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Article

LC-MS and NMR Based Plant Metabolomics: A Comprehensive Phytochemical Investigation of Symphytum anatolicum

by
Hilal Kılınc
1,
Gilda D’Urso
2,
Annunziata Paolillo
2,
Ozgen Alankus
3,
Sonia Piacente
2,* and
Milena Masullo
2
1
Department of Geological Engineering, Engineering Faculty, Dokuz Eylul University, Buca, 35370 İzmir, Turkey
2
Dipartimento di Farmacia, Università degli Studi di Salerno, Via Giovanni Paolo II, Fisciano, 84084 Salerno, Italy
3
Chemistry Department, Faculty of Science, Ege University, Bornova, 35100 Izmir, Turkey
*
Author to whom correspondence should be addressed.
Metabolites 2023, 13(10), 1051; https://doi.org/10.3390/metabo13101051
Submission received: 24 August 2023 / Revised: 22 September 2023 / Accepted: 26 September 2023 / Published: 4 October 2023
(This article belongs to the Special Issue Progress in Metabolomic Analysis in Medicinal Plants)
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Versions Notes

Abstract

:
The application of metabolomics to the study of plants is growing because of the current development of analytical techniques. The most commonly used analytical technology driving plant metabolomics studies is Mass Spectrometry (MS) coupled to liquid chromatography (LC). In recent years, Nuclear Magnetic Resonance (NMR) spectroscopy, not requiring a previous chromatographic separation, has been receiving growing attention for metabolite fingerprinting of natural extracts. Herein, an integrated LC-MS and 1H NMR metabolomic approach provided a comprehensive phytochemical characterization of Symphytum anatolicum whole plant, taking into account both primary and specialized metabolites. Moreover, the NMR analyses provided direct quantitative information. Species belonging to the Symphytum genus, known as comfrey, have shown several biological activities including anti-inflammatory, analgesic, hepatoprotective, antifungal, and antibacterial. The LC-MS profile showed the presence of 21 main specialized metabolites, belonging to the classes of flavonoids, phenylpropanoids, salvianols, and oxylipins. The 1H NMR spectrum revealed the occurrence of metabolites including organic acids, phenolics, flavonoids, sugars, and amino acids. A quantitative analysis of these metabolites was performed and their concentration was obtained with respect to the known concentration of TSP, by means of the software package Chenomx which allows quantification of individual components in the NMR spectra. Furthermore, the phenolic content, antioxidant activity, glucosidase, and tyrosinase inhibitory activity of S. anatolicum extract were evaluated. The resulting bioactivity profile suggests how S. anatolicum represents a source of metabolites with health-promoting activity.

Graphical Abstract

1. Introduction

Metabolomics is an omics approach that can be used to acquire comprehensive information on the composition of food and medicinal plants. The use of metabolomics in ecology is more recent, with some exceptions [1]. The metabolome is the quantitative collection of all the low molecular weight compounds present in a cell organism in a particular physiological or developmental state. Early studies used analytical standards to determine the presence or abundance of a limited set of pre-determined metabolites in a sample. The field has now shifted towards untargeted metabolomics, which instead attempts to detect and identify all the metabolites in a sample [1]. The two most commonly used analytical technologies driving quantitative plant metabolomics studies are Mass Spectrometry (MS) and Nuclear Magnetic Resonance (NMR) spectroscopy [2].
Due to its high sensitivity, MS is by far the technology of choice in most plant metabolomics studies especially when coupled to powerful chromatographic techniques (e.g., liquid chromatography–mass spectrometry (LC-MS)). NMR spectroscopy is largely used in the field of quality evaluation of various food and medicinal plants, and it is widely used for the characterization and structure determination of natural products. NMR spectrum can provide a wealth of accurate qualitative and quantitative information even regarding the components of a mixture [3]. In most cases, in contrast to GC-MS and LC-UV/MS techniques, the NMR approach does not require separation or isolation of analytes from a mixture. Hence, the loss of the whole metabolite information caused by the filtration of chromatographic columns can be avoided (such loss is very likely for botanicals since they have a wide range of distributions both of molecular weight and polarity) [4].
Both approaches provide complementary as well as supplementary information on the metabolite profiles of plants and herein they have been employed to provide a comprehensive phytochemical characterization of Symphytum anatolicum, an endemic Turkish plant, less investigated if compared to the well-known Symphytum officinale (comfrey).
The genus Symphytum L. (Boraginaceae) is represented by perennial plants and includes about 35 species [5,6,7]. Turkey which hosts different climatic conditions in a wide area, has a rich plant diversity and the Symphytum genus is represented by 18 species among which Symphytum tuberosum L., Symphytum officinale L., Symphytum caucasicum Bieb., and Symphytum anatolicum Boiss [8].
Various species of Symphytum have shown anti-inflammatory, analgesic, hepatoprotective, antifungal, and antibacterial activity [5,9]. Different formulations obtained from the roots of S. officinale are used as a topical anti-inflammatory remedy and in the treatment of arthritis [10,11].
Furthermore, Symphytum spp. are reported to be an excellent remedy for fractures and injuries, facilitating the joining of broken bones and reducing the pain of needling [12].
Symphytum anatolicum Boiss. is an ornamental and medicinal plant growing in Europe, Asia, and North America. The plant was first collected by d’Urville and named S. asperrimum d’Urv, then Boissier changed its name to S. anatolicum Boiss [8,13].
The extracts of S. anatolicum roots exhibited antioxidant activity and protective effects against tyrosinase and α-amylase [14], aerial parts of S. anatolicum showed a high inhibitory capacity, especially against acetylcholinesterase and α-glucosidase enzymes [15,16]. S. anatolicum is also used in wound healing and the treatment of sprains and bruises [5].
Indeed, the genus contains many important bioactive constituents, including alkaloids, flavonoids, triterpenes, tannins, sterols, polysaccharides, and amino acids [5]. Among alkaloids, pyrrolizidine-type alkaloids are found in this genus [5]. Chemical composition, biological activities, applications, and uses of different species of Symphytum are reported in the literature, whereas few are studies regarding the chemical composition of S. anatolicum [14,15]. Therefore, this investigation was aimed at providing a comprehensive phytochemical characterization of S. anatolicum whole plant, by an integrated LC-MS and 1H NMR metabolomic approach. Furthermore, phenolic content, antioxidant activity, glucosidase, and tyrosinase inhibitory activity of S. anatolicum MeOH extract were evaluated. The results of antioxidant and enzyme inhibitory assays suggested how S. anatolicum represents a source of bioactive compounds with health-promoting properties.

