Phytochemical analysis and biological activities of in vitro cultured Nidularium procerum, a bromeliad vulnerable to extinction.

This study reports the first phytochemical and biological characterization in treatment of adrenocortical carcinoma cells (H295R) of extracts from Nidularium procerum, an endemic bromeliad of Atlantic Forest vulnerable to extinction. Extracts of dry leaves obtained from in vitro-grown plants were recovered by different extraction methods, viz., hexanoic, ethanolic, and hot and cold aqueous. Chromatography-based metabolite profiling and chemical reaction methods revealed the presence of flavonoids, steroids, lipids, vitamins, among other antioxidant and antitumor biomolecules. Eicosanoic and tricosanoic acids, α-Tocopherol (vitamin E) and scutellarein were, for the first time, described in the Nidularium group. Ethanolic and aqueous extracts contained the highest phenolic content (107.3 mg of GAE.100 g-1) and 2,2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH) radical scavenging activity, respectively. The immunomodulatory and antitumoral activities of aqueous extracts were assessed using specific tests of murine macrophages modulation (RAW 264.7) and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay against adrenocortical carcinoma cell line, respectively. The aqueous extract improved cell adhesion and phagocytic activities and phagolysossomal formation of murine macrophages. This constitutes new data on the Bromeliaceae family, which should be better exploited to the production of new phytomedicines for pharmacological uses.


Results and Discussion
phytochemical screening. The phytochemical screening of crude extracts from the leaves of in vitro cultivated N. procerum revealed the presence of some secondary metabolites, according to the solvent used ( Table 1). The Ethanolic (ET), Hot Aqueous (HA-100 °C) and Cold Aqueous (CA-25 °C) extracts showed positive results for alkaloids, with the appearance of red orange precipitated complexes on Dragendorff test. Two qualitative tests (i.e., Wagner and Mayer) were also carried out for this chemical group, confirming the positive results. Furthermore, the aqueous extracts showed defined turbidity (HA) and precipitate (CA), whereas ET showed only opalescence, indicating that aqueous extracts could also be effective for alkaloid extraction.
The Liberman-Buchard test revealed the presence of steroids/triterpenoids in Hexanoic (HE) and ET extracts. HE showed the formation of yellow color, indicating the possible presence of a methyl group on carbon 14 21 . In the ET, a green color was observed, related with a carbonyl function in carbon 3 and double bound between carbons 5 and 6 or 7 and 8 in the extracted compounds 22 .
The flavonoid group was observed in ET, HA and CA extracts, with the appearance of yellowish green and intense yellow, respectively, by Shinoda test. In addition, the ferric chloride assay confirmed the presence of tannins in these extracts. The ET showed a blueish black color, indicating the presence of pyrogallol tannins or  Table 1. Preliminary screaning of hexane, ethanolic and aqueous extracts of Nidularium procerum Lindm shoots. Blank spaces mean that the test was not performed on the extract. (+) small quantity positive response was obtained for the chemical group in the extract. (++) medium quantity positive response was obtained for the chemical group in the extract. (+++) positive response of greater quantity was obtained for the chemical group in the extract. (−) negative response was obtained for that chemical group in the extract.
Lipid profile -gas cromatography (GC-MS). The lipidic profile of N. procerum was investigated in the same apolar extractors used in GC-MS assay, whereas in the polar phase, it was analyzed in aqueous solvents, used in biological tests. The major identified constituents were Linolelaidic acid methyl ester (C18:2 -Omega 6), Methyl palmitate (C16:0 -Palmitic Acid), Cis-9-Oleic acid methyl ester (C18:1 -Oleic acid) and ɣ-Linolenic acid methyl ester (C18:3 -Gamma linolenic acid/Omega 6) ( Table 3). Omega-6 Linolelaidic acid, an isomer of Linoleic acid found in spinach, broccoli, potatoes soya bean, cotton seed oil and sunflower oil 35 , was the major component found in the extracts. Furthermore, palmitic, oleic and ɣ-Linolenic acids are lipidic compounds commonly detected in Bromeliads 36 Other minor constituents detected were stearic and palmitoleic acids, previously reported in A. erctifolius L.B.Sm. 32 , B. pinguin L. 36 (Table 3) and, to our knowledge, it was the first time these compounds are found in bromeliads leaves extracts. Eicoisanoic acid was already described in A. erectifolius bromeliad (24,2 mk/Kg in Fibers) 32 and reported for having anticancer and antiinflamatory potential 37 ; while tricosanoic acid was present in hexane extract of leaves from Ananas cosmosus bromeliad, which demonstrated potential cytotoxic against tumoral cell lines 38 .
