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ORIGINAL ARTICLE
Year : 2010  |  Volume : 6  |  Issue : 24  |  Page : 331-334 Table of Contents     

Biological screening of araripe basin medicinal plants using Artemia salina Leach and pathogenic bacteria


1 Programa de Pós-Graduação em Bioprospecção Molecular, Departamento de Química Biológica, Laboratório de Pesquisa de Produtos Naturais, Universidade Regional do Cariri, Rua Cel. Antônio Luiz 1161, Pimenta, 63105-000 Crato-CE, Brazil
2 Vice-Reitoria de Pesquisa e Pós-Graduação, Universidade de Fortaleza, Av. Washington Soares 1321, Edson Queiroz, 60811-905, Fortaleza-CE, Brazil

Date of Submission02-Mar-2010
Date of Decision26-Mar-2010
Date of Web Publication20-Oct-2010

Correspondence Address:
José Galberto M da Costa
Programa de Pós-Graduação em Bioprospecção Molecular, Departamento de Química Biológica, Laboratório de Pesquisa de Produtos Naturais, Universidade Regional do Cariri, Rua Cel. Antônio Luiz 1161, Pimenta, 63105-000 Crato-CE
Brazil
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Source of Support: FUNCAP and CNPq, Conflict of Interest: None


DOI: 10.4103/0973-1296.71792

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   Abstract 

Background: Many medicinal plant species from the Araripe Basin are widely known and used in folk medicine and for commercial manufacturing of phytotherapeutic products. Few ethnobotanical and pharmacological studies have been undertaken in this region, however, in spite of the great cultural and biological diversity found there. Materials and Methods : Extracts of 11 plant species collected from Cearα state, Brazil, were subjected to the brine shrimp lethality test in order to detect potential sources of novel cytotoxic, antitumor compounds. The larvicidal activity, based on the percentage of larval mortality, was evaluated after 24 h exposure to the treatments. Results: All species tested showed good larvicidal activity as compared to a reference compound and literature data. The extract from Vanillosmopsis arborea was the most active with an LC 50 of 3.9 μg/ml. Best results were shown by Lantana montevidensis against Pseudomonas aeruginosa [minimum inhibitory concentration (MIC) 8μg/ml] and Escherichia coli (MIC 32 μg/ml), Zanthoxylum rhoifolium against E. coli (MIC, 256 μg/ml) and Staphylococcus aureus (MIC 64 μg/ml) and Croton zenhtneri against S. aureus (MIC 64 μg/ml). Conclusion: Chemical tests indicated that a wide variety of natural product classes was present in those extracts that showed significant activities in the bioassays.

Keywords: Araripe Basin, Artemia salina, ethanol extracts, larvicidal activities, pathogenic bacteria


How to cite this article:
da Costa JM, Campos AR, Brito SA, Pereira CB, Souza EO, Rodrigues FG. Biological screening of araripe basin medicinal plants using Artemia salina Leach and pathogenic bacteria. Phcog Mag 2010;6:331-4

How to cite this URL:
da Costa JM, Campos AR, Brito SA, Pereira CB, Souza EO, Rodrigues FG. Biological screening of araripe basin medicinal plants using Artemia salina Leach and pathogenic bacteria. Phcog Mag [serial online] 2010 [cited 2019 Nov 18];6:331-4. Available from: http://www.phcog.com/text.asp?2010/6/24/331/71792


   Introduction Top


Although progress has been made through conventional chemistry and pharmacology in producing effective drugs, the plant kingdom may provide useful sources of new anti-ulcer compounds for development as pharmaceutical entities or, alternatively, as simple dietary adjuncts to existing therapies. [1] The use of natural resources by rural communities in northeastern Brazil has been examined in greater depth. These communities practice subsistence agriculture, cattle ranching, and harvest both woody and non-woody forest products, sometimes associated with agroforest systems. [2]

Despite a less diversified flora, when compared with other regions of Brazil, Cearα presents numerous species widely used in popular medicine. The cytotoxicity and antitumoral effects, such as those produced by antifungal activity of extracts from Cearα's flora, have been reported. [3]

Many medicinal plant species from the Araripe Basin are widely known and used in folk medicine and for commercial manufacturing of phytotherapeutic products. Few ethnobotanical and pharmacological studies have been undertaken in this region, however, in spite of the great cultural and biological diversity found there. In an effort to discover new lead compounds, many research groups screen plant extracts to detect secondary metabolites with relevant biological activities.