2. Materials and Methods

2.1. Chemical and Reagents

MeOH and water for HPLC were purchased from VWR (Milan, Italy). Acetonitrile, HCOOH, and water for LC-MS analysis were purchased from Merck (Merck KGaA, Darmstadt, Germany). MeOH-d4 (99.95%), D2O (99.9% containing 0.75 wt.% 3-(trimethylsilyl)propionic-2,2,3,3-d4, sodium salt), Folin–Ciocalteu, 1,1-diphenyl-2-picrylhydrazyl (DPPH), 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (Trolox), diammonium 2,20-azinobis(3-ethylbenzothiazoline-6-sulfonate) (ABTS), quercetin 3-O-glucoside, vitamin C, kojic acid, L-tyrosine, acarbose and 4-nitrophenyl α-D-glucopyranoside (p-NPG) were purchased by Sigma-Aldrich (Milan, Italy). α-glucosidase from Saccharomyces cerevisiae and tyrosinase from mushrooms were purchased from Sigma-Aldrich (Milan, Italy).

2.2. Plant Material

Whole plants of Symphytum anatolicum Boiss. (Boraginaceae) were collected in Bozdağ (GPS coordinates latitude: 38.354274, longitude: 28.089896), Izmir, Turkey, after the beginning of the flowering period (April–May period). A voucher specimen was deposited in the Herbarium of Science Faculty, Ege University, Izmir, Turkey (EGE 12571).

2.3. General Procedures

Semi-preparative HPLC separations were carried out using a Symmetry Prep TM-C18 (78 mm × 300 mm, 7 μm) column on a Waters system (Milford, CT, USA) equipped with an R-401 refractive index detector and using a Phenomenex C18 Synergy-Hydro-RP (250 mm × 10 mm, 10 μm) column on an Agilent 1260 Infinity system (Agilent Technologies, Palo Alto, CA, USA), equipped with a binary pump (G-1312C) and a UV detector (G-1314B). TLC was performed on silica gel F254 (Macherey-Nagel Deltek, Naples, Italy) plates (20 cm × 10 cm), and mixtures of CHCl3–CH3OH–H2O (80:20:2, 70:30:3, 61:32:7) (VWR international PBI S.r.l., Milan, Italy) were used as mobile phases. Detection was carried out by spraying cerium (IV) sulphate followed by heating at 100 °C for 5 min. HR/ESI-MS data were acquired on an LTQ Orbitrap XL mass spectrometer (Thermo Fisher Scientific, Bremen, Germany) operating in negative-ion mode. A Thermo Scientific™ Multiskan SkyHigh Microplate Spectrophotometer was used for spectrophotometric assays.

2.4. LC-ESI/LTQOrbitrap/MS Analysis

LC-MS was performed using a system of Liquid Chromatography coupled to Electrospray Ionization and High-Resolution Mass Spectrometry (LC-ESI/HRMS) characterized by a quaternary Accela 600 pump and an Accela autosampler coupled to an LTQOrbitrap XL mass spectrometer (LTQ-Orbitrap XL, Thermo Fisher Scientific, Bremen, Germany) working in negative ion mode. A Phenomenex C18 Kinetex Evo-RP (150 mm × 2.1 mm, 5 µm) column at a flow rate of 0.2 mL/min was selected; water plus 0.1% formic acid and acetonitrile plus 0.1% formic acid were used as mobile phase A and B, respectively. A linear gradient method from 5 to 95% of B in 35 min was performed. The autosampler was set to inject 4 μL of methanol extract (1 mg/mL). The mass range was from m/z 120 to 1600 with a resolution of 30,000. A data-dependent scan experiment was performed for fragmentation, selecting precursor ions corresponding to the first and the second most intense ions from the LC-HRMS spectrum and using collision energy at 30%, a minimum signal threshold of 300, and an isolation width of 2.0.

