Carapa guianensis Aublet (Andiroba) Seed Oil: Chemical Composition and Antileishmanial Activity of Limonoid-Rich Fractions

Leishmaniasis is a complex of diseases caused by protozoa of the genus Leishmania and affects millions of people around the world. Several species of plants are used by traditional communities for the treatment of this disease, among which is Carapa guianensis Aubl. (Meliaceae), popularly known as andiroba. The objective of the present work was to conduct a chemical study of C. guianensis seed oil and its limonoid-rich fractions, with the aim of identifying its secondary metabolites, particularly the limonoids, in addition to investigating its anti-Leishmania potential. The chemical analyses of the C. guianensis seed oil and fractions were obtained by electrospray ionization mass spectrometry (ESI-MS). The cytotoxic activity was tested against peritoneal macrophages, and antileishmanial activity was evaluated against promastigotes and intracellular amastigotes of Leishmania amazonensis. All the C. guianensis seed oil samples analyzed exhibited the same pattern of fatty acids, while the limonoids 7-deacetoxy-7-hydroxygedunin, deacetyldihydrogedunin, deoxygedunin, andirobin, gedunin, 11β-hydroxygedunin, 17-glycolyldeoxygedunin, 6α-acetoxygedunin, and 6α,11β-diacetoxygedunin were identified in the limonoid-rich fractions of the oil. The C. guianensis seed oil did not exhibit antileishmanial activity, and cytotoxicity was higher than 1000 μg/mL. Three limonoid-rich oil fractions demonstrated activity against promastigotes (IC50 of 10.53±0.050, 25.3±0.057, and 56.9±0.043μg/mL) and intracellular amastigotes (IC50 of 27.31±0.091, 78.42±0.086, and 352.2±0.145 μg/mL) of L. amazonensis, as well as cytotoxicity against peritoneal macrophages (CC50 of 78.55±1.406, 139.0±1.523, and 607.7±1.217 μg/mL). The anti-Leishmania activity of the limonoid-rich fractions of C. guianensis can be attributed to the limonoids 11β-hydroxygedunin and 6α,11β-diacetoxygedunin detected in the chemical analysis.


Introduction
Leishmaniasis is characterized as zoonotic disease in which humans can be involved in a secondary or accidental manner. They are noncontagious, infectious-parasitic diseases, caused by several species of protozoa of the genus Leishmania. Although the efficacy of the drugs available for leishmaniasis depends on which clinical form is being treated and also on the specific geographical location, there remains a need for better therapeutic results for different clinical forms, as well as Leishmania-HIV coinfection [1].
Leishmaniasis is classified as neglected disease, and the treatment recommended by the World Health Organization still has many side effects, making patient adherence difficult and contributing to increased cases of resistance to several strains of Leishmania. For this reason, new therapeutic alternatives have been sought, including the use of natural products [2].

BioMed Research International
The use of medicinal plants as an alternative for leishmaniasis treatment is quite common in endemic areas. In an ethnobotanical survey carried out in the northeast of Brazil, forty-nine plant species identified for the topical treatment of skin ulcerations caused by species of the genus Leishmania were identified [3]. Herbal medicines are numerous and frequently used, according to the local population, and their practical effectiveness has been observed [4,5].
Among many medicinal plants in Brazil, Carapa guianensis Aublet (andiroba in Portuguese or crabwood in English) offers several benefits to populations resident in the Amazon, due to the medicinal properties of the oil extracted from its seeds, its use in the timber industry, and its ecological value [6]. The Carapa (Meliaceae) genus has been described as one of the most used by Amazonian communities for the treatment of leishmaniasis [7].
C. guianensis has already demonstrated its effects against protozoa of the genera Plasmodium and Trypanosoma, due to the limonoids that exist in the oil [8][9][10]. Limonoids are a structurally diverse series of tetranortriterpenoids found primarily in the Meliaceae family. Much of the research on the biological activities of limonoids has been motivated by the desire to find compounds that are useful for agricultural or medicinal applications [11].
While a study described the activity of C. guianensis nanoemulsion on L. amazonensis and L. infantum [17], the chemical compounds that acted on the parasites were not defined, creating a need for a more detailed investigation of the limonoid-rich fractions of C. guianensis seed oil in terms of their leishmanicidal activity. As a result of the medicinal properties already reported for this species, the common treatments used for leishmaniasis in the Amazon region, and the reports in literature, the present study proposed to evaluate the chemical compounds present in the oil and limonoid-rich fractions of C. guianensis seed oil and to verify which compounds are involved in their anti-Leishmania activity.

