Maritime Halophyte Species from Southern Portugal as Sources of Bioactive Molecules

Extracts of five halophytes from southern Portugal (Arthrocnemum macrostachyum, Mesembryanthemum edule, Juncus acutus, Plantago coronopus and Halimione portulacoides), were studied for antioxidant, anti-inflammatory and in vitro antitumor properties. The most active extracts towards the 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical were the methanol extracts of M. edule (IC50 = 0.1 mg/mL) and J. acutus (IC50 = 0.4 mg/mL), and the ether extracts of J. acutus (IC50 = 0.2 mg/mL) and A. macrostachyum (IC50 = 0.3 mg/mL). The highest radical scavenging activity (RSA) against the 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) radical was obtained in the ether extract of J. acutus (IC50 = 0.4 mg/mL) and H. portulacoides (IC50 = 0.9 mg/mL). The maximum total phenolic content (TPC) was found in the methanol extract of M. edule (147 mg gallic acid equivalents (GAE)/g) and in the ether extract of J. acutus (94 mg GAE/g). Significant decreases in nitric oxide (NO) production were observed after incubation of macrophages with lipopolysaccharide (LPS) and the chloroform extract of H. portulacoides (IC50 = 109 µg/mL) and the hexane extract of P. coronopus (IC50 = 98.0 µg/mL). High in vitro cytotoxic activity and selectivity was obtained with the ether extract of J. acutus. Juncunol was identified as the active compound and for the first time was shown to display selective in vitro cytotoxicity towards various human cancer cells.

and mouth, dermal itching caused by insect bites, for treating wounds and burns and also for the treatment of sinusitis, diarrhea, infantile eczema and tuberculosis [7,8]. Sourfig is native to the coastal areas of South Africa and was introduced in southern and western Europe, including the Algarve, for soil stabilization and landscaping along railroad tracks and in sand banks. Because of its highly successful reproduction and dispersal capacity, sourfig became an invasive species in several parts of the world, including Europe, Australia, California and the Mediterranean. As physical (e.g., manual removal of plants) and chemical (i.e., use of herbicides) control are currently being used to decrease its populations, a more useful approach should include the use of the harvested plant as a source of beneficial secondary metabolites. The results obtained in this work are in accordance with previous in vitro studies showing that M. edule is endowed with strong antioxidant compounds, possibly of a polyphenolic nature [9][10][11][12]. Those properties suggests that biomass from M. edule could be used as source of antioxidants, thus contributing to the sustainable control of this invasive species.
A high radical scavenging activity (RSA) against DPPH • was also obtained with the methanol extract of J. acutus (IC 50 = 0.4 mg/mL), and the diethyl ether extracts of J. acutus (IC 50 = 0.2 mg/mL) and A. macrostachyum (IC 50 = 0.3 mg/mL; Table 1). Concerning the 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) (ABTS) free radical, the lowest IC 50 values were obtained in the diethyl ether extract of J. acutus (IC 50 = 0.4 mg/mL) and H. portulacoides (IC 50 = 0.9 mg/mL, Table 1). The species J. acutus is traditionally used for the treatment of infection and inflammation [13], and is endowed with antioxidant compounds, such as phenolics (e.g., 8,8′-bidehydrojuncusol) and flavones (e.g., luteolin), which were isolated from methanol extracts of the rhizomes [14]. The C3 shrub A. macrostachyum L. is also considered to be a medicinal plant [15], containing metabolites with RSA of the DPPH radical, and also iron reducing and copper chelating activities [12]. H. portulacoides is an obligate halophyte able to maintain growth in salinities up to 1 M NaCl [16]. Leaf waxes of H. portulacoides contain long chain chloroalkanes [17], and volatile organic compounds were detected in the root exudates [18]. Moreover, in a recent work it was found that the lipophilic fraction of leaves and stems of H. portulacoides was mainly composed of long chain aliphatic acids, alcohols and sterols, while the major component of the roots was a triterpenic ketone, whereas the leaves had a high content of phenolic compounds, mostly sulfated flavonoids [19]. However, to the best of our knowledge, there are no reports of the biological activity of this species.
The extracts with the highest total phenolic content (TPC) were the methanol extract of M. edule (147 mg gallic acid equivalents (GAE)/g DW) and the diethyl ether extract of J. acutus (93 mg GAE/g DW), which was correlated with a high RSA (Table 1). This is in agreement with several reports of positive correlations between the content of phenolics of halophyte extracts and its capacity to scavenge free radicals [10,20,21]. However, in other extracts and species no correlation between these parameters was observed, similar to the findings of Conforti et al. [22] in hydroalcoholic extracts of Mediterranean dietary plants. This suggests that the RSA of these samples might be due to combined action of phenolic compounds with other components such as peptides and organic acids [23].

