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Article

Antileishmanial Potential of Tropical Rainforest Plant Extracts

by
Lianet Monzote
1,
Abel Piñón
1 and
William N. Setzer
2,*
1
Parasitology Department, Institute of Tropical Medicine "Pedro Kouri", 10400 Havana, Cuba
2
Department of Chemistry, University of Alabama in Huntsville, Huntsville, AL 35899, USA
*
Author to whom correspondence should be addressed.
Medicines 2014, 1(1), 32-55; https://doi.org/10.3390/medicines1010032
Submission received: 9 October 2014 / Revised: 11 November 2014 / Accepted: 12 November 2014 / Published: 19 November 2014
(This article belongs to the Special Issue Medicinal Plants and Phytomedicines)
Versions Notes

Abstract

:
A total of 115 different plant extracts from our collection, representing 96 plant species, have been evaluated for in vitro antileishmanial activity against L. amazonensis promastigotes. In addition, the extracts were screened for cytotoxic activity against BALB/c mouse macrophages in order to assess a selectivity index. Crude extracts that showed a selectivity index (CC50 for macrophage / IC50 for promastigotes) ≥ 5 or with IC50 < 12.5 μg/mL against promastigotes, a total of 28 extracts, were further screened for anti-amastigote activity. A total of 25 extracts showed promising activity against L. amazonensis promastigotes with low cytotoxic activity. Ten of these extracts showed selectivity indices, (CC50 for macrophages / IC50 for amastigotes) greater than 10 and are considered “hits”, worthy candidates for further phytochemical exploration: Conostegia xalapensis methanol bark extract, Endiandra palmerstonii bark extract, Eugenia monteverdensis acetone bark extract, Eugenia sp. “fine leaf” acetone bark extract, Exothea paniculata chloroform bark extract, Mallotus paniculatus ethanol bark extract, Matelea pseudobarbata ethanol extract, Quercus insignis ethanol bark extract, Sassafras albidum dichloromethane bark extract, and Stemmadenia donnell-smithii acetone bark extract.

1. Introduction

Leishmaniasis is a collection of chronic infectious diseases caused by different species of parasitic Leishmania protozoa and are transmitted by sandflies (Phlebotomus spp. and Lutzomyia spp.) [1,2]. The disease, considered to be a “neglected disease”, currently affects around 12 million people, with nearly 350 million people at risk of infection around the world. The clinical forms of leishmaniasis have been classified as cutaneous, mucocutaneous, or visceral. Additionally, global climate change will likely affect the geographical range of Leishmania infections in North America [3] and Europe [4]. Indeed, Phlebotomus sandfly distribution in Europe has shifted as far north as Germany [5] while Lutzomyia sandflies are now found as far north as Ohio [6], Maryland, and Delaware [7].
Current proven chemotherapy includes the pentavalent antimonials meglumine antimoniate (glucantime) and sodium stibogluconate (pentostam) [8], miltefosine, amphotericin B, or pentamidine [9]. However, all of these treatments are associated with undesirable side effects, induction of parasite resistance, and relatively high cost in developing countries. Due to the limitations of current chemotherapeutic regimes, along with the absence of suitable vaccines, there is a persistent need for alternative and readily available chemotherapies for treatment of leishmaniasis.
Natural products have overwhelmingly contributed to the pharmacopeia of the world and continue to provide new and effective anti-infective agents [10,11,12]. Recently, several reviews have appeared demonstrating the potential of higher plants and phytochemicals as treatment options for leishmaniasis [13,14,15,16,17,18,19]. In this current work, we present the in vitro screening of 115 different extracts from higher plants (96 species) collected from rainforests of north Queensland, Australia, Abaco Island, Bahamas, Costa Rica, southeastern U.S., and Zimbabwe, against Leishmania amazonensis.

2. Experimental Section

2.1. Plant Materials and Reference Drugs

Plant materials from 96 species of plants (Table 1) were collected and extracted as previously described [20,21,22]. The crude extracts were dissolved in dimethylsulfoxide (DMSO) at 20 mg/mL. The reference drugs amphotericin B (Imefa, Havana, Cuba) and pentamidine (Richet, Buenos Aires, Argentina) were also used.

2.2. Parasite Cultures

L. amazonensis (MHOM/77BR/LTB0016) was kindly provided by the Department of Immunology, Oswaldo Cruz Foundation (FIOCRUZ), Brazil. Parasites were routinely isolated from mouse lesions and maintained as promastigotes at 26 °C in Schneider’s medium (SIGMA, St. Louis, MO, USA) containing 10% heat-inactivated fetal bovine serum (HFBS) (SIGMA, St. Louis, MO, USA), 100 μg of streptomycin/mL, and 100 U penicillin/mL. The parasites were not used after the tenth passage.

2.3. Anti-Promastigote Assay

Schneider’s medium (50 µL) was distributed in each well of a 96-well plate. In the first well of each lane, 48 µL of medium and 2 µL of tested extracts were added. The extract solutions were serially diluted (1:1) down each lane of the 96-well plate with medium (removing 50 μL of test solution and diluting with 50 μL medium). Then, 50 µL of exponentially growing cells at 2 × 105 promastigotes/mL were added to each well to give final concentrations ranging from 12.5 to 200 μg/mL. After an incubation of 72 hours at 26 °C, 20 µL of 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide (MTT) (SIGMA, St. Louis, MO, USA) was added. MTT solutions were prepared at 5 mg/mL in PBS, filtered and sterilized just prior to use. After incubation for an additional 4 h, the formazan crystals were dissolved by addition of 100 μL of DMSO. The optical density was determined using a spectrophotometer (Sirio S Reader, 2.4-0, Italy), at a test wavelength of 560 nm and a reference wavelength of 630 nm [23,24] and median inhibitory concentrations (IC50) were calculated.