Fatty acids play an important role in biological functions of living organisms, contributing to the prevention and treatment of some diseases. Diets with oleic, linolenic, linoleic and linoleic conjugates have been shown to reduce plasma cholesterol levels, in addition to affecting some physiological reactions, such as immune response and inhibition of tumor growth 39 , decreased risk of coronary heart disease, and protective action against stroke, age-related cognitive decline and Alzheimer disease 40,41 . Moreover, Omega-6 fatty acids has gained attention in medicine studies for showing potential in preventing sarcopenia, modulate cancer, atherosclerosis, obesity, immune function and diabetes 40,42 . This is the first time the lipid profile of N. procerum was described, improving the knowledge of its chemical compounds.
Chlorophyll quantification. Leaves of in vitro cultivated N. procerum showed a greater concentration of chlorophyll b (215.06 ± 14.8 µg.g −1 of fresh mass) than chlorophyll a (170.75 ± 18.5 µg.g −1 of fresh leaves). In comparison with Nidularium campo-alegrense Lem (56.4 ± 11.2 µg.g −1 fresh mass) and Aechmea ornate Baker (97.1 ± 11.2 µg.g −1 fresh mass) wild-type bromeliads 43 , N. procerum presented higher amounts of both chlorophylls. The photosynthetic mechanism of plants grown during in vitro culture is not completely active and the leaves have a reduced capacity to synthesize organic compounds 44 . Then, plants can compensate this failure with greater amounts of photosynthetic pigments, as they tend to increase its concentration, with reduced light intensity. Furthermore, bromeliads usually grow under the canopy and the leaves of shade plants often have higher content of chlorophylls than sun species 45 .
Despite the low ratio between chlorophylls a/b (0.79 ± 0.1 µg.g −1 ), when compared to N. campo -alegrense Lem (3.07 µg.g −1 ) and A. ornate Baker (2.94 µg.g −1 ) grown in normal conditions 43 , the higher amount of pigments can be related to the improvement of biological activity of the extracts. Chlorophyll compounds have been described as potential antioxidants with effective activity against lipidic peroxidation, DNA degradation and some cases of anemia 46,47 . Furthermore, recent works showed that chlorophyll derivatives, such as chlorophyllide, are also closely correlated to enhanced selectivity and improved cytotoxic activity against a range of carcinoma cells 48 . www.nature.com/scientificreports www.nature.com/scientificreports/ total phenolic content. The ET extract presented the highest concentration (107.27 mg of gallic acid/100 g), followed by CA (96.82 mg of GAE/100 g) and HA (78.57 mg of GAE/100 g). Similar results (70.73 mg of GAE/100 g) were reported in fresh fruit extracts of wild-type Bromelia anticantha Berto 49 .
In general, phenolics have gained attention due to their antioxidant, antimutagenic, anticancer and anti-inflammatory capacities 50 . The aromatic benzene rings with substituted hydroxyl groups are responsible for their biological activity through the capacity to eliminate or absorb free radicals, and to chelate reactive oxygen species molecules formators. Furthermore, the effectiveness is generally proportional to the number of hydroxyl (OH) groups present in their aromatic rings 51 . phenols content. The phenolic profile of aqueous extracts was evaluated in HPLC, in order to identify some antioxidants present in the solvents applied in the biological tests. The compounds were identified and quantified by comparing their retention times and absorption spectrum data in ultraviolet, which presented UV-band characteristic for gallic acid, p-coumaric acid, rutin, daidzein, quercetin, trans-cinnamic acid and genistein ( Table 4).