2.5. Extraction and Isolation Procedures

Air-dried and powdered whole plant material (390 g) was extracted with hexane (2.5 L for two days), dichloromethane (2.5 L for two days), and methanol (2 × 2.5 L. each for two days) at room temperature (25 °C). After filtration and evaporation of solvent to dryness in vacuum, the dichloromethane (0.98 g) and methanol (12.64 g) extracts were obtained.
Two grams of MeOH extract were fractionated on a Sephadex LH-20 (GE Healthcare, Sigma Aldrich, Milan, Italy) column (100 cm × 5 cm), using MeOH as mobile phase, affording 186 fractions (8 mL), and monitored by TLC.
Further purifications were carried out by semipreparative HPLC-RI in isocratic conditions with MeOH-H2O at different percentages, at a flow rate of 2 mL/min. Fractions were dried and then dissolved in MeOH in a concentration of 10 mg/100 μL for the injections. The fractions 78–83 (71.8 mg) were chromatographed using MeOH–H2O (40:60) as mobile phase to produce compound 15 (1.4 mg, tR = 12.8 min). Fractions 84–103 (111.3 mg) were chromatographed using MeOH-H2O (40:60) as mobile phase to yield compounds 16 (1.2 mg, tR = 8.3 min), 11 (1.6 mg, tR = 11.6 min), 9 (1.8 mg, tR = 22.3 min). The fractions 116–128 (105.9 mg) were further chromatographed using MeOH-H2O (35:65) as mobile phase to produce compounds 7 (1.7 mg, tR = 32.1 min). The fractions 153–162 (24.9 mg) gave compound 17. The fractions 181–186 (2.6 mg) gave compound 18.
A total of 200 mg of MeOH extract was analyzed by an RP-HPLC-UV system. The mobile phase consisted of solvent A (H2O + 0.1% formic acid) and solvent B (CH3CN + 0.1% formic acid), at a flow rate of 2.0 mL/min. The HPLC gradient started at 5% B, after 5 min % B was 5%, after 15 min it was at 20%, after 20 min % B was at 50%, after 10 min it was at 100% as it was held for 5 min, to produce compounds 6 (1.1 mg, tR = 20.2 min), 3 (1.3 mg, tR = 23.1 min), 4 (2.4 mg, tR = 28.5 min), 5 (1.8 mg, tR = 29.9 min), 13 (1.4 mg, tR = 32.4 min), 8 (2.5 mg, tR = 32.8 min), 10 (2.4 mg, tR = 34.1 min), 14 (3.3 mg, tR = 36.4 min) and 12 (1.1 mg, tR = 39.7 min). The isolated compounds were injected into the LC-MS instrument and were used as standards, confirming their identification in the LC-MS profile of the extract (Table 1).

2.6. NMR Analysis and Data Processing

NMR experiments were acquired on a Bruker Ascend-600 NMR spectrometer (Bruker BioSpin GmBH, Rheinstetten, Germany) equipped with a Bruker 5 mm PATXI probe. DQF-COSY, HSQC, HMBC, and ROESY spectra were acquired in methanol-d4 (99.95%, Sigma-Aldrich), and standard pulse sequences and phase cycling were used. The 1D and 2D NMR data were processed by TOPSPIN 3.2 software.
For 1H NMR analysis, the extract (5.1 mg) was dissolved in 537 μL of phosphate buffer (1 M KH2PO4, D2O, and 2 mM NaN3 to prevent microbial contamination) after that, 13 μL of 44 mM TSP (trimethylsilyl propanoic acid) was added as internal standard and finally filled into a 5mm NMR tube. Experiments were run at 300 K in automation mode after loading individual samples on a Bruker Automatic Sample Changer, interfaced with the software IconNMR (Bruker). To suppress the residual water signal, a zgesgp Bruker standard pulse sequence was applied. A total of 80 transients (with 4 dummy scans) were collected into 64 k data points with a relaxation delay set to 5.0 s. The spectra were automatically Fourier transformed using an exponential window with a line broadening of 0.5 Hz. Phase and baseline were corrected using Chenomx NMR Suite 9.0 (Chenomx Inc., Edmonton, AB, Canada). Compounds were identified using the Chenomx and Human Metabolome Database (HMDB) 600 MHz libraries [17]. The metabolite concentrations were determined using the concentration of a known reference signal (TSP) [18].

