Extracts of Eryngium foetidum Leaves from the Amazonia Were Efficient Scavengers of ROS and RNS

Eryngium foetidum L. is an edible plant widespread in Amazonian cuisine and its leaves have high levels of promising phenolic compounds for the production of extracts to be used as natural antioxidant additives. In this study, the in vitro scavenging capacity of three freeze-dried extracts of E. foetidum leaves, obtained by ultrasound-assisted extraction using green solvents [water (H2O), ethanol (EtOH), and ethanol/water (EtOH/H2O)], was investigated against the most common reactive oxygen species (ROS) and reactive nitrogen species (RNS) generated in both physiological and food systems. Six phenolic compounds were identified, chlorogenic acid (2198, 1816 and 506 μg/g) being the major compound for EtOH/H2O, H2O, and EtOH extracts, respectively. All E. foetidum extracts were efficient in scavenging all the ROS and RNS (IC50 = 45–1000 µg/mL), especially ROS. The EtOH/H2O extract showed the highest contents of phenolic compounds (5781 μg/g) and showed the highest efficiency in scavenging all the reactive species, with high efficiency for O2•− (IC50 = 45 μg/mL), except for ROO•, for which EtOH extract was the most efficient. Therefore, E. foetidum leaf extracts, especially EtOH/H2O, showed high antioxidant potential to be used as natural antioxidants in food formulations and are promising for nutraceuticals products.


Introduction
Eryngium foetidum L., one of the main non-conventional vegetables grown in Brazil [1] (also known as Plantas Alimentícias Não-Convencionais, PANCs, in Portuguese), is native to the Amazonia biome and Central America [2]. It is a vegetable widely used as a condiment in Amazonian cuisine and has attracted the attention of researchers because its use in traditional medicine to treat different pathologies and due to the presence of bioactive compounds with promising antioxidant properties [3][4][5][6][7][8][9].
Exogenous antioxidant compounds absorbed from the diet, as well as endogenous antioxidants produced by the human body, can inhibit or delay cell damage by scavenging reactive oxygen species (ROS) and reactive nitrogen species (RNS). Although ROS and RNS have beneficial physiological effects, such as cell signaling, ROS and RNS can impair the normal functioning of cells when overproduced in the physiological system as a result of oxidative stress [10]. Although the endogenous defense mechanisms of the human body, such as glutathione and the enzymatic systems superoxide dismutase, catalase, and glutathione peroxidase, are able to reduce the oxidative damage induced by the overproduction of ROS and RNS [10][11][12], endogenous antioxidants are generally not enough, and it is therefore necessary to supply antioxidants from exogenous sources.

Leaves of Eryngium foetidum
The leaves of E. foetidum were obtained from a vegetable farm in Santa Izabel do Pará, Brazil (Latitude: −1.29938, Longitude: −48.161, 1 • 17 58 S, 48 • 9 40 W) in July, 2017. The access to the selected plants was registered in the Brazilian National System for the Management of Genetic Heritage and Associated Traditional Knowledge (SisGen, A89EDD3). The leaves (approximately 500 g) were washed with distilled water, left to dry at room temperature (25 • C) for 2 h, frozen at −18 • C and freeze-dried (Liotop, L101, São Paulo, Brazil) at −60 • C in continuous vacuum for 24 h. The freeze-dried leaves were crushed, packaged in plastic bags under vacuum, and stored at −18 • C, protected from light exposure.

Extracts of Eryngium foetidum Leaves
The ultrasound-assisted method used to produce three extracts of E. foetidum leaves was carried out using three green solvents, as suggested elsewhere [23], with modifications. The following solvents were used: ethanol (EtOH), ethanol/water mixture (1:1, w/v) (EtOH/H 2 O), and water (H 2 O), and they were chosen considering the permissibility of residue in extracts after evaporation, following the Commission Directive 95/45/EC of the European Communities [24]. For each extract, the leaves were mixed with the solvent (1:10, w/v), and the phenolic compounds were extracted during 5 min in an ultrasound bath (Quimis, model 03350, São Paulo, Brazil) with a fixed frequency of 25 KHz, at room temperature. After the time in the ultrasonic bath, the extracts were centrifuged (Heraeus multifuge X1r centrifuge, Thermo Electron Led GMBH, São Paulo, Brazil) at 11,627.2× g for 5 min at room temperature, and the supernatant fraction was collected. The solid residues were subjected to seven more extractions under the same conditions and all centrifuged liquid fractions were combined to compose the extract. Then, the extracts containing EtOH and EtOH/H 2 O were dried and concentrated, respectively, under reduced pressure in a rotary evaporator (T < 38 • C), and the ethanol free extracts were frozen at −18 • C followed by freeze-drying (Liotop, L101, São Paulo, Brazil). All the freeze-dried extracts were stored at −18 • C until analysis, in amber flasks saturated with N 2 flow. The extraction procedure was performed in triplicate (n = 3) for each solvent.