Anti-Inflammatory Activity
To evaluate the in vitro anti-inflammatory activity of the extracts, the effect of nontoxic concentrations on the nitric oxide (NO) production was measured in lipopolysaccharide (LPS) stimulated RAW264.7 macrophage cells. LPS is in this context an endotoxin responsible for septic shock syndrome, which stimulates the production of inflammatory mediators such as NO, a radical often associated with the expression of pro-inflammatory proteins, namely iNOS and cyclooxygenase (COX-2) [24]. Thus, a reduction in NO production is indicative of the potential of the extracts to attenuate an inflammatory response. A significant decrease in NO production was observed upon incubation of macrophages with LPS and the chloroform extract of H. portulacoides (IC 50 = 109 µg/mL) as well as the hexane extract of P. coronopus (IC 50 = 98 µg/mL; Table 2), which suggests the presence of compounds with anti-inflammatory potential in these samples. This is the first report describing the anti-inflammatory potential of H. portulacoides and P. coronopus. However, other species of the Plantago genus, namely P. altissima and P. lanceolata, have already been described as containing anti-inflammatory molecules capable to inhibit COX-1 and 12-lipoxygenase (12-LOX) [25]. Interestingly, the application of the water extract of M. edule (3.9-125 µM) significantly increased the NO production (Table 2), which suggests that this extract contains compounds able to stimulate the response of RAW264.7 macrophages against LPS stimulation. Ordway et al. [26] observed that the methanol extract of M. edule exhibited an immunomodulatory effect, since it was able to stimulate THP-1 human monocyte-derived macrophages to kill ingested Staphylococcus aureus, and to promote the release of lymphokines associated with cellular immune functions, namely interferon gamma (IFN-γ). Although the compounds responsible for those activities are still unknown, such bioactivity could be useful for tuning and modification of the responses from the immune system, through the stimulation of the macrophage-mediated immune response. In this way, the aqueous extract of M. edule could be used as an immunostimulant, aiding infection resolution, in accordance with its in vitro antibacterial potential as described by Martins et al. [27].