2.7. Total Phenolic Content, DDPH, and TEAC Assays

Folin-Ciocalteu, DPPH, and TEAC (Trolox Equivalent Antioxidant Capacity) assays for the extract have been performed as previously reported [19]. The total phenolic content of the extracts was determined by Folin–Ciocalteu assay; gallic acid was used as a reference compound (calibration equation: y = 0.0027x + 0.0982, R2 = 0.9929). All the experiments were performed in triplicate, and results were expressed as the means of gallic acid equivalents (GAE mg/g dried extract).
For the TEAC assay, the extract was tested at concentrations of 250, 500, 750, and 1000 μg/mL. A total of 1.5 mL of diluted ABTS was added to 15 μL of each sample solution. The assay was carried out in triplicates. Quercetin 3-O-glucoside was used as reference standard. The results are presented as TEAC values, that is the concentration (mM) of a standard Trolox solution with the same antioxidant capacity as 1 μg/mL of the tested extract.
The stables radical DPPH• was used to assess the antiradical activity of the extract following the procedure previously described [20]. Vitamin C was the positive control, while methanol was the negative control. A total of 37.5 μL of the methanol solution containing different concentrations of methanol extract has been added to 1.5 mL of daily prepared DPPH• solution (0.025 g/L in MeOH). Absorbance has been measured at 517 nm 10 min after starting the reaction. The DPPH• concentration in the reaction medium has been calculated from a calibration curve (range = 10–200 mg/mL) analyzed by linear regression (y = 0.257x + 5.55; R2 = 0.990). All experiments were conducted in triplicate.

2.8. α-Glucosidase Inhibition Assay

The α-glucosidase inhibitory activity was tested by using 96 well plates and following protocols previously reported [21]. The extract and acarbose were dissolved in MeOH and were tested at the final concentrations of 20 μg/mL, 8 μg/mL, 6 μg/mL, and 2 μg/mL. A total of 10 μL of each stock solution together with 15 μL of α-glucosidase from Saccharomyces cerevisiae (2 U/mL, 0.1 M potassium phosphate buffer, pH 6.8) were mixed in 150 μL of 0.1 M potassium phosphate buffer (pH 6.8). After 5 min of incubation at 37.0 °C, 75 μL of p-NPG (2.5 mM), as substrate, was added to the mixture, and the solution was incubated at 37.0 °C for another 10 min. The absorbance of the generated p-nitrophenol was measured at 405 nm using a UV spectrometer. The sample was replaced with 10 μL of buffer (potassium phosphate buffer) for the negative control. The experiment was conducted in triplicate. The IC50 value (μg/mL) represents the concentration inhibiting the α-glucosidase activity by 50%.
The α-glucosidase inhibitory activity was calculated by using the following formula:
inhibition (%): [(XA − XB)/XA] × 100
XA is the absorbance of the control and XB is the absorbance of the sample.

2.9. Tyrosinase Inhibition Assay

The tyrosinase inhibitory activity was evaluated using a method described by Oh et al. [22]. 30 microliters of the sample (300, 100, 50, and 25 µg/mL), and 50 µL of 100 U/mL mushroom tyrosinase were treated in 96-well plates and incubated at 37 °C for 15 min. Subsequently, 50 µL of 1 mM L-tyrosine was added and then reacted at 37 °C for 15 min. The amount of dopachrome formed was measured at 495 nm. Each sample has been tested in triplicate and the tyrosinase inhibitory activity was calculated using the following equation:
tyrosinase inhibition (%) = [1 − (S − S0)/(C − C0)] × 100
where S is the absorbance of the sample, tyrosinase, and L-tyrosine; S0 is the absorbance of the sample and L-tyrosine; C is the absorbance of tyrosinase and L-tyrosine, and C0 is the absorbance of L-tyrosine. Kojic acid, a known tyrosinase inhibitor, was used as a positive control.

2.10. Statistical Analysis of Data

Data are reported as means ± mean standard error (SEM) of at least three independent experiments. Each experiment was conducted in triplicate. A p-value less than 0.05 was considered significant.

