Target guided isolation, in-vitro antidiabetic, antioxidant activity and molecular docking studies of some flavonoids from Albizzia Lebbeck Benth. bark
© Ahmed et al.; licensee BioMed Central Ltd. 2014
Received: 8 November 2013
Accepted: 30 April 2014
Published: 13 May 2014
Albizzia Lebbeck Benth. is traditionally important plant and is reported to possess a variety of pharmacological actions. The present research exertion was undertaken to isolate and characterized the flavonoids from the extract of stem bark of Albizzia Lebbeck Benth. and to evaluate the efficacy of the isolated flavonoids on in-vitro models of type-II diabetes. Furthermore, the results of in-vitro experimentation inveterate by the molecular docking studies of the isolated flavonoids on α-glucosidase and α-amylase enzymes.
Isolation of the flavonoids from the methanolic extract of stem bark of A. Lebbeck Benth was executed by the Silica gel (Si) column chromatography to yield different fractions. These fractions were then subjected to purification to obtain three important flavonoids. The isolated flavonoids were then structurally elucidated with the assist of 1H-NMR, 13C-NMR, and Mass spectroscopy. In-vitro experimentation was performed with evaluation of α-glucosidase, α-amylase and DPPH inhibition capacity. Molecular docking study was performed with GLIDE docking software.
Three flavonoids, (1) 5-deoxyflavone (geraldone), (2) luteolin and (3) Isookanin were isolated from the EtOAc fraction of the methanolic extract of Albizzia lebbeck Benth bark. (ALD). All the compounds revealed to inhibit the α-glucosidase and α-amylase enzymes in in-vitro investigation correlating to reduce the plasma glucose level. Molecular docking study radically corroborates the binding affinity and inhibition of α-glucosidase and α-amylase enzymes.
The present research exertion demonstrates the anti-diabetic and antioxidant activity of the important isolated flavonoids with inhibition of α-glucosidase, α-amylase and DPPH which is further supported by molecular docking analysis.
Type 2 diabetes mellitus (T2D) is one of the fastest growing epidemics of our time [1–3]. This disease affected nearly 150 million adults worldwide in 2000. T2D is characterized by decreased insulin sensitivity leading to insulin resistance in its target tissues (mainly liver, skeletal muscle and adipose tissues) [4–6]. On the other hand, impaired glucose-induced insulin secretion (GIIS) with a decrease in pancreatic -cell mass will eventually lead to chronic hyperglycaemia . Both genetic and environmental factors are involved in the aetiology of T2D and dysfunction of fatty-acid (FA) metabolism appears to be an early key event leading to insulin resistance .
Insulin dependent diabetes mellitus (IDDM) or juvenile-onset diabetes accounts for about 10% of diabetes. The main symptoms include high blood sugar, excessive thirst, frequent urination, increased appetite, fatigue, weight loss, poor wound healing, blurred vision etc. the only treatment of this type available is insulin injections. The risk of hypoglycemia is greatly increased. In 2011 about 366 million people suffered with diabetes globally and this is expected to increase to 552 million by 2030 . One recent study by ICMR-INDIA reported that about 62.4 million type-II diabetic people are from India. This statistics are expected to increase to 101 million by the year 2030 .
A change in diet, lifestyle and exercise will help to a great extent in management of diabetes at the early stages with little lesser impact at the later stages of life. Quite a lot of minerals have been found to benefit diabetes either due to deficiencies or their favorable effect on metabolism of glucose .
Plant-based products have been popular all over the world for centuries. In diabetics, some herbal alternatives are proven to provide symptomatic relief and assist in the prevention of the secondary complications of the disease. Some herbs have also been proven to help in the regeneration of beta cells and in triumph over insulin resistance. Apart from normalizing the blood glucose level, some the Indian Medicinal plants are also reported to possess antioxidant and cholesterol lowering action .
Therefore, herbal medication is the most widespread used unconventional therapy for diabetes treatment. Alternatives are considered necessary because of inability of current therapies to contribute normoglycemia and prevention of diabetic complications. Due to high cost of modern treatment and medications and dependency of about 85-95% of rural population in developing countries on traditional medicines for their primary health care necessitates the alternative strategies for the prevention and treatment of diabetes. Moreover herbs are known for their safety, efficacy, cultural acceptability and lesser side effects besides maintaining normal blood glucose level in diabetic patients .
Preparation of standardized medicinal herbs is urgently needed for future studies and therapies. To date, over 600 traditional plant treatments for diabetes have been reported but only a small number of these have received scientific and clinical evaluation to assess their efficacy. However, the hypoglycemic effect of some herbal extracts have been confirmed in human and animal models of type-II diabetics and some of the conventional drugs have been derived from the active molecules of these medicinal plants. For example, metformin a less toxic biguanide and potent oral hypoglycemics was developed from plant Galgea officinals. The need of basic information about the availability of antidiabetic plants in India for researchers for their scientific quest is fanatically felt.
Due to capability of antioxidants to assuage oxidative stress in cells and helps in the prevention and treatment of many diseases of humans, the exploration for antioxidants has attracted much attention in the past decades and many medicinal plants are considered to have colossal antioxidant potential .