Phenolic Compounds Composition by HPLC-DAD
The freeze-dried extracts of E. foetidum leaves were solubilized in methanol/water (80:20, v/v) and injected into an Agilent HPLC (Agilent 1260 Infinity model, Santa Clara, CA, USA) equipped with a quaternary pump (G1311C), an automatic injector (G7129), an oven (G1316A), and a DAD detector (G1328C). The phenolic compounds were separated on a Synergi Hydro C 18 column (Phenomenex, 4 µm, 250 × 4.6 mm), using a linear gradient of water/formic acid (99.5: 0.5, v/v) and acetonitrile/formic acid (99.5: 0.5 v/v) as mobile phase, according to the procedure described in detail by [25]. The UV-visible spectra were obtained between 200 and 600 nm, and chromatograms were processed at 270, 320, and 360 nm. The phenolic compounds were quantified by external standards, and the limits of detection (LOD) and quantification (LOQ) were calculated using the parameters of the analytical curves [26]. The six-point analytical curves (3.12-100 µg/mL, in duplicate) were quercetin (360 nm, R 2 = 0.99, LOD = 0.15 µg/mL and LOQ = 0.62 µg/mL), luteolin (320 nm, R 2 = 0.99, LOD = 0.15 µg/mL and LOQ = 0.62 µg/mL), and chlorogenic acid (320 nm, R 2 = 0.99, LOD = 0.15 µg/mL and LOQ = 0.62 µg/mL). The contents of phenolic compounds were expressed in µg/g of extract (dry basis), considering three independent extraction procedures (n = 3). The phenolic compounds were tentatively identified by combining the following information: elution order and retention time on the C 18 column, comparison with authentic standards analyzed under the same conditions, and UV-Visible spectra in comparison with the same compounds previously identified and quantified by our research group by mass spectrometry using electrospray as ionization source and sequential fragmentation data (HPLC-DAD-ESI-MS n ) [8].

In Vitro Antioxidant Capacity of E. foetidum Extracts to Scavenge ROS and RNS
Except for the 1 O 2 -quenching assay, all the other assays were carried out in a microplate reader (Synergy HT, BioTek, Winooski, VT, USA), equipped with a thermostat, by fluorescence, absorbance, or chemiluminescence measurements. No interference were observed among the extracts at the highest tested concentration for each assay with the specific probes. Chlorogenic acid, quercetin, and ascorbic acid were used as positive controls. Each ROS/RNS-scavenging assay corresponds to four independent experiments, each performed in triplicate (n = 3), at six different concentrations of E. foetidum extracts.
The results were expressed as percentage of inhibition (mean ± standard error of the mean, SEM) and the extract concentrations that were able to decrease the effect of each ROS and RNS by 50% (IC 50 ) were obtained from the curves of the percentage of inhibition versus antioxidant concentration using Origin Pro v8 software (OriginLab Corporation, Northampton, MA, USA).

Singlet Oxygen ( 1 O 2 )-Quenching Assay
The 1 O 2 -quenching capacity of E. foetidum extracts was determined by monitoring the inhibition of L-tryptophan degradation during 1 O 2 generation by photosensitization of MB [8]. Five concentrations of E. foetidum extracts (125 to 1000 µg/mL) were tested, along with quercetin (0.78 to 4.75 µg/mL) and chlorogenic acid (0.78 to 4.75 µg/mL) as positive controls. Kinetic data obtained from the intensity of tryptophan absorbance decay (219 nm) were fitted to a first-order reaction (Equation (1)), using the Origin Pro 8 software and the rate constants were calculated (Equation (2)). The percentage of protection that E. foetidum extract (EXT) (or positive controls) offered to tryptophan (TRP) was calculated using Equation (3).
where Y is the TRP absorbance; Y∞ is the TRP absorbance at infinite time; A is the preexponential factor; k is the pseudo-first order rate constant; x is the reaction time; t 1⁄2 is the half-life time (min); k TRP obs is the observed pseudo-first order rate constant fitted to the TRP decay curve (obtained in the blank experiment without the antioxidant); and k TRP+EXT obs is the observed pseudo-first order rate constant fitted to the TRP decay curve in the presence of E. foetidum extracts.