Cytotoxic Activity
The evaluation of the cytotoxic activity of the extracts was made in vitro through the application of the samples to a human hepatocarcinoma cell line (HepG2) for 72 h at a concentration of 125 µg/mL, followed by determination of cell viability using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. A significant reduction in HepG2 cell viability was observed after application of the hexane extract of P. coronopus (39%) and the diethyl ether and chloroform extracts of M. edule (50% and 58% of cellular viability, respectively; Figure 1).
The use of several Plantago species by humans against cancer has been reported by different authors, and includes the species P. coronopus, P. lanceolata, P. major, P. ovate and P. hirtella [28]. A methanol extract of P. coronopus significantly reduced the viability of human breast (MCF-7) and melanoma (UACC-62) cell lines [29]. In the same way, several compounds with antiproliferative activity against mouse T-cell lymphoma cells were isolated from M. edule, namely β-amyrin, uvaol, oleanolic acid, monogalactosyldiacylglycerol, catechin, epicatechin and procyanidin B5 [30].
The best result was achieved with the diethyl ether extract of J. acutus, which reduced cell viability to 7.7%; similar to the results obtained with the positive control compound, the drug etoposide ( Figure 1). The chloroform and methanol extracts of J. acutus also showed low tumor cell viabilities of 22% and 37%, respectively ( Figure 1). Juncus is the largest genus in the Juncaceae family comprising more than 200 species that usually grow in maritime environments, such as salt marshes, or in badly drained soils under different climatic conditions [31]. It has been claimed that several species belonging to the Juncus genus exhibit medicinal properties: the medulla of J. effusus (L.) is used as an antipyretic and sedative agent whereas the rhizomes of J. maritimus are recommended for insomnia [31]. The species J. rigidus has diuretic effects and is useful in the treatment of stomach disorders [2]. Leaves from J. acutus are used in the province of Almeria (Spain) to treat warts [32], in oriental traditional medicine the seeds of Juncus sp. are used for the treatment of diarrhea and fruits are used in infusions to alleviate cold symptoms [31].
Several biological activities have been ascribed to extracts made from different species of Juncus, namely cytotoxicity, antitumoral, anti-eczematic, anti-inflammatory, anti-algal, antioxidant and hepatoprotective [2,31]. Juncus species are known to contain secondary metabolites of different classes, namely coumarins, flavonoids, sterols, terpenes, phenolic acids, stilbenes, carotenoids and phenanthrenes [2,31]. The rhizomes of J. acutus are known to contain phenanthrenoids with anti-inflammatory activity [33], while the aerial parts are endowed with phenolic glycosides displaying anti-eczematic activity [13]. Regarding in vitro antitumoral activity, it was shown that a hydroalcoholic extract of the tops of the species J. roemerianus was active against the National Cancer Institute's murine P-388 lymphocytic leukemia [34]. However, to the best of our knowledge, until now there has been no information about the cytotoxic activity of J. acutus towards human tumoral cells.
Given the promising results obtained with the diethyl ether extract of J. acutus, the IC 50 values and the selectivity index (SI) towards cells of non-tumoural origin (S17, murine bone marrow) were also determined and are summarized in Table 3. According to dos Santos et al. [35], natural extracts are considered promising sources of antitumoral compounds when they exhibit IC 50 values lower than 30 µg/mL. That was the case of the J. acutus extract, with an IC 50 value of 6.2 µg/mL in HepG2 cells, significantly lower than that obtained in the S17 cell line (IC 50 , 34.4 µg/mL, p < 0.05). Moreover, the SI displayed by J. acutus (5.5) was similar to the one observed for etoposide (SI = 5.4, Table 3).
In order to identify the compound responsible for the cytotoxic activity, the extract from J. acutus was submitted to a bio-guided fractionation, affording 10 fractions from which fractions 2 to 8 were cytotoxic to HepG2 and S17 cells (Figure 2). Fraction 2 displayed the highest selectivity against HePG2 cells (SI = 7.1), and was further fractionated until an active and apparently pure compound was obtained. The chemical structure of the isolated compound was established using spectral data obtained with FT-IR, 1 H-NMR, 13 C-NMR and mass spectrometry. Values represent the mean ± SEM of at least three experiments performed in triplicate (n = 9); * Indicates significant differences (p < 0.01) as compared with S17 cells. The chemical shifts from 1 H and 13 C-NMR spectra were consistent with the compound juncunol ( Figure 4) [36].
This compound was previously identified in J. acutus and J. roemerianus [36][37][38][39], and displayed phytotoxicity against the microalga Selenastrum capricornutum [38], but low activity against the growth of Agrobacterium tumefaciens using the potato disc assay, and also in the brine shrimp assay [36,37]. However, to the best of our knowledge, nothing was known until now about the in vitro cytotoxic activity of juncunol against human cancer cells. The cytotoxicity of pure juncunol was further tested in different tumoral cell lines and the selectivity towards S17 and mTEC (mouse thymic epithelial) cells was assessed (Table 4).   Table 4. Effect of the application of juncunol and etoposide on the viability of tumoral (HepG2) and non-tumoral cell lines (S17 and mTEC), expressed as IC 50 values (µM /mL), and selectivity index (SI). In addition to HepG2 cells, juncunol was able to significantly reduce the viability of human breast and cervical cell lines, while maintaining a high SI towards S17 (SI values of 17 and 14 respectively) and mTEC cell lines (SI values of 16 and 13, respectively; Table 4). Juncusol, a dihydrophenanthrene closely related to juncunol was isolated from J. roemerianus and was demonstrated to significantly reduce the viability of different cell lines, such as human epidermoid carcinoma of the nasopharynx (NCI 90 KB: IC 50 = 0.3 µg/mL), B-16 mouse melanoma (IC50 = 12.5 µg/mL) and also of L-1210 mouse lymphocytic leukaemia (IC 50 = 12.5 µg/mL) [34], but no assays were performed in order to establish the selectivity of that compound. The IC 50 values obtained in our work (HePG2 = 4.6 µg/mL; MDA-MB-468 = 5.6 µg/mL and HeLa = 6.9 µg/mL) were lower than those obtained with juncusol suggesting a higher in vitro cytotoxicity of juncunol. Nevertheless, one must bear in mind that different cell lines and methodologies were tested.