Albizzia Lebbeck Benth. is traditionally important medicinal plant. Albizia lebbeck Benth. (Mimosaceae), commonly known as Sirisa in Sanskrit, is a tall, unarmed, and deciduous tree distributed throughout India from the plains up to 900 m in the Himalayas. In Siddha system of medicine the bark and flowers of this plant are used to treat arthritis . The stem bark of Albizia lebbeck Benth (ALD). is used to treat diarrhea , poisoning, edema, asthma and bronchitis . The leaves of this plant contain alkaloids, flavonoids, tannins and saponins which have brilliant therapeutic importance .
A research work indicates that flavonoids isolated from Albizzia Julibrissin showed significant antioxidant activity. Present research exertion explores the possible hypoglycemic and lipid lowering properties of some of the flavonoids which were previously isolated and characterized from bark of Albizzia Julibrissin have shown to produce powerful antioxidant effects .
In the present study we hypothesized that the function of the bark for the treatment of type –II diabetes may be mediated with the compounds in the plants with antioxidant activity, because oxidative stress is considered to be major cause in the development of type-II diabetes . An in-vitro evaluation was therefore undertaken and antioxidant and antidiabetic activities of the isolated flavonoids were evaluated by and α-glucosidase, α-amylase and DPPH inhibition assay. Furthermore, the mechanism of action of the isolated compounds was explored by molecular docking analysis.
General experimental procedures
1H and 13C NMR spectra were recorded on a Bruker Advance II NMR spectrometer at 400 MHz for proton and 100 MHz for carbon utilizing TMS as internal standard. Solvent used was DMSO-d6. EIMS were recorded WATERS, Q-TOF micromass.
The bark of Albizzia Lebbeck Benth. was collected in the month of December 2012 from Herbal Garden of Department of Pharmaceutical Sciences, Faculty of Health Sciences, SHIATS-Deemed University, Allahabad, Uttar Pradesh. The botanical identity of the plant was confirmed with the help of Pharmacognosist, Department of Pharmaceutical Sciences, Faculty of Health Sciences, SHIATS-Deemed University, Allahabad, Uttar Pradesh. The voucher specimen was deposited in the Department of Pharmacognosy, Faculty of Health Sciences, SHIATS-Deemed University, Allahabad, Uttar Pradesh. (Voucher No. ALD/B/2012/12/0018).
Preparation of extracts
The bark of Albizzia Lebbeck Benth. was chopped into small pieces, cleaned, powdered, air-dried, sieved (Mesh size = 40) and stored in air tight container at room temperature. The powdered plant material (14.2 kgs) was then extracted sequentially with Ethyl Acetate (EtOAc), dichloromethane (CH2Cl2), and methanol (MeOH) using soxhlation method. The extract (1.89 kg) was concentrated to dryness using Rotary Evaporator (Rotavapor, R-210/R-215, Buchi). The percentage yield of Ethyl Acetate (EtOAc), dichloromethane (CH2Cl2), and methanol extract was found to be 0.27%, 1.63% and 16.39% respectively.
Preliminary phytochemical evaluation
In order to confirm the presence of different types of compounds, some important colorimetric tests were used to reveal the families of the compounds. The presence of saponins, flavonoids and reducing compounds were revealed by Shibata Test and Fehling’s test . The Presence of tannins was confirmed using FeCl3 and Stiasny’s reagent according to the Soro et al. .
Phytochemical screening of Albizzia Lebbeck Benth. Stem bark. (ALD)
As our research exertion was focused on the isolation of flavonoids, phytochemical screening of Albizzia Lebbeck Benth. bark was carried out for the presence of flavonoids.
Test for flavonoids
Presence of flavonoids was inveterate by the method developed by Saeed et al. . Filtrate was obtained by suspending 50 mg of the ALD extract in 100 ml of distilled water. From the filtrate 10 ml was pipette out and 5 ml of the dilute ammonia solution was added to the filtrate followed by few drops of concentrated H2SO4. Yellow color confirms the presence of flavonoids.
Determination of total flavonoid content
Total flavonoid content was determined following a method by Perk et al.. 0.3 ml of the extract, 3.4 ml of 30% methanol, 0.15 ml of NaNO2 (0.5 M) and 0.15 ml of AlCl3.6H2O (0.3 M) were mixed in a 10 ml test tube. 1 ml of NaOH (1 M) was added after an interval of 5 minutes. The solution was then mixed well and the absorbance was measured against a reagent blank at 506 nm with UV spectrophotometer type Shimadzu UV–vis 1800. The flavonoid content was calculated from a quercetin standard curve and expressed in mg quercetin equivalent per g of dry weight (DW).
