- Research article
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In vitro evaluation of the α-glucosidase inhibitory potential of methanolic extracts of traditionally used antidiabetic plants
BMC Complementary and Alternative Medicine volume 19, Article number: 74 (2019)
Different plant parts of Roylea cinerea (D. Don) Baill. (Lamiaceae), Clematis grata Wall. (Ranunculaceae), Cornus capitata Wall. (Cornaceae) are traditionally used in the management of diabetes and various other diseases.
The air-dried plant parts from different plants were coarsely powdered and macerated in methanol to obtain their crude extracts. The crude extracts were evaluated for their α-glucosidase inhibitory activity. On the basis of results obtained, the methanolic crude extract of Cornus capitata Wall. was further sequentially fractionated in hexane, diethyl ether, ethyl acetate, n-butanol. Fractions obtained were also evaluated for their α-glucosidase inhibitory potential. The kinetic study was performed using Lineweaver Burk plot to evaluate the type of inhibition. Furthermore, in silico analysis was also carried with active sites of the enzyme (PDB ID: 3WY1) using Autodock4.
Among all the plant extracts, Cornus capitata extract showed maximum inhibitory activity. Therefore its methanolic extract was further fractionated with the help of different solvents and the maximum activity was shown by the ethyl acetate fraction (IC50 50 μg/mL). Kinetic analysis indicated that Vmax and Km were increased indicating a competitive type of inhibition. In docking studies, among different constituents known in this plant, betulinic acid showed minimum binding energy (− 10.21 kcal/mol). The kinetic and docking studies have strengthened the observation made in the present study regarding the α-glucosidase inhibitory activity of Cornus capitata.
The study provided partial evidence for pharmacological basis regarding clinical applications of Cornus capitata in the treatment of diabetes suggesting it to be a suitable candidate for the treatment of postprandial hyperglycemia.
Diabetes is the world’s fastest-growing metabolic endocrine disorder with compromised carbohydrate and lipid metabolism. The defected metabolism can be attributed to the impaired insulin secretion, insulin action or both. Alpha-glucosidase inhibitors are one of the effective class of antidiabetic therapeutics capable of ameliorating hyper-glycemia especially postprandial hyperglycemia over alpha-amylase inhibitors . Postprandial hyperglycemia is a sudden elevation in glucose levels in the blood after a meal. Major constituents of the human diet are comprised of carbohydrates such as starch and sucrose. The membrane-bound α-glucosidase enzyme, localized in the epithelium of small intestine hastens the digestion of oligosaccharides and disaccharides into simple glucose, after which it gets absorbed and enter into the bloodstream . Inhibition of α-glucosidase enzyme can help in delaying digestion of carbohydrates, thereby reducing the levels of glucose in blood . Several drugs are available as α-glucosidase inhibitors such as acarbose and miglitol that inhibit the absorption of carbohydrates from the gut. These inhibitors can prevent or mask the manifestation of the disease. There are several studies reported for such inhibitors being beneficial to prevent or delay impaired glucose tolerances in diabetes. Though being effective, these drugs have been reported to cause severe side effects such as gastrointestinal discomforts including diarrhea and flatulence .
Natural products of plant origin are known for their dual role both as preventive and therapeutic agents, combined with their less toxicity and side effects. Traditionally different plants are used throughout the world by the local population for the treatment of various ailments . Cornus capitata Wall. (Cornaceae) is widely available in different regions of the world such as China and India. Studies have shown that it has several constituents present in its aerial parts such as cornin and phlorin from leaves, others include n-hentriacontane, 7-hydrocadeline, triacontanol, stigmastranone, lupeol, triacontanoic acid, betulin, epibetulin, betulinic acid, epibetulinic acid, tetracosanoic acid, maslinic acid, arjunolic acid, sitosterol-β-D-glucoside, gallic acid isolated from stem [6, 7]. It is used as fuel, for animal bedding and its fruits are edible . It has been reported for its traditional use in the management of diabetes in Mandi district of Himachal Pradesh . Clematis grata Wall. (Ranunculaceae), is used by indigenous people of Bana valley (Jammu and Kashmir) for its antioxidant, antimicrobial, and antidiabetic activities . Its crushed leaves are used as a paste for the treatment of skin diseases such as eczema, warts, carbuncles  and boils . Two important constituent viz., clematoside-S and triterpenoids saponins have been reported from the roots of Clematis grata Wall. . Roylea cinerea (D. Don) Baill. (Lamiaceae) found in Western Himalayas had been used by the local population in the management of various diseases including diabetes, fever, skin diseases [9, 13]. Rutin, isoquercetin, nicotiflorin and martynoside are some constituents reported from its aerial parts . Thus, the present study was conducted with an objective to unravel the α-glucosidase inhibitory effect of Cornus capitata Wall. (leaves), Clematis grata Wall. (whole plant), Roylea cinerea (D. Don) Baill.(leaves and stem) based on their traditional use for the management of diabetes [9, 10]. Kinetic study and in silico analysis was also carried out to further investigate the mechanism of inhibition.