Cell lines
Taken together, our results indicate that juncunol is a good candidate for further studies on its potential use as an anticancer drug or as a valuable lead compound for the semi-synthesis or total synthesis of effective novel drugs. Assays are currently being conducted in order to elucidate its mode of action.

Plant Material and Preparation of the Extracts
Five species of halophytes were collected in the south of Portugal, near Faro beach and Ludo, in May 2010, namely A. macrostachyum, M. edule, J. acutus, P. coronopus and Halimiones portulacoides. Taxonomical classification was confirmed by Dr. Manuel J. Pinto (National Museum of Natural History, University of Lisbon, Botanical Garden, Portugal). Voucher specimens are being kept in a herbarium in the MarBiotech laboratory. Samples were oven dried for three days at 40 °C and powdered, and the extracts were prepared sequentially as follows: the dried powder was mixed with hexane (1:10, w/v) and homogenized during 2 min. using a disperser IKA Ultra-Turrax T10B, at room temperature (RT). Samples were then centrifuged (10 min, 5000× g, RT), and the supernatants were recovered. The extraction was repeated three more times and the supernatants were combined and filtered (Whatman No, 4). The remaining biomass was consecutively extracted with diethyl ether, chloroform, methanol and water. The organic extracts were evaporated under reduced pressure, and aqueous extracts were freeze dried. Dried extracts were weighed, dissolved in DMSO to obtain a final concentration of 50 mg/mL and stored at 4 °C.

RSA by the DPPH • Assay
The antioxidant activity was assessed by the DPPH • assay, according to the method of Brand-Williams et al. [40], as described by Moreno et al. [41]. Samples (22 µL) at concentrations ranging from 0.125 to 10 mg/mL were mixed with 200 µL of a methanol DPPH • solution (120 µM) in 96-well microplates and incubated for 30 min at RT, in the dark. Absorbance was measured at 517 nm using a Biotek Synergy 4 microplate reader and results were expressed as antioxidant activity (%), relative to a control containing DMSO and as half maximal inhibitory concentration (IC 50 , mg/mL). BHT (E320) was used as the positive control at the same concentrations of the biological samples.

RSA by the ABTS •+ Assay
The RSA against ABTS •+ was evaluated according to Re et al. [42]. A stock solution of ABTS •+ (7.4 mM) was prepared in potassium persulfate (2.6 mM), and left in the dark for 12-16 h at RT. The ABTS •+ solution was then diluted with ethanol to get an absorbance of 0.7 at 734 nm (Biotek Synergy 4). The samples (10 µL), at concentrations ranging from 125 to 1000 µg/mL, were mixed with 190 µL of ABTS •+ solution in 96-well microplates, and after 6 min of incubation the absorbance was measured at 734 nm (Biotek Synergy 4, Biotek, Winooski, VT, USA). Results were presented as antioxidant activity (%) relative to a control containing DMSO, and as IC 50 values (mg/mL). BHT was used as a positive control at the same concentrations of the extracts.

