Nowadays, in spite of great developments in organic synthesis and new biotechnological processes, a notable increase in phytotherapeutic practice can be observed. Approximately 25% of the medicines prescribed in the industrialized countries originate from plants and about 120 compounds of natural origin, obtained from approximately 90 species of plants, are used in modern therapy [1
]. Furthermore, natural products are involved in the development of about 44% of all new drugs [1
]. In Brazil, approximately 80,000 species of plants are described, offering a wide range of raw material for the discovery of new drugs [1
]. Clearly, given this enormous variety of species, this potential source of new drugs is far from completely explored and only 17% of this group of plants has been the focus of systematic studies in search of biological compounds [2
]. The World Health Organization (WHO) estimates that 65–80% of the people in developing countries use traditional medicine for primary health care and 85% of that involves the use of plant extracts. The WHO recommends research into the use of the local flora for therapeutic purposes, with the intention of reducing the number of people excluded from effective therapy in the government health systems, which could constitute an economically viable alternative treatment of several diseases, especially in developing countries [3
The abusive and indiscriminate use of antimicrobial compounds over many years is the main factor responsible for the appearance of the phenomenon of bacterial resistance to such compounds [5
]. Several alternatives have been suggested to solve this problem such as the search for new antimicrobials in plant species [6
]. Some plants synthesize substances to defend themselves when attacked by bacteria, fungi, parasites, viruses or other agents. These compounds are products of their secondary metabolism and of particular interest are those with antimicrobial properties such as: terpenoids (monoterpenes, sesquiterpenes, diterpenes and saponins), phenolics (simple phenols, tannins, dibenzofurans and flavonoids), nitrogenated compounds (alkaloids, cyclic peptides and glycosides), coumarin and camphor [8
(Huber) Cuatrec. (Humiriaceae) is a native tree of the Brazilian Amazon rainforest and is found scattered over the whole Amazonian Basin. The family Humiriaceae was described by Antoine Laurent de Jussieu and includes 50 species classified in eight genera, spread in tropical areas of America, and one specie in tropical West Africa. The plant is known in the Amazon as “uchi
”, “uxi-amarelo”, “cumatê”, “axuá”, “pururu”, “uxi-liso”, “uxi-ordinário” or “uchi-pucu” [12
]. The erect trees have pale gray bark and reach between 25 and 30 meters in height, with a stem diameter over one meter. The bark is widely commercialized at fairs, markets and even drugstores, being prescribed in the form of tea, for arthritis, cholesterol, diabetes, diarrhea treatments and as an anti-inflammatory [14
]. The phytochemical screening of the bark revealed the predominance of tannins, coumarins and saponins as the main classes of secondary metabolites [15
]. In previous work, Luna et al.
] isolated, from crude ethanolic extracts of the bark, two coumarins (bergenin and dimethyl bergenin) and two pentacyclic triterpenoids of the oleanane series (maslinic acid and methyl maslinate).
In this study we determined total tannin contents and investigated the antimicrobial and cytotoxic activities of various extracts of powdered bark of E. uchi.