2.4. Cytotoxicity Assay

The cytotoxic median concentration (CC50) of the extracts was determined on mouse peritoneal macrophages, which are the host cells for the amastigote form of the parasite, aiming to investigate macrophage toxicity caused by the extracts [23]. Resident macrophages were collected from peritoneal cavities of normal BALB/c mice in ice-cold RPMI 1640 medium (SIGMA, St. Louis, MO, USA) supplemented with antibiotics, and seeded at 30,000 cells/well. The cells were incubated for 2 h at 37 °C in 5% CO2. Non-adherent cells were removed by washing with phosphate-buffered saline (PBS), and then 2 μL of extract/DMSO solutions were added to 98 μL medium with 10% HFBS and antibiotics. Then, five two-fold dilutions were carried out taking 50 µL each time and adding an additional 50 µL of medium to give test concentrations of the extracts ranging from 12.5 to 200 μg/mL. The cells were incubated with the test solutions for 72 h. Macrophages treated with DMSO were included as controls. The cytotoxicity was determined using the colorimetric assay with MTT as previously described; 15 μL MTT solution added to each well. After incubation for an additional 4 h the formazan crystals were dissolved by addition of 100 μL of DMSO and the optical density was determined.

2.5. Selectivity Index

The selectivity index (SI) ratio (CC50 for macrophage / IC50 for promastigotes) was used to compare the toxicity of the extracts for murine macrophages and the activity against Leishmania promastigotes. Extracts with a SI ≥ 5 or with IC50 < 12.5 μg/mL against promastigotes were selected for further anti-amastigote determination.

2.6. Anti-Amastigote Assay

The peritoneal macrophages were harvested and plated at 106 cells/mL in 24-well Lab-Tek plates (Costar®, Washington, DC, USA) and incubated at 37 °C under an atmosphere of 5% CO2 for 2 h. Non-adherent cells were removed by washing with PBS. Stationary-phase of L. amazonensis promastigotes were added at a 4:1 parasite/macrophage ratio and the cultures were incubated for an additional 4 h. The cell monolayers were washed three times with PBS to remove free parasites. Then, 1990 μL of RPMI completed medium and 10 μL of the different extracts dissolved in DMSO were added to each well. Four two-fold dilutions were carried out taking 1000 µL each time to give test concentrations of the extracts ranging from 12.5 to 100 μg/mL, in duplicate cultures, incubating for an additional 48 h [25]. The parasites were then fixed in absolute methanol, stained with Giemsa, and examined under light microscopy. The number of intracellular amastigotes was determined by counting the amastigotes in 25 macrophages per sample, and the results were expressed as percent of reduction of the infection rate in comparison to that of the controls. The infection rates were obtained by multiplying the percentage of infected macrophages by the number of amastigotes per infected macrophages [26] and the IC50 value was determined. A second SI was calculated: CC50 for macrophages / IC50 for intracellular amastigotes (see Table 1).

2.7. Statistical Analyses

The IC50 of the tested extracts and reference drugs against L. amazonensis promastigotes and amastigotes and the CC50 on peritoneal macrophages from BALB/c mice were obtained from dose-response curves fit to the data by means of the linear equation model using the STATISTICA for Windows Program (Release 4.5, StatSoft, Inc., Tulsa, OK, USA, 1993). The evaluations were performed in triplicate and the results are expressed as means ± standard deviations.