Collection
Area and Obtaining C. guianensis Seeds Oil. C. guianensis seed oil was obtained from extractive producers in Axixá, Maranhão, Brazil (latitude 02 ∘ 41 18 and 02 ∘ 56 53 south, longitude 44 ∘ 02 43 and 44 ∘ 09 51 west). In relation to the climatic characteristics of the study area, the municipal region of Axixá has an average annual temperature of 26.1 ∘ C, while annual rainfall varies from 1,600 to 2,400 mm, and relative air humidity corresponds to about 85%. The collection was carried out in the rainy season in January 2017. Botanical identification was performed out in the Laboratory of Botany and Herbarium of the Universidade Estadual do Maranhão, voucher n ∘ 4.896. The entire process of obtaining C. guianensis seed oil was carried out in an artisanal manner.
The extraction of the C. guianensis seed oil went through the steps of fruit collection, cooking, pulping, and mass treatment for the extraction of oil. After the pulp was removed from the andiroba nuts, the mass was macerated daily to obtain the oil. Five-point oil samples from the same region were collected for chemical analysis. To perform the in vitro experiments, the oils were diluted in DMSO (Sigma, USA) at 200x, the highest tested concentration, with the experiments performed with a maximum concentration of 0.5% of DMSO.

Obtaining of Limonoid-Rich Fractions from C. guianensis
Seed Oil. C. guianensis seed oil (10 g) was fractionated on a silica gel chromatographic column (Merck 60, 0.040-0.063 mm) using a gradient solvent mixture of ethyl acetate in hexane as eluent. The fractions were submitted to chemical analysis by mass spectrometry.

Electrospray Ionization Mass Spectrometry (ESI/MS).
Electrospray ionization mass spectra were obtained using a Q-TOF mass spectrometer (Bruker, Amazon SL-ion trap). To identify the fatty acid profile of C. guianensis seed oil, direct infusions were performed from the dilution of 20 L of the oils in 1 mL of toluene for negative mode (ESI-) analyses. The fractions were submitted to chemical analysis by mass spectrometry after the addition of 800 L MeOH:H 2 O solution (1:1) with 0.1% formic acid for positive mode (ESI+) and 0.1% NH 4 OH for negative mode (ESI-) analyses. The operating conditions were 3.0-4.0 kV capillary voltage, 100 ∘ C temperature source, and cone voltage of 20-40 V. The diluted samples were injected by automatic injection with a continuous flow of 10 L/min.

Parasite
Culture. The isolate of Leishmania amazonensis (MHOM/BR/76/MA-76) was maintained in the Laboratório de Imunomodulação e Protozoologia by serial passages in BALB/c mice. Periodically, parasites were isolated from the lesions and maintained in Schneider's Insect Medium (Sigma, USA) supplemented with 10% fetal bovine serum (FBS) (Gibco, USA), penicillin (100 UI/mL), and streptomycin (100 g/mL) (Sigma, USA) at 26 ∘ C in a BOD incubator. To guarantee the infectivity of the promastigote forms, only cultures with a maximum of 6 passages in vitro were used.

Animals.
Female BALB/c mice aged 4-6 weeks were obtained from the Instituto de Ciência e Tecnologia em Biomodelos from Instituto Oswaldo Cruz, Rio de Janeiro. All animal experiments were conducted according to the guidelines for experimental procedures of the Fundação Oswaldo Cruz (License L53/2016). During the experiments, all mice were kept at a controlled temperature, receiving food and water ad libitum.