Total Phenolic Content (TPC)
The TPC of the extracts was determined by the F-C colorimetric assay [43]. The experiments were performed in 96-well plates: 5 µL of each extract at a concentration of 10 mg/mL were mixed with 100 µL of diluted F-C (1:10, v/v in water). After 5 min, 100 µL of a sodium carbonate solution (75 g/L, in water) were added, and the mixture was incubated at RT for 90 min in the dark. Absorbance was measured at 725 nm in a microplate reader (Biotek Synergy 4). TPC was calculated based on a standard curve of gallic acid and the results were expressed as milligrams of gallic acid equivalents per gram of dry weight (mg GAE/g DW).

Quantification of NO
Exponentially growing RAW264.7 cells were plated at 2.5 × 10 5 cells/well in 96-well tissue plates and allowed to adhere overnight. Afterwards, cells were treated with concentrations of the extracts allowing cellular viability higher than 80%, in serum-and phenol-free culture medium, for 24 h together with LPS (100 ng/mL) [44]. Control cells were treated with DMSO at the highest concentration used in test wells (0.5%), and NO production in cell culture medium was measured spectrophotometrically by the Griess method [45]. In brief, 100 µL of the culture supernatants were mixed with 100 µL of Griess reagent (1% (w/v) sulphanilamide + 0.1% of NED and 2.5% (v/v) phosphoric acid), incubated for 20 min at RT in the dark, and absorbance was measured at 540 nm on a microplate reader (Biotek Synergy 4). The NO concentration was determined using a calibration curve prepared with several known concentrations (1.7, 3.1, 6.2, 12.5, 25, 50 and 100 µM) of sodium nitrite as standard. Results were expressed as NO production (%) relative to LPS-stimulated RAW264.7 cells, and as IC 50 values (µg/mL).

Cell Viability Assay
Exponentially growing HepG2 and S17cells were plated in 96-well tissue plates at a density of 5 × 10 3 cells/well and incubated for 24 h. Then, extracts were applied at various concentrations (3.9, 7.8, 15.6, 31.2, 62.5 and 125 µg/mL) for 72 h. Control cells were treated with DMSO at the highest concentration used in test wells (0.5%), and cell viability was determined by the MTT colorimetric assay [46]. Briefly, 2 hours prior to the end of the incubation period 20 μL of MTT (5 mg/mL in PBS) were added to each well and further incubated at 37 °C. Then, 150 μL of DMSO was added to each well in order to dissolve the formazan crystals and absorbance was measured at 590 nm (Biotek Synergy 4). Results were expressed in terms of cell viability (%) and IC 50 values (µg/mL). The selectivity index (SI) of the extracts was estimated using the following equation: SI = VNT/VT, where VNT and VT indicate cell viability on non-tumoral cells (S17) and tumoral cells (HepG2), respectively [47].

Bioguided Fractionation and Isolation of the Bioactive Compound
The active crude extract of J. acutus (5 g) was subjected to silica gel (120 mesh) column chromatography (25 cm × 2 cm i.d), and eluted with different proportions of n-hexane, a mixture of n-hexane and ethyl acetate (90:10; 85:15; 4:1; 75:25; 7:3; 3:2 and 1:1), ethyl acetate and a mixture of chloroform and methanol (1:1). Fractions with similar TLC profiles using GF254 (Merck) as stationary phase and n-hexane/EtOAc 3:1 and 4:1 as mobile phase, were pooled yielding 10 fractions, which were tested for cytotoxic activity and selectivity as described on the Section 3.8. Based on the results, fraction 2 (0.76 g) was selected and subjected to a new silica 60 mesh column chromatography (14 cm × 2 cm i.d) and sequentially eluted with n-hexane and a mixture of n-hexane and ethyl acetate (98:2 and 95:5) affording 3 fractions, which were again evaluated for cytotoxicity. Fraction 3 (100 mg), an orange solid powder, was active and contained a pure compound, which was stored at 4 °C until further use.