3. Results and Discussion

A total of 115 different plant extracts from our collection, representing 96 plant species, have been screened for in vitro antileishmanial activity against L. amazonensis. In addition, the extracts were screened for cytotoxic activity against BALB/c mouse macrophages in order to assess a selectivity index. The antileishmanial and cytotoxic activities are summarized in Table 1. A total of 18 extracts showed activity against L. amazonensis promastigotes with IC50 values < 12.5 μg/mL. An additional 25 extracts showed antileishmanial activities ranging from IC50 17.4 μg/mL to 63.4 μg/mL. Of the plant extracts that were active against L. amazonensis promastigotes, 18 were non-toxic to BALB/c mouse macrophages (CC50 > 200 μg/mL). In addition, 10 others were only slightly toxic to the mouse macrophages, showing selectivity indices (CC50 for macrophage / IC50 for promastigotes) ≥ 5, and were considered for further testing against L. amazonensis amastigotes. Additional screening against L. amazonensis amastigotes revealed ten extracts with IC50 ≤ 21.0 μg/mL against the parasites and non-toxic to the mouse macrophages (CC50 > 200 μg/mL). That is, the selectivity indices (CC50 for macrophage / IC50 for amastigotes) for these extracts were all > 10. It is generally considered that for plant extracts showing SI > 10, the antiprotozoal activity is not due to general cytotoxicity and are promising extracts for further phytochemical analysis [27,28,29].
The methanol bark extract of Conostegia xalapensis (Melastomataceae) showed good leishmanicidal activity (IC50 < 12.5 μg/mL against both promastigotes and amastigotes), but was neither cytotoxic to BALB/c mouse macrophages nor human tumor cells [21]. Thus, this plant extract shows excellent selectivity and apparently low acute toxicity. To our knowledge, no phytochemical work has been carried out on this plant; it is not known what compounds may be responsible for the antileishmanial activity. Although the dichloromethane bark extract of Quercus insignis (Fagaceae) was inactive, the ethanol bark extract exhibited notable antileishmanial activity against L. amazonensis promastigotes and amastigotes (IC50 = 17.8 and 21.0 μg/mL, respectively). Q. insignis ethanol bark extract showed no in vitro toxicity to mouse macrophage cells or human tumor cells [21]. The phytochemistry of this tree has not been examined.
Interestingly, both the chloroform and methanol bark extracts of Exothea paniculata (Sapindaceae) from Monteverde, Costa Rica, showed good activity against L. amazonensis with little cytotoxicity on BALB/c mouse macrophages, but neither the acetone bark extract nor the methanol bark extract of E. paniculata from Abaco Island, Bahamas was leishmanicidal. The chloroform extract of E. paniculata from Monteverde showed the most promise with IC50 < 12.5 μg/mL against both the promastigote and amastigote forms of L. amazonensis, but non-toxic to macrophage cells. There have been no reported studies on the phytochemical composition of E. paniculata.
An ethanol extract of the aerial parts of Matelea pseudobarbata (Apocynaceae) was shown to be non-cytotoxic to mouse macrophages, but notably leishmanicidal against L. amazonensis promastigotes and amastigotes (IC50 < 12.5 μg/mL). Additionally, this extract was non-cytotoxic to Hep-G2, MCF-7, MDA-MB-231, and PC-3 tumor cell lines [21]. Apparently little else is known about this vine. The acetone bark extract of Stemmadenia donnell-smithii (Apocynaceae) was also antileishmanial (IC50 < 12.5 μg/mL) and non-toxic to the mouse macrophage. S. donnell-smithii is cytotoxic to human tumor cells, however [21]. A decoction of S. donnell-smithii bark is used as a traditional medicine in Guatemala to treat malaria [30]. Several indole alkaloids have been isolated from S. donnell-smithii, including (+)-quebrachamine, voacangine, isovoacangine, voacamine, tabernanthine, ibogamine, and stemmadine [31] and may be responsible for the leishmanicidal activity of S. donnell-smithii. An extract of Tabernaemontana catharinensis, rich in voacangine (53%) has shown antileishmanial activity against L. amazonensis [32]. Voacamine has shown antiplasmodial activity [33] and a molecular docking study revealed voacamine to dock strongly to Leishmania N-myristoyl transferase as a molecular target [34].
Two different species of Eugenia (Myrtaceae) from Monteverde, Costa Rica, showed good antileishmanial activity. Thus, the acetone bark extracts of E. monteverdensis and Eugenia sp. “fine leaf” were active against L. amazonensis promastigotes (IC50 = 23.9 and < 12.5 μg/mL, respectively), while neither was cytotoxic to BALB/c mouse macrophages (CC50 > 200 μg/mL). Furthermore, E. monteverdensis acetone bark extract was inactive against MCF-7 and Hs 578T human breast tumor cells (unpublished results from this laboratory), and Eugenia “fine leaf” acetone bark extracts was inactive on several human tumor cell lines (Hep-G2 MDA-MB-231, Hs 578T, and 5637) [21]. Consistent with these results, the ethanol bark extracts of E. austin-smithii and a Eugenia sp. from the Alberto Manuel Brenes Biological Reserve, Costa Rica, showed antileishmanial activity [35]. The acetone bark extract of E. austin-smithii has been found to be cytotoxic to Hs 578T, 5637, and BHK cells [21]. Both the hexane and methanol fruit extracts of E. umbelliflora were leishmanicidal to L. amazonensis and L. braziliensis promastigotes [36]. E. uniflora has been screened for antileishmanial activity. The ethanol leaf extract was marginally active against L. braziliensis promastigotes (65% inhibition at 100 μg/mL) [37], but inactive against L. amazonensis or L. chagasi promastigotes [38]. The leaf essential oil of E. uniflora showed good antileishmanial activity against both promastigotes and amastigotes of L. amazonensis (IC50 = 3.04 and 1.92 μg/mL, respectively) [39], but E. uniflora bark essential oil was inactive against L. donovani promastigotes [40].