2. Results and Discussion
Considering that the aim of the present study was to evaluate the antibacterial effect of powdered bark extracts of E. uchi
and given the antimicrobial activity described for the tannins [17
], it was important to estimate the contents of this group of substances in the extracts (Table 1
and Figure 1
Thus, the extracts were selected according to their total tannins contents, to be subjected to the biological tests. The 5% extract with the highest total tannins content was prepared by maceration (23.62% ± 1.0); the 10% extract with highest total tannins content was prepared by percolation (32.85% ± 1.62), this being the extract with the overall highest total tannins content, and the 20% extract with highest total tannins content was prepared by turboextraction (24.77% ± 2.54). Besides these three extracts, the 10% infusion (26.06% ± 4.27) and the 20% decoction (20.27% ± 1.16) were included in the biological tests because popular use is almost totally based on the consumption of teas. It was found that for some extraction processes (decoction and maceration) the total tannins content in the 5% extracts was very close to that in the 20% extracts (H0
< 0.05). This makes the 5% extract attractive from the economic point of view, because smaller amounts of plant material are consumed. The values of total tannins (TT) found in the extracts of powdered barks of E. uchi
, all around 21%, compare favorably with the values found by Yamaguti-Sasaki et al
. (2007) [23
], who used 5% aqueous extract (16.16% ± 0.44), crude acetone:water extract (31.15% ± 1.46) and semi-purified fractions (30.05% ± 0.54; 17.09% ± 0.52) of the seeds of Paullinia cupana
H. B. K. var sorbilis
The results of the antimicrobial activity tests are presented in Table 2
. The control solution (DMSO:BHI) did not produce inhibition haloes against the microorganisms studied, indicating that this solvent does not interfere in the antimicrobial activity results for the extracts. In the disk-diffusion test in agar, with either templates or filter paper discs; no significant bacterial growth inhibition was observed, except a small activity in the extracts against S. aureus
and activity of the 10% infusion extract against C. albicans
. It should be noted that since the tannins form complexes with proteins [24
], it is possible that local precipitation occurred, impeding the tannins from diffusing in the culture medium, and thus masking their real activity, despite the presence of Tween 80®
. In general, plant extracts contain low concentrations of highly active compounds and a great number of other compounds that may have promising activities, but which need an appropriately sensitive test to be detected [27
]. It is also possible that yet other substances exist in the extracts that interfere with the real antimicrobial potential of the tannins. Thus, it would be very interesting to fractionate the extracts, isolate the compounds and obtain a more accurate assessment.
The minimum inhibitory concentration (MIC) was determined for the strain S. aureus. There was bacterial growth in the wells selected as positive growth control and solvent control (DMSO) and no bacterial growth in the wells that did not receive the inoculums (negative controls), indicating the sterility of the culture medium and of the extracts. The antibiotic was shown to be effective (MIC of 0.78 μg/mL), but the extracts showed no activity at any of the dilutions.
In the cytotoxicity tests with fibroblast cells, none of the tested extracts were shown to be toxic, and all the cell survival values were 100%. Thus, the IC50 of all the extracts was higher than the highest tested concentration (0.2 mg/mL).
DPPH is a stable free radical that interacts with antioxidant substances, which transfer electrons or atoms of hydrogen to DPPH, neutralizing (“scavenging”) the free radical. This process can be observed as a change in the color of the reaction agent from violet to yellow and a reduction in the absorbance at 517 nm [28
]. The ANOVA demonstrated that the tested extracts showed similar scavenging activities among themselves and statistically significantly lower (P
< 0.05) from that of Ginkgo biloba
extract and other standards such as gallic acid, vitamin C and rutin. However, the DPPH scavenging activities of the isolated pure substances were higher and the results do not disqualify the antioxidant activity of the tested samples (Table 3
). The results here represent a basis for the quality control of this plant drug, as there are no reference values described in the literature for the bark of E. uchi
Parametric and nonparametric correlation tests were done between total phenols content, total tannins content and antioxidant activity. The results are presented in Table 4
These results suggest that there was no relationship between the total tannins content in extracts and their antioxidant activity (values close to zero) and that there was a significant negative relationship between total phenols and total tannins and among total phenols and antioxidant activity.
The high antioxidant activity coupled with low cytotoxicity of the extracts, in addition to the previously reported lack of acute oral toxicity [29
], and selective anti-inflammatory activity [30
], encourage further studies in search of possible potential anti-cancer activities.
3. Experimental Section
3.1. Plant Material
Powdered bark of Endopleura uchi (Huber) (Humiriaceae) was acquired from the Sítio da Mata company (lot: Uxi03/01; N°Inscr. Prod.: 024.308.176; crop: 01/09/2005; expiry: 30/09/2008), located on the Cajuru highway, Cassia dos Coqueiros (SP), Brazil.