Extraction and isolation of compounds 1–3
4′,7-Dihydroxy-3′-methoxyflavone (Geraldone) [Compound 1]
Amorphous yellow powder, UV λmax (MeOH) (log ϵ): 236 (4.18), 316 (sh. 4.03), 337 (4.07); +AlCl3: 237 (4.12), 316 (sh. 4.06). 337 (4.13); +AlCl3 +HCl: 236 (4.15), 317 (sh. 4.08), 337 (4.14), 406 (sh. 3.16); +NaOMe: 254 (4.16), 319 (sh. 3.87), 3.68 (3.99) +NaOAc: 247 (4.19), 356 (4.17); +NaOAc +H3BO3: 236 (4.18), 317 (sh.4.04), 336 (4.17) nm; C16H12O5, M.P.: 226–228 0C; O.P.: [α]D20 -2°; 1H NMR (400 MHz, DMSO, TMS) δ ppm: 5.35-5.34 (d, 1H, J = 0.01 Hz), 5.32-5.30 (d, 1H, J = 0.02 Hz), 5.29-5.27 (d, 1H, J = 0.02 Hz), 4.68 (d, 1H, J = 0.02 Hz), 4.55 (s, 1H), 4.23-4.22 (d, 1H, J = 0.01 Hz), 3.83-3.82 (d, 1H, J = 0.01 Hz), 3.78-3.74 (m, 2H), 3.57 (s, 3H); 13C NMR (100 MHz, DMSO) δ ppm: 177.20, 150.27, 109.61, 76.74, 69.25, 60.21, 55.37, 49.89, 39.87, 38.45, 37.54, 33.87, 31.66, 30.05, 29.01, 28.70; M/Z: 455.1 (100%), 456.1 (30.23%), 281.0 (6.97%).
3′, 4′, 7, 8-tetrahydroxyflavanone (Isookanin) [Compound 2]
Amorphous orange powder: UV ;λmax (MeOH) (log ϵ): 239 (sh. 4.19), 280 (4.01), 378 (3.65); +NaOMe: 251 (4.01), 294 (sh. 3.78), 337 (4.16), 432 (3.47); AICI3 + HCI: 230 (sh. 4.19), 281 (4.01), 428 (3.73); AICI3: 248 (3.83), 291 (sh. 3.63), 313 (3.81), 350 (sh. 3.17), 472 (2.73); +NaOAc : 234 (sh. 4.16), 259 (4.13), 286 (4.14), 320 (3.85), 368 (3.62); +NaOAc +H3BO3: 241 (sh. 4.18), 289 (4.01), 302 (4.00), 394 (3.69) nm, M.P.: 221–224 0C; O.P.: [α]D20 -3°; 1H NMR (400 MHz, DMSO, TMS) δ ppm: 8.24(s, 1H), 4.68-4.67 (d, 1H, J = 0.01 Hz), 4.55-3.58 (d, 1H, J = 0.97 Hz), 3.53-2.99 (m, 2H), 2.98-2.01 (m, 2H), 1.99-099 (m, 3H), 093–0.62 (m, 2H); 13C NMR (100 MHz, DMSO) δ ppm: 177.18, 174.41, 150.23, 129.65, 127.70, 109.58, 76.73, 41.94, 39.25, 38.24, 33.88, 29.05, 27.12, 26.59, 17.93; M/Z: 455 (100%), 456.1 (30.23%), 284.9 (13.95%).
2-(3, 4-dihydroxyphenyl)-5, 7-dihydroxy-4H-chromen-4-one (Luteolin) [Compound 3]
Amorphous yellow powder; UV λmax (MeOH) (log ϵ): 252 (4.18), 268 (sh. 4.27), 341 (4.18); AICI3: 276 (4.22), 306 (sh. 3.91), 427 (4.32); +NaOMe: 231 (sh. 4.87), 261 (4.69), 327 (sh. 4.19), 401 (4.62); +AICI3 +HCI: 266 (sh. 4.12), 275 (4.18), 293 (4.10), 361 (4.13), 392 (4.13); +NaOAc 271 (4.23), 363 (4.16); +NaOAc +H3BO3: 266 (4.28), 372 (4.19) nm, M.P.: 189–194 0C; O.P.: [α]D20 -3°; 1H NMR (400 MHz, DMSO, TMS) δ ppm:4.48 (s, 1H), 3.83-3.38 (m, 2H), 2.51-2.09 (M, 2H), 1.83-1.47 (m, 2H), 1.38-1.1.09 (m, 3H); 13C NMR (100 MHz, DMSO) δ ppm: 177.18, 150.24, 129.66, 109.58, 76.73, 69.75, 41.95, 39.87, 36.68, 33.62, 31.67, 28.92, 22.09, 14.33, 13.92; M/Z: 246.8 (100%), 455 (74.41%), 285.0 (11.62%).
Structural elucidations of the isolated compounds
Molecular formula of compound 1 was construed as C16H12O5 on the basis of NMR and EIMS spectral analysis. The UV spectrum exhibited characteristic absorbance bands of flavones at 236 nm and 254 nm. The compound 1 showed the M + peak at m/z 455.1 consistent with the presence of one hydroxyl group in ring-A and both methoxy and hydroxyl groups in ring-B, respectively. The 1H NMR spectrum of compound 1 depicts thirteen hydrogen atoms and showed signals due to presence of one hydroxyl group in ring-A and methoxy and hydroxyl groups are found to be present in ring-B. The 1H-NMR spectrum of I showed signals due to a methoxy group at δ 3.57 (3H, s), H-3 at δ 5.29-5.27 (1H, s), and two aromatic ABX coupled systems at δ 5.35 (1H, d, J = 0.01 Hz), 5.32 (1H, d, J = 0.02 Hz), and 4.68 (1H, d, J = 0.02 Hz) assigned to H-5, -6, and -8, and δ 4.23 (1H, d, J = 0.01 Hz), 3.83 (1H, d, J = 0.01 Hz), and 3.78 (1H, d, J = 0.01 Hz) assigned to H-2′, -6′, and -5′, confirming the presence of mono substitution in ring-A and disubstitution in ring-B. Based on these evidences, the compound 1 was identified as 4′, 7-Dihydroxy-3′-methoxyflavone.