The bark of Endiandra palmerstonii (Lauraceae) from far north Queensland was extracted using a chloroform/ethanol mixed solvent [22]. The crude extract showed promising antileishmanial activity (IC50 < 12.5 μg/mL on promastigotes and 18.7 μg/mL on amastigotes) and no cytotoxicity on BALB/c mouse macrophages (CC50 > 200 μg/mL). The extract was also non-cytotoxic to Hep-G2 human liver tumor cells [22]. There have been no phytochemical investigations reported for this tree species.
Two different bark extracts of Mallotus (Euphorbiaceae) from far north Queensland, Australia, M. mollisimus (CHCl3/EtOH mixed solvent bark extract) and M. paniculatus (EtOH bark extract), showed promising antileishmanial activity coupled with selectivity. M. paniculatus ethanol bark extract was the more promising with IC50 < 12.5 μg/mL on both promastigotes and amastigotes, and no cytotoxicity to macrophage cells. Previous screening for cytotoxicity against a panel of human tumor cell lines revealed M. paniculatus ethanol bark extract to be non-cytotoxic to Hep-G2, MDA-MB-231, Hs 578T, and 5673 cells [22]. Thus, this plant extract is apparently non-toxic to mammalian cells while remarkably toxic to the parasite. The triterpenoid 29-nor-3,22-hopanedione has been isolated from the stem bark of M. paniculatus, but no bioactivities were reported for this compound [41]. M. oppositifolius leaves are used in traditional medicine in the Ivory Coast to treat intestinal helminths, but the leaf extracts were inactive against L. donovani promastigotes [42].
Both the dichloromethane bark extract and the ethyl acetate bark extract of Sassafras albidum (Lauraceae), collected from north Alabama, showed notable antileishmanial activities against promastigotes (IC50 < 12.5 and 19.4 μg/mL, respectively), and the dichloromethane extract had a median inhibitory concentration of 20.5 μg/mL against amastigotes of L. amazonensis. In addition, the extracts were non-toxic to macrophage cells. Although the essential oil compositions of S. albidum have been investigated [43,44], apparently the non-volatile bark components have not. S. albidum bark oil is rich in α-pinene, β-pinene, 1,8-cineole, and α-terpineol [44]. Many essential oils and components have shown antiprotozoal activities [45], including α-pinene [46] and α-terpineol [47].
The acetone bark extract of Acacia choriophylla (Fabaceae) from Abaco Island, Bahamas, showed a selectivity index >3. The dichloromethane bark extract of the same tree showed similar activity. Both of these crude extracts had been previously screened for in vitro cytotoxic activity against 5637 bladder tumor and Hs 578T breast tumor cells (unpublished results from our laboratory) and were non-cytotoxic, so neither seems to be acutely toxic to human cells. The phytochemistry of this tree has not been examined.
The acetone bark extract of Tabebuia bahamensis (Bignoniaceae) was active against L. amazonensis promastigotes and amastigotes with IC50 values of 17.4 and 23.8 μg/mL, respectively. This bark extract was screened for cytotoxic activity against a panel of human tumor cell lines, including SK-Mel-38 (melanoma), Hep-G2 (hepatocellular carcinoma), MDA-MB-231 (mammary adenocarcinoma), and 5637 (bladder carcinoma), and was found to be inactive against all cell lines screened (unpublished results from our laboratory). T. umbellata is used traditionally in Bahia, Brazil to treat cutaneous leishmaniasis (L. braziliensis) infections [48]. Likewise, T. serratifolia bark is used in Peru to treat leishmaniasis, and T. serratifolia chloroform bark extract did show in vitro activity against L. infantum promastigotes [49]. Naphthoquinones from T. avellanedae [50] and T. serratifolia [49] have shown antileishmanial activity against L. major and L. infantum, respectively. Thus, the antileishmanial activity of T. bahamensis bark extract may also be due to naphthoquinones.
The bark resin from Agathis atropurpurea (Araucariaceae) exhibited good antileishmanial activity (IC50 < 12.5 and 19.3 μg/mL, respectively against L. amazonensis promastigotes and amastigotes) along with weak cytotoxic activity against BALB/c mouse macrophage cells. This resin had shown cytotoxic activity against SK-MEL-28 human melanoma cells, but was inactive against the Hep-G2, MDA-MB-231, Hs 578T, MCF-7, and PC-3 cell lines [22]. The resin is rich in diterpenoids, including agatholic acid [51].
