New Potential Use of Protium spruceanum in Hyperglycemia: α-Glucosidase Inhibition and Protection against Oxidative Stress

Abstract

The high prevalence of diabetes and obesity encourages research for the development of α-glucosidase inhibitors from natural sources. This study evaluated the activity of fractions obtained from Protium spruceanum branches. Anti-α-glucosidase activity was investigated in vitro using 4-nitrophenyl-α-D-glucopyranoside as the substrate, while free-radical scavenging activity was evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2’-azinobis-3-ethylbenzotiazoline-6-sulfonic acid (ABTS) assays. Furthermore, a model of oxidative stress promoted by H₂O₂ in fibroblasts was employed, and cell viability was determined by sulforhodamine B. Fractions inhibited α-glucosidase activity effectively, highlighting the hydromethanolic fraction (HMF). Quercitrin, isolated from the HMF, was identified by spectroscopy and quantified by a validated high performance liquid chromatography with diode array detector (HPLC-DAD) method and exhibited free radical scavenging activity comparable to the HMF. However, this flavonoid showed low anti-α-glucosidase effect, suggesting a synergism effect among several components of the HMF. This proposal is also supported by the docking results obtained by PyRx software. The compounds present in the HMF showed a noncompetitive inhibition at the in silico simulation. Finally, the HMF also protected fibroblasts against cell death induced by oxidative stress. This is the first evidence of the capacity of P. spruceanum branches to inhibit α-glucosidase activity and to counteract oxidative stress. These results encourage the use of this Brazilian plant against hyperglycemia-correlated diseases.

Keywords:
Protium spruceanum ; Burseraceae; α-glucosidase activity; oxidative stress; flavonoids; free-radical scavenging activity

Introduction

The worldwide changes in caloric intake and diet composition contribute to the increasing prevalence of obesity.¹ This metabolic disorder leads to low-grade inflammation and chronic oxidative stress which may cause hyperglycemia, leading to type 2 diabetes mellitus (T2DM).² Inhibition of α-glucosidase is one suitable strategy for the prevention and treatment of various metabolic disorders, such as obesity and T2DM.^1,3 Moreover, antioxidant activity may contribute to the patient care, slowing the low-grade inflammation associated with these diseases.²

α-Glucosidase is an intestinal enzyme which catalyzes the cleavage of saccharides to glucose. Thus, its inhibitors are useful to decrease postprandial hyperglycemia.⁴ Efforts have been made to find effective α-glucosidase inhibitors from natural sources by studying medicinal plants.^3,5 Protium spruceanum (Benth.) Engler, a Brazilian medicinal plant popularly known as “breu”, occurs in Atlantic, Amazon, and Cerrado forests.^6,7 In traditional medicine, preparations from its resin, leaves, and bark are administered as tea, inhalation and topical applications to treat mainly inflammatory diseases.⁸

Studies of the anti-inflammatory, antinociceptive, and antimicrobial activities of extracts from P. spruceanum have already been reported.^7-10 On the contrary, no ethnopharmacological description of this species for the treatment of T2DM is available in the literature. However, its extracts may have antidiabetic potential due to their high content of phenolic compounds.⁸ In addition, the need for new treatments for T2DM highlights the usefulness of the study of the α-glucosidase inhibitory action of P. spruceanum, since it has never been investigated.

The present study evaluated the in vitro α-glucosidase inhibitory activity of two fractions obtained from P. spruceanum branches. Furthermore, identification and quantification of quercitrin, one of the major bioactive compounds isolated from the hydromethanolic fraction (HMF), were also performed, and then in silico analysis of enzyme interaction with the identified compounds was obtained. Finally, the oxidative stress protection of the most active fraction HMF was investigated.