3.4. Antimicrobial Assays
The agar disk diffusion technique (both with “templates” and “paper discs”) was employed to test for antimicrobial activity against strains of Bacillus subtilis (ATCC 9372), Staphylococcus aureus (ATCC 25923), Staphylococcus epidermidis (ATCC 27853), Escherichia coli (ATCC 25922), Shigella sonnei (clinical isolate) and Candida albicans (ATCC 64548). A colony of each bacterial strain used, or 150 μL of a previously prepared bacterial suspension was inoculated in Brain Heart Infusion (BHI) broth and incubated at 37 °C for 24 hours. The turbidity of each bacterial cell suspension was then adjusted with saline to match the 0.5 McFarland scale (∼1.5 × 108 CFU/mL). Five colonies of Candida albicans were inoculated in Sabouraud broth and incubated at 35 °C for 24–48 hours. The turbidity of the yeast cell suspension was then adjusted to 0.5 on the McFarland scale (1× 106–5 × 106 CFU/mL) with sterile saline. Ampicillin (50 μg/mL) was used as a positive control for the bacterial strains and amphotericin B for the Candida albicans strain. The later was prepared by dissolving 16 mg of amphotericin B in 10 mL of dimethylsulfoxide (DMSO) and diluting this, twice, in the proportion 1:5 (w/v), obtaining the stock solution 64 μg/mL.
The agar diffusion tests were performed as in the approved standards M2-A8 and M44-A of the Clinical and Laboratory Standards Institute, with modifications [33
]. Bacterial and yeast inoculums were prepared as described previously adjusting the turbidity to the McFarland scale. Müller-Hinton agar (MHA) for bacteria, or MHA supplemented with 2% glucose and 0.5 μg/mL methylene blue for yeast, were poured into sterilized Petri dishes, having been seeded with previously prepared inocula (150 μL of bacterial suspension or 100 μL of yeast suspension). Disk diffusion templates (6 wells of 6 mm internal diameter) or paper discs (6 mm diameter) were placed on the seeded plates. To each well, 50 μL of ampicillin/amphotericin B solution, 50 μL of each E. uchi
extract (10 mg/mL, resuspended in DMSO) and 50 μL of DMSO:BHI solution (1:1 v/v) as a negative control were added. Sterilized filter paper discs (Whatman®
grade No. 1) were individually impregnated with 40 μL of each 10 mg/mL extracts solution (resuspended in DMSO), 40 μL of DMSO:BHI (1:1, v/v) as negative control and 40 μL of ampicillin or amphotericin B as positive controls. The plates were incubated at 37 °C for 24–48 hours. The inhibition of the bacterial and/or fungal growth was determined by measuring the haloes around of the wells and discs with the aid of a digital calliper, and expressed as the average of three independent experimental determinations.
3.5. Broth Micro-Dilution Assay for Minimum Inhibitory Concentrations (MIC)
The minimum inhibitory concentration (MIC) of the extracts that presented some activity against the tested microbial strains was determined by the broth micro-dilution method, as described in the M7-A6 reference guideline of the Clinical and Laboratory Standards Institute, with modifications [35
The test was carried out in BHI broth for bacterial strains or RPMI-1640 (adjusted to pH 7.0 with 3-(N-morpholino) propanesulfonic acid (MOPS) buffer, 0.165 mol/L) for the yeast in 96-well flat-bottomed microtitration plates, containing 0.1 mL medium in each well. The extracts were prepared in DMSO at an initial concentration of 200 mg/mL and diluted in DMSO:BHI (1:5, v/v) to obtain 10 mg/mL in test solutions. Sample solutions (0.1 mL) were two-fold serially diluted in the plates with liquid medium. The working inoculum suspension (0.1 mL) was added to give a final inoculum concentration of 1 × 105–5 × 105 and 0.55 × 103–2.5 × 103 CFU/mL, for bacteria and yeast assays, respectively. Ampicillin final dilutions ranging from 12.5 μg/mL to 0.012 μg/mL and amphotericin B final dilutions ranging from 16 μg/mL to 0.015 μg/mL were used for bacteria and yeast, respectively, as positive control. Negative contamination controls using only medium (BHI or RPMI), and with or without extract were used in the tests. The plates were incubated at 37 °C for 24 and 48 hours for bacteria and yeast, respectively. No inhibitory effects were observed in the presence of DMSO at the highest concentration used. To perform the visual reading, 20 μL of 0.01% (w/v) resazurin (Sigma®) was added to each well. The plates were incubated for a further 30 minutes, and estimated visually for any change in color from blue to pink, indicating reduction of the dye due to microbial growth. The lowest concentration that remained blue was taken as the MIC. Experiments were performed in duplicate.