Four species of Melicope (Rutaceae) from north Queensland, Australia, were screened for antileishmanial activity. M. broadbentiana and M. vitiflora bark extracts were inactive, but M. jonesii chloroform bark extract and M. rubra ethanol bark extract showed promising activity against L. amazonensis promastigotes. Further screening revealed no selectivity for L. amazonensis amastigotes over mouse macrophages, however. Both M. jonesii and M. rubra bark extracts showed in vitro cytotoxicity to human tumor cells [22]. Although the leaf essential oils of M. jonesii and M. rubra have been investigated [52], there are no reports on the bark phytochemistry. The chloroform bark extract of Polyosma alangiacea (Escalloniaceae) from far north Queensland, Australia was somewhat leishmanicidal (IC50 = 60.9 μg/mL) against promastigotes, but non-cytotoxic to mammalian cells, either mouse macrophages or human tumor cells [22]. The phytochemistry of P. alangiacea bark has not been reported.
The chloroform bark extract of an, as yet, undescribed species of Myrcianthes “black fruit” (Myrtaceae) from Monteverde, Costa Rica, does show promise with leishmanicidal IC50 of < 12.5 and 18.3 μg/mL, respectively, against promastigotes and amastigotes of L. amazonensis. The aerial parts of the liana Ruyschia phylladenia (Marcgraviaceae), collected from Monteverde, Costa Rica, were extracted with dichloromethane. The extract inhibited L. amazonensis promastigotes (IC50 < 12.5 μg/mL) and amastigotes (IC50 = 22.0 μg/mL). Although this extract was cytotoxic to human tumor cells [21] no cytotoxicity on BALB/c mouse macrophages was observed.
The dichloromethane bark extract of Cupania glabra (Sapindaceae), collected from Monteverde, Costa Rica, had shown remarkable in vitro cytotoxic activity against several human tumor cell lines, which was attributed to the fatty alcohol glycoside cupanioside [53]. The ethanol bark extract of this tree, on the other hand, was devoid of cytotoxic activity [21], and in this work, the ethanol extract was leishmanicidal (IC50 = 17.6 and 27.0 μg/mL on promastigotes and amastigotes, respectively) and non-toxic to BALB/c mouse macrophages. Consistent with these results, the crude methanol bark extract of C. dentata from the Yucatan peninsula of Mexico showed in vitro antileishmanial activity against L. mexicana promastigotes (IC50 = 13 μg/mL) [54]. Interestingly, the crude hexane bark extract of C. cinerea showed in vitro leishmanicidal activity against L. donovani axenic amastigotes [29], possibly attributable to the diterpene glycoside cupacinoside [55]. Similarly, the hexane leaf extract of C. vernalis was active against L. donovani promastigotes [56]. Extracts of C. macrophylla from Costa Rica, on the other hand, were inactive against Leishmania promastigotes [35].
The crude ethanol bark extract of Diospyros digyna (Ebenaceae) showed in vitro antileishmanial activity against L. amazonensis promastigotes and amastigotes with IC50 = 25.0 and 29.2 μg/mL, respectively. Additionally, D. digyna extract was not cytotoxic to either BALB/c mouse macrophages or MCF-7, UACC-257, MDA-MB-231, or M-14 human tumor cells (unpublished results from this laboratory). Diospyrin, a bis-naphthoquinone isolated from D. montana, has shown in vitro activity against L. donovani promastigotes [57] and L. major promastigotes [58]. This compound has been shown to be a topoisomerase I inhibitor of L. donovani [59] and initiates apoptosis in L. donovani [60]. Antileishmanial bis-naphthoquinones have also been isolated and characterized from D. assimilis chloroform root extract from India (in vitro assay against L. donovani axenic amastigotes) [61] and D. burmanica methanol wood extract from Myanmar (in-vitro assay against L. major promastigotes) [62].
The crude ethanol bark extract of Erythrina lanceolata (Fabaceae) showed promising antileishmanial activity (IC50 < 12.5 μg/mL against promastigotes) without cytotoxic activity against BALB/c mouse macrophages or a number of human tumor cell lines (Hep-G2, MDA-MB-231, MCF-7, Hs 578T, PC-3, SK-MEL-28), or baby hamster kidney (BHK) cells [21]. In contrast, the crude dichloromethane bark extract was not leishmanicidal but cytotoxic to all cells tested [21]. The hydroalcoholic extract of E. speciosa from Brazil was tested for antileishmanial activity against both L. amazonensis promastigotes and amastigotes, but was inactive [63]. Likewise, the methanol wood extract of E. suberosa from Myanmar was inactive against L. major promastigotes [64], and the ethanol bark extract of E. variegata from New Caledonia was inactive against L. donovani promastigotes [65].
The acetone bark extract of Inga sierrae (Fabaceae) from Monteverde, Costa Rica, showed leishmanicidal activity (IC50 = 25.7 μg/mL) with reduced cytotoxic activity (CC50 = 130.6 μg/mL). Several Inga species are used in traditional medicine to treat leishmaniasis. I. edulis leaves are used by the Kichwa in Ecuador [29] while I. edulis bark is used by the Wayãpi people of French Guiana [66] to treat leishmaniasis. The Chachi people of Ecuador also use I. oerstediana leaves and bark [29] and I. bourgoni bark is also used by the Wayãpi [66] to treat leishmaniasis.
The methanol bark extract from Pappea capensis (Sapindaceae) collected in Matabeleland, Zimbabwe, also showed promising antileishmanial activity (IC50 < 12.5 μg/mL). Rhynchosia resinosa (Fabaceae) methanol root extract, from Matabeleland, Zimbabwe, did not exhibit cytotoxic activity toward BALB/c mouse macrophages, but was active against L. amazonensis amastigotes with an IC50 of 27.7 μg/mL. The methanol bark extract of R. edulis from Monteverde, Costa Rica was shown to be inactive against L. amazonensis (this work), while the methanol extract of the whole plant of R. reniformis from Karak, Pakistan was also non-leishmanicidal [67].