Activity against Promastigote Forms of L. amazonensis.
Promastigotes of L. amazonensis (10 6 parasites/mL) from a 2-4 day old culture were placed in 96-well plates with different concentrations of oil and limonoid-rich fractions of C. guianensis seed oil (3.9 to 500 g/mL) in a final volume of 200 L per well for 72 h. They were then incubated in a BOD oven at 26 ∘ C. Wells without parasites and wells with only parasites with 1% DMSO were used as controls. The parasite viability was evaluated by the modified colorimetric method based on the tetrazolium dye MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) (Sigma, USA) [18]. MTT (5 mg/mL) was added to each well in a volume equal to 10% of the total. After 5 h, 150 L of DMSO was added to each well to dissolve the formazan crystals. The absorbance was read on a spectrophotometer at a wavelength of 570 nm. Data were normalized according to the formula: % survival = Abs. sample-Abs. blank / Abs. control-Abs. blank × 100. The results were used to calculate IC 50 (50% inhibition of parasite growth) by nonlinear regression with GraphPad Prism 6.0. Amphotericin B was used as a reference drug.

Cytotoxicity Assay.
Peritoneal murine macrophages cultured in RPMI medium were pipetted into 96-well plates at a density of 10 5 cells/mL. After 24 hours of incubation at 37 ∘ C in 5% CO 2 , the culture medium from each well was withdrawn, supplemented with different dilutions of the oil or limonoidrich fractions of C. guianensis seed oil (7.8 to 1000 g/mL), and incubated again. As a control, wells were maintained with only 1% DMSO cells or with medium only. After 24 hours, cell viability was measured by MTT colorimetric assay as previously described [19].

Activity against Intracellular Amastigotes of L. amazonensis and Selectivity Index (SI).
Peritoneal macrophages were cultured in 24-well plates (1 mL/well; 5×10 5 cells/mL) containing glass coverslips and incubated for two hours at 37 ∘ C and 5% CO 2 . Nonadherent macrophages were removed and promastigote forms of L. amazonensis (5x10 6 cells/mL) were added to each well for 24 hours at 34 ∘ C and 5% CO 2 . Noninternalized promastigotes were removed via PBS lavage and the cells were treated for 24 h with limonoid-rich fractions of C. guianensis seed oil (LF3: 5 to 20 g/mL; LF4: 6.25 to 100 g/mL; LF5: 25 to 200 g/mL) or amphotericin (0.5 to 4 g/mL). Wells without treatment were kept as controls. The coverslips with cells were then fixed with Bouin solution, stained with Giemsa (Merck, USA), and examined by light microscopy. IC 50 was calculated with the GraphPad Prism 6.0 software package from the nonlinear regression curve of the concentration log of the limonoid-rich fractions of the oil by the normalized response of the number of intracellular amastigotes in 200 cells. The percentage of infected cells was obtained from the number of infected cells divided by two. The mean number of amastigotes per cell was obtained from the number of intracellular amastigotes in 200 cells divided by the number of infected cells. The selectivity index was calculated from the ratio of CC 50 versus the IC 50 for intracellular amastigotes.

Statistical Analysis.
The numerical results were expressed as mean ± standard deviation and were organized into tables or plotted in graphs. IC 50 and CC 50 were calculated from the nonlinear regression curve from the log of the inhibitor concentration versus the normalized response. Data were statistically analyzed by the Kruskal-Wallis test and Dunn's multiple comparison test and differences were considered significant when p<0.05. All analyses were performed with GraphPad Prism 6 software (GraphPad Software Inc.).

Phytochemical Profile of C. guianensis Seed
Oils. The five samples of C. guianensis seed oil had their phytochemical profiles compared by mass spectrometry using the direct infusion technique (ESI/MS). Figure 1 shows the mass spectra obtained for the oils in the negative mode, with the presence of molecular ions m/z 255, 279, 281, 283, and 311 corresponding to the deprotonated ions [M-H] of the palmitic, linoleic, oleic, stearic, and arachidic acids, respectively [20]. The presence of the ions in m/z 511, 537, and 563 characterizes the dimeric forms [2M-H] of palmitc, margaric and oleic acids, respectively. The comparison of the spectra revealed that the composition of free and dimeric fatty acids is very similar to the 5 types of oils analyzed, being altered only, even if just a little, in the intensity of some ions, which may indicate a small variation in the concentrations of these free and dimeric fatty acids.