Superoxide Radical (O 2
•− )-Scavenging Assay O 2 •− was generated by the NADH/PMS/O 2 system and the O 2 •− -scavenging capacity was determined by monitoring the effect of the E. foetidum extracts (or positive controls) on the NBT reduction induced by O 2 •− at 560 nm, after 10 min of incubation at room temperature [23]. The concentrations of the E. foetidum extracts varied from 3.91 to 125 µg/mL; for quercetin it was from 0.001 to 30 µg/mL, and for chlorogenic acid it was from 12.5 to 250 µg/mL. The results were expressed as percentage inhibition of the reduction of NBT to formazan.

Hypochlorous Acid (HOCl)-Scavenging Assay
The HOCl-scavenging capacity of E. foetidum extracts was measured by monitoring the inhibition of the increase in fluorescence resulting from the oxidation of DHR 123 to rhodamine 123 as induced by HOCl [23]. The fluorescence measurement was observed at the excitation wavelength at 485 ± 20 nm and emission at 528 ± 20 nm. HOCl was prepared by adjusting the pH of a NaOCl solution 1% (w/v) to 6.2 with the dropwise addition of 10% H 2 SO 4 , and the concentration was determined by spectrophotometry at 235 nm (ε = 100 M −1 ·cm −1 ). The E. foetidum extracts were tested from 31.5 to 650 µg/mL, quercetin from 0.001 to 30 µg/mL, and chlorogenic acid from 0.24 to 7.81 µg/mL.

Hydrogen Peroxide (H 2 O 2 )-Scavenging Assay
The H 2 O 2 -scavenging capacity was determined by monitoring the effect of E. foetidum extracts on the inhibition of chemiluminescence observed during the H 2 O 2 -induced oxidation of lucigenin [23]. The readings were carried out after 5 min of reaction in the presence of E. foetidum extract (3.91 to 125 µg/mL), quercetin (0.001 to 30 µg/mL), or chlorogenic acid (12.50 to 250 µg/mL).

Peroxyl Radicals (ROO • )-Scavenging Assay
The evaluation of ROO • -scavenging capacity was determined as described elsewhere [23] and measured by monitoring the effect of E. foetidum extracts on the inhibition of fluorescence decay of fluorescein resulting from ROO • -induced oxidation. The reaction media was pre-incubated at 37 • C for 15 min. The fluorescence signal was monitored every minute at the emission wavelength at 528 ± 20 nm, with excitation at 485 ± 20 nm, until total fluorescence decay. Trolox was used as positive control. The protection provided by the antioxidants was calculated using the difference between the area under the fluorescence decay curve in the presence of antioxidants and in its absence. The ROO • -scavenging capacity was expressed as the ratio between the slope of each extract (or positive control) and the slopes obtained for Trolox curves, as previously described [27].

Peroxynitrite Anion (ONOO − )-Scavenging Assay
The ONOO − -scavenging capacity was determined by monitoring the effect of E. foetidum extracts on the inhibition of the increase in fluorescence resulting from the oxidation of DHR 123 to non-fluorescent rhodamine 123 as induced by ONOO − [23]. ONOO − was chemically synthesized as described elsewhere [28]. The fluorescence measurement was monitored at the excitation wavelength at 485 ± 20 nm and emission at 528 ± 20 nm, after 2 min of incubation at 37 • C. Parallel tests were carried out in the presence of 25 mM NaHCO 3 to simulate physiological conditions. The E. foetidum extracts were tested from 400 to 900 µg/mL, and chlorogenic acid from 0.06 to 1.95 µg/mL.

Statistical Analysis
All the results (mean ± standard deviation or standard error of the mean) were calculated and submitted to analysis of variance (one-way ANOVA) and the means were compared by Tukey's test, or Student's test, at the significance level of 95% (p < 0.05) with Statistica 8.1 (Statsoft) software.

Composition of Phenolic Compounds in the E. foetidum Extracts
HPLC-DAD analysis of the freeze-dried extracts of E. foetidum leaves allowed the separation ( Figure 1) and quantification (Table 1) of six phenolic compounds.