Both the dichloromethane and ethanol extracts of the aerial parts of Conradina canescens (Lamiaceae) from north Florida showed promising antileishmanial activity. The dichloromethane extract did show some cytotoxicity on BALB/c mouse macrophages (CC50 = 63.7 μg/mL) as well as MCF-7 and MDA-MB-231 human breast tumor cells (unpublished results from our laboratory). The essential oil composition of C. canescens has been reported [68], but there have been no reports regarding the non-volatile components. The major components in the essential oil were 1,8-cineole, camphor, α-pinene, p-cymene, cis-pinocamphone, myrtenal, myrtenol, verbenone, and myrtenyl acetate. 1,8-Cineole is inactive against Leishmania spp. [69] but α-pinene is active [46]. Myrtenal, camphor, and verbenone have shown antitrypanosomal activity [70].
Table
Table 1. Antileishmanial (Leishmanial amazonensis promastigotes) and cytotoxic screening of tropical rainforest plant extracts.
Table 1. Antileishmanial (Leishmanial amazonensis promastigotes) and cytotoxic screening of tropical rainforest plant extracts.
Plant NameOriginExtractRef.L. amazonensis promastigotesIC50 (μg/mL)BALB/c Mouse macrophageCC50 (μg/mL)Selectivity Index (CC50/IC50)L. amazonensis amastigotes IC50 (μg/mL)Selectivity Index (CC50/IC50)
Acacia choriophylla Benth.Abaco aacetone barkb63.4 ± 4.9> 200> 361.5 ± 4.6> 3
Acacia choriophylla Benth.AbacoCH2Cl2 barkb74.1 ± 2.4197.6 ± 1.43--
Acnistus arborescens (L.) Schltdl.Monteverde cacetone bark[21]> 20036.8 ± 3.4---
Acronychia acronychioides (F. Muell.) T. HartleyPaluma dEtOH bark[20]> 20047.3 ± 7.6---
Agathis atropurpurea B. HylandF. No. Qld. ebark resin[22]< 12.5118.4 ± 0.8> 919.3 ± 2.56
Albizia adinocephala (Donn. Sm.) Britton & Rose ex RecordMonteverdeacetone barkb> 200> 200---
Alchornea latifolia Sw.MonteverdeEtOH bark[21]> 200> 200---
Alloxylon flammeum P. Westpm & CrispF. No. Qld.CHCl3/EtOH bark[22]> 20055.5 ± 9.1---
Alphitonia petriei Braid & C. WhitePalumaEtOH bark[20]> 200> 200---
Alzatea verticillata Ruiz & Pav.MonteverdeEtOH bark[21]> 200> 200---
Apodytes brachystylis F. Muell.PalumaEtOH bark[20]< 12.5< 12.51--
Archidendron vaillantii (F. Muell.) F. Muell.PalumaEtOH bark[20]92.0 ± 8.1< 12.50--
Ardisia compressa KunthMonteverdeEtOH bark[21]> 200146.2 ± 6.3--
Ardisia palmana Donn. Sm.Monteverdeacetone bark[21]143.7 ± 11.196.6 ± 2.6---
Ardisia revoluta KunthMonteverdeacetone bark[21]> 20070.5 ± 6.2---
Ardisia revoluta KunthMonteverdeCH2Cl2 bark[21]44.0 ± 2.949.2 ± 1.51--
Ardisia solomonii LundellMonteverdeCH2Cl2 barkb> 20026.3 ± 2.3---
Ardisia solomonii LundellMonteverdeCH2Cl2 barkb28.1 ± 2.0< 12.5---
Balanops australiana F. Muell.PalumaEtOH bark[20]49.0 ± 4.3< 12.50--
Beilschmiedia sp. “choncho blanco”MonteverdeEtOH bark[21]> 200> 200---
Bocconia frutescens L.MonteverdeMeOH bark[21]> 200168.0 ± 4.5---
Bravaisia integerrima (Spreng.) StandleyMonteverdeCHCl3 bark[21]76.6 ± 0.521.6 ± 5.00--
Bridelia mollis Hutch.MatabelelandfMeOH barkb> 200> 200---
Byrsonima crassifolia (L.) KunthMonteverdeacetone barkb> 20066.2 ± 0.8---
Cardwellia sublimis F. Muell.PalumaEtOH bark[20]> 200> 200---
Cavendishia bracteata (Ruiz & Pav. ex J. St.-Hil.) HoeroldMonteverdeacetone barkb38.4 ± 6.976.0 ± 5.62--
Cestrum megalophyllum DunalMonteverdeEtOH bark[21]> 20028.6 ± 1.1---
Chionanthus panamensis (Standl.) StearnMonteverdeacetone bark[21]> 20078.2 ± 6.4---
Conostegia xalapensis (Bonpl.) D. DonMonteverdeMeOH bark[21]< 12.5> 200> 16< 12.5> 16
Conradina canescens A. GrayFloridagCH2Cl2 aerial partsb< 12.563.7 ± 5.0> 520.5 ± 5.03
Conradina canescens A. GrayFloridaEtOH aerial partsb33.6 ± 5.9202.8 ± 6.8630.6 ± 3.97
Cryptocarya corrugata C. White & FrancisPalumaEtOH bark[20]> 20088.7 ± 5.3---
Cryptocarya densiflora BlumePalumaEtOH bark[20]> 200> 200---
Cupania glabra Sw.MonteverdeEtOH bark[21]17.6 ± 5.3> 200> 1127.0 ± 4.5> 7
Daphandra repandula (F. Muell.) F. Muell.F. No. Qld.CHCl3/EtOH bark[22]> 200< 12.5---
Dendropanax gonatopus (Donn. Sm.) A.C. Sm.MonteverdeMeOH leaf[23]> 20072.4 ± 7.2---
Diospyros digyna Jacq.MonteverdeEtOH barkb25.0 ± 2.9152.9 ± 8.8629.2 ± 1.25
Diospyrus sp. “fluted trunk”MonteverdeEtOH barkb> 20057.4 ± 3.5---
Drymonia conchocalyx Hanst.MonteverdeEtOH aerial parts[21]> 200111.1---
Drypetes lasiogyna F. Muell.PalumaEtOH bark[20]47.6 ± 2.2125.8 ± 8.23--
Elaeodendron matabelicum Loes.MatabelelandMeOH barkb> 200125.7 ± 9.0---
Endiandra palmerstonii (F.M. Bailey) C.T. White & FrancisF. No. Qld.CHCl3/EtOH bark[22]< 12.5> 200> 1618.7 ± 3.7> 11
Erythrina lanceolata Standl.MonteverdeCH2Cl2 bark[21]> 2006.9 ± 1.2---
Erythrina lanceolata Standl.MonteverdeEtOH bark[21]< 12.5129.5 ± 3.4> 1022.3 ± 3.46
Eugenia monteverdensis BarrieMonteverdeacetone barkb23.9 ± 2.8> 200> 820.7 ± 4.5> 10
Eugenia sp. “fine leaf”Monteverdeacetone bark[21]< 12.5> 200> 16< 12.5> 16
Euphorbia elata BrandegeeMonteverdeMeOH bark[21]> 20048.3 ± 3.6---
Euphorbia elata BrandegeeMonteverdeacetone bark[21]> 20021.6 ± 2.2---
Exothea paniculata (Juss.) Radlk.Abacoacetone barkb> 20049.8 ± 1.8---
Exothea paniculata (Juss.) Radlk.AbacoMeOH barkb> 200> 200---
Exothea paniculata (Juss.) Radlk.MonteverdeCHCl3 barkb< 12.5> 200> 16< 12.5> 16