3.6. Cytotoxicity Assay
Cytotoxicity was tested on rabbit corneal fibroblasts (SIRC, CCL-60). These cells were maintained in culture bottles incubated at 37 °C with 5% CO2 in Eagle medium (pH 7) supplemented with 15% fetal bovine serum, without sodium bicarbonate. The extract samples were prepared by dissolving 10 mg of 20% decoction, 10% infusion, 5% maceration (EtOH 50%), 10% percolation (EtOH 50%) and 20% turboextraction (EtOH 50%) in 1 mL of DMSO. These initial stock solutions were diluted (1:5, v/v) in Eagle medium, to obtain the test solutions.
For cytotoxicity evaluation, the cells were collected, centrifuged (1500 rpm, 10 minutes) counted and adjusted to the concentration 1 × 105
cells/mL in Eagle medium. The cells were incubated in 96-well flat-bottomed microtitration plates at 37 °C in an atmosphere of 5% CO2
for 72 h. E. uchi
samples, diluted in DMSO:Eagle (1:10, v/v), were added. The extracts were serially diluted (1:1, v/v) across the plate resulting in an initial concentration of 200 μg/mL to a final concentration of 39 μg/mL. The plate was incubated for 24 hours at 37 °C in a humid atmosphere with 5% CO2
]. After this, 15 μL of resazurin aqueous solution (0.1 mg/mL) was added. The plate was incubated in a humid atmosphere with 5% CO2
at 37 °C. The wells were read visually after 3 hours by distinguishing the original blue color (absence of living cells) from pink (presence of living cells) and with a microplate fluorescence reader (Spectra Fluor Plus, Analysis program Magellin), with filters of 530 and 590 nm [39
3.7. Scavenging Activity of DPPH Radical
The assay of antioxidant activity of the extracts was based on the scavenging activity of 2.2-diphenyl-1-picrylhydrazyl solution (DPPH) [40
]. Gallic acid, rutin and vitamin C were used at a concentration of 250 μg/mL (in methanol), as antioxidants [41
]. A Ginkgo biloba
L. extract (Santosflora®
) was also used in this test, at the concentration of 250 μg/mL (in methanol), for its recognized antioxidant activity [42
]. The tests were performed on the extracts: 20% decoction; 10% infusion; 5% maceration (EtOH 50%); 10% percolation (EtOH 50%) and 20% turboextraction (EtOH 50%). To 1 mL of the sample solutions, 2.5 mL of 0.004% DPPH in methanol solution were added. The resulting solutions were homogenized by vortex and kept in the dark for 30 minutes at room temperature. A solution of DPPH in methanol (2.5:1, v/v) was used as negative control, and methanol was used as blank. Absorbance was measured at 517 nm in a Shimadzu-1603 spectrophotometer, with quartz cuvettes of 1 cm light pathway. The anti-radical activity was calculated by the equation: percent radical scavenging activity = (Abscontrol
× 100, where Abs
3.8. Statistical Analysis
The results were expressed as the average of three determinations ± standard deviation, using Microsoft Office Excel 2007®. When necessary, analysis of variance (ANOVA) was performed, with P < 0.05. The Spearman and Kendall-Tau tests (α = 0.05) were performed with Stat Plus Professional 2009® to verify correlation coefficient among total tannins content, total phenols content and antioxidant activity.