The physicochemical properties of compound 2 were found to be amorphous, orange powder. The UV spectrum depicted characteristic absorbance bands of flavones at 239 and 337 nm. At position C-7 and 4, free hydroxyl groups were found which was confirmed by the presence of shift of band-II and I with NaOAc and NaOMe. The 1H- and 13C-NMR spectral data exhibited characteristic signals for the ABX system at 5H 1.99 (dd, J = 0.01 Hz, H-3 eq) and 2.98 (d, J = 0.01 Hz) and 5H 3.53 (d, J =0.02 Hz, H-2), along with an oxygen bearing methine at 6c 109.58 (C-2), a carbonyl group at 5c 127.70 (C-4) and a methylene at 5c 150.23 (C-3), assigned to positions 2 and 3 on a flavanone. The chemical shift value at 6c 109.58, corresponding to a carbonyl resonance indicated the absence of the hydroxyl group in position 5. The 1H NMR spectrum of compound 2, two aromatic protons in the aromatic rings at δ 3.53 and 2.98 were assigned to H-5 and H-6 on ring-A. Hydroxy groups were found to be at C-7, 8, 3 and 4. Based on the above parameters compound 2 was portrayed as 3′, 4′, 7, 8-tetrahydroxyflavanone.
In vitro intestinal α-glucosidase activity test
α- glucosidase and α-amylase inhibition activity of Compounds 1, 2 and 3
α-Glucosidase from saccharomyces cerevisiae
α-Amylase from bacillus subtilis
Compound 1 (7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-chromen-4-one)
93.91 ± 1.21***
93.98 ± 1.02***
Compound 2 ((S)-2-(3,4-dihydroxyphenyl)-7,8-dihydroxychroman-4-one)
73.14 ± 1.30**
84.36 ± 0.60***
Compound 3 (2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one)
92.59 ± 1.36***
90.10 ± 0.58***
43.77 ± 1.67
37.65 ± 0.94
In vitro bacterial α-amylase activity test
In order to investigate the inhibitory activity of isolated compounds from Albizzia Lebbeck Benth. bark, α-amylase activity was performed according to the method of Chen J et al. . Samples (ALD or acarbose) were mixed and pre-incubated in 20 mM sodium phosphate buffer (pH 6.7) for 5 min at 37°C. After that the volume of reaction mixture was made up to 2 ml by incorporation of 1 ml of .2% (w/v) starch dissolved in the buffer, and the whole reaction mixture was incubated for 5 min at 37°C. After the incubation, 1 ml of di-nitro salicylic acid (DNS) color reagent was incorporated and kept in boiling water bath precisely for 5 min. Then, the temperature of this mixture was decreased to room temperature by cooling it on ice and added another 6 ml of deionized water. α-Amylase activity was determined by measuring the absorbance of the mixture at 540 nm (Table 1).
Spectrophotometric DPPH inhibition assay
DPPH radical scavenging activity of isolated Compounds 1, 2 and 3
IC50 ± SD (μM)
Compound 1 (7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-chromen-4-one)
21.5*** ± 0.39
Compound 2 ((S)-2-(3,4-dihydroxyphenyl)-7,8-dihydroxychroman-4-one)
31.8** ± 0.22
Compound 3 (2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one)
29.26** ± 0.63
17.3 ± 1.10
Molecular docking analysis
Mode of inhibition of Compounds 1, 2 and 3 on the α-glucosidase enzyme was further assessed by molecular docking analysis.
Preparation of protein structure
The 3D coordinates of crystal structure of B. cereus oligo- 1,6—glucosidase (PDB ID: 1UOK) was downloaded from the RCSB protein data bank (http://www.rcsb.org/pdb) set up at Brookhaven National Laboratory in 1971. It is a worldwide repository of information about the 3D structures of large biological molecules, including proteins and nucleic acids. Water molecules were removed from the protein 1UOK before the instigation of molecular docking. The protein structure was corrected by the utilization of alternate conformations and valence monitor options as some crystallographic disorders as well as some unfilled valance atoms were present in the protein file. The resultant protein file was subjected to energy minimization by applying Chemistry at HARvard Macromolecular Mechanics (CHARMm) force fields. CHARm is a program which provides a large suite of computational tools that encompass numerous conformational and path sampling methods, free energy estimates, molecular minimization, dynamics, and analysis techniques, and model-building capabilities (http://www.charmm.org/). After the energy minimization the protein file was subjected to define and edit binding site option available on tools panel to explore the plausible binding site within the protein (1UOK). Five binding sites were explored with different fitting points. The binding site (Site 1) consist of maximum fitting point (Fitting points = 275) was selected.