Statistical Analysis
All the results (mean ± standard deviation or standard error of the mean) were calculated and submitted to analysis of variance (one-way ANOVA) and the means were compared by Tukey's test, or Student's test, at the significance level of 95% (p < 0.05) with Statistica 8.1(Statsoft) software.
Chlorogenic acid is a biologically active phenolic compound and is one of the phenolic acids widely found naturally in certain plant species, such as Camelia sinensis, also being Antioxidants 2023, 12, 1112 7 of 13 one of the main phenolic compounds of coffee. Chlorogenic acid has versatile properties as it acts both as a nutraceutical and food additive. As a nutraceutical, it exhibits antioxidant, anti-inflammatory and anti-hypertensive properties, among others, which can contribute to the prevention and treatment of several associated pathologies [29][30][31][32]. On the other hand, as food additive, chlorogenic acid inhibits lipid oxidation, prevents degradation of other bioactive compounds, has antimicrobial activity, and can act as prebiotic [17,29].
Among the tested extracts, the EtOH/H 2 O extract presented the highest contents of phenolic compounds (5581 µg/g extract), followed by the H 2 O extract (3416 µg/g extract).
The sum of the identified phenolic compounds in the EtOH extract (1104 µg/g extract) was three and five times lower than the total contents observed for the H 2 O and EtOH/H 2 O extracts, respectively ( Table 1). The differences among the contents found in the extracts were expected and are commonly associated in the literature with the polarities of the studied solvents, which modulate the type of extracted compounds based on the affinity with the solvent [33][34][35][36][37][38]. Furthermore, depending on the food matrix, the combination of two or more solvents during extract preparation may allow the extraction of higher amounts of certain types of phenolic compounds than isolated solvents [39][40][41]. In addition, the extraction of different classes of phenolic compounds considering the use of solvents with different polarities has been widely discussed in the literature [42][43][44][45].
According to our study (Figure 2), the highest efficiency to extract the most polar phenolic compounds (phenolic acids) was observed for H 2 O, which has the highest polarity among the solvents. On the other hand, flavones were better extracted with EtOH (the lowest polarity), and the addition of water decreased the ability of ethanol to solubilize this type of phenolic compounds. Interestingly, the mixture of water and ethanol yielded the highest contents of flavonols, being represented in our study by quercetin glucuronide (Table 1).
Chlorogenic acid is a biologically active phenolic compound and is one of the phenolic acids widely found naturally in certain plant species, such as Camelia sinensis, also being one of the main phenolic compounds of coffee. Chlorogenic acid has versatile properties as it acts both as a nutraceutical and food additive. As a nutraceutical, it exhibits antioxidant, anti-inflammatory and anti-hypertensive properties, among others, which can contribute to the prevention and treatment of several associated pathologies [29][30][31][32]. On the other hand, as food additive, chlorogenic acid inhibits lipid oxidation, prevents degradation of other bioactive compounds, has antimicrobial activity, and can act as prebiotic [17,29].
Among the tested extracts, the EtOH/H2O extract presented the highest contents of phenolic compounds (5581 μg/g extract), followed by the H2O extract (3416 μg/g extract).
The sum of the identified phenolic compounds in the EtOH extract (1104 μg/g extract) was three and five times lower than the total contents observed for the H2O and EtOH/H2O extracts, respectively ( Table 1). The differences among the contents found in the extracts were expected and are commonly associated in the literature with the polarities of the studied solvents, which modulate the type of extracted compounds based on the affinity with the solvent [33][34][35][36][37][38]. Furthermore, depending on the food matrix, the combination of two or more solvents during extract preparation may allow the extraction of higher amounts of certain types of phenolic compounds than isolated solvents [39][40][41]. In addition, the extraction of different classes of phenolic compounds considering the use of solvents with different polarities has been widely discussed in the literature [42][43][44][45].
According to our study (Figure 2), the highest efficiency to extract the most polar phenolic compounds (phenolic acids) was observed for H2O, which has the highest polarity among the solvents. On the other hand, flavones were better extracted with EtOH (the lowest polarity), and the addition of water decreased the ability of ethanol to solubilize this type of phenolic compounds. Interestingly, the mixture of water and ethanol yielded the highest contents of flavonols, being represented in our study by quercetin glucuronide (Table 1).

