In vitro antimalarial activity of extracts of some plants from a biological reserve in Costa Rica
Misael Chinchilla1*, Idalia Valerio1, Ronald Sánchez2*, Víctor Mora2, Vanessa Bagnarello1, Laura Martínez1, Antonieta Gonzalez2, Juan Carlos Vanegas1 & Álvaro Apestegui1
Treatment with the usual antimalarial drugs, have induced parasite resistance, reinforcing the need to finding natural antimalarial components that would be found on plants from the forest. Therefore, we decided to look for these components in Costa Rican plants from a protected forest area. Fresh and dry extracts of roots, bark, leaves, flowers and fruits of 25 ]]>
in vitro for the presence of substances with antimalarial activity. By studying the inhibition of P. berghei schizogony, we assessed the antimalarial activity of several plant extracts: Aphelandra aurantiaca, A. tridentata (Acanthaceae); Xanthosoma undipes (Araceae); Iriartea ]]>
(Arecaceae); Neurolaena lobata (Asteraceae); Senna papillosa, Pterocarpus hayessi, Lonchocarpus pentaphyllus (Fabaceae); Nectandra membranacea, Persea povedae, Cinamomum chavarrianum (Lauraceae); Hampea appendiculata (Malvaceae); Ruagea glabra, Guarea glabra (Meliaceae); Psidium guajava (Myrtaceae); Bocconia frutescens (Papaveraceae); Piper friedrichsthalii (Piperaceae); Clematis dioica (Ranunculaceae); Prunus annularis (Rosaceae); Siparuna thecaphora (Siparunaceae); Solanum arboreum,Witheringia solanácea (Solanaceae); ]]>
Ticodendrum incognitum (Ticodendraceae); Heliocarpus appendiculatus (Tiliaceae) and Myriocarpa longipes (Urticaceae). We used different parts of the plants as well as fresh and dried extracts for testing IC50. The solid content of the extracts ranged from 1-71.9μg/mL. The fresh extracts showed stronger activity than the dry ones. Since the plants showing the strongest antimalarial activity are very common in Central America, and some similar genera of these plants have shown ]]>
El tratamiento con las drogas antimaláricas de uso común han inducido resistencia por ]]>
in vitro en busca de sustancias con actividad antimalárica. Las plantas estudiadas fueron: Aphelandra ]]>
(Acanthaceae); Xanthosoma undipes (Araceae); Iriartea deltoidea (Arecaceae); Neurolaena lobata (Asteraceae); Senna papillosa, Pterocarpus hayessi, Lonchocarpus pentaphyllus (Fabaceae); Nectandra membranacea, Persea povedae, Cinamomum chavarrianum (Lauraceae); Hampea appendiculata ]]>
Ruagea glabra, Guarea glabra (Meliaceae); Psidium guajava (Myrtaceae); Bocconia frutescens (Papaveraceae); Piper friedrichsthalii (Piperaceae); Clematis dioica (Ranunculaceae); Prunus annularis (Rosaceae); Siparuna thecaphora (Siparunaceae); Solanum arboreum, ]]>
(Solanaceae); Ticodendrum incognitum (Ticodendraceae); Heliocarpus appendiculatus (Tiliaceae) y Myriocarpa longipes (Urticaceae). Los extractos frescos y secos de las diferentes partes de las plantas fueron estudiadas y se determinó la IC50, el cual osciló entre 1-71.9mg/mL; los extractos frescos mostraron mayor actividad antimalárica. Las plantas que presentaron mayor actividad son muy comunes en ]]>
de discusión en este tema. Además este es el primer estudio sistemático de esta naturaleza realizado en un área boscosa circunscrita y protegida de Costa Rica.
Palabras clave: malaria, antimaláricos, in vitro, plantas, Costa Rica, Plasmodium berghei.
Malaria is a very important tropical disease, with a reported human morbidity approaching 300-500 million worldwide and a mortality of 1-2 million deaths per year (WHO ]]>
Plasmodium falciparum, the most pathogenic representative of this species, is responsible for the great majority of cases (Tramputz et al. 2003, Batista et al. 2009, Kakkilaya 2008). Confirming this fact, the geographical areas where this species is more frequent, such as Africa, also have the greater incidence of deaths due to malaria infection.
From 1973-1983, ]]>
et al. 2010). ]]>
Unfortunately, continuous and frequent treatments with antimalarial drugs, such as chloroquine, have induced parasite resistance (Baird 2004), reinforcing the need for finding more natural antimalarial components. We believe that the best candidates for that would be found on plants from the forest.