3. Results

3.1. LCESI/Orbitrap/MS/MS Analysis of MeOH extract of S. anatolicum

The methanol extract of S. anatolicum was investigated by preliminary analysis using an extremely sensitive analytical technique such as liquid chromatography coupled to high-resolution tandem mass spectrometry in negative ionization mode, using a mass spectrometer with electrospray source coupled to Orbitrap mass analyzer (LC-ESI-FT-MS). The LC-ESI-FT-MS profile (Figure 1) showed the presence of 21 main specialized metabolites, belonging to the classes of flavonoids, phenylpropanoids, salvianols, and oxylipins. Initially, some peaks were tentatively identified, based on their accurate masses, on the characteristic fragmentation pattern, and by comparing the results obtained with the data reported in the literature on S. anatolicum and in databases (database “KNApSAcK”). Compound 2 showed a precursor ion [M-H]− at m/z 377.0857, supporting the molecular formula C18H18O9. Comparing the results of mass spectra with the library and the literature data, compound 2 was identified as dan shen suan C. Compounds 3 and 4 have been identified as 2,5-dihydroxybenzoic acid and 4-hydroxybenzoic acid, already reported in S. anatolicum [14]. The analysis of the fragmentation spectra of compounds 7–11 made it possible to ascertain the presence of sugar units in different positions of the aglycone, determining characteristic neutral losses from precursor ions of 162 and 132 Da, corresponding to the dehydrated form of hexose and pentose, respectively, allowing to identify the compounds as kaempferol or quercetin glycosides. Compounds 5, 7, 8, 10, and 14 had already been reported in the species S. anatolicum [15] and were identified as caffeic acid (5) (C9H8O4), rutin (7) (C27H30O16), quercetin-3-O-glucoside (8) (C21H20O12), kaempferol 3-O-glucoside (10) (C21H20O11), rosmarinic acid (14) (C18H16O8). The molecular formula together with the fragmentation spectra of compounds 15–18 allowed us to identify them as salvianolic acid A (C26H22O10) and C (C26H20O10) (15,16), previously reported in S. anatolicum, and salvianolic acid B (17) (C36H30O16), previously reported in S. officinale [15,23]. Compound 18 showed a precursor ion [M-H]− at m/z 551.1200 supporting a molecular formula C28H24O12; the fragmentation pattern was similar to those of salvianolic acids with the presence of fragment ions at m/z 519.0928 corresponding to the neutral loss of 32 Da assigned as MeOH unit, allowing us to suppose esterification of the carboxyl group in the furan ring of lithospermic acid, and at m/z 339.0498, corresponding to the neutral loss of 180 Da assigned as caffeic acid unit. Thus compound 18 was identified as monomethyl lithospermate, for the first time reported in Symphytum species. Salvianolic acids can be divided into monomers and polymers (dimers, trimers, and tetramers) based on the number of phenyls present in their structures [24]. In general, the polymers of salvianolic acids generate product ions in the tandem mass spectra due to successive or simultaneous loss of C9H6O3 (162.0317 Da), C9H8O4 (180.0423 Da) and C9H10O5 (198.0528 Da), corresponding respectively to caffeoyl unit, caffeic acid or to the loss of dan shen suan C. Compounds 19–21 showed a typical fragmentation pattern ascribable to oxylipins, fatty acids differing from each other in the degree of unsaturation and number of hydroxyl groups. The product ions generated by one or more consecutive neutral losses of 18 Da allowed us to define the number of hydroxyl groups present in the oxylipine structure. By detecting characteristic product ions, such as those at m/z 171 (C9H15O3) and m/z 201 (C10H17O4), or those at m/z 253 (C15H25O3), 229 (C12H21O4), 223 (C14H23O2) and 199 (C11H19O3), these hydroxyl groups could be located at the head (precisely at the C9 and C10 positions) or at the tail of the oxylipin (precisely at C12, C13, C15 and C16) [25]. Furthermore, along with the molecular formula and RDB (Double Bond/Ring Equivalents) value, the fragmentation pattern allowed in some cases to establish the position of the double bond. In this way, the compounds were identified as those reported in Table 1. In order to accurately determine the structures of the compounds present in the methanol extract of S. anatolicum, the extract was purified by chromatography, using Sephadex LH-20, HPLC-UV, and HPLC-RI. In detail, the methanol extract was first fractionated by size exclusion chromatography on Sephadex LH-20, and the obtained fractions were further purified by HPLC; for some fractions, a refractive index (RI) detector was used, and for some other fractions a UV detector.
The isolated compounds have been shown in Table 1 (Figure 2).

3.2. NMR Analysis of MeOH Extract of S. anatolicum

To obtain complete information not only about the occurrence of specialized metabolites but also of primary metabolites, the MeOH extract of S. anatolicum was investigated by an approach based on 1H NMR analysis [19,20,26]. NMR is one of the most useful analytical techniques which can contribute to the field of metabolomics. The 1H NMR spectrum of the extract showed the presence of various classes of metabolites. NMR has a universal detection capability, since any molecule containing one or more atoms with a non-zero magnetic moment (such as 1H, 13C, 14N, 15N, and 31P), is potentially detectable by NMR, providing unbiased detections and covering compounds of all organic chemical classes in plant extracts. 1H NMR is a non-destructive technique and is characterized by a simple sample preparation and rapid analysis. It can simultaneously identify diverse groups of specialized metabolites as well as abundant primary compounds [26]. A comprehensive inspection of the 1H NMR spectrum based on its characteristic signals allowed the identification of organic acids, phenolics, flavonoids, sugars, and amino acids. A total of 21 metabolites were identified by comparison with the literature data, the Chenomx database, and on the basis of 2D NMR spectra. The identified metabolites are displayed in Figure 3. The most intense signals were observed in the region ranging from 3.00 to 5.00 ppm, representing the carbohydrate constituents (sucrose, fucose, and maltotriose) [27]. In the low-frequency region, characteristic peaks of the amino acids alanine, valine, and isoleucine were detected while other two amino acids, tyrosine, and N-methyl-aspartic acid were identified in the mid to high-frequency region (Figure 3).
Along with primary metabolites, the occurrence of specialized metabolites was revealed. For the complete and unambiguous assignment of some compounds, standard two-dimensional NMR experiments, namely COSY, TOCSY, and HSQC, were performed. To make some identifications and assignments more robust, the obtained results were integrated with the information provided by the reference library of Chenomx and the NMR spectra available in the Human Metabolome Database [18,28].
The principal peak areas of the spectrum afforded an immediate measure of metabolite concentration allowing all the metabolites to be quantified based on a single internal standard. Indeed, the concentration of the identified metabolites was obtained, with respect to the known concentration of TSP, by means of the well-established software package, Chenomx [29]. This latter software is based on a highly sophisticated targeted profiling technology that allows an easy deconvolution of complex NMR spectra into their individual components that can be quantified with good accuracy [18].
The metabolites average molar concentrations, expressed both as mM and as mg/g MeOH extract, showed a high sugar content (sucrose, fucose, and maltotriose with a concentration of 10.13, 8.25, and 19.06 mg/g extract, respectively). Allantoin, a metabolite deriving from uric acid oxidation [30], was identified in S. officinale and S. cordatum extracts [5]. Allantoin is a safe and non-toxic compound, used in cosmetics for its soothing, skin softening, cell proliferation stimulating, and injured tissue repairing properties [5]. Overall, allantoin is a versatile ingredient with a range of biological effects such as wound healing, anti-inflammatory, antioxidant, and antidiabetic [31,32]. Herein, the MeOH extract of S. anatolicum revealed a content in allantoin of 2.47 mg/g extract.
Regarding specialized metabolites, the extract appeared a good source of rosmarinic acid (3.18 mg/g extract) as well as of rutin (8.58 mg/g extract).