In the human body, antioxidants are efficient against some metabolic disorders that compromise the corporal homeostasis, such as lipidic and protein peroxidation, DNA degradation and cell membrane alteration 59 . The antioxidant power of N. procerum extracts can be attributed to the molecular structure of compounds, inparticular polyphenolics. They can inhibit free radicals and chelate metals, acting in entire oxidative process. Gallic acid has three hydroxyl radicals attached in its aromatic ring, which are considered to be closely related to its antioxidant, cytotoxic and antiproliferative potential 60 . In comparison to other phenolic acids, trihydroxilated derivatives displays grater biological activities than phenolic acids with fewer hydroxyl radicals in their molecular structure, such as p-coumaric, trans-ferulic and trans-caffeic acids 61 . Furthermore, compounds such as chlorophylls, alkaloids and some fatty acids, appear to contribute to the antioxidant activity, due to their ability in delocalize the unpaired electrons of free radicals 62 . immunomodulatory activity. Many plant extracts have long been described as possessing anti-inflammatory and immunomodulatory actions. The first line of human body defense against invading pathogens is the innate immune system, through macrophage cells. In the present study, murine macrophages were assessed in vitro by morphological indicators, such lysosomal volume, adhesion and phagocytic capacity, as well as metabolic activities of hydrogen peroxide and superoxide anion (Fig. 1). The macrophage adhesion response showed that the lowest concentration (2 µg.mL −1 ) of HA extract elicited a significant raise (p < 0.05) of about 32% of its activity (Fig. 1A). On the other hand, CA extract showed no significant impact at 2 µg.mL −1 , but increased the adhesion capacity at a higher concentration tested (1000 µg.mL −1 ) in over 28% of isolated macrophages. The adhesion alteration capacity of cells may be linked to the biological compounds present in HA extract. Fatty acids and polyphenols, especially flavonoids and tannins, can change properties of the plasma membrane, altering its fluidity capacity, as well as the distribution of adhesion molecules within the plasma membrane, such β1 (CD29) and β2 (CD18/11a, b, c) integrins 63 . β1 (CD29) and β2 (CD18/11a, b, c) are molecules involved in mediate the adherence of phagocyte cells to endothelium cell receptors.
Cells treated with 10 µg.mL −1 HA elicited a significant increase in the phagocytic capacity of macrophages (p < 0.05), while in CA extract, no significant effect was observed at all concentrations tested (Fig. 1B). Similar results were reported in cells treated with methanolic extracts of Garcinia mangostana L. and Annona muricate L 64 . Triterpenes, isocoumarins, steroids and flavones described in this study (e.g., stigmasterol, rutin, daidzein and genistein) can induce activities in phagocytic cells, by activating surface receptors, such Fc gamma (FcɣRI, FcɣRIIA and FcɣRIIB), starting the "zippering" phagocytosis 65 and also increasing the expression of complement receptors-CR1, CR3 and CR4-promoting the "sinking" phagocytosis 66 . Furthermore, unsaturated fatty acids have previously shown to improve phagocytosis ability 67 , and according to Table 3, HA presented higher content of unsaturated fatty acids (73%) than CA (60%).
The phagolysosomal formation of macrophages was stimulated when the cells were treated with lower concentrations of extracts (p < 0,05), raising ~25% of neutral red uptake in both HA and CA, at 20 µg.mL −1 (Fig. 1C). This held the dose-dependent response and the proportional increase rate observed previously in phagocytosis activity. Lysosomes play the role of digesting intracellular components and also break down phagocytosed material, through the fusion of phagosome to hydrolase-containing lysosomal vesicles 68 , improving the defense cell mechanism.
Reactive oxygen species, such as hydrogen peroxide (H 2 O 2 ) and superoxide anion (O 2 − ), are generated in the first minutes of macrophage stimulation, during the so-called "respiratory burst" 69 . They are involved in the inflammation process, acting as efficient protectors; however, uncontrolled or excessive ROS production can further promote oxidative stress -a disruption in the redox balance system that contributes to damaging the body´s own cells and tissues 70 .