Experimental

All solvents were purchased from a commercial supplier (Sigma-Aldrich, St. Louis, USA). The nuclear magnetic resonance (NMR) data were acquired using a Nuclear Bruker Ascend 400 Instrument (Malvern Panalytical, Malvern, UK). The free-radical scavenging activity was evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) and 2,2’-azinobis- 3-ethylbenzotiazoline-6-sulfonic acid (ABTS) assays (Sigma-Aldrich, St. Louis, USA). A model of oxidative stress promoted by H₂O₂ in fibroblasts was employed, and cell viability was determined by sulforhodamine B (Sigma-Aldrich, St. Louis, USA). The anti-α-glucosidase activity was analyzed using 4-nitrophenyl-α-D-glucopyranoside as substrate (Sigma-Aldrich, St. Louis, USA). The absorbance measurements were performed with a Victor X3 2030 Multilabel Reader (PerkinElmer, Waltham, MA, USA). ¹H NMR and mass spectra of the isolated compound quercitrin are available in the Supplementary Information section.

Plant material and extraction

The access for the research was registered at SisGen, Brazilian National System of Genetic Resource Management and Associated Traditional Knowledge under number A2B5290. Thin branches of P. spruceanum were collected in July 2016 at Lavras, Minas Gerais, Brazil (coordinates 21º17’33.6” S and 44º59’15.1” W, 21º18’11.9” S and 44º59’18.8” W). The speciment was identified by Dr Vivette Appolinário Rodrigues Cabral from the Departamento de Ciências Florestais, Universidade Federal de Lavras. A voucher was deposited in the Herbarium of Universidade Federal de Lavras (16399 HESAL). The branches were dried at room temperature and powdered using a knife mill. The ethanol extract was obtained by ultrasonic-assisted extraction at room temperature of the fragmented material (300.0 g) with 2 L of ethanol 95 ºGL, and then the hexane fraction (HF) (2.3 g, 11.5%) and hydromethanolic fraction (HMF) (18.1 g, 90.6%) were obtained by liquid-liquid partition of the extract, as previously reported.⁸

Quercitrin isolation

A portion of the HMF (2 g) was obtained by chromatography on silica gel 60 (70-230 mesh, glass column 2 × 30 cm), eluted with a solvent system of increasing polarity with hexane, ethyl acetate and methanol to afford 52 fractions (HMF.F1 to F52) of 10 mL each. The fraction HMF.F52 (200 mg), eluted with hexane:ethyl acetate:methanol 30:50:20, was submitted to size exclusion chromatography (Sephadex LH 20, column 2.5 cm × 60 cm, methanol) to afford 26 fractions (SPF.1 to 26). Fraction SPF.15-19 was applied to preparative high performance liquid chromatography (p-HPLC) with column C-18 Luna (250 mm × 2.2 mm × 5 µm), with water (solvent A) and methanol (solvent B) as mobile phase (from 40% B to 100% B, from 0 to 40 min) with a flow rate of 8 mL min^-1 to give Fr.IVT-1 (5.2 mg) at retention time 20 min.

Structure elucidation

The Fr.IVT-1 structure was proposed by interpretation of its spectroscopic data (UV, NMR, and mass spectrometry (MS/MS)) and comparison with the literature.

Quercitrin (quercetin-3-O-rhamnoside)

Yellow powder; UV-Vis (methanol) λ_max / nm 264, 348; ¹H NMR (500 MHz, methanol-d₄) d 6.36 (d, J1.82 Hz, H-6), 6.19 (d, J 2.08 Hz, H-8), 7.36 (d, J 1.82 Hz, H-2’), 6.91 (d, J 8.30 Hz, H-5’), 7.31 (dd, J 8.43, 1.95 Hz, H-6’), 5.35 (s, H-1”), 3.16-3.17 (m, H-2”), 3.75 (dd, J 9.47, 3.50 Hz, H-3”), 4.21-4.22 (m, H-4”), 3.45 (d, J 1.56 Hz, H-5”), 0.94 (d, J 5.97 Hz, H-6”); liquid chromatography coupled to mass spectrometry (LC-MS/MS) negative mode m/z 447.32 [M - H]⁻, 301.76 [M - H - rhamnose]⁻, 273.23 [M - H - rhamnose - CO]⁻, 257.12 [M - H - rhamnose - CO₂]⁻, 151.20 [M - H - rhamnose - C₈O₃H₆]⁻ and LC-MS positive mode m/z 449.41 [M + H]⁺, 303.26 [M + H - rhamnose]⁺.