In Vitro Antioxidant Capacity of Eryngium foetidum Extracts to Scavenge ROS and RNS
In general, all the extracts of E. foetidum leaves were able to inhibit the oxidizing effects of the tested reactive species (Table 2) in a concentration-dependent manner, except for the H 2 O extract, which did not show quenching ability at the highest tested concentration (1000 µg/mL). Among the extracts, the EtOH/H 2 O presented the highest antioxidant efficiency, probably due to its high contents of phenolic compounds, mainly phenolic acids (≈75% of the total sum) (Table 1). Recently, phenolic acids have received special attention due to their relevant pharmacological contributions associated with improvement of health as consequence of their antioxidant and anti-inflammatory properties, providing protection against diseases related to oxidative stress [17,30,46]. In addition to physiological effects, phenolic acids were also reported as efficient antioxidants in food systems [47].
The EtOH/H 2 O extract showed superior efficiency in quenching 1 O 2 (IC 50 at 76 µg/mL) as compared to the EtOH extract (IC 50 at 1000 µg/mL), while the H 2 O extract did not show any antioxidant activity at the highest tested concentration (1000 µg/mL). The quenching efficiency observed for the EtOH/H 2 O extract of E. foetidum was 3.5 times higher than S. diploconos extract (IC 50 = 269 µg/mL) [48] and close to the values reported for Caesalpinia crista leaf extracts (IC 50 = 61 µg/mL) [49], but much lower than chlorogenic acid and quercetin (  [50][51][52][53][54], and cause deleterious biological effects [52,[55][56][57]. In foods, 1 O 2 oxidizes amino acids and vitamins, yet it reacts very quickly with polyunsaturated fatty acids and aromatic amino acids due to the high reactivity of π electrons of double bonds; the greater the unsaturation of fatty acids, the higher the reaction rate with 1 O 2 [15]. Thus, natural extracts with bioactive compounds with high 1 O 2 -quenching capacity are highly desirable as promising natural ingredients for food formulations to increase the stability of foods. Regarding O 2 •− , the EtOH/H 2 O extract of E. foetidum leaves presented the highest antioxidant capacity (IC 50 = 45 µg/mL) ( Table 2), which was 1.9 and 2.3 times superior when compared to the EtOH and H 2 O extracts, respectively, but less efficient than chlorogenic acid (20 µg/mL) and quercetin (12.9 µg/mL). Conversely, Souza et al. [22] reported no antioxidant activity in a methanolic extract of E. foetidum at the highest tested concentration of 4 mg/mL. However, this extract exhibited similar antioxidant efficiency to walnut leaf extracts (Ruglans regia), whose IC 50 was 47 µg/mL [58], and superior efficiency to Vismia cauliflora leaf extract (51 µg/mL) [59].
Among the ROS, O 2 •− is considered an important precursor of a variety of other highly reactive pro-oxidant species [10] can be used to delay oxidative processes, including lipid peroxidation, which is one of the main pathways to food deterioration during processing and storage [11]. Concerning HOCl, the EtOH/H 2 O extract was about twice as effective as compared to the EtOH and H 2 O extracts. When compared to the literature, this E. foetidum extract was more efficient than Caesalpinia crista leaf extracts (IC 50 at 170 µg/mL) [49]. However, Souza et al. [22] reported higher antioxidant efficiency in the methanolic extract of E. foetidum (13 µg/mL) than the extracts obtained in our study (IC 50 from 118 to 222 µg/mL). The importance of being an efficient HOCl-scavenger is mainly due to the fact that this ROS, by itself, is considered a strong oxidant that reacts with O 2 •− to generate • OH, another highly reactive ROS known as a potent pro-inflammatory agent [61], and which also decreases food stability as consequence of lipid peroxidation [15].
In relation to H 2 O 2 , statistic differences (p > 0.05) were observed among the three extracts, and the EtOH/H 2 O extract showed once more its high scavenging capacity, at approximately 2.5 to 3.5 times higher than the EtOH and H 2 O extracts, respectively. Importantly, the EtOH/H 2 O extract (IC 50 at 110 µg/mL) was as effective as chlorogenic acid (IC 50 at 100 µg/mL) in scavenging H 2 O 2 , yet almost three times less efficient than ascorbic acid ( Table 2). The EtOH/H 2 O extract of E. foetidum showed higher antioxidant capacity for scavenging H 2 O 2 than leaf extracts of Castanea sativa and Quercus robur (IC 50 at 410 and 251 µg/mL, respectively) [62], leaf extracts of Vismia cauliflora (IC 50 at 289 µg/mL), a medicinal plant species abundant in the Amazonia [59], and leaf extracts of Meyna spinosa, a medicine plant from India (IC 50 at 127 µg/mL) [63]. Contrasting again, Souza et al. [22] stated that no antioxidant activity was observed in the methanolic extract of E. foetidum at the highest tested concentration of 4 mg/mL. H 2 O 2 is a reactive species capable of crossing cell membranes and oxidizing various cellular compartments, the source of many of its toxic effects [64]. In foods, H 2 O 2 can indirectly cause lipid peroxidation, because H 2 O 2 is also a precursor of • OH [15].