In this regard, several simple bioassays have been developed for screening purposes, [4] and some of them were used in this screening. Thus, Artemia salina larvae have been used as a target organism to detect bioactive compounds in plant extracts and toxicity to this crustacean has a good correlation with anti-tumor [5] and anti-Trypanosoma cruzi[6] activities. More recently, it has been shown that there is a very good correlation between the median lethal concentrations (LC 50 ) of plant extracts to brine shrimp larvae and the median lethal doses (LD 50 ) of the same extracts, administered orally in mice. [7]

As part of our program to evaluate medicinal plants from northeastern Brazilian flora, the aim of this study was to screen medicinal plant extracts that could be useful for the development of new tools for the control of infectious diseases. While pursuing this goal, we initiated a systematic evaluation of extracts from the Araripe Basin plant species, the brine shrimp (A. salina Leach) lethality assay (BSLA).


   Materials and Methods Top


Plants and sample preparation

A total of 11 plant species were collected randomly from the medicinal plant garden of the Universidade Regional do Cariri and Floresta Nacional do Araripe, Brazil. The taxonomic identities of these plants were confirmed by a botanist and the voucher specimen numbers of the plants were deposited in the Herbαrio Caririense Dαrdano de Andrade Lima. Different parts of the plants (leaves, barks and stem barks) were dried, powdered and exhaustively extracted with ethanol at room temperature for 2 days.

Phytochemical prospection

Phytochemical tests to detect the presence of heterosides, saponins, tannins, flavonoids, steroids, triterpenes, coumarines, quinones, organic acids and alkaloids were performed following the method described by Matos. [8] These tests are based on visual observation of color modification or precipitate formation after addition of specific reagents.

Brine shrimp cytotoxicity assay

A. salina encysted eggs were incubated in artigical seawater under light at 28°C. After incubation for 24 h, nauplii were collected with a Pasteur pipette and kept for an additional 24 h under the same conditions to reach the metanauplii stage. The samples (triplicate) to be assayed were dissolved in Tween 80 and diluted serially (1000, 250, 125, 100, 75 μg/ml) in seawater. Ten nauplii were added to each set of tubes containing the samples. Controls containing Tween 80 in seawater were included in each experiment. K 2 Cr 2 O 7 was used as a positive control. Twenty-four hours later, the number of survivors was counted.

Lethal concentration determination

The lethal concentrations of plant extracts resulting in 50% mortality of the brine shrimp (LC 50 ) and 95% confidence intervals were determined from the 24-h counts and the dose-response data were transformed into a straight line by means of a trendline fit linear regression analysis; the LC 50 was derived from the best-fit line obtained. [9]

Antibacterial assays

The antibacterial activities of the extracts were investigated by employing a microdilution method, recommended by NCCLS M7-A6. [10] The assay was carried out with four bacterial species obtained from Fundaηγo Oswaldo Cruz-FIOCRUZ: Staphylococcus aureus (ATCC 6538), Pseudomonas aeruginosa (ATCC 15442), Klebsiella pneumoniae (ATCC 10031) and  Escherichia More Details coli (ATCC 25922).

Brain Hear Infusion (BHI 3.8%) broth was used for bacterial growth (24 h, 35 ± 2°C). The inoculum was an overnight culture of each bacterial species in BHI broth diluted in the same media to a final concentration of approximately 1 Χ 10 8 Colony Forming Unit - CFU/ml (0.5 nephelometric turbidity units - McFarland scale). After this, the suspension was diluted to 1 Χ 10 6 CFU/ml in 10% BHI. Hundred milliliters of each dilution was distributed in 96-well plates plus extracts in different concentrations, achieving 5 Χ 10 5 UFC/ml as the final concentration of the inoculum. Extracts were dissolved in distilled water and dimethyl sulfoxide (DMSO) to a concentration of 103 mg/ml. Further serial dilutions were performed by addition of BHI broth to reach a final concentration in the range of 512 - 8 mg/ml. All experiments were performed in triplicate, and the microdilution trays were incubated at 35 ± 2°C for 24 h. Antibacterial activity was detected using a colorimetric method by adding 25 ml of resauzurin, staining (0.01%) aqueous solution in each well at the end of the incubation period. The minimal inhibitory concentration (MIC) was defined as the lowest essential oil concentration able to inhibit the bacterial growth, as indicated by resauzurin staining (bacterial dead cells are not able to change the staining color when visually observed - blue to red).