Quercitrin quantification

The analysis was performed using a Waters Alliance HPLC-DAD system equipped with a C-18 column (Luna, 4.6 × 250 mm, 5 µm particle size, Phenomenex, California, USA) at 30 ºC. The mobile phase was comprised by 0.5% acetic acid in Milli-Q purified water (solvent A) and methanol (solvent B). The flow rate was 1.0 mL min^-1 and the injected volume was 20 µL, using the gradient (10-20% B/0-5 min, 20-40% B/5-10 min, 40-50% B/10-15 min, 50-60% B/15-20 min, 60-100% B/20-30 min, 100-10% B/30-35 min, 100% B/35-40 min). A wavelength of 254 nm was used for the analysis. HMF solutions were prepared in methanol at the concentration of 10 mg mL^-1. A quercitrin standard solution of 500 µg mL^-1 in methanol was used to get the range of concentrations 5-250 µg mL^-1. The analytical method was validated to demonstrate the selectivity, linearity, precision (repeatability), accuracy, and limits of detection and quantification.¹¹

Free radical scavenging assays

The antioxidant activity was evaluated by two photocolorimetric in vitro methods using the free radical indicators 2,2-diphenyl-1-picrylhydrazyl (DPPH), and 2,2’-azinobis-3-ethylbenzotiazoline-6-sulfonic acid (ABTS). The plant fractions, quercitrin and gallic acid (positive control) were solubilized in ethanol (240.0 µg mL^-1) and different aliquots were diluted to obtain the final solutions (0.5 to 40.0 µg mL^-1).

DPPH assay was performed according to the previously described method, with minor modifications.¹² 100 µL of the DPPH solution at 0.008% m/v in ethanol were added to each sample and the final volume was adjusted to 240 µL with ethanol. The control was obtained using 100 µL of DPPH and 140 µL of ethanol. All samples were incubated for 30 min at room temperature (25 ± 2 ºC) protected from light. The absorbance (Abs) was acquired at a wavelength of 490 nm.

The ABTS assay was performed according to the method previously described.¹³ The solution was obtained by mixing ABTS (7.4 mmol L^-1) with potassium persulfate (2.6 mmol L^-1) and kept for 16 h at room temperature, protected from light. On the day of analysis, this solution was diluted with ethanol to obtain an absorbance of 0.70 (± 0.02) at 650 nm. Then, 120 µL of ABTS were added to the samples. The final volume was adjusted to 150 µL with the addition of ethanol. The control was obtained from 120 µL of ABTS and 30 µL of ethanol. The readings were performed at 650 nm after incubation of the samples for 6 min at room temperature (25 ± 2 ºC) and protected from light.

All assays were performed in triplicate. The ability to scavenge free radicals was calculated as the scavenging percentage (% I), using the formula: I (%) = (Abs control - Abs sample/Abs control) × 100. The concentration required to obtain a 50% antioxidant effect (EC₅₀) was calculated using GraphPad Prism.^14,15 Antioxidant activity index (AAI) was calculated as: AAI = Final concentration of DPPH (µg mL^-1)/EC₅₀ (µg mL^-1). The antioxidant activity was classified as weak (AAI < 0.5), moderate (0.5 ≤ AAI < 1.0), strong (1.0 ≤ AAI < 2.0) and very strong (AAI ≥ 2.0).¹⁶

α-Glucosidase inhibition assay

The α-glucosidase inhibition was studied using 4-nitrophenyl-α-D-glucopyranoside (p-NPG) as substrate and α-glucosidase from Saccharomyces cerevisiae, type I lyophilized powder. Each sample was incubated with α-glucosidase and 0.1 M phosphate buffer solution (PBS pH 6.8) for 10 min at 37 °C. The reaction started by adding 4 mM p-NPG, and the absorbance values were measured at 405 nm for 30 min.¹⁷ Acarbose (2 mM) was used as positive control. The results were expressed as the half maximal inhibitory concentration (IC₅₀) calculated using GraphPad Prism.¹⁵

