, vol. 104, no. 5, pp. 1053–1059, 2009.View at: Publisher Site | Google Scholar
A. E. Consolini and M. G. Sarubbio, “Pharmacological effects of Eugenia uniflora (Myrtaceae) aqueous crude extract on rat's heart,” Journal of Ethnopharmacology, vol. 81, no. 1, pp. 57–63, 2002.View at: Publisher Site | Google Scholar
C. B. Alice, V. M. F. Vargas, G. A. A. B. Silva et al., “Screening of plants used in south Brazilian folk medicine,” Journal of Ethnopharmacology, vol. 35, no. 2, pp. 165–171, 1991.View at: Google Scholar
P. Weyerstahl, H. Marschall-Weyerstahl, C. Christiansen, B. O. Oguntimein, and A. O. Adeoye, “Volatile constituents of Eugenia uniflora leaf oil,” Planta medica, vol. 54, no. 6, pp. 546–549, 1988.View at: Google Scholar
F. N. Victoria, E. J. Lenardão, L. Savegnago et al., “Essential oil of the leaves of Eugenia uniflora L.: antioxidant and antimicrobial properties,” Food and Chemical Toxicology, vol. 50, no. 8, pp. 2668–2674, 2012.View at: Publisher Site | Google Scholar
A. E. Consolini, O. A. N. Baldini, and A. G. Amat, “Pharmacological basis for the empirical use of Eugenia uniflora L. (Myrtaceae) as antihypertensive,” Journal of Ethnopharmacology, vol. 66, no. 1, pp. 33–39, 1999.View at: Publisher Site | Google Scholar
I. A. Ogunwande, N. O. Olawore, O. Ekundayo, T. M. Walker, J. M. Schmidt, and W. N. Setzer, “Studies on the essential oils composition, antibacterial and cytotoxicity of Eugenia uniflora L.,” International Journal of Aromatherapy, vol. 15, no. 3, pp. 147–152, 2005.View at: Publisher Site | Google Scholar
A. C. L. Amorim, C. K. F. Lima, A. M. C. Hovell, A. L. P. Miranda, and C. M. Rezende, “Antinociceptive and hypothermic evaluation of the leaf essential oil and isolated terpenoids from Eugenia uniflora L. (Brazilian Pitanga),” Phytomedicine, vol. 16, no. 10, pp. 923–928, 2009.View at: Publisher Site | Google Scholar
D. P. Costa, E. G. A. Filho, L. M. A. Silva et al., “Influence of fruit biotypes on the chemical composition and antifungal activity of the essential oils of Eugenia uniflora leaves,” Journal of the Brazilian Chemical Society, vol. 21, no. 5, pp. 851–858, 2010.View at: Google Scholar
G. F. Ibikunle, A. C. Adebajo, F. G. Famuyiwa, A. J. Aladesanmi, and C. O. Adewunmi, “In-vitro evaluation of anti-trichomonal activities of Eugenia uniflora leaf,” African Journal of Traditional, Complementary and Alternative Medicines, vol. 8, no. 2, pp. 170–176, 2011.View at: Google Scholar
K. K. Santos, S. R. Tintino, C. E. Souza et al., “Anti-Trypanosoma cruzi and cytotoxic activities of Eugenia uniflora L.,” Experimental Parasitology, vol. 131, no. 1, pp. 130–132, 2012.View at: Publisher Site | Google Scholar
NIST 05, Mass Spectral Library (NIST/EPA/NIH), National Institute of Standards and Technology, Gaithersburg, Md, USA, 2005.
R. P. Adams, Identification of Essential Oil Components By Gas Chromatography/Mass Spectrometry, Allured, Carol Stream, Ill, USA, 4th edition, 2007.