Contrasting the results, the EtOH extract was the most efficient extract for scavenging ROO • radicals, almost twice as efficient as the H 2 O extract and trolox. The H 2 O extract presented the same capacity to scavenge ROO • as observed for trolox, while the EtOH/H 2 O extract showed the least scavenging efficiency. As ROO • are widely known to be generated during lipid peroxidation of unsaturated fatty acids, independently of their localization, either as part of cell membranes or in food sources and formulations, these ROS have high physiological and food relevance. When compared to the literature, the EtOH extract showed higher antioxidant capacity (1.75) than hydroalcoholic extracts of artichoke leaves (Cynara cardunculus L.) (0.31) [65], and extracts of pulp (0.053), peels (0.72), and seeds (0.068) of Bactris setosa fruits [66]. Our results certainly highlight the promising potential of E. foetidum extracts to be added in food formulations to extend the shelf life of processed products by delaying lipid peroxidation.
Previous studies have already pointed to the high efficiency of chlorogenic acid in protecting cells against oxidative damages caused by H 2 O 2 , 1 O 2 , and O 2 •− , clearly demonstrating its ability to scavenge ROS [67,68], which gives support to stimulate further deep research to understand the contribution of E. foetidum plants as a bioactive compound source.
Concerning RNS, Table 3 shows that all the extracts of E. foetidum leaves were able to inhibit the oxidative/nitrosative effects of the tested RNS in a concentration-dependent manner, but with much lower efficiency than the positive controls. To the best of our knowledge, this is the first study reporting the RNS-scavenging capacity of E. foetidum extracts.
Either in the presence or absence of NaHCO 3 , the EtOH/H 2 O extract presented the highest ONOO --scavenging capacity, while EtOH and H 2 O extracts showed similar IC 50 values with no statistical difference (Table 3). In the experiments with the presence of NaHCO 3 to simulate the presence of CO 2 in the physiological system, the antioxidant capacity tended to decrease as the IC 50 values increased. Overall, the E. foetidum extracts were less efficient in scavenging RNS than ROS (Table 2). By comparison, the extracts of Vismia cauliflora leaves, a medicinal plant also from the Amazonia, presented a much higher ONOO − -scavenging capacity (5.8 µg/mL) [59] than the E. foetidum extracts, while gallic acid (IC 50 at 876 µg/mL) was only 1.6 times more efficient [49]. As chlorogenic acid showed a very high antioxidant efficiency (IC 50 at 0.23 µg/mL), either in the presence or absence of NaHCO 3 , it is probable that other nonidentified compounds in the E. foetidum extracts might have interfered with the observed antioxidant effect.
Peroxynitrite is one of the most potentially harmful RNS, and it is generated in vivo by the reaction of nitric oxide ( • NO) with O 2 •− . ONOO − can undergo homolysis of the O−O bond, generating extremely reactive • NO 2 and • OH [69,70]. The formation of • OH by ONOO − homolysis is approximately one million times faster than the metal-catalyzed generation of • OH from H 2 O 2 via the Fenton reaction [71]. Another highly relevant factor is that ONOO − participates in one-and two-electron oxidation reactions with lipids, proteins and DNA, playing a key role in the process of cell/tissue injury under pathological conditions [14]. These factors together justify systematic further research to uncover natural efficient scavengers of such relevant RNS.

Conclusions
The study clearly demonstrated that extracts of E. foetidum leaves showed efficient antioxidant capacity to scavenge biologically relevant ROS and RNS. The EtOH/H 2 O extract presented the highest phenolic compound contents, highlighting chlorogenic acid as the major compound, and, in general, the higher antioxidant performance. Our results suggested that the E. foetidum extracts have promising compounds to be used in food formulations to delay lipid peroxidation, or even for drug design purposes to efficiently scavenging ROS during oxidative stress.
Therefore, this study stated the importance of further systematic research on the biological properties of E. foetidum, which can be seen as a promising Amazonian plant to be rationally exploited by sustainable means for obtaining natural antioxidants.