Molecular docking

Molecular docking studies of the compounds identified in the HMF by Amparo et al.⁸ were conducted using the PyRx software,¹⁸ according to Shahzad et al.¹⁹ Saccharomyces cerevisiae isomaltase (SCI) (PDB code: 3A4A) α-glucosidase crystal structure was obtained from protein data bank (PDB). The 3D structures of the identified compounds (catechin, isoquercitrin, procyanidin B, quercetin-3-O-rhamnoside, quercitrin, and rutin) and acarbose (positive control) were obtained from PubChem data bank. The files were converted to (*.pdb) using Biovia Discovery Studio²⁰ prior to docking analysis. The grid box-centered parametric values were x = 21.2783, y = -0.7737, z = 18.6460, and the size values were x = 57.60, y = 59.83, and z = 72.29. A default exhaustiveness value of 8 was used. Graphical depictions were prepared using Biovia Discovery Studio (2.1.0).²⁰

Oxidative stress protection

The effect of the HMF on cell death caused by oxidative stress induced by hydrogen peroxide (H₂O₂) was evaluated according to the previously described method, with minor modifications.^21-23 The assay was performed using murine L929 fibroblasts cultured in Roswell Park Memorial Institute (RPMI) 1640 medium containing 10% fetal bovine serum and gentamicin (60 µg L^-1), at 37 ºC, with 5% CO₂. Cells were added in 96-well plates (1 × 10⁵cellsperwell) and incubated for 24 h for adhesion. Firstly, the cytotoxicity of the HMF (concentrations from 2.00 to 0.03 mg mL^-1 in RPMI, 1.0% dimethyl sulfoxide (DMSO)) and H₂O₂ (from 500.0 to 7.8 mM) were evaluated in order to select the concentrations to be used in the cytoprotection test. Cells with RPMI and with RPMI 1.0% DMSO were used as controls. After incubation for 4 h, cell viability was evaluated by the sulforhodamine B assay.²⁴ HMF concentrations that maintained at least 70% of cell viability in the cytotoxicity test were used to evaluate their effect on oxidative stress. The oxidative stress was induced by H₂O₂ at concentrations considered toxic (viability less than 70%). To assess protection against oxidative stress, cells were treated simultaneously with HMF and H₂O₂. The controls were cells with H₂O₂ not treated with the extract and cells without any treatment. After incubation for 4 h, cell viability was evaluated by sulforhodamine B assay. In parallel, the cytotoxic concentration of the HMF for 50% of the cells (CC₅₀) was calculated by a non-linear regression equation using GraphPad Prism.¹⁵ The selectivity index (SI) was calculated by the ratio CC₅₀/IC₅₀.

Statistical analysis

The results are presented as mean ± standard deviation (SD). The data were evaluated by one-way analysis of variance (ANOVA) using GraphPad Prism 6.¹⁵ Level of significance was set at p < 0.05.

Results and Discussion

P. spruceanum is a Brazilian medicinal plant which exhibits several favorable pharmacological effects due to its high content of phenolic compounds.⁸ The current research evaluated two fractions from extracts of P. spruceanum branches to estimate their potential use in hyperglycemic disorders, such as obesity and T2DM.

Analyzed fractions exhibited free radical scavenging activity by DPPH and ABTS assays (Table 1). The ability to scavenge free radicals is important for the treatment of T2DM, since the excess of radicals is associated with alterations of lipid and protein structures, leading to cellular damage typical of obesity and T2DM.²

Table 1
Free-radical scavenging activity of the two P. spruceanum fractions detected by DPPH and ABTS assays

Sample	DPPH			ABTS
	EC50 / (µg mL-1)	AAI		EC50 / (µg mL-1)
HF	37.76 ± 5.91a	0.8 ± 0.1a		72.84 ± 9.65a
HMF	8.56 ± 0.52b	3.7 ± 0.2b		1.93 ± 0.29b
Quercitrin	7.60 ± 0.38b	3.9 ± 0.2b		5.06 ± 0.23b
Gallic acid	0.91 ± 0.03c	36.5 ± 1.1c		0.52 ± 0.11c

• Results are expressed as mean ± standard deviation (n = 3). Different letters mean p < 0.05 in each column by one-way ANOVA test. DPPH: 2,2-diphenyl-1-picrylhydrazyl; ABTS: 2,2-azinobis-3-ethylbenzotiazoline-6-sulfonic acid; EC₅₀: 50% antioxidant effect; AAI: antioxidant activity index; HF: hexanic fraction; HMF: hydromethanolic fraction.