   Results and Discussion Top


Since demonstrating activity in a bioassay is the first necessary step in the drug development process from ethnomedical systems, some extracts from reputed medicinal plants were screened for in vitro toxicity using brine shrimp test and antibacterial activities, in order to search for biological activity. This method allows the use of smaller extract quantities and the testing of a larger number of samples and dilutions in a short time. The species studied were Plectranthus amboinicus (#3037), Plectranthus barbatus (#3038), Zanthoxylum rhoifolium (#38231), Stryphnodendron rotundifolium (#33621), Lantana camara (#1662), Lantana montevidensis (#1663), Guapira graciliflora (#4023), Croton zenhtneri (#1619), Dimorphandra gardineriana (#1527), Vanillosmopsis arborea (#43291), and Piper tuberculatum (#43042), as shown in [Table 1].
Table 1: Parts of the plant used in the preparation of extracts, amounts and yield and identification of the main chemical classes

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It was also important to separate and identify the active constituents chemically. [Table 1] presents a summary of the classes of compounds that we have shown by chemical tests to be present in the plants used in this survey. The LC 50 values obtained after the analysis of extracts from medicinal plants from the northeast of Brazil are shown in [Table 2]. All plant extracts analyzed demonstrated toxicity to brine shrimp (LC 50 < 1000 μg/ml). These results suggested the presence of bioactive plant compounds and required further examination using elaborate bioassays which would detect pharmacological proprieties of a more specific nature.
Table 2: Larvicidal activities of ethanol extracts of various plant species against the larvae of A. salina

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According to Meyer et al, who classified crude extracts and pure substances into toxic (LC 50 value < 1000 μg/ml) and non-toxic (LC50 value > 1000 μg/ml), all extracts tested showed good brine shrimp larvicidal activity.

Several new antibacterial agents are currently being developed in response to the emergence of bacterial resistance to existing drug. New vegetal sources presenting with antimicrobial activity and low toxicity could be a viable alternative to poor communities inhabiting the areas where the species are found, due to their low cost and easy accessibility. [11] The antibacterial activity of ethanolic extract of various plants presented significant results against the pathogenic microorganisms tested.

In relation to the antibacterial assay, L. montevidensis was the most active, presenting lower MICs against P. aeruginosa (MIC = 8 μg/ml), one of the most clinically important microorganisms because of its high resistance potential to conventional antibiotics. The extract was effective against E. coli (MIC 32 μg/ml) too. Similar studies done with this species have demonstrated activity against standard pathogenic and multiresistant strains of E. coli (Ec 27) (16 μg/ml). [12]

Z. rhoifolium extract was effective against the gram-negative E. coli (MIC 256 μg/ml) and the gram-positive S. aureus (MIC 64 μg/mL). Previous studies indicated that the leaves and fruit essential oils were bioactive against S. aureus, K. pneumoniae and  Salmonella More Details sp.; however, the essential oil from the flowers was inactive. [13] In the antimicrobial study, it was verified that among the analyzed strains, S. aureus, Salmonella choleraesuis and Shigella flexneri were sensitive to the essential oil, with inhibition halos of 15, 13 and 10 mm, respectively. [14]

C. zenhtneri presented significant activity only against the gram-positive S. aureus (MIC 64 μg/ml). The essential oil from the leaves of this species demonstrated antibacterial activity against E. coli, S. aureus, Streptococus β-haemolyticus, but the best result was against S. flexneri (CIM 50 μg/ml. [15] It was evidenced that five species presented activity against only one strain, P. barbatus against S. aureus (CIM 128 μg/ml), S. rotundifolium against E. coli (CIM 128 μg/ml), L. camara against E. coli (CIM 256 μg/ml), G. graciliflora against K pneumoniae (CIM 512μg/ml), D. gardineriana against S. aureus (CIM 128 μg/ml).

V. arborea was sensitive against all strains only at the highest concentration, showing a low antibacterial activity, whereas P. amboinicus and P. tuberculatum were not active against the used strains as shown [Table 3].
Table 3: Antibacterial activity of ethanol extracts of various plant species

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The most promising extracts for the activity of toxicity were the aqueous extracts of V. arborea, P. barbatus and P. amboinicus, which have been used in the traditional medicine as analgesic and anti-inflammatory agents. In addition, the extracts of Z. rhoifolium, S. rotundifolium, L. camara, L. montevidensis, G. graciliflora, C. zenhtneri, D. gardineriana and P. tuberculatum showed significant lethality to brine shrimp.

These extracts can be regarded as promising candidates for a plant-derived antitumor compound. In fact, the essential oil of V. arborea was found to present the highest larvicidal activity. [16] The activity results of species belonging to Piperaceae family were found to be consistent with existing phytochemical knowledge of these plants as a source of cytotoxic and antitumor compounds. [17] It is possible that a broad range of structurally diverse compounds contributes to the overall pharmacological activity of the extracts and synergistic effects between active principles may exist.

The antibacterial activity demonstrated in this study for some extracts are relevant, since the best results against gram-negative strains that are often more resistant than gram-positive. This fact may be correlated with the polarity of the polar chemicals (tannins, flavonoids and alkaloids) present in extracts that can interact with the chemical composition of the polar cell structure of this bacterial type.


   Acknowledgment Top


The authors are grateful to FUNCAP and CNPq for grants and fellowships.