Besides, the World ]]>
et al. 2005). Quinine was the first natural drug found for malaria treatment, but because of its high toxicity, its use is limited to only some very qualified cases (WHO 2010). For P. falciparum resistant strains, the alternative treatment actually is the ]]>
Artemisia. (Kakkilaya 2008, WHO 2010). Research has continued in laboratories of many developed as well as undeveloped countries (Saxena et al. 2003). Several studies regarding this matter have made important contributions to this subject in the past in Costa Rica (Castro et al. 1996, Chinchilla et al. 1998, 2001, 2003). ]]>
While, in Africa and Asia there have been many studies that have reported active substances against P. falciparum (Pillay et al. 2008, Soh & Benoit-Vical 2007). In Latin-America most of the studies came from South America (Krettli et al. 2001, Botsaris 2007, Valadeu et al. 2009 among others) and very ]]>
et al. 2002, Franssen et al. 1997); we believe that our study represents a new contribution to this scientific area.
WHO and OPS (Organización Panamericana de la Salud) recommend, as an oficial model for research ]]>
Plasmodium berghei strains (Ramesar et al. 2008).
Based on the previous knowledge, we decided to perform a more integral study of Costa Rican plants for antimalarial activity. We choose to work in a more protected and less disturbed forest area called “Reserva Biológica Alberto Manuel ]]>
This study have three fundamental objectives: 1) Reveal the natural diversity present in REBAMB, 2) Demonstrate the importance of our biodiversity in ethnobotany, especially concerning the treatment of important diseases, such as malaria, and finally, 3) disseminate our studies, in an attempt to help the discovery of new drugs that could improve human health. ]]>
Material and methods
Plants: A total of 25 different plants (Table 1) were collected from October 2007-December 2008 in the biological reserve, previously mentioned (REBAMB), owned by the University of Costa Rica. This reserve is located 42km Northeast from ]]>
Plants were selected according to previous works (Sittenfeld et al. 1999, ]]>
et al. 2008) that showed that extracts obtained from insects feeding from certain plants, had antimalarial activity. Identification and selection of those host families and species was definitive in choosing the plants for this study.
All the plants were identified by an expert botanist, who based his findings on previous publications (Gómez-Laurito & Ortíz 2004, Barrantes 2004), the ]]>
In all cases, the samples obtained consisted of bark, roots, young and mature leaves, as well as flowers and ripe or unripe fruits. All these materials were placed in ]]>
plastic bags and transported in a cold container to the laboratory.
Each part of the plant was further divided into two portions: one was kept as fresh material, while the other was dried for subsequent analysis. ]]>
Preparation of extracts: The fresh material coming from all parts of the plants was carefully washed and then finely chopped; the other portion was dried and prepared as a coarse powder in order to ease extraction. For screening purposes, we used 15g of fresh or 10g of dried material. They were placed in separate 250mL amber bottles, and then extracted with 100mL of 70% ethanol for a week at ]]>
In vitro antimalarial assay:
• Parasite strain: A P. bergheis strain (NK 65) obtained from American Type Culture Collection (ATCC) was used to assess the antimalarial activity of the extracts. This strain was kept alive by weekly re-infection in Swiss mice following the recommendations given by WHO for these type of studies. • Experimental animals: Male and female mice (Mus musculus Swiss) weighing 22-24g originally obtained from the University of Costa Rica were used through the experiments. The animals were maintained in an air-conditioned environment in the animal house of UCIMED, feeding with standard pet food and drinking wáter ad libitum. They were caged in groups of 5-10 and all studies were performed in agreement with international rules for laboratory animal use, under the ACCMAL control in Costa Rica. • Inoculum: Parasitized erythrocytes were obtained from a previously infected mouse by cardiac puncture using heparin as anticoagulant and then diluted in RPMI 1640 medium, supplemented with 10% fetal calf serum plus antibiotics (RPMI 1640). Animals were inoculated by intraperitoneal injection with a blood suspension (0.2 mL) containing 106-107 parasitized erythrocytes. After 24h infection, mice showing a parasitic presence in blood of ten to 15% of the erythrocytes infected with ring stages, were used in all the in vitro studies. • In vitro antimalarial assays: We followed general procedures for P. berghei cultura and also for testing in vitro antimalarial effect (Ager et al. 1984, Deharo et al. 2000). Briefly, erythrocytes (final cell suspensión 1%, v/v, blood/culture medium), from a one day infected mice, suspended in RPMI 1640 medium, were mixed with the intact plant extracts (0.05mL blood and 0.05mL diluted extract per well), the mixture was transferred to plates and then incubated in a candle jar at 37°C for 24h in a low speed shaker (Mini-Shaker 3D Boeco, Germany). For each experiment we used a positive control with chloroquine in standard concentration and a negative control with only culture medium.
To determine the IC50 (minimal concentration that inhibits 50% of parasite schizogony), we made serial dilutions of the extract according to the dry weight obtained in each case. After the incubation period, we made blood smears from each well, stained with Giemsa dye, and the number of schizonts was determined by counting at least 500 red blood cells under the microscope´s 100X objective. The percentage of the parasite schizogony inhibition was calculated by the following formula (Deharo et al. 2000): ]]>
Schizogony inhibition (%) = schizonts in control - schizonts with extract x 100/ schizonts in control.