Preparation of ligand
The structures of compounds 1, 2 and 3 (4′, 7-Dihydroxy-3′-methoxyflavone, 3′, 4′, 7, 8-tetrahydroxyflavanone and Luteolin) was drawn using ChemBioDraw software. ChemBioDraw™ is a software from PerkinElmer for development of chemical structures of bioactive compounds. The prepared ligand was then subjected to add the hydrogen bonds and the energy has been minimized using CHARm force field. The ADMET properties of all the three isolated compounds which satisfy the Lipinski properties were measured primarily for the toxicity parameters using TOPKAT. Lipinski rule of five is a rule to evaluate drug likeness to determine if a chemical compound has a certain pharmacological or biological activity to make it an orally active drug in humans .
To find out the accurate binding model for the active site of α-glucosidase enzyme, molecular docking analysis was performed using ligand fit of GLIDE software from Schrodinger (http://www.schrodinger.com/). Molecular docking analysis was performed using crystal structure of oligo-1, 6-glucosidase (dextrin 6-alpha-glucanohydrolase, EC 220.127.116.11) from Bacillus cereus and crystal of pig pancreatic alpha-amylase. The structure of α-glucosidase (PDB: 1UOK) and crystal structure of α-amylase (PDB: 1PPI) were obtained from Protein Data Bank (http://www.rcsb.org). The mechanism of ligand position is based on the fitting points. Fitting points are incorporated into the hydrogen bonding groups on the ligand and the proteins. The ligand fit module  from GLIDE software was utilized to execute the molecular docking analysis, based on shape-based searching and Monte Carlo methods. At the time of docking, variable trials Monte Carlo conformation was applied where the number of steps depends on the number of rotatable bonds present in the compounds/ligands. By default the torsion number is 2, the maximum minimizations steps is 300 and maximum successive failure is 110. During the docking process the top ten conformations were engendered for each of the compound after the minimization of the energy. Each of the saved conformation was evaluated and ranked by using the scoring functions including LigScore1, LigScore2, PLP1, PLP2, Jain, PMF and Dock Score. All the compounds/ligands which forms good hydrophobic and hydrogen bond interactions with Phe163, Asp199, Val200, Phe203, Met228, Glu255, Pro257, Phe281, Asp285, Asp329 and Arg415.
Results and discussion
Among all of the plant constituents, flavonoids are the most scrutinized group for their effect on the health concerns. A recent study supports the efficacy of flavonoids in the treatment of diabetes mellitus by influencing the β-cell mass and function as well as insulin signaling . Several researches suggested having beneficial and shielding effect against cancer  stress, hypertension and heart disorders [30, 31].
The flavonoids are low molecular weight bioactive phenols actively participate in the cell wall synthesis [32–35]. Flavonoids were revealed to regulate insulin secretion, insulin signaling, carbohydrate digestion and glucose uptake in insulin-sensitive tissues through various intracellular signaling pathways . One recent study has assessed the relationship between the flavonoids and the risk of diabetes. This study confirms that the men and women received the flavonoids were at lower risk of diabetes .
Intestinal α-glucosidases (maltase, isomaltase and sucrase) are membrane bound enzymes integrated in the epithelium of the small intestine and are implicated for the final step of carbohydrate hydrolysis to produce absorbable monosaccharide. Starch is the major dietary carbohydrate source of glucose and diabetic complications depends upon the rate and extent of digestion of glucose from starch by the pancreatic α-amylase and intestinal α-glucosidase . Disaccharides and oligosaccharides are broken down by the pancreatic α-amylase before the intestinal α-glucosidase enzyme catalyzes the breakdown of disaccharides into glucose which is then later absorbed into the systemic circulation. Inhibition of these enzymes would slow down the breakdown of starch into the simpler saccharides in the gastrointestinal tract, thus reducing the postprandial hyperglycemia [39, 40]. α-Glucosidase inhibitors were also reveled to possess property to prevent dysfunction of β-cell insulin secretion in diabetic patients [41, 42].
In the present research exertion α-glucosidase inhibitory activity was determined against the enzyme obtained from yeast (S. cerevisiae). α-amylase was procured from bacteria (B. subtilis). Acarbose (10 mg/ml) was used as standard. The results clearly suggest that flavonoids obtained from Albizzia Lebbeck Benth. bark i.e. compounds 1–3 inhibited the α-glucosidase and α-amylase to a significant extent (Table 1).