It can be observed that HMF displayed higher scavenging activity than HF (Table 1). A higher activity of polar plant extracts compared to nonpolar ones is frequently observed, since polar solvents favor the extraction of phenolic compounds which are well-known for the antioxidant activity.²⁵ Indeed, previous studies have shown that hydromethanolic extracts from P. spruceanum branches have a high content of flavonoids and tannins.⁸ These phenolic compounds are among the main natural antioxidants which trap free radicals by mechanisms that involve the catechol group (o-diphenolic group) and other functional groups that are important for antioxidant activity, such as double conjugated bonds and hydroxyl groups.²⁶

The antioxidant activity index (AAI) confirmed that the effect of HMF can be considered as very strong (AAI > 2.0), although its EC₅₀ is higher than the gallic acid reference compound (Table 1). This AAI value highlights the antioxidant activity of HMF from P. spruceanum branches, especially when compared with fractions derived from orange (Citrus sinensis), that is popularly known as an antioxidant and have an AAI between 1.1 and 1.4.²⁷

Furthermore, the fractions of P. spruceanum branches inhibited the α-glucosidase activity (Figure 1), the main enzyme responsible for the hydrolysis of complex carbohydrates and glucose intestinal absorption.²⁸ This experimental finding is the first evidence of the anti-α-glucosidase activity of fractions obtained from Protium genus.

Figure 1
(a) Concentration-dependent inhibition of α-glucosidase activity by P. spruceanum hexanic and hydromethanolic fractions (HF and HMF, respectively), and quercitrin. (b) Effects of HMF on the α-glucosidase kinetics. Acarbose (2 mM) was used as positive control. Control: no treatment. Data are expressed as mean ± standard deviation (n = 3-5). *p < 0.05 vs. control by one-way ANOVA test.

Among the fractions, HMF showed higher activity than HF, inhibiting α-glucosidase activity at lower concentrations. The higher activity of HMF may be related to the presence of flavonoids, which were detected in large amounts in polar extracts of P. spruceanum.⁸ Several compounds of this class of secondary metabolites have been considered as potential antidiabetic agents due to the anti-α-glucosidase activity and the ability to regulate the glucose homeostasis.²⁹

In fact, HMF at 0.5, 1.0 and 5.0 µg mL^-1 significantly inhibited the α-glucosidase activity, as well as the positive control acarbose (Figure 1a). Acarbose can be considered the main α-glucosidase inhibitor since it is currently used as a hypoglycemic drug in the treatment and prevention of diabetes. However, the long-term use of acarbose may cause abdominal distention, vomiting and diarrhea, and therefore natural products may represent a choice with minor side effects.³⁰

The IC₅₀ values for α-glucosidase inhibition were 0.4 and 34.7 µg mL^-1 for HMF and HF, respectively. Thus, both fractions showed a great α-glucosidase inhibitory activity when compared to acarbose reference drug, for which an IC₅₀ of 449 µM (289 µg mL^-1) is reported in the literature.³¹ Furthermore, HMF showed a IC₅₀ lower than 52 extracts obtained from several species as reported in the review performed by Kumar et al.³ The suitable anti-α-glycosidase activity obtained with low concentrations of HMF suggests that this fraction may be appropriate for the treatment of hyperglycemia-correlated pathologies.

The α-glucosidase kinetics reveals that the inhibitory effect of the HMF is a time- and concentration- dependent process (Figure 1b). In detail, HMF (0.5, 1.0 and 5.0 µg mL^-1) significantly decreased the enzymatic activity during 45 min of incubation; furthermore, at 1 and 5 µg mL^-1 it exhibited higher inhibitory activity than 2 mM acarbose (Figure 1b). Other plant derivatives also demonstrated a time- and concentration-dependent inhibition of α-glucosidase kinetics, such as extracts from Vernonia amygdalina, used in traditional African medicine to treat diabetes.²⁸ Nevertheless, HMF exhibits a greater potential than V. amygdalina extracts, which showed IC₅₀ higher than the HMF from P. spruceanum.