HA extract (10 µg.mL −1 ) was capable to inhibit 36% the production of hydrogen peroxide (H 2 O 2 ) in macrophage cells ( Fig. 2A), while CA did not differ in comparison to the control at any concentration tested (p < 0.05). In the same way, HA (10 µg.mL −1 ) significantly reduced 38% of the production of superoxide anion (Fig. 2B), and different from that described in the H 2 O 2 assay, CA was capable of inhibiting the production of O 2 − in all concentrations (p < 0,05), with maximum reduction (40%) of activity at 2 µg.mL −1 . This may be related to the potential of some flavonoids, such as rutin and quercetin, present in higher concentrations in CA extracts (3.41 and 0.71 µg.g −1 respectively) than HA, in the inhibition of xanthine oxidase and phosphoinositide 3-Kinase γ enzymes 71 . Furthermore, the higher concentration of H 2 O 2 in relation to superoxide anion radical could be involved through the formation of enzyme-flavonoids hydrogen bonds, inhibiting the antioxidant activity of some peroxidase enzymes, such as catalase 72 . Some molecules described in N. procerum extracts, especially flavonoids and derivatives, can act in different mechanisms of enzymes responsible for the oxidative burst in cells. The inhibition of ROS is related to their structure, the number and orientation of the hydroxyl group and the antioxidant potential of each compound; employing in its ability to permeate cell membrane and modulate the pathway signaling of NADPH-oxidase, phospholipase D, protein kinase C-(PKC) alpha, among others 73 . Plant extract compounds can also increase the expression of genes associated with the antioxidative system, such Cu/Zn-SOD, Mn-SOD, catalase, and GPx genes, suppressing oxidative stress by increasing antioxidant activity of enzymes 74 .
The ability to modulate all macrophage parameters found in N. procerum extract can be promising to help fight inflammation and even maintain cell homeostasis under different conditions. Leaf aqueous extract of N. procerum was also shown to interfere in different functions of host response capacity against injuries, such the inhibition of lipid body formation, PGE2 and cytokine production of in vivo pleural leukocytes 12 . Taken together, these data indicate that the substances described in the leaves of N. procerum proved to be efficient in modulating significant responses mediated by macrophages. This can be a potential alternative as a therapeutic agent applied Scientific RepoRtS | (2020) 10:7008 | https://doi.org/10.1038/s41598-020-64026-z www.nature.com/scientificreports www.nature.com/scientificreports/ in the prevention and treatment of pathologies related to the immune system. In addition, previous studies demonstrated that plant-derived compounds are able to alter the immunosuppressive status of patients, increasing antitumor immunity, promoting the proliferation of immune cells and accelerating macrophage phagocytosis 75 . To the best of our knowledge, there is no study on the anti-tumor activity of N. procerum extract. Studies  Antitumoral activity. The key results obtained by MTT assay in H295R and the non-tumoral African green monkey kidney (VERO) cell lines exposed from 2 µg.mL −1 to 1000 µg.mL −1 for 24 h are summarized in Fig. 3. Both HA and CA showed significant decrease in tumor cell viability at all concentrations tested (Fig. 3A). The maximum mortality rate was 24,7% (CA at 100 µg.mL −1 ) and 34,4% -(HA at 250 µg.mL −1 ). On the other hand, there was no statistical difference among extracts and control in the viability of non-tumor cells (VERO) (Fig. 3B). The levels of extracts also showed no statistical differences, with no interaction among them. Molecules, such as phenolics described in this study, can either inhibit or stimulate the oxidative damage process, depending on the dose, structure, target molecule and environment 77 . In the present work, both HA and CA showed no cytotoxicity against normal cells, which makes these extracts promising as sources for the development of alternative drugs.
Antitumoral activity has already been found in some species or Bromeliaceae, such as A. comosus L. 78 , Tillandsia recurvata Baker 79 and Bromelia fastuosa Lindl. 15 . The antitumoral activity was attibuted to cysteine proteinases (e.g., bromelain and fastuosain) as well as flavonoids, including penduletin, cirsimaritin and HLBT-100 33,79 . Biological compounds are related to the suppression of some metastatic markers, resulting in regulation of mitogen activated protein kinase and protein kinase B 80 . Genistein, present in higher amounts in both HA and CA (Table 4), is also related to the inhibition of protein tyrosine kinase and topoisomerase II, and elimination of oxygen free radicals 81,82 , inhibiting the bioavailability of sex hormones, platelet aggregation, angiogenesis, as well as modulating the apoptosis of malignant cell lines 83 . The biological activities of genistein are also related to the intramolecular hydrogen bonding formed by 5-hydroxyl and 4-ketonic oxygen 84,85 . These characteristics may be related to the cytotoxic potential of HA and CA extracts.