Docking results based on the LigScore1, LigScore2, PLP1, PLP2, Jain, PMF and Dock Score of the compounds 1, 2 and 3 into the α-glucosidase enzyme (PDB: 1UOK)
Internal energy (kcal/mol)
4′,7-Dihydroxy-3′-methoxyflavone (Compound 1)
3′,4′,7,8-tetrahydroxyflavanone (Compound 2)
Luteolin (Compound 3)
Docking results based on the LigScore1, LigScore2, PLP1, PLP2, Jain, PMF and Dock Score of the Compounds 1, 2 and 3 into the α-amylase enzyme (PDB: 1PPI)
Internal energy (kcal/mol)
4′,7-Dihydroxy-3′-methoxyflavone (Compound 1)
As concluding remarks, the isolated flavonoids from Albizzia Lebbeck Benth. bark showed a high potential as inhibitors of α-glucosidase, α-amylase and DPPH. In-vitro evaluation of these compounds clearly depicts the inhibition of both the enzymes responsible for high blood glucose level as well as the inhibition of formation of ROS (Reactive Oxygen Species) accountable for the development of type-II diabetes. Inhibition of these enzymes was further supported by the molecular docking analysis. Thus 7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-chromen-4-one, (S)-2-(3,4-dihydroxyphenyl)-7,8 dihydroxychroman-4-one) and (2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one) showed to the potential to decrease the fasting and postprandial glucose levels in type-II diabetes patients.
Our invitro experimentation and molecular docking studies results demonstrated that isolated flavonoids from Albizzia Lebbeck Benth. bark significantly inhibits the α-glucosidase, α-amylase and DPPH enzymes. Therefore, the present study suggests a basis for the possible use of Albizzia Lebbeck Benth. bark as functional food. Consequently, in-vivo antidiabetic research exertion of isolated flavonoids is underway in our laboratory to explore the other plausible mechanism of action to restrain the hyperglycemia and hyperlipidemia in the STZ (streptozotocin) induced diabetic rats.
Authors wish to thanks Prof. Dr. Mohammad Ali for helping in structural elucidation of the compounds and to Sam Higginbottom Institute of Agriculture, Technology & Sciences for providing essential infrastructural facilities.
- Astrup A: Healthy lifestyles in Europe: prevention of obesity and type II diabetes by diet and physical activity. Public Health Nutr. 2001, 4: 499-515.View ArticlePubMedGoogle Scholar
- Bazzano L, Serdula MLS: Prevention of type 2 diabetes by diet and lifestyle modification. J Am Coll Nutr. 2005, 24: 310-319. 10.1080/07315724.2005.10719479.View ArticlePubMedGoogle Scholar
- Ahmed D, Sharma M, Mukerjee A, Ramteke PW, Kumar V: Improved glycemic control, pancreas protective and hepatoprotective effect by traditional poly-herbal formulation “Qurs Tabasheer” in streptozotocin induced diabetic rats. BMC Complement Altern Med. 2013, 13: 10-10.1186/1472-6882-13-10.View ArticlePubMedPubMed CentralGoogle Scholar
- Boden G, Shulman G: Free fatty acids in obesity and type 2 diabetes: defining their role in the development of insulin resistance and beta-cell dysfunction. Eur J Clin Invest. 2002, 32: 14-23. 10.1046/j.1365-2362.32.s3.3.x.View ArticlePubMedGoogle Scholar
- Kumar V, Ahmed D, Gupta PS, Anwar F, Mujeeb M: Anti-diabetic, anti-oxidant and antihyperlipidemic activities of Melastoma malabathricum Linn. leaves in streptozotocin induced diabetic rats. BMC Complement Altern Med. 2013, 13: 222-10.1186/1472-6882-13-222.View ArticlePubMedPubMed CentralGoogle Scholar
- McGarry JD: Banting lecture 2001: dysregulation of fatty acid metabolism in the etiology of type 2 diabetes. Diabetes. 2002, 51: 7-18. 10.2337/diabetes.51.1.7.View ArticlePubMedGoogle Scholar
- Ferrannini E, Gastaldelli A, Miyazaki Y, Matsuda M, Mari A, DeFronzo R: Beta-cell function in subjects spanning the range from normal glucose tolerance to overt diabetes: a new analysis. J Clin Endocrinol Metab. 2005, 90: 493-500. 10.1210/jc.2004-1133.View ArticlePubMedGoogle Scholar
- Whiting DR, Guariguata L, Weil C, Shaw J: IDF Diabetes Atlas: Global estimates of the prevalence of diabetes for 2011 and 2030. Diabetes Res Clin Pract. 2011, 94: 311-321. 10.1016/j.diabres.2011.10.029.View ArticlePubMedGoogle Scholar