Spectral and Chromatographic Analysis
IR spectra were recorded on a Bruker spectrophotometer (Bruker, Coventry, UK) in a range of 500-4000 cm −1 . GC-MS analysis was performed using Agilent 6890N Gas Chromatograph connected to Agilent 5973 Mass Spectrometer (Agilent, Santa Clara, CA, USA) operated at 70 eV. The isolated compound was dissolved in CDCl 3 (99.8% D) and analyzed at 27 °C at 600.03 MHz for 1 H and 150.88 MHz for 13 C. NMR-spectra were acquired using a 600 MHz Bruker Avance III HD equipped with a cryogenically cooled 5 mm dual probe optimized for 13 C and 1 H. Proton spectra were acquired using 30°-pulses, a spectral width of 12 kHz, collecting 16 scans with a length of 65,536 data points with a relaxation delay of 1.0 s. Carbon spectra were acquired with 30°-pulses, a spectral width of 36 kHz, collecting 256 scans with a length of 65,536 data points and with a relaxation delay of 2.0 s. FIDs were exponentially multiplied with a line broadening factor of 0.3 Hz ( 1 H) and 1.0 Hz ( 13 C) before Fourier transform. Signals were assigned using information obtained by COSY, HSQC, HMBC (65 ms and 100 ms mixing time) experiments. Standard parameters and sequences were used as delivered with the software Topspin (version 3.2, Bruker). HR-ESIMS were performed on a microQTOF-QII mass spectrometer (Bruker Daltonik GmbH) equipped with an electrospray ionization interface (ESI). The sample were introduced using a RP-HPLC system (Agilent 1200, Agilent, Santa Clara, CA, USA) employing a steep gradient of acetonitrile in water with 0.1% formic acid. A small portion of the eluate was directed towards the ESI where it was ionized using a capillary voltage of 4100 V, a drying temperature of 200 °C, nebulizer pressure of 2.0 bar and a drying gas flow of 7 L/min. Mass spectra were externally calibrated using a standard of sodium formate clusters introduced just before the analysis.

Statistical Analysis
The results were expressed as mean ± SEM, and the experiments were conducted in triplicate. Analysis of variance (ANOVA) was used to assess differences using the SPSS statistical package for Windows (release 15.0, SPSS INC), and significance between means was analyzed by the Tukey HSD test (p < 0.05). The IC 50 values were calculated by sigmoidal fitting of the data in the GraphPad Prism V 5.0 program (GraphPad Software, La Jolla, CA, USA).

Conclusions
Halophytes are endowed with a vast array of compounds displaying important biological activities, such as antioxidant, antimicrobial and antitumoral, and therefore could be useful in the prevention and treatment of a variety of diseases, namely cancer, chronic inflammation, atherosclerosis and cardiovascular disorders. In this context, halophytic species have been increasingly considered as an important source of novel active agents with applications in the food and pharmaceutical industries [2]. In this work five maritime halophytic species abundant on the southern coast of Portugal were evaluated for their potential as sources of antioxidant, anti-inflammatory and cytotoxic compounds. M. edule and J. acutus revealed a strong antioxidant potential and a high content of phenolic compounds, while H. portulacoides and P. coronopus displayed a high capacity to attenuate NO release in LPS-stimulated macrophages, suggesting a possible anti-inflammatory activity. J. acutus exhibited a strong in vitro selective cytotoxic activity against HepG2 cells, a human hepatocarcinoma cell line highly resistant to drugs and toxins [48], and therefore, it was fractionated until the bioactive compound was isolated and identified as juncunol (1,7-dimethyl-5-vinyl-9,10-dihydrophenanthren-2-ol). For the first time, juncunol was shown to display a high selective in vitro cytotoxicity towards various human cancer cell lines and hence, can be considered a potential chemotherapeutic agent or a scaffold for the semi-synthesis or total synthesis of effective new anticancer drugs. Assays are currently being conducted in order to elucidate the mechanisms responsible for the cytotoxic activity displayed by juncunol.