Furthermore, some tannins, alkaloids, saccharides and fatty acids, especially polyunsaturated, have proved to be efficient as antitumoral agents, inducing autophagy of cells and other pathways 86,87 . Until now, there have been only a few studies in the biological activity of N. procerum and none of them included the chemical compounds related to it, nor their potential as antitumor agents. Adrenocortical carcinoma is a rare and aggressive neoplasm with pour prognosis 88,89 , in which most patients diagnosed with advanced disease had a median survival time of less than 12 months and a 5-year survival rate of less than 15% among patients with metastatic disease 90 . In this scenario, the biological activity reported for N. procerum shows potential for the development of alternative treatments against adrenocortical carcinoma, which needs to be further explored through isolation and/or microencapsulation of bioactive compounds.

conclusions
The extracts obtained from the leaves of in vitro grown N. procerum were chemically characterized for the first time, showing the presence of phenolic compounds, steroids, fatty acids, polysaccharides, α-Tocopherol and scutellarein. These compounds showed good antioxidant activity and promoted the immunomodulation of murine macrophages. The crude extracts also showed potential against adrenocortical carcinoma cells, without cytotoxicity to non-tumoral cells, making it a potential candidate for alternative therapies against this tumoral line. However, further studies should be carried out to isolate and characterize N. procerum-derived compounds to improve cytotoxic activity as well as to prevent other human diseases caused by free radicals and other pathways.  91 . Shoots (2 cm height) from clusters previously micropropagated in vitro were used as explants and subcultured in vitro to elongation and rooting for 90 days, free of plant growth regulators, up to the formation of a complete explant (basal and aerial part)-becoming available for extraction of leaves compounds, protocol adapted from Kim et al. 80 . Plantlets were removed from culture chambers and the leaves were cut into small pieces and 1 g of fresh leaf mass was macerated and extracted in 10 mL of specific solvent, over 24 hours, under 80 rpm agitation and 25 °C in a dark room. The extracts were filtered with Whatman n° 1 filter paper, lyophilized and stored at −20 °C for further characterizations and applications. chemical characterization of Nidularium procerum extracts. The chemical investigation of N. procerum compounds were carried out in different solvents, in order to detect the maximum range of substances extracted as summarized in the flowchart below (Fig. 4). The analyses were performed based on the results obtained in preliminary phytochemical screening and finally focused on aqueous extracts used in biological tests. The antioxidant, immunomodulatory and antitumoral potential of the aqueous fractions were explored due to their lack of toxicity and the low-cost of the process. phytochemical screening. The phytochemical tests were carried out in four different extracts from N. procerum: hexane (Analytical standard-VETEC), ethanolic (Analytical standard-VETEC), hot aqueous (100 °C) and cold aqueous (25 °C). The screening was performed according to Iqbal et al. 92 . Identification of alkaloids was determined using Dragendorff, Mayer and Wagner´s test, reducing sugars using Fehling´s reagent, quinones by Bornträger´s test, saponins by permanent foam appearance, mucilage by gelatinous consistency after cooled, coumarins using Bajlet´s test, steroids/triterpenoids using Liebermann-Buchard´s test, resins by precipitation test, flavonoid by Shinoda´s test and tannins/phenols using Ferric Chloride´s test.  www.nature.com/scientificreports www.nature.com/scientificreports/ Chlorophyll quantification. Fresh leaves (5 g) were macerated in 10 mL acetone (P.A. VETEC). The solution was filtered with Whatman n° 1 filter paper and stored at −6 °C for five minutes. The absorbance was measured with spectrophotometry at 470, 662, 645, and 652 nm to chlorophyll a, b, relation between and chlorophyll a/b, respectively 93 . The assays were carried out in triplicate and the results were expressed in μg.g −1 of fresh weight. total phenol content. Total phenolic contents of ET, HA and CA extracts were determined using Folin-Ciocalteu method 94 and the standard curve was performed