- Anjana RM, Pradeepa R, Deepa M, Datta M, Sudha V, Unnikrishnan R, Bhansali A, Joshi SR, Joshi PP, Yajnik CS, Dhandhania VK, Nath LM, Das AK, Rao PV, Madhu SV, Shukla DK, Kaur T, Priya M, Nirmal E, Parvathi SJ, Subhashini S, Subashini R, Ali MK, Mohan V: On behalf of the ICMR–INDIAB Collaborative Study Group. Prevalence of diabetes and prediabetes (impaired fasting glucose and/or impaired glucose tolerance) in urban and rural India: Phase I results of the Indian Council of Medical Research-India DIABetes (ICMR-INDIAB) study. Diabetologia. 2011, 54: 3022-3027. 10.1007/s00125-011-2291-5.View ArticlePubMedGoogle Scholar
- Nelson ME, Rejeski WJ, Blair SN, Duncan PW, Judge JO, King AC, Macera CA, Castaneda-Sceppa C: Physical activity and public health in older adults: recommendation from the American College of Sports Medicine and the American Heart Association. Circulation. 2007, 116 (9): 1094-View ArticlePubMedGoogle Scholar
- Bailey C, Day C: Metformin: its botanical background. Pract Diab Int. 2004, 21: 115-117. 10.1002/pdi.606.View ArticleGoogle Scholar
- Krishnaiah D, Sarbatly R, Nithyanandam R: A review of the antioxidant potential of medicinal plant species. Food Bioprod Process. 2010, 89: 217-233.View ArticleGoogle Scholar
- Mudaliar KSM: Siddha Materia Medica. 1936, Chennai: Department of Indian Medicine and Homeopathy, 799-800.Google Scholar
- Nadkarni AK: Dr. K.M. Nadkarni’s Indian Materia Medica. 1954, Bombay, India: Popular Book DepotGoogle Scholar
- Gupta RS, Chaudhary R, Yadav RK, Verma SK, Dhobal MP: Effect of Saponins of Albizia lebbeck Benth. Bark on the reproductive system of male albino rats. J Ethnopharmacol. 2005, 96: 31-36. 10.1016/j.jep.2004.07.025.View ArticlePubMedGoogle Scholar
- Mohammad F, Singh PP, Irchhaiya R: Review On Albizia Lebbeck A Potent Herbal Drug. Int Res J Pharm. 2012, 3: 5-Google Scholar
- Jung MJ, Kang SS, Jung HA, Kim GJ, Choi JS: Isolation of flavonoids and a cerebroside from the stem bark of Albizzia julibrissin. Arch Pharm Res. 2004, 27: 593-599. 10.1007/BF02980155.View ArticlePubMedGoogle Scholar
- Akgul E, Ilham N, Halifeoglu IL: Plasma lipid peroxide levels and antioxidant enzyme activities in type II diabetics: relationship with diabetic microagiopatic complications. Atherosclerosis. 1997, 130 (suppl 1): 9-View ArticleGoogle Scholar
- Karumi Y, Onyeyili PA, Ogugbuaja VO: Identification of active Principles of M. balsamina (Balsam Apple) Leaf Extract. Int J Med Sci. 2004, 4: 179-182.Google Scholar
- Soro TY, Traore F, Datte JY, Nene-Bi AS: Activité antipyrétique de l’extrait aqueux de Ximenia americana. Phytother. 2009, 7: 297-303. 10.1007/s10298-009-0507-3.View ArticleGoogle Scholar
- Naima S, Khan MR, Maria S: Antioxidant activity, total phenolic and total flavonoid contents of whole plant extracts Torilis leptophylla L. BMC Complement Altern Med. 2012, 12: 221-10.1186/1472-6882-12-221.View ArticleGoogle Scholar
- Park Y-S, Jung S-T, Kang S-G, Heo BK, Arancibia-Avila P, Toledo F, Drzewiecki J, Namiesnik J, Gorinstein S: Antioxidants and proteins in ethylene-treated kiwifruits. Food Chem. 2008, 107: 640-648. 10.1016/j.foodchem.2007.08.070.View ArticleGoogle Scholar
- Feng J, Yang XW, Wang RF: Bio-assay guided isolation and identification of α-glucosidase inhibitors from the leaves of Aquilaria sinensis. Phytochemistry. 2011, 72: 242-247. 10.1016/j.phytochem.2010.11.025.View ArticlePubMedGoogle Scholar
- Wan L-s, Chen C-p, Xiao Z-q, Wang Y-l, Min Q-x, Yue Y, Chen J: In vitro and in vivo anti-diabetic activity of Swertia kouitchensis extract. J Ethnopharmacol. 2013, 147: 622-630. 10.1016/j.jep.2013.03.052.View ArticlePubMedGoogle Scholar
- Zhang Y, Li Q, Xing H, Xuefeng L, Zhao L, Kankan Q, Bi K: Evaluation of antioxidant activity of ten compounds in different tea samples by means of an on-line HPLC–DPPH assay. Food Res Int. 2013, 53: 847-856. 10.1016/j.foodres.2013.03.026.View ArticleGoogle Scholar
- Lipinski CA, Lombardo F, Dominy BW, Feeney PJ: Drug-like properties and the causes of poor solubility and poor permeability. J Pharmacol Toxicol Methods. 1997, 44: 235-249.View ArticleGoogle Scholar
- Venkatachalam CM, Jiang X, Oldfield T, Waldman M: LigandFit: a novel method for the shape-directed rapid docking of ligands to protein active sites. J Mol Graph Model. 2003, 21: 289-307. 10.1016/S1093-3263(02)00164-X.View ArticlePubMedGoogle Scholar
- Lee SJ, Kim HE, Choi SE, Shin HC, Kwag WJ, Lee BK, Cho KW, Kang Y: Involvement of Ca2 +/calmodulin kinase II (CaMK II) in genistein-induced potentiation of leucine/glutamine-stimulated insulin secretion. Mol Cells. 2009, 28: 167-174. 10.1007/s10059-009-0119-7.View ArticlePubMedGoogle Scholar