3.3. Evaluation of Phenolic Content and Antioxidant Activity

Considering the chemical profile of the extract, the phenolic content was determined by the Folin-Ciocalteu method [26], before evaluating the radical scavenging activity. The result of the total phenolic content determination indicated a phenolic content, expressed as milligrams of gallic acid equivalents per gram of extract, of 21.40 mg GAE/g (±0.35). Successively, the antioxidant activity of S. anatolicum extract was tested by TEAC and DPPH assays. The methanol extract displayed a radical scavenging activity (TEAC value of 1.80 ± 0.05 mM) higher than that of quercetin 3-O-glucoside (0.69 ± 0.05 mM), used as a reference compound. The DPPH assay displayed antioxidant activity with an EC50 value of 115.7 ± 0.93 µg/mL). Ascorbic acid was used as a reference compound (EC50 = 4.4 ± 0.03 µg/mL).

3.4. α-Glucosidase Inhibitory Activity

Symphytum is a medicinal herb that has been used for centuries to treat a variety of ailments, including diabetes. This species contains several active compounds such as allantoin and rosmarinic acid, which have been shown to have antidiabetic effects [5,33]. The antidiabetic effects of Symphytum species like S. officinale and S. anatolicum have been extensively studied, showing high α-glucosidase inhibitory activity [15,34]. The inhibitory effect of the extract of the whole plant of S. anatolicum was evaluated against α-glucosidase and showed a potent inhibitory activity (IC50 = 18.28 ± 0.31 μg/mL), comparable to that exerted by acarbose (IC50 = 17.05 ± 0.25 μg/mL), used as a positive control.

3.5. Tyrosinase Inhibitory Activity

Tyrosinase is an enzyme that plays a key role in melanin synthesis. It catalyzes two distinct reactions occurring during this process: the hydroxylation of tyrosine and the oxidation of 3,4-dihydroxyphenylalanine (L-DOPA) to o-dopaquinone [35,36]. It is reported that the abnormal and uncontrolled production and distribution of melanin can cause many dermatological disorders, such as lentigines, melasma, and post-inflammatory hyperpigmentation [36,37]. In recent years, there has been a growing interest in the search for new tyrosinase inhibitors [38]. Herein, S. anatolicum extract was investigated for its potential inhibitory activity against mushroom tyrosinase. Results showed that MeOH extract presented an interesting tyrosinase inhibitory activity (IC50 = 20.59 ± 0.30 µg/mL). Kojic acid, considered a strong inhibitor of tyrosinase, was used as a reference (IC50 = 23.18 ± 0.35 µg/mL).