Activity against Promastigote and Cytotoxicity of Oil
and Limonoids-Rich Fractions of C. guianensis Seed Oil. C. guianensis seed oil did not exhibit leishmanicidal activity against L. amazonensis promastigote forms and did not present cytotoxicity even in the highest analyzed concentrations, 500 and 1000 g/mL, respectively. On the other hand, the limonoid-rich fractions LF3, LF4, and LF5 exhibited  leishmanicidal activity, with fraction LF3 and LF5 presenting the lowest and highest IC 50 value among them. The cytotoxicity of limonoid-rich fractions LF3, LF4, and LF5 demonstrated the same pattern of activity against promastigotes, with the CC 50 increasing from LF3 to LF5. The fractions LF1, LF2, and LF6 did not exhibit activity against promastigote forms or cytotoxicity at the analyzed concentrations. Amphotericin had IC 50 for promastigote and CC 50 values similar to those described in literature (Table 1).

Activity against Intracellular Amastigote and SI of Limonoid-Rich Fractions of C. guianensis Seeds Oil.
The same limonoid-rich fractions that were active against promastigotes also exhibited activity against intracellular amastigote forms, although they had higher IC 50 values than those obtained for the promastigote forms. The intracellular amastigote IC 50 values for LF3, LF4, and LF5 ranged from 27.31±0.091 to 352.2±0.180 g/mL, with fraction LF3 having the lowest result of the three. The selectivity index was also higher for LF3 than for LF4 and LF5 ( Table 1). Analysis of the parameters of infection showed that LF3 had the most consistent activity against the intracellular amastigote, inducing a reduction in the number of amastigotes per 200 cells, the percentage of infected cells, and the mean amastigotes per cell at 20 g/mL. LF4 decreased the number of amastigotes per 200 cells and the percentage of infected cells at 100 g/mL, while LF4 only decreased the mean number of amastigotes per cell at 200 g/mL (Figure 4). A reduction in intracellular amastigotes in peritoneal macrophages infected with L. amazonensis and treated with LF3, LF4, and LF5 at these concentrations was clearly observed with light microscopy ( Figure 5).

Discussion
The present study investigated the effect of oil and limonoidrich fractions of C. guianensis seed oil on promastigotes and intracellular amastigotes of L. amazonensis. The chemical constituents of the C. guianensis seed oil involved in the activity and cytotoxicity against BALB/c peritoneal macrophages were also identified. Different combinations of solvents and parts of plant may have different biological effects due to the variety and relative concentrations of compounds present in the final extract. Information on solvents, plant tissues, and methods of preparation and extraction is therefore important for standardization between studies. Unfortunately, studies that report the composition of vegetal material and associate the same with biological activity are scarce, especially in the Amazon region [24].
According to our results, C. guianensis seed oil exhibited anti-Leishmania activity higher than 500 g/mL for the promastigote form after 72 hours of treatment. A recent study with C. guianensis seed oil nanoemulsion revealed activity against promastigotes after 48 hours of treatment,  with an IC 50 of 260±29 g/mL [17]. Although the oil used to prepare the nanoemulsion is also of Amazonian origin, as in the present study, only classes of chemical compounds such as limonoids and the fatty acids palmitic oil, oleic acid, and linoleic acid have been described in oil that originated the nanoemulsion. In addition, nanoemulsion may facilitate the entry of C. guianensis seed oil compounds and favored leishmanicidal activity. It is noteworthy that C. guianensis seed oil used in our experiments did not also demonstrate in vitro cytotoxicity, a characteristic that was not evaluated in nanoemulsion.
The 6 limonoid-rich fractions obtained from the C. guianensis seed oil were analyzed for antileishmanial activity and the chemical constituents in each were identified. The LF1, LF2, and LF6 fractions had an IC 50 higher than 500 g/mL, similar to the oil. The LF3, LF4, and LF5 fractions were able to decrease the IC 50 in comparison with the results of the C. guianensis seed oil, both for the promastigote forms and the intracellular amastigotes, demonstrating the potential of limonoids of the gedunin group, especially 11hydroxygedunin 6 ,11 -diacetoxygedunin, which was more concentrated in these fractions. It was found that the activity Table 1: Activity against the promastigotes and intracellular amastigotes of Leishmania amazonensis, cytotoxicity in BALB/c peritoneal macrophages, and selectivity index of oil and limonoid-rich fractions of Carapa guianensis seed oil.