Considering the anti-α-glucosidase activity of HMF, molecular docking analyses were performed for the compounds previously identified in this fraction by Amparo et al.⁸ All compounds showed fitting binding affinity, interacting with the protein chains mainly by hydrogen bonding (Figure 2). The binding site of the flavonoids was predicted to be close to the active site (glucose binding site), except for the tannin procyanidin B (Figure 2). Thus, the binding of catechin, isoquercitrin, quercitrin, quercetin-3-O-glucuronide and rutin may preclude the entrance of the substrate, preventing the enzyme activity. This observation suggests that these compounds may act as noncompetitive inhibitors, in contrast to acarbose that is a competitive inhibitor.^32,33 Several natural phenolic compounds displayed α-glucosidase inhibition by a noncompetitive interaction. Comparing to the competitive type, noncompetitive inhibitors offer the advantage of not being affected by high concentrations of the substrate.³⁴

Figure 2
3D diagram showing the superimposed binding site (a) and diagrams of interactions; (b) of the compounds of the hydromethanolic fraction (HMF) obtained from Protium spruceanum branches with the α-glucosidase enzyme. *Binding energy values are in kcal mol^-1.

In consideration of the fact that quercitrin exhibited the highest α-glucosidase affinity (-10.5 kcal mol^-1) among the studied compounds (Figure 2), this compound was isolated and quantified in the HMF. The flavonoid was obtained as a yellow powder and its spectroscopic data (UV, NMR, and MS/MS) were according to that of quercetin-3-O-rhamnoside (quercitrin) reported in the literature.^35,36 Quercitrin has already been isolated from other Protium species, such as P. javanicum and P. heptaphyllum.^37,38 However, this flavonoid has not yet been isolated and quantified from P. spruceanum.

Validation results of the quantification method for quercitrin showed linearity in the range from 5 to 250 µg mL^-1 with limits of detection and quantification of 0.62 and 1.89 µg mL^-1, respectively. The method was precise and accurate since it showed relative standard deviation (RSD) values minor of 5% (Table 2). In addition, the purity angle (1.267) was lower than the purity threshold (2.284), indicating the specificity of the method. Thus, the validated method was used to quantify quercitrin in the HMF. The quercitrin content in the HMF was 2.6 ± 0.1 mg g^-1 (0.26% m/m). The amount is higher than that found in the methanolic extract of Hypericum perforatum nonflowering shoots, which showed considerable α-glucosidase inhibitory activity correlated with quercetin and kaempferol glycosides.³⁹

Table 2
Validation parameters for quercitrin quantification

Specificity
Purity angle	1.267
Purity threshold	2.284
Linearity
r2	0.9999
Equation	$\mathit{y}=31807\mathit{x}-2115$
Significance	p = < 0.0001 (a ≠ 0)
Linearity	p = 1.0000 (linear)
Precision (repeatability)
Concentration / (µg mL-1)	RSD
5	4.94
10	4.88
50	1.40
100	1.37
250	1.45
Limit of detection / (µg mL-1)	0.62
Limit of quantification / (µg mL-1)	1.89

• r²: R-squared (coefficient of determination); p: level of statistical significance; RSD: relative standard deviation.

Moreover, the isolated quercitrin exhibited free-radical scavenging activity comparable to the HMF (Table 1). The scavenging mechanism of quercitrin includes hydrogen donating of its phenolic hydroxyl groups to stabilize free radicals and thus prevent the oxidation of lipids, proteins, and deoxyribonucleic acid (DNA).⁴⁰ About the anti-α-glucosidase effect, quercitrin showed a concentration-dependent inhibition similar to HMF (Figure 1a). The IC₅₀ value of quercitrin for α-glucosidase inhibition was 8.69 µg mL^-1, equivalent to 19 µM. The quercitrin IC₅₀ is at least 20 times higher than that of the HMF, indicating that quercitrin is only one of the bioactive compounds responsible for the α-glucosidase inhibition demonstrated by the fraction as well as its activity may be greater when combined with other compounds. Thus, the data suggest a possible synergistic effect that is also supported by the docking results, since all compounds showed binding affinity higher or equal than the positive control acarbose (-8.0 kcal mol^-1) (Figure 2). The α-glucosidase inhibitory activity of other extracts containing quercitrin has already been reported, e.g., Agrimonia pilosa, used to treat T2DM in Chinese traditional medicine, which has also antioxidant activity.⁴¹