4. Discussion

The comprehensive investigation of S. anatolicum whole plant extract was performed by LC-MS and NMR analysis to highlight the occurrence of both specialized and primary metabolites. The LC-MS analysis, more sensitive than the NMR, allowed us to identify 21 phenolic compounds, belonging to phenolic acids, flavonoids, and lignans.
Rosmarinic acid (14) corresponded to one of the highest peaks observed in the LC-MS profile, in agreement with previous investigations on S. anatolicum and also on Symphytum genus [5,14,15]. Compared to the previous investigation reported for S. anatolicum [14,15], allantoin (1), dan shen suan C (2), benzoic acid (6), saponarin (9), 3,5-dicaffeoylquinic acid (3,5-O-DCQA, 12), monomethyl lithospermate (18) and oxylipins (19–21) are reported here for the first time in the species. Among these compounds, allantoin is considered a marker of comfrey, and monomethyl lithospermate (18) was previously reported in Arnebia radix and Lithospermum erythrorhizon, belonging to the Boraginaceae family [39,40].
Regarding allantoin (1), although reported as a main compound in the Symphytum genus [5], it did not appear as a high peak in the LC-MS profile acquired in negative ionization mode. Its relevant content, reported as responsible for the wound-healing property of Symphytum spp., was evident in the NMR analysis (Figure 3 and Table 2) which, compared to the LC-MS analysis, evidenced primary metabolites as amino acids, sugars, and organic acids. Among amino acids, N-methyl-aspartic acid was previously described by GC-MS in the fruits of Lycium chinense and Lycium barbarum, also known as Lycii Fructus [40].
Moreover, rutin (7) and rosmarinic acid (14), identified by LC-MS analysis, were also evident in the NMR profile. These results highlight how the two analytical techniques, LC-MS and NMR, afford complementary information that combined offer an in-depth knowledge of the plant metabolome.
In this work, NMR analysis allowed also the quantitative analysis of S. anatolicom methanol extract. NMR analyses provide direct quantitative information because the intensity of the proton signal is proportional to the molar concentration of the metabolites. In previous studies, Sarikurkcu et al. reported the quantitative analysis of phenolic compounds in the methanol extract of S. anatolicum roots by an LC-MS approach using the Multiple Reaction Monitoring (MRM) experiments [14]; rosmarinic acid represented one of the major compounds isolated, in agreement with the literature data for the comfrey roots [5]. Taking into account that the plant material was the whole plant, the quantitative analysis of rosmarinic acid in the methanol extract of S. anatolicum was comparable to that reported by Sarikurkcu [14].
The phenolic content, expressed as mg GAE/g of extract, was in agreement with that reported for the aerial parts and the roots of S. anatolicum [14,15]. DPPH and ABTS assays revealed a significant antioxidant activity. Furthermore, comparing our results with the literature, it was observed that methanol extract from the whole plant of S. anatolicum showed higher DPPH assay than the methanol extract of the roots [14].
Enzyme inhibitory surveys, such as inhibitors of α-glucosidase and tyrosinase, are regarded as key strategies for reducing the risk of many severe health problems. So, α-glucosidase and tyrosinase inhibitory activity was tested for the methanol extract of the whole plant. Our results showed that the methanol extract of the whole plant presented a higher tyrosinase inhibitory activity than the roots [14]. This could be attributed to the fact that different molecules are biosynthesized from different plant organs, so the inhibitory activity depends on the chemical profile of each raw material.

5. Conclusions

Considering the innumerable potentialities of the Symphytum species and their widespread use in the world, it is extremely important to define their phytochemical profile and bioactivity. The metabolome varies among species, and organs, due to genetic and environmental factors, and its investigation may provide better mechanistic understanding in ecological and evolutionary contexts. The metabolome lies at the interface between genes and the environment, and for this reason, by comprising the composition, abundance, and interplay of many thousands of metabolites, it provides a direct and multidimensional measure of the molecular mechanisms through which evolutionary and ecological processes shape plant functioning [1]. Over recent decades, advances in analytical methods have led to the advent of metabolomics, and each of these shows advantages and disadvantages.
1H NMR can provide comprehensive characteristic fingerprints of herbal products and it is widely used to analyze plant metabolites [20]. Noteworthy, a combined approach of NMR and LC-MS analysis provides a comprehensive phytochemical investigation of S. anatolicum.
The results of the antioxidant and enzyme inhibitory assays of the present study demonstrate the methanol extract of S. anatolicum as a source of bioactive compounds with health-promoting properties. These findings provide promising evidence for further investigation into the specific bioactive compounds responsible for the α-glucosidase and tyrosinase inhibitory effects. Therefore, the methanol extract of S. anatolicum shows a significant therapeutic potential for the treatment of metabolic and dermatological disorders.

Author Contributions

Conceptualization, M.M. and S.P.; methodology, H.K., G.D. and M.M.; software, G.D. and A.P.; validation, H.K., G.D. and M.M.; formal analysis, H.K., G.D. and A.P.; investigation, H.K., G.D. and A.P.; resources, S.P.; data curation, H.K. and M.M.; writing—original draft preparation, H.K., G.D. and M.M.; writing—review and editing, O.A. and S.P.; supervision; project administration, S.P.; funding acquisition, S.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available in the main article.

Conflicts of Interest

The authors declare no conflict of interest.