 
   References Top

1.Schmeda-Hirschmann G, Yesilada E. Traditional medicine and gastroprotective crude drugs. J Ethnopharmacol 2005;100:61-6.  Back to cited text no. 1  [PUBMED]  [FULLTEXT]  
2.Albuquerque UP, Medeiros PM, Almeida AL, Monteiro JM, Neto EM, Melo JG, et al. Medicinal plants of the caatinga (semi-arid) vegetation of NE Brazil: A quantitative approach. J Ethnopharmacol 2007;114:325-54.   Back to cited text no. 2      
3.Faria MH, Carvalho TG, Rabenhorst SH, Sidrim JJ, Moraes-Filho MO. Cytotoxic and antifungal properties of medicinal plants from Ceara, Brazil. Braz J Biol 2006;66:1133-5.   Back to cited text no. 3  [PUBMED]  [FULLTEXT]  
4.Hostettmann K. Assays for Bioactivity. Methods in Plant Biochemistry. San Diego: Academic Press; 1991. p. 6.   Back to cited text no. 4      
5.McLaughlin JL, Rogers LL, Anderson JE. The use of biological assays to evaluate botanicals. Drug Inf J 1998;32:513-24.  Back to cited text no. 5      
6.Zani CL, Chaves PP, Queiroz R, Mendes NM, Oliveira AB, Cardoso JE, et al. Brine Shrimp lethality assay as a Prescreening system for anti-Trypanosoma cruzi activity. Phytomedicine 1995;2:47-50.  Back to cited text no. 6      
7.Parra AL, Yhebra RS, Sardiρas IG, Buela LI. Comparative study of the assay of Artemia salina L. and the estimate of the medium lethal dose (LD50 value) in mice, to determine oral acute toxicity of plant extracts. Phytomedicine 2001;8:395-400.  Back to cited text no. 7      
8.Matos FJ. Introduηγo ΰ Fitoquνmica experimental. 2 nd ed. Fortaleza: Ediηυes UFC; 2000.  Back to cited text no. 8      
9.Meyer BN, Ferrigni NR, Putnam JE, Jacobsen LB, Nichols DE, McLeughlin JL. Brine shrimp: A convenient general bioassay for active plant constituents. Planta Medica 1982;45:31-4.  Back to cited text no. 9      
10.National Committee for Clinical Laboratory Standards; Methods for Dilution Antimicrobial Susceptibility Tests for bacteria that grow aerobically, Approved Standard M7-A6, 6 th ed. NCCLS: Wayne; 2003.  Back to cited text no. 10      
11.Barreto FS, Sousa EO, Campos AR, Costa JG, Rodrigues FF, Antibacterial activity of Lantana camara Linn and Lantana montevidensis brig extracts from Cariri-Cearα, Brazil. J Young Pharm 2010; 2:1:42-4.  Back to cited text no. 11      
12.Costa JG, Rodrigues FF, Angιlico EC, Pereira CK, Souza EO, Germana FR, et al. Composiηγo quνmica e avaliaηγo da atividade antibacteriana e toxicidade do σleo essencial de Croton zehntneri (variedade estragol). Rev Bras Farmacogn 2008;18:583-6.  Back to cited text no. 12      
13.Costa JG, Rodrigues FF, Silva MR, Campos AR, Lemos TL, Lima SG. Chemical Composition, Antibacterial and Larvicidal Activities of Zanthoxylum rhoifolium Lam Fruits Essential Oil. J Essential Oil Bearing Plants 2008;11:571-6.  Back to cited text no. 13      
14.Gonzaga WA, Weber AD, Giacomelli SR, Simionatto E, Dalcol II, Dessoy EC, et al. Composition and Antibacterial Activity of the Essential Oils from Zanthoxylum rhoifolium. Planta Medica 2003; 69:773-5.  Back to cited text no. 14      
15.Costa JG, Rodrigues FF, Angιlico EC, Pereira CK, Sousa EO, Caldas GF, et al. Composiηγo quνmica e avaliaηγo da atividade antibacteriana e toxicidade do σleo essencial de Croton zehntneri (variedade estragol). Rev Bras Farmacogn 2007;18:583-6.  Back to cited text no. 15      
16.Furtado RF, Lima MG, Neto MA, Bezerra JN, Silva MG. Atividade Larvicida de σleos essenciais contra Aedes aegypti Linnaeus (Diptera:Culiciidae). Neot Entomol 2005; 34:843-7.  Back to cited text no. 16      
17.Parmar VS, Jain SC, Bisht KS, Jain R, Taraj P, Tha A, et al. Phytochemistry of the genus Piper. Phytochemistry 1997;46:597- 673.  Back to cited text no. 17      



 
 
    Tables

  [Table 1], [Table 2], [Table 3]


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