In view of the great anti-α-glucosidase activity of HMF, this fraction was also evaluated whether it could protect fibroblasts from oxidative damage induced by reactive oxygen species (ROS) and subsequent cell death. Apoptosis and necrosis due to high oxidative stress generated by hyperglycemia also play a role in the progression of diabetic complications, culminating in tissue injury in the heart, retina and kidneys.⁴² Fibroblasts are present in all these tissues and H₂O₂ has been reported to induce apoptosis of these cells.^43,44 The assay was performed using H₂O₂ at 500, 250 and 125 mM, concentrations able to reduce cell viability below 70% (Figure 3a). HMF decreased cell viability only at very high concentrations and the CC₅₀ was 1.58 mg mL^-1. This low cytotoxicity highlights the use of the HMF as an antioxidant agent and inhibitor of α-glucosidase, since the IC₅₀ for both activities was much lower than its CC₅₀.

Figure 3
Effects of hydromethanolic fraction (HMF) of Protium spruceanum branches against H₂O₂-induced oxidative stress on L929 fibroblasts. (a) Cytotoxicity of H₂O₂ or HMF. (b) Cell viability after simultaneous treatment with both HMF and H2O2 for 4 h. Control: untreated cells. H₂O₂ control: H₂O₂-induced cell viability without HMF. Results are expressed as mean ± SD (n = 3). *p < 0.05 vs. H₂O₂ control by one-way ANOVA test.

In these experimental conditions, the HMF treatment prevented the H₂O₂-induced cell death (Figure 3b). This cytoprotective effect obtained with the simultaneous incubation of H₂O₂ and HMF suggests that the protection may be due to a direct interaction between HMF and H₂O₂ via free-radical scavenging.²⁵ This idea is also supported by the data obtained with DPPH and ABTS assays. The HMF protection against oxidative stress was observed at 0.50, 0.25 and 0.12 mg mL^-1 with 125 mM H₂O₂ (Figure 3b), while with 250 and 500 mM H₂O₂ the HMF inhibited the damage only at higher concentrations, showing a concentration-dependent protective activity. The minimum active concentration of HMF vs. 125 mM H₂O₂ was 0.12 mg mL^-1, which is at least 13 times lower than the CC₅₀ of the fraction.

This research is the first report showing the cytoprotection against H₂O₂-induced oxidative stress of P. spruceanum branches. In view of the fact that oxidative stress contributes to the progression of diabetic complications, the cytoprotective effect of HMF also suggests its potential use in T2DM treatment.

Conclusions

This research shows for the first time the inhibitory activity of polar fractions of P. spruceanum branches on α-glucosidase activity. Quercitrin, isolated from the hydromethanolic fraction (HMF), exhibits free-radical scavenging activity comparable to the fraction, but with a lower anti-α-glucosidase effect, indicating a possible synergism among the various compounds in the mixture. This observation is supported by the docking results, in which identified compounds showed a noncompetitive inhibition, with binding affinity higher or similar to acarbose. In addition to the anti-α-glucosidase activity, HMF can also protect fibroblasts against H₂O₂-induced oxidative stress. Overall, the data suggest that P. spruceanum extracts could be useful to develop new medicines to treat hyperglycemia-correlated pathologies.

Acknowledgments

Fundação de Amparo à Pesquisa de Minas Gerais (FAPEMIG) (PCI-00359-18), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), University of Padova (DOR 2019) were acknowledge.

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Publication Dates

• Publication in this collection
  01 Oct 2021
• Date of issue
  Oct 2021

History

• Received
  05 Mar 2021
• Accepted
  21 June 2021