Exothea paniculata (Juss.) Radlk.MonteverdeMeOH barkb33.2 ± 3.6159.1 ± 7.5532.3 ± 7.55
Forestiera carthaginense Donn. Sm.MonteverdeCHCl3/EtOH bark[21]> 200> 200---
Inga sierrae Britton & KillipMonteverdeacetone bark[21]25.7 ± 1.9130.6 ± 2.5529.9 ± 5.54
Lonchocarpus oliganthus F.J. HermMonteverdeacetone bark[21]20.6 ± 2.629.8 ± 4.81--
Lonchocarpus orotinus PittierMonteverdeacetone barkb> 200176.8 ± 5.9---
Macaranga subdentata Benth.PalumaCHCl3/EtOH leaf[20]> 200> 200---
Machaerium biovulatum MicheliMonteverdeacetone bark[21]> 200120.8 ± 4.5---
Mallotus mollissimus (Geiseler) Airy ShawF. No. Qld.CHCl3/EtOH bark[22]20.9 ± 0.3> 200> 1025.2 ± 1.0> 8
Mallotus paniculatus (Lam.) Muell. Arg.F. No. Qld.EtOH bark[22]< 12.5> 200> 16< 12.5> 16
Matelea pseudobarbata (Pittier) WoodsonMonteverdeEtOH aerial parts[21]< 12.5> 200> 16< 12.5> 16
Melicope broadbentiana BaileyPalumaCHCl3/EtOH bark[20]23.7 ± 4.379.7 ± 0.33--
Melicope jonesii T.G. HartleyF. No. Qld.CHCl3 bark[22]< 12.535.5 ± 8.6> 333.4 ± 5.01
Melicope rubra (Lauterb. & K. Schum) T.G. HartleyF. No. Qld.EtOH bark[22]< 12.529.6 ± 0.4> 222.0 ± 2.01
Melicope vitiflora (F. Muell.) T. HartleyPalumaEtOH bark[20]> 20062.6 ± 3.6---
Mucuna urens (L.) DC.MonteverdeMeOH bark[21]> 20063.6 ± 4.2---
Myrcianthes sp. “black fruit”MonteverdeCHCl3 bark[21]< 12.548.8 ± 2.0> 418.3 ± 4.43
Neea psychotrioides Donn. Sm.MonteverdeCHCl3 bark[21]> 200> 200---
Neolitsea dealbata (R. Br.) Merr.PalumaEtOH bark[20]> 200> 200---
Ocotea sp. “los llanos”Monteverdeacetone barkb> 200> 200---
Octea meziana C.K. AllenMonteverdeacetone bark[21]> 200132.1 ± 6.8---
Ormosia cruenta RuddMonteverdeacetone bark[21]> 200198.5 ± 2.1---
Pappea capensis Eckl. & Zeyh.MatabelelandMeOH barkb< 12.555.6 ± 7.4> 4< 12.5> 4
Phoradendron cf. Flavens
(Sw) Griseb.		MonteverdeCH2Cl2/EtOH aerial parts[21]> 200> 200---
Phoradendron robustissimum EichlerMonteverdeCH2Cl2/EtOH aerial parts[21]44.1 ± 4.9166.44--
Phoradendron robustissimum EichlerMonteverdeCH2Cl2/EtOH flowers[21]> 200> 200---
Piper aequale VahlMonteverdeacetone leaf[21]81.1 ± 1.435.9 ± 7.60--
Polyosma alangiacea F. muell.F. No. Qld.CHCl3 bark[22]60.9 ± 8.9> 200> 346.2 ± 3.7> 4
Psychotria parvifolia Benth.Monteverdeacetone barkb> 200> 200---
Quercus insignis M. Martens & GaleottiMonteverdeCH2Cl2 bark[21]> 200161.4 ± 6.3---
Quercus insignis M. Martens & GaleottiMonteverdeEtOH bark[21]17.8 ± 2.3> 200> 1121.0 ± 3.0> 10
Rhynchosia edulis Griseb.MonteverdeMeOH bark[21]> 200144.9 ± 1.2---
Rhynchosia resinosa Hochst. ex BakerMatabelelandMeOH rootb54.1 ± 4.2> 200> 427.7 ± 5.4> 7
Ruyschia phylladenia SandwithMonteverdeCH2Cl2 aerial parts[21]< 12.5> 200> 1622.0 ± 5.9> 9
Salacia petenesis LundellMonteverdeEtOH bark[21]> 20035.4 ± 0.8---
Salacia sp. “liana”MonteverdeCH2Cl2 bark[21]> 20079.2 ± 3.8---
Salacia sp. “liana”MonteverdeMeOH bark[21]>20091.5 ± 0.3---
Sapium glandulosum (L.) MorongMonteverdeacetone bark[21]> 200> 200---
Sapium glandulosum (L.) MorongMonteverdeCH2Cl2 bark[21]> 20073.3 ± 5.6---
Sapium glandulosum (L.) MorongMonteverdeEtOH bark[21]> 200> 200---
Sassafras albidum (Nutt.) NeesAlabamahCH2Cl2 barkb< 12.5> 200> 1620.5 ± 0.6> 10
Sassafras albidum (Nutt.) NeesAlabamaEtOAc barkb19.4 ± 3.8> 200> 10
Saurauia montana SeemMonteverdeacetone leaf[21]> 200> 200---
Sinclaria polyantha (Klatt) Rydb.MonteverdeCHCl3/EtOH leaf[21]> 200> 200---
Sorocea trophoides W.C. BurgerMonteverdeMeOH bark[21]> 200> 200---
Stauranthus perforatus Leibm.MonteverdeEtOH bark[21]> 200> 200---
Stemmadenia donnell-smithii (Rose) WoodsonMonteverdeacetone bark[21]< 12.5> 200> 16< 12.5> 16
Stenocarpus sinuatus (Loudon) Endl.F. No. Qld.CHCl3/EtOH bark[22]39.0 ± 1.036.8 ± 0.31--
Stockwellia quadrifida .J. Carr, S.G.M. Carr, & B. HylandF. No. Qld.EtOH bark[22]> 200> 200---
Struthanthus cf. oerstedii (Oliv.) Standl.MonteverdeCHCl3/EtOH leaf[21]> 200> 200---
Styphnolobium monteviridis M. Sousa & RuddMonteverdeMeOH leaf[21]> 200194.8 ± 7.3---
Styphnolobium monteviridis M. Sousa & RuddMonteverdeMeOH bark[21]> 200105.3 ± 7.4---
Symplocos limoncillo Humb. & Bonpl.MonteverdeEtOH bark[21]> 200> 200---
Syncarpia glomulifera (Smith) NiedenzuPalumaCHCl3 bark[20]> 200> 200---
Syncarpia glomulifera (Smith) NiedenzuPalumaEtOH bark[20]> 200> 200---
Syzygium gustavioides (F.M. Bailey) B. HylandF. No. Qld.CHCl3/EtOH bark[22]> 200> 200---
Tabebuia bahamensis (Northr.) BrittonAbacoacetone barkb17.4 ± 3.5> 200> 1123.8 ± 5.7> 8
Weinmannia pinnata L.MonteverdeEtOH bark[21]> 200> 200---
Xanthophyllum octandrum (F. Muell.) DominPalumaEtOH bark[20]33.7 ± 3.620.6 ± 0.61--
Zanthoxylum rhoifolium Lam.MonteverdeMeOH barkb34.2 ± 2.3122.0 ± 7.04--
Zanthoxylum setulosum P. WilsonMonteverdeMeOH bark[21]188.9 ± 1.6> 200---
Zanthoxylum setulosum P. WilsonMonteverdeMeOH bark[21]> 200> 200---
Zanthoxylum setulosum P. WilsonMonteverdeCHCl3 bark[21]> 200> 200---
Zanthoxylum sp. aff. Juniperinum PoeppMonteverdeEtOH bark[21]< 12.514.9 ± 2.2> 1--
Zanthoxylum veneficum F.M. BaileyF. No. Qld.CHCl3/EtOH bark[22]> 20066.9 ± 7.9---
Amphotericin B---0.030 ± 0.0035.8 ± 0.51930.030 ± 0.003193
Pentamidine---0.37 ± 0.0111.7 ± 1.7321.3 ± 0.19
a Abaco Island, Bahamas. b Unpublished. c Monteverde, Costa Rica. d Paluma, north Queensland, Australia. e Far north Queensland, Australia. f Matabeleland, Zimbabwe. g Navarre, Florida, USA. h Huntsville, Alabama, USA.