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Metabolites 13 01051 g001
Figure 1. LC-ESI-FT-MS profile of Symphytum anatolicum methanol extract in negative ion mode.
Figure 1. LC-ESI-FT-MS profile of Symphytum anatolicum methanol extract in negative ion mode.
Metabolites 13 01051 g001
Metabolites 13 01051 g002
Figure 2. Compounds occurring in Symphytum anatolicum methanol extract.
Figure 2. Compounds occurring in Symphytum anatolicum methanol extract.
Metabolites 13 01051 g002
Metabolites 13 01051 g003
Figure 3. 1H NMR spectrum of Symphytum anatolicum methanol extract.
Figure 3. 1H NMR spectrum of Symphytum anatolicum methanol extract.
Metabolites 13 01051 g003
Table 1. Compounds identified in Symphytum anatolicum extract by LC-ESI-FT-MS, LC-ESI-FT-MS/MS analysis, and NMR spectroscopy.
Table 1. Compounds identified in Symphytum anatolicum extract by LC-ESI-FT-MS, LC-ESI-FT-MS/MS analysis, and NMR spectroscopy.
N°Rt[M-H]−Molecular FormulappmMS/MSIdentity
11.54157.0362C4H6O3N4−0.63140.01/114.03/97.00Allantoin *
21.86377.0857C18H18O9−2.6197.0471dan shen suan C *
34.40153.0184C7H6O41.9-2,5-dihydroxybenzoic acid
45.60137.0240C7H6O31.4-4-hydroxybenzoic acid
57.14179.0346C9H8O41.1-caffeic acid
67.26121.0301C7H6O23.0-benzoic acid
79.26609.1460C27H30O160.8301.0356rutin
89.62463.0879C21H20O120.7301.0341quercetin-3-O-glucoside
99.98593.1509C27H30O150.5285.0405saponarin
1010.20447.0930C21H20O110.67285.0407kaempferol 3-O-glucoside
1110.43447.1348C15H28O15−0.44285.0407kaempferol 3-O-galactoside
1210.62515.1190C25H24O120.19353.08723,5-O-DCQA
1311.12193.0505C10H10O42.5-ferulic acid
1411.24359.0770C18H16O81.11161.0249/179.0359/197.0472rosmarinic acid
1511.85493.1136C26H22O100.40295.0613salvianolic acid A
1612.69491.0980C26H20O100.40311.0564salvianolic acid C
1712.80717.1460C36H30O160.69519.0928/339.0498/321.0403salvianolic acid B
1813.23551.1200C28H24O122.8519.0922/371.0768/353.0666/339.0506monomethyl lithospermate
1913.85327.2180C18H32O52.7309.2076/291.1965/211.1346/171.10309,12,13-TriHODE (10,15) *
2014.76329.2333C18H34O51.51171.1030/229.1445/293.2128/311.22289,12,13 triHOME (10) *
2115.15327.2179C18H32O52.5229.1445/211.1346/171.1030/291.1965Oxo-9,10DiHOME (11) *
* Compounds detected and identified by LC-MS analysis.
Table 2. Metabolites average molar concentrations in S. anatolicum methanol extract.
Table 2. Metabolites average molar concentrations in S. anatolicum methanol extract.
mMmg/g MeOH Extract
Amino acids
Alanine0.0148 ± 0.00520.1293 ± 0.0454
Isoleucine0.0254 ± 0.00850.3266 ± 0.1093
Tyrosine0.1716 ± 0.00183.0483 ± 0.0320
N-Methyl-aspartic acid0.2474 ± 0.03493.5686 ± 0.5034
Valine0.0424 ± 0.00370.4870 ± 0.0425
Sugars
Sucrose0.3021 ± 0.002810.1381 ± 0.0940
Fucose0.5127 ± 0.03748.2515 ± 0.6019
Maltotriose0.3855 ± 0.029319.0634 ± 1.4489
Organic acids
Pyrrolidonecarboxylic acid0.3492 ± 0.09754.4201 ± 1.2341
Succinic acid0.1020 ± 0.01541.1607 ± 0.1752
4-Hydroxybenzoic acid0.0129 ± 0.00520.1734 ± 0.0699
Malonic acid0.3249 ± 0.02873.2506 ± 0.2871
Glutaric acid0.0509 ± 0.02000.6543 ± 0.2571
Fumaric acid0.0663 ± 0.00230.7414 ± 0.0257
Malic acid0.0986 ± 0.02511.2962 ± 0.3300
Phenolic compounds
Rutin0.1435 ± 0.01528.5889 ± 0.9098
Rosmarinic acid0.0900 ± 0.00623.1791 ± 0.2190
3,4-dihydroxyhydrocinnamic acid0.0934 ± 0.00631.6482 ± 0.1112
Others
Myo-inositol0.2131 ± 0.09993.7639 ± 1.7645
Hydroquinone0.0160 ± 0.00210.1727 ± 0.0227
Allantoin0.1595 ± 0.02372.4726 ± 0.3674
The concentration of the identified metabolites was obtained, with respect to the known concentration of TSP, by means of Chenomx.
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Kılınc, H.; D’Urso, G.; Paolillo, A.; Alankus, O.; Piacente, S.; Masullo, M. LC-MS and NMR Based Plant Metabolomics: A Comprehensive Phytochemical Investigation of Symphytum anatolicum. Metabolites 2023, 13, 1051. https://doi.org/10.3390/metabo13101051

AMA Style

Kılınc H, D’Urso G, Paolillo A, Alankus O, Piacente S, Masullo M. LC-MS and NMR Based Plant Metabolomics: A Comprehensive Phytochemical Investigation of Symphytum anatolicum. Metabolites. 2023; 13(10):1051. https://doi.org/10.3390/metabo13101051

Chicago/Turabian Style

Kılınc, Hilal, Gilda D’Urso, Annunziata Paolillo, Ozgen Alankus, Sonia Piacente, and Milena Masullo. 2023. "LC-MS and NMR Based Plant Metabolomics: A Comprehensive Phytochemical Investigation of Symphytum anatolicum" Metabolites 13, no. 10: 1051. https://doi.org/10.3390/metabo13101051

APA Style

Kılınc, H., D’Urso, G., Paolillo, A., Alankus, O., Piacente, S., & Masullo, M. (2023). LC-MS and NMR Based Plant Metabolomics: A Comprehensive Phytochemical Investigation of Symphytum anatolicum. Metabolites, 13(10), 1051. https://doi.org/10.3390/metabo13101051

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