using 0.39, 3.9, 7.8, 15.6, 31.2, 62.5 and 125 μg. mL −1 of gallic acid. The results were expressed in mg of gallic acid equivalent (GAE) in 100 g of fresh weight. phenolic content -high performance liquid chromatography. The phenolic content of aqueous extracts was separated in HPLC using an Agilent Technology 1200 Series system, coupled to a diode array detector (DAD) at wavelengths 235, 260, 275, 280, 290, 311, 357, 370 nm and a scanning from 190 nm to 600 nm. A ZorbaxElipse XDB-C18 (4,6 ×150 mm, 5-micron) column was used at 0,7 mL min −1 flow. The mobile phase was 2,5% acetic acid (solvent A) and methanol (solvent B). The elution gradient was carried out as follows: 90% A/10% B, 0-13 min; 75% A/25% B, 13-28 min; 15% A/85% B, 28-32 min; 10% A/90% B, 32-36 min. Chlorogenic acid, caffeic acid, ferulic acid, tocopherol, genistein, transcinnamic acid, catechin, rutin, p-coumaric acid, gallic acid, resveratrol and epicatechin (SIGMA) were used as standards. To obtain the calibration curve, all standard reagents were solved in mobile phase and used at 1, 2, 5, 8 and 10 ppm. The samples were microfiltered trough a hydrophilic membrane GV (Durapore) made of polyvinylidene difluoride (PVDF), with a pore size of 0,22 μm. The resulting chromatogram values were plotted and a linear equation was generated by calculating the average of triplicate runs for each compound. The equations were used to quantify the phenolic compound contents of the samples. The injection volume was 10 µL. All the assays were also performed in triplicate.

In vitro antioxidant activity
Scavenging ability on DPPH. The antioxidant potential of the aqueous extracts was determined by their ability of quenching the free radical DPPH 69 . A Trolox (Sigma) standard solution was diluted from 0.25 to 25 mg/ ml and used as positive control to the assay, mixing 200 μL of each concentration in 800 μl of 0.004% methanol solution of DPPH. After 30 min of incubation in absence of light at room temperature, the absorbances were read against blank at 517 nm using a SP-2000 spectrophotometer. The same protocol was used for the HA and CA treatments. DPPH solution was used as negative control with the solvent extraction. Tests were carried out in triplicate and the percentage of free radical inhibition was calculated by the following Eq. (1): Where A blank is the negative control and A sample is the absorbance of extracts. The results were expressed in extract concentration producing 50% inhibition (IC 50%), calculated from the graph of the DPPH scavenging effect against the extract concentration.
ABtS assay. The ABTS assay was carried out using a radical cation decolorization protocol 95 . The ABTS radical had to be pre-formed by the reaction between 5 mL ABTS 7 mM (Sigma) with 88 μL of 140 mM potassium persulfate, stored in the dark at room temperature for 16 hours. The ABTS solution (1 mL) was previously diluted in 50 mL of ethanol P.A. (Alphatec) to obtain an absorbance of 0.700 at 734 nm. In absence of light, 10 μL of each aqueous plant extract were added to 500 μL ABTS solution. After 6 minutes, the absorbance was read in the spectrophotometer (SP 2000) at 734 nm. Distilled water was used as blank and as negative control. All measurements were carried out in triplicates. The scavenging capability of tests compounds was calculated using the following Eq. (2): Where λ 734-Sample is the absorbance of control without radical scavenger and λ 734-Control the remaining ABTS in the presence of scavenger. Trolox was used as standard.
immunomodulatory activity. Macrophage activity was assessed by its reactive oxygen species production -superoxide anion and hydrogen peroxide, cell adhesion, phagocytic efficiency and phagolysosomal formation 96 . Murine macrophages cells were cultured in Dulbecco's Modified Eagle's medium (DMEM-Sigma Aldrich) supplemented with 10% fetal bovine serum (FBS -Gibco and 1% antibiotic solution (10.000 U.mL −1 penicilin and 10 mg.mL −1 streptomycin -Gibco ® ), maintained in a humidified atmosphere with 5% CO 2 at 37 °C until 80-90% confluence was reached. The cells were divided at 10 5 cells/well in 96-well plate (Biofil) and exposed into the following experimental groups: cells without treatment (C), Hot Aqueous (HA) and Cold Aqueous Extract (CA), both at concentrations 2, 10, 20, 100 and 1000 μg.mL −1 for 24 h at same conditions of growing. The analyses were performed in 12 repetitions.