For calculations and statistical analysis the Probit method (Deharo et al. 2000, Diaz et al. 2004) was used. To classify the activity levels of each extract the Rasoanaivo table (1999) was used. Accordingly the term “very active” means a IC50 less than 5μg/mL; active from >5-50μg/ mL; “weakly active” from >50-100μg/mL and “inactive” more than 100μg/mL.
Results
The crude alcoholic extracts obtained from the different plant structures of the 25 varieties studied (Table 1) showed some antimalarial activity (Fig. 1). The plants with the highest activity consistently showed it in both fresh and dried material. Not all plant structures showed the antimalarial effect. Figure 2 show the percentages of plants with one, two, three, four or more structures with potential effect against P. berghei.
There were more plants showing antimalarial activity in only one type of structure, (Figs. 2, 3) but three plants showed it in four or more parts. When comparing extracts of fresh and dried plant with antimalarial activity (Fig. 3), no significant differences were found for structures, except in flowers and young leaves where the dry material showed higher antimalarial activity. Root fresh extracts showed more activity as well.
IC50 tests on fresh (Table 2) and dried extracts (Table 3) yielded the results presented in figure 4. Fresh material (Fig. 4A) showed the highest antimalarial activity (“very active”) as compared to the other categories; it was also independent of the part of the plant studied. In contrast, for dry samples (Fig. 4B), the “active” category presented higher values than the others, again regardless of the plant structure studied. ]]>
Discussion
Several authors have pursued the search for natural products with antimalarial effect in plants in the past and in recent years (Rafatro et al. 2005, Ogbonna et al. 2008, Pillay et al. 2008, Kayser
et al. 2003). The rationale for such studies is based on the resistance of the parasites to conventional treatment as observed in the case of malaria (Fidock et al. 2008).
This resistance began with P. falciparum near the ‘60s and today is extremely common, ]]>
P. vivax (Baird 2004, Anstey et al. 2009) the most common species found outside Africa (Wells et al. 2010) and in Costa Rica, were reports account for 95-98% of the cases (Vargas 2001).
]]>
Malaria parasites also exhibit resistance to Fansidar, a treatment involving Sulfadoxine and Pyrimethamine, that act inhibiting the formation of nucleic acids (Bloland 2001, Hastings 2004, Kakkilaya 2008).
Based on the foregoing, we started in Costa Rica the search for antimalarial components in plants, as ]]>
et al. 1998, 2001, Castro et al. 1996).
In conducting this research, we took into account not only the traditional observations on the treatment of malaria and its symptoms, but also the findings of a previous study (Chinchilla et al. 2008), in which, antimalarial ]]>
Very few papers in other countries mention plants with higher antimalarial activity than the ones found in ]]>
et al. 1999), and no other researchers have done any work with them.
H. appendiculata is found only in Panama, Honduras and Costa Rica (Tropicos 2010) and T. incognitum is a ]]>
S. thecaphora, N. membranaceae and B. frutescens have a greater distribution in the Americas, but were not found in any other places (Tropicos 2010). In Africa and Asia there has been an intense and enthusiastic search for active compounds against P. falciparum especially (Aderounmu 2002, Mariath et al. 2009, Titanji et al. ]]>
et al. 2001, Rodríguez-Pérez et al. 2006, Batista et al. 2009, Valadeau et al. 2009 among others) and very few from Central America (Franssen 1997, Kohler et al. 2002). Antimalarial components have been found in
S. andina, S. pauciflora, S. tonduziana and S. aspera, but not in S. thecaphora. The present study represents an important contribution to this field since the data obtained, together with that already reported, has shown to be inedited.
Most of the studies mentioned, have ]]>
Almost every one of the studies referred before used dried material for extraction. Since the traditional way of using plants for healing is by using fresh material (Blair & Madrigal 2005, Togola et ]]>
2005) we included this modality as part of our research. Shows that the activity in different structures of the plant was very similar independently of the use of the dry or fresh extract. However, when analyzing the potency of IC50, the fresh material showed, except for bark and mature leaves, a dominance of the condition “very active” over “active”. The opposite is true for dry extracts; it can be deducted that although the antimalarial activity was detectable in both types of extracts, the potency of this activity appears to decrease by drying the structure. The implication of this observation concludes that if only dry samples ]]>
Since this study was performed in a biological reserve, there is a guarantee for the permanence, for many years, of plants with active components against malaria. In addition, all samples were collected in a fairly restricted area, which reduces the risk of changes due to external factors such as climate, soil type and other (Martin 2001). Factors such as stage of development of the ]]>
This work seeks to offer a contribution to Ethnobotany applied to Medical Sciences in Costa Rica, as has been done in many other countries (Martin 2001). Studies in ]]>
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