4. Conclusions

Of the 115 extracts screened, 25 (21.7%) showed promising activity against L. amazonensis promastigotes with low cytotoxic activity. Additional antileishmanial screening against L. amazonensis amastigotes revealed ten of these extracts (8.7%) to be considered “hits”, with selectivity indices, CC50 (macrophage)/IC50 (amastigotes) greater than 10 that are worthy candidates for further phytochemical exploration: Conostegia xalapensis methanol bark extract, Endiandra palmerstonii bark extract, Eugenia monteverdensis acetone bark extract, Eugenia sp. “fine leaf” acetone bark extract, Exothea paniculata chloroform bark extract, Mallotus paniculatus ethanol bark extract, Matelea pseudobarbata ethanol extract, Quercus insignis ethanol bark extract, Sassafras albidum dichloromethane bark extract, and Stemmadenia donnell-smithii acetone bark extract. The good antileishmanial activity coupled with low cytotoxicity to mammalian cells indicates promise in terms of therapeutic index. Phytochemical analyses are currently underway in our laboratories. The results of this study demonstrate the medicinal potential of tropical rainforests and may provide complementary, safe, and affordable therapeutics for treatment of leishmaniasis. A total of 85 extracts were inactive or unspecific, which constitute 74% of tested samples, and reinforces the need to screen large series of natural products to find promising ones.

Acknowledgments

We thank Forest Heights Academy, Marsh Harbour, for allowing us the use of their laboratory facilities on Abaco. We are grateful to the Queensland Forest Service and to the Queensland National Parks and Wildlife Service for allowing access to State Forest and National Park lands. We thank Betsy R. Jackes and Anthony K. Irvine for plant identification in north Queensland, Australia. We are very grateful to the Monteverde Cloud Forest Preserve and the Tropical Science Center for granting us permission to collect plant materials under a cooperative rights agreement and to the Commission for the Development of Biodiversity of Costa Rica’s Ministry of the Environment, Energy, and Telecommunications for Research Permit R-001-2006-OT-CONAGEBIO. We are grateful to Maynor Vargas Arguedas for permission to collect plant materials on the property of Hotel El Bosque, Monteverde. We thank William A. Haber and Robert O. Lawton for plant identification in Monteverde, Costa Rica. Financial support for the collection and extraction of plant materials was provided, in part, by grants from the National Institutes of Health (R15-AIOD39740-01, R15-GM46120-01A1, R15-CA74343-01, R15-GM57646-01A, R15-AI059001-01) and private donations. This work was performed as part of the activities of the Research Network Natural Products against Neglected Diseases (ResNetNPND), (http://www.resnetnpnd.org/Start/).

Author Contributions

L.M. and W.N.S. conceived and designed the project; L.M. and A.P. performed the experiments; L.M. and W.N.S. analyzed the data; W.N.S. wrote the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

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Monzote, L.; Piñón, A.; Setzer, W.N. Antileishmanial Potential of Tropical Rainforest Plant Extracts. Medicines 2014, 1, 32-55. https://doi.org/10.3390/medicines1010032

AMA Style

Monzote L, Piñón A, Setzer WN. Antileishmanial Potential of Tropical Rainforest Plant Extracts. Medicines. 2014; 1(1):32-55. https://doi.org/10.3390/medicines1010032

Chicago/Turabian Style

Monzote, Lianet, Abel Piñón, and William N. Setzer. 2014. "Antileishmanial Potential of Tropical Rainforest Plant Extracts" Medicines 1, no. 1: 32-55. https://doi.org/10.3390/medicines1010032

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