S. M. P. Carneiro, F. A. A. Carvalho, L. C. L. R. Santana, A. P. L. Sousa, and M. H. Chaves, “The cytotoxic and antileishmanial activity of extracts and fractions of leaves and fruits of Azadirachta indica (A Juss.),” Biological Research, vol. 45, no. 2, pp. 111–116, 2012.View at: Publisher Site | Google Scholar
M. D. G. F. de Medeiros, A. C. da Silva, A. M. D. G. L. Citó et al., “In vitro antileishmanial activity and cytotoxicity of essential oil from Lippia sidoides Cham,” Parasitology International, vol. 60, no. 3, pp. 237–241, 2011.View at: Publisher Site | Google Scholar
S. E. Löfgren, L. C. Miletti, M. Steindel, E. Bachère, and M. A. Barracco, “Trypanocidal and leishmanicidal activities of different antimicrobial peptides (AMPs) isolated from aquatic animals,” Experimental Parasitology, vol. 118, no. 2, pp. 197–202, 2008.View at: Publisher Site | Google Scholar
F. C. C. Grando, C. A. Felício, A. Twardowschy et al., “Modulation of peritoneal macrophage activity by the saturation state of the fatty acid moiety of phosphatidylcholine,” Brazilian Journal of Medical and Biological Research, vol. 42, no. 7, pp. 599–605, 2009.View at: Google Scholar
M. M. Iwu, J. E. Jackson, and B. G. Schuster, “Medicinal plants in the fight against leishmaniasis,” Parasitology Today, vol. 10, no. 2, pp. 65–68, 1994.View at: Publisher Site | Google Scholar
L. G. Rocha, J. R. G. S. Almeida, R. O. Macêdo, and J. M. Barbosa-Filho, “A review of natural products with antileishmanial activity,” Phytomedicine, vol. 12, no. 6-7, pp. 514–535, 2005.View at: Publisher Site | Google Scholar
S. M. De Morais, A. A. Craveiro, M. I. L. Machado, J. W. Alencar, and F. J. A. Matos, “Volatile constituents of Eugenia uniflora leaf oil from northeastern Brazil,” Journal of Essential Oil Research, vol. 8, no. 4, pp. 449–451, 1996.View at: Google Scholar
J. G. S. Maia, E. H. A. Andrade, M. H. L. Da Silva, and M. G. B. Zoghbi, “A new chemotype of Eugenia uniflora L. from North Brazil,” Journal of Essential Oil Research, vol. 11, no. 6, pp. 727–729, 1999.View at: Google Scholar
J. H. G. Lago, E. D. Souza, B. Mariane et al., “Chemical and biological evaluation of essential oils from two species of myrtaceae—Eugenia uniflora L. and Plinia trunciflora (O. Berg) Kausel,” Molecules, vol. 16, no. 12, pp. 9826–9837, 2011.View at: Google Scholar
R. Chang, S. A. L. de Morais, D. R. Napolitano, K. C. Duarte, V. B. Guzman, and E. A. do Nascimento, “A new approach for quantifying furanodiene and curzerene. A case study on the essential oils of Eugenia uniflora (pitangueira) leaves,” Brazilian Journal of Pharmacognosy, vol. 21, no. 3, pp. 392–396, 2011.View at: Publisher Site | Google Scholar
A. M. Adio, “Germacrenes A-E and related compounds: thermal, photochemical and acid induced transannular cyclizations,” Tetrahedron, vol. 65, no. 8, pp. 1533–1552, 2009.View at: Publisher Site | Google Scholar
D. P. Costa, S. C. Santos, J. C. Seraphin, and P. H. Ferri, “Seasonal variability of essential oils of Eugenia uniflora leaves,” Journal of the Brazilian Chemical Society, vol. 20, no. 7, pp. 1287–1293, 2009.View at: Google Scholar
A. T. Henriques, M. E. Sobral, A. D. Caudaro, E. E. S. Schapoval, V. L. Bassani, and G. Lamaty, “Aromatic plants from Brazil II. The chemical composition of some Eugenia essential oils,” Journal of Essential Oil Research, vol. 5, no. 5, pp. 501–505, 1993.View at: Publisher Site | Google Scholar
B. Teixeira, A. Marques, C. Ramos et al., “European pennyroyal (Mentha pulegium) from portugal: chemical composition of essential oil and antioxidant and antimicrobial properties of extracts and essential oil,” Industrial Crops and Products, vol. 36, no. 1, pp. 81–87, 2012.View at: Publisher Site | Google Scholar
D. C. Arruda, F. L. D'Alexandri, A. M. Katzin, and S. R. B. Uliana, “Antileishmanial activity of the terpene nerolidol,” Antimicrobial Agents and Chemotherapy, vol. 49, no. 5, pp. 1679–1687, 2005.View at: Publisher Site | Google Scholar
R. Di Pasqua, G. Betts, N. Hoskins, M. Edwards, D. Ercolini, and G. Mauriello, “Membrane toxicity of antimicrobial compounds from essential oils,” Journal of Agricultural and Food Chemistry, vol. 55, no. 12, pp. 4863–4870, 2007.View at: Publisher Site | Google Scholar
Y. Tariku, A. Hymete, A. Hailu, and J. Rohloff, “Essential-oil composition, antileishmanial, and toxicity study of Artemisia abyssinica and Satureja punctata ssp. punctata from Ethiopia,” Chemistry and Biodiversity, vol. 7, no. 4, pp. 1009–1018, 2010.View at: Publisher Site | Google Scholar
J. S. Armstrong, “Mitochondrial membrane permeabilization: the sine qua non for cell death,” BioEssays, vol. 28, no. 3, pp. 253–260, 2006.View at: Publisher Site | Google Scholar