Compounds
IC 50 ( g/mL) promastigote CC 50 ( g/mL) peritoneal macrophage IC 50 ( g/mL) intracellular amastigote IS C. guianensis seed oil >500 >1000 10  of the limonoid-rich fractions against the promastigote forms was more effective than against the intracellular amastigote forms. In contrast, C. guianensis nanoemulsion oil exhibited better results against amastigote forms [17]. When treating L. amazonensis-infected macrophages with andiroba nanoemulsion for 24 hours (200-300 g/mL), it significantly reduced L. amazonensis infection levels in macrophages (54% and 96%, respectively); however the chemicals involved in this activity could not be identified. The plant C. guianensis belongs to the Meliaceae family, which is chemically distinguished by its production of limonoids, highly oxygenated tetranortriterpenoid compounds with a wide range of biological activities [11]. Compounds of this type are found in only four other families of the plant kingdom: Rutaceae, Cneoraceae, Simaroubaceae, and Ptaeroxylaceae where 1,300 limonoids have already been described, with more than 35 different carbon structures [11,[25][26][27]. C. guianensis seed oil is composed of palmitic, oleic, and linoleic acid, in addition to an unsaponifiable fraction composed mainly of limonoids, which are probably responsible for their biological activity [28].
According to the classification that covers the majority of the limonoids isolated from the Meliaceae family, these can be divided into main groups, according to the carbon skeleton pattern presented [25,29,30]. The present study was able to identify previously undescribed limonoids for C. guianensis seed oil belonging to the gedunin group, such as the 17-glycolyldeoxygedunin. The limonoids found in the oil fractions were part of the andirobin and gedunin group. These chemical compounds are probably involved in the profile of leishmanicidal activity observed in the fractions evaluated.
Limonoids of different plant species have already demonstrated antiparasitic activity [31,32]. Extracts and fractions rich in limonoids have already demonstrated activity on promastigotes and amastigotes of L amazonensis, such as Azadirachta indica A. Juss. [33], a representative of the Meliaceae family that has already had its limonoids isolated, such as gedunin and nimbolide [10,34].
The LF3 and LF4 fractions, respectively, had better leishmanicidal activity, probably due to the presence of the 11hydroxygedunin and 6 ,11 -diacetoxygedunin limonoids. A compound that may have influenced the activity of the LF3 fraction is the 6 ,11 -diacetoxygedunin, which was absent in the LF5 fraction and present in low amounts in LF4 fraction. The presence of 11 -hydroxygedunin in LF5 and the concomitant presence of 11 -hydroxygedunin and 6 ,11 -diacetoxygedunin in LF4 may be the responsible for their activities. The LF5 fraction had better activity against the promastigote form, demonstrating a significant activity reduction against the intracellular amastigote and low cytotoxicity against peritoneal macrophages. It was necessary to increase the concentration by up to 6 times in comparison with the promastigote form, revealing low permeability and diffusion through cell membrane. The limonoid structure may be related to the potential for activity and may in some situations make them more or less active. Some groups of limonoids may be two to three times more active than other limonoids [35]. Treatment with the LF3, LF4, and LF5 fractions was able to reduce infection levels in L. amazonensis cells. However, they also showed cytotoxicity, meaning caution is required with the use of limonoid-rich fractions from C. guianensis seed oil. Certain rings in the limonoid nucleus may be critical to the activity of these compounds. Alterations in ring A of the limonoid nucleus may lead to a loss of cytotoxic activity for neoplasic cells, for example, while changes in the D ring can be tolerated without any apparent loss of activity [36]. In this way, assays with the fractions in the nanoemulsion form as a carrier system are likely to improve the specificity of the chemical compounds against the L. amazonensis parasite. These results demonstrated that the limonoid-rich fractions of C. guianensis seeds oil were able to promote leishmanial activity. However, more studies should focus on the detailed characterization, quantification, and projection of a versatile and simple natural or synthetic limonoid route.

Conclusions
The analysis of the mass spectra obtained from the oil allowed the identification of fractions rich in limonoids derived from C. guianensis seed oil. Limonoid-rich fractions showed leishmanicidal activity against the promastigotes and amastigotes of L. amazonensis. The anti-Leishmania activity was assigned to the limonoids 11 -hydroxygedunin and 6 ,11 -diacetoxygedunin, identified in the active limonoidrich fractions of C. guianensis seed oil.

Data Availability
The data used to support the findings of this study are included within the article.