- Cantero G, Campanella C, Mateos S, Cortés F: Topoisomerase II inhibition and high yield of end reduplication induced by the flavonoids luteolin and quercetin. Mutagenesis. 2006, 5: 321-325.View ArticleGoogle Scholar
- Ross JA, Kasum CM: Dietary flavonoids: Bioavailability, metabolic effects, and safety. Annu Rev Nutr. 2002, 22: 19-34. 10.1146/annurev.nutr.22.111401.144957.View ArticlePubMedGoogle Scholar
- Gui-Yuan L, Yan-Ping Z, Jian-Li G, Jing-Jing Y, Jing L, Zhi-Ru Z, Bo L, Ruan-Juan Z, Su-Hong C: Combined antihypertensive effect of luteolin and buddleoside enriched extracts in spontaneously hypertensive rats. J Ethnopharmacol. in pressGoogle Scholar
- Fernandez SP, Wasowski C, Loscalzo LM, Granger RE, Johnston GA, Paladini AC, Marder M: Central nervous system depressant action of flavonoid glycosides. Eur J Pharmacol. 2006, 539: 168-176. 10.1016/j.ejphar.2006.04.004.View ArticlePubMedGoogle Scholar
- Heim KE, Tagliaferro AR, Bobliya DJ: Flavonoids antioxidants: chemistry, metabolism and structure–activity relationship. J Nutr Biochem. 2002, 13: 572-584. 10.1016/S0955-2863(02)00208-5.View ArticlePubMedGoogle Scholar
- Hollman PC, Katan MB: Dietary flavonoids: intake, health effects and bioavailability. Food Chem Toxicol. 1999, 37: 937-942. 10.1016/S0278-6915(99)00079-4.View ArticlePubMedGoogle Scholar
- Cushnie TP, Lamb AJ: Antimicrobial activity of flavonoids. Int J Antimicrob Agents. 2005, 26: 343-356. 10.1016/j.ijantimicag.2005.09.002.View ArticlePubMedGoogle Scholar
- Hanhineva K, Torronen R, Bondia-Pons I, Pekkinen J, Kolehmainen M, Mykkanen H, Poutanen K: Impact of dietary polyphenols on carbohydrate metabolism. Int J Mol Sci. 2010, 11: 1365-1402. 10.3390/ijms11041365.View ArticlePubMedPubMed CentralGoogle Scholar
- Wedick NM, Pan A, Cassidy A, Rimm EB, Sampson L, Rosner B, Willet W, Hu FB, Sun Q, Dam RMV: Dietary flavonoid intakes and risk of type 2 diabetes in US men and women. Am J Clin Nutr. 2012, 95: 925-933. 10.3945/ajcn.111.028894.View ArticlePubMedPubMed CentralGoogle Scholar
- Dhital S, Lin AH-M, Hamaker BR, Gidley MJ, Muniandy A: Mammalian mucosal α-glucosidases coordinate with α-amylase in the initial starch hydrolysis stage to have a role in starch digestion beyond glucogenesis. PLoS One. 2013, 8 (4): e62546-10.1371/journal.pone.0062546.View ArticlePubMedPubMed CentralGoogle Scholar
- Kwon YI, Apostolidis E, Kim YC, Shetty K: Health benefits of traditional corn, beans and pumpkin: In vitro studies for hyperglycemia and hypertension management. J Med Food. 2007, 10: 266-275. 10.1089/jmf.2006.234.View ArticlePubMedGoogle Scholar
- Kim JS, Kwon CS, Son KH: Inhibition of alpha glucosidase and amylase by luteolin, a flavonoid. Biosci Biotechnol Biochem. 2000, 64: 2458-2461. 10.1271/bbb.64.2458.View ArticlePubMedGoogle Scholar
- Baron AD: Postprandial hyperglycaemia and a-glucosidase inhibitors. Diabetes Res Clin Pract. 1998, 40: 51-55.View ArticleGoogle Scholar
- Casirola DM, Ferraris RP: a-Glucosidase inhibitors prevent diet induced increases in intestinal sugar transport in diabetic mice. Metabolism. 2006, 55: 832-841. 10.1016/j.metabol.2006.02.011.View ArticlePubMedGoogle Scholar
- Liu RH, Adom KK: Antioxidant activity of grains. J Agric Food Chem. 2002, 50: 6182-6187. 10.1021/jf0205099.View ArticlePubMedGoogle Scholar
- Maria SMR, Fabiano ANF, Ricardo EA, de Brito ES: Free radical scavenging behavior of some north-east Brazilian fruits in a DPPH system. Food Chem. 2009, 114: 693-695. 10.1016/j.foodchem.2008.09.098.View ArticleGoogle Scholar
- Anderson RA, Evans ML, Ellis GR, Graham J, Morris K, Jackson SK, Lewis MJ, Rees A, Frenneaux MP: The relationship between post-prandial lipaemia, endothelial function and oxidative stress in healthy individuals and patients with type 2 diabetes. Atherosclerosis. 2001, 154: 475-483. 10.1016/S0021-9150(00)00499-8.View ArticlePubMedGoogle Scholar
- Devasagayam TPA, Tilak JC, Boloor KK, Sane KS, Ghaskadbi SS, Lele RD: Free radicals and antioxidants in human health: current status and future prospects. J Assoc Physicians India. 2004, 52: 794-804.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6882/14/155/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.