A. L. Silva, C. M. Adade, F. M. Shoyama et al., “In vitro leishmanicidal activity of N-dodecyl-1, 2-ethanediamine,” Biomedicine and Pharmacotherapy, vol. 66, no. 3, pp. 180–186, 2012.View at: Google Scholar
B. Purkait, A. Kumar, N. Nandi et al., “Mechanism of amphotericin B resistance in clinical isolates of Leishmania donovani,” Antimicrobial Agents and Chemotherapy, vol. 56, no. 2, pp. 1031–1141, 2012.View at: Publisher Site | Google Scholar
M. Vermeersch, R. I. Da Luz, K. Toté, J. P. Timmermans, P. Cos, and L. Maes, “In vitro susceptibilities of Leishmania donovani promastigote and amastigote stages to antileishmanial reference drugs: practical relevance of stage-specific differences,” Antimicrobial Agents and Chemotherapy, vol. 53, no. 9, pp. 3855–3859, 2009.View at: Publisher Site | Google Scholar
C. Di Giorgio, F. Delmas, V. Akhmedjanova et al., “In vitro antileishmanial activity of diphyllin isolated from Haplophyllum bucharicum,” Planta Medica, vol. 71, no. 4, pp. 366–369, 2005.View at: Publisher Site | Google Scholar
H. Martinez-Rojano, J. Mancilla-Ramirez, L. Quiñonez-Diaz, and N. Galindo-Sevilla, “Activity of hydroxyurea against Leishmania mexicana,” Antimicrobial Agents and Chemotherapy, vol. 52, no. 10, pp. 3642–3647, 2008.View at: Publisher Site | Google Scholar
Y. Tariku, A. Hymete, A. Hailu, and J. Rohloff, “Essential-oil composition, antileishmanial, and toxicity study of Artemisia abyssinica and Satureja punctata ssp. punctata from Ethiopia,” Chemistry and Biodiversity, vol. 7, no. 4, pp. 1009–1018, 2010.View at: Publisher Site | Google Scholar
A. H. Klimp, E. G. E. De Vries, G. L. Scherphof, and T. Daemen, “A potential role of macrophage activation in the treatment of cancer,” Critical Reviews in Oncology/Hematology, vol. 44, no. 2, pp. 143–161, 2002.View at: Publisher Site | Google Scholar
M. R. Piemonte and D. F. Buchi, “Analysis of IL-12, IFN-γ and TNF-α production, a5b1 integrins and actin filaments distribution in peritoneal mouse macrophages treated with homeopathic medicament,” Journal of Submicroscopic Cytology and Pathology, vol. 33, no. 1, pp. 255–263, 2002.View at: Google Scholar
F. Niedergang and P. Chavrier, “Signaling and membrane dynamics during phagocytosis: Many roads lead to the phagos(R)ome,” Current Opinion in Cell Biology, vol. 16, no. 4, pp. 422–428, 2004.View at: Publisher Site | Google Scholar
W. L. Lee, R. E. Harrison, and S. Grinstein, “Phagocytosis by neutrophils,” Microbes and Infection, vol. 5, no. 14, pp. 1299–1306, 2003.View at: Publisher Site | Google Scholar
S. J. Green, M. S. Meltzer, J. B. Hibbs, and C. A. Nacy, “Activated macrophages destroy intracellular Leishmania major amastigotes by an L-arginine-dependent killing mechanism,” Journal of Immunology, vol. 144, no. 1, pp. 278–283, 1990.View at: Google Scholar
E. Osorio, G. J. Arango, N. Jiménez et al., “Antiprotozoal and cytotoxic activities in vitro of Colombian Annonaceae,” Journal of Ethnopharmacology, vol. 111, no. 3, pp. 630–635, 2007.View at: Publisher Site | Google Scholar
S. Kamhawi, “Phlebotomine sand flies and Leishmania parasites: friends or foes?” Trends in Parasitology, vol. 22, no. 9, pp. 439–445, 2006.View at: Publisher Site | Google Scholar
P. Tripathi, V. Singh, and S. Naik, “Immune response to leishmania: paradox rather than paradigm,” FEMS Immunology and Medical Microbiology, vol. 51, no. 2, pp. 229–242, 2007.View at: Publisher Site | Google Scholar
L. V. Costa-Lotufo, G. M. A. Cunha, P. A. M. Farias et al., “The cytotoxic and embryotoxic effects of kaurenoic acid, a diterpene isolated from Copaifera langsdorffii oleo-resin,” Toxicon, vol. 40, no. 8, pp. 1231–1234, 2002.View at: Publisher Site | Google Scholar
R. M. Aparicio, M. J. García-Celma, M. Pilar Vinardell, and M. Mitjans, “In vitro studies of the hemolytic activity of microemulsions in human erythrocytes,” Journal of Pharmaceutical and Biomedical Analysis, vol. 39, no. 5, pp. 1063–1067, 2005.View at: Publisher Site | Google Scholar
L. A. Lexis, R. G. Fassett, and J. S. Coombes, “α-tocopherol and α-lipoic acid enhance the erythrocyte antioxidant defence in cyclosporine A-treated rats,” Basic and Clinical Pharmacology and Toxicology, vol. 98, no. 1, pp. 68–73, 2006.View at: Publisher Site | Google Scholar
J. R. Muñoz-Castañeda, J. Muntané, M. C. Muñoz, I. Bujalance, P. Montilla, and I. Tunez, “Estradiol and catecholestrogens protect against adriamycininduced oxidative stress in erythrocytes of ovariectomized rats,” Toxicology Letters, vol. 160, no. 3, pp. 196–203, 2006.View at: Publisher Site | Google Scholar