The entire plant or its different parts can be used in the form of a whole plant, crude extract, and aqueous decoctions. In the present study, the whole plant was selected in case of herbs, leaves and stem in case of shrubs and leaves in case of trees on the basis of availability of phytoconstituents . Plant materials viz., (Cornus capitata Wall. (leaves), Clematis grata Wall. (Whole plant), Roylea cinerea (D. Don) Baill. (Leaves and stem) were collected, identified and submitted as a voucher specimen (Accession no. 7373, 7374 and 7376 respectively) for authenticity in Herbarium, Department of Botanical and Environmental Sciences, Guru Nanak Dev University, Amritsar, Punjab (Additional file 1: Table S1). The identification was done by taxonomist Dr. Amarjit Singh Soodan and Mr. Ram Prasad (Senior lab technician), of Department of Botanical and Environmental Sciences, Guru Nanak Dev University, Amritsar, Punjab. Each plant material was air dried, coarsely powdered and subjected to maceration for 48 h in methanol. The methanolic extracts were further concentrated with a rotary evaporator (IKA® RV 10). The extracts were stored at − 20 °C until use. Crude methanolic extract was dissolved in distilled water. Further, an equal volume of Hexane was added and the mixture was shaken vigorously. The mixture was allowed to separate into layers. The upper layer (Hexane) was collected and concentrated on rotary evaporator to obtain Hexane fraction. Similarly, the aqueous layer was further subjected to fractionation via series of solvents on the basis of polarity viz., Diethyl-ether<Ethyl acetate<n-butanol. Polar solvents help in the extraction of hydrophilic compounds and non-polar solvents aids in the extraction of lipophilic compounds [15, 16].
α-Glucosidase inhibitory assay
Plant extracts were evaluated for α-glucosidase inhibitory activity according to the method given by Pistia Brueggeman and Hollingsworth, 2001  with slight modifications. Plant extracts (50 μL) at varying concentrations (12.5 to 400 μg/mL) was incubated with 10 μL of the α-glucosidase (maltase) ex. Yeast (Sisco Research Laboratories Pvt. Ltd.) enzyme solution (1 U/mL) for 20 min at 37 °C with an additional 125 μL of 0.1 M phosphate buffer (pH 6.8). After 20 min, the reaction was started with the addition of 20 μL of 1 M pNPG (substrate) and the mixture was incubated for 30 min. The reaction was terminated with the addition of 0.1 N of Na2CO3 (50 μL) and final absorbance was measured at 405 nm using Biotek multi-well plate reader. Acarbose was used as a positive control at varying concentrations (12.5 to 400 μg/mL). Enzyme activity was calculated as:
(ODBLANK-ODSAMPLE)/ODBLANK x 100
One unit of the enzyme can be defined as the amount of enzyme (α-glucosidase) required for the formation of one μmol of product (p-Nitrophenol) from the substrate (p-nitrophenyl-α-D-glucopyranoside) per minute. IC50 (concentration required to inhibit 50% of the enzyme activity) was calculated using regression equation obtained through plotting concentration in the range 12.5–400 μg/mL (x-axis) and %inhibition (y-axis) for different extracts and fractions.
Lineweaver-Burk plot was plotted for methanolic extract of Cornus capitata Wall. with IC50 of 12.45 μg/mL. The substrate p-nitrophenyl-α-D-glucoside was used in varying concentrations (2 mM, 1 mM, 0.5 mM, 0.25 mM and 0.125 mM). Enzyme concentration was kept constant (1 U/mL) and molar extinction coefficient for calculating enzyme activity was 17.4 mM− 1 . Inhibition type was determined with Lineweaver-Burk plots and calculated using the Michaelis Menten equation.
Rearranging the equation for Line-weaver Burk plot (linear, y = ax+b).
Where V0 is the initial rate of reaction, Km is the Michaelis Menten constant, Km/Vmax is the slope, and the y-intercept (1/Vmax) was calculated using Eq. 2.
The methanolic extract of Cornus capitata Wall. exhibited maximum α-glucosidase inhibitory activity, therefore the docking studies were carried out for the chemical constituents already reported in this plant. The chemical structure and molecules for which docking was carried out are mentioned in Additional file 1: Table S2. In this study, the protein structure of the target enzyme α-glucosidase (3WY1) and a binding pocket for polyacrylic acid was obtained from the protein data bank (www.rcsb.org) (Fig. 1). The 3WY1 protein consists of 3 ligands namely polyacrylic acid (ID: PRU), glycerol (ID: GOL) and magnesium ion (ID: MG). The preparation of the target enzyme with the AutoDock4 involved the addition of hydrogen atoms to the target enzyme, which is a necessary step for the computation of partial atomic charge. Hetero-atoms present in the protein structure 3WY1 were removed prior to autodock analysis. Gasteiger charges were considered for each atom present in the target. It executes automated docking of user-specified ligands into protein binding pocket. Three-dimensional affinity grid size − 10.620, − 15.320, 17.310 (x, y, and z) on the geometric center of the target protein was used. Docking algorithm was run using Cygwin software, to obtain the binding energy data. Visualization and analysis of the results were done using UCSF chimera 1.11rc. Ligand structures were obtained from PubChem (https://pubchem.ncbi.nlm.nih.gov/search/search.cgi) and prepared using chemsketch tool.
The data for inhibitory activity of plant extracts and their formulations for α-glucosidase enzyme are presented as mean ± standard error. The data was further analyzed using one-way analysis of variances (ANOVA) and Tukey’s test for multiple comparison tests assuming variances are equal using IBM SPSS version 16.0 software.
In vitro α-glucosidase inhibitory activity
Crude methanolic extracts of (Cornus capitata Wall. (leaves), Clematis grata Wall. (Whole plant) and Roylea cinerea (D. Don) Baill. (leaves and stem) were evaluated for their α-glucosidase inhibitory activity. The methanolic extract of Cornus capitata Wall. was sequentially extracted with different solvents to obtain fractions. It was observed that Cornus capitata Wall. (leaves), Clematis grata Wall. (Whole plant), Roylea cinerea (D. Don) Baill. (leaves and stem) extracts exhibited 98.37, 5.05, 10.50 and 7.01% inhibitory activity at 50 μg/mL respectively (Table 1 and Fig. 2). Among the different plants, Cornus capitata Wall. extract exhibited maximum inhibitory activity with 98.37% inhibition (IC50 12.5 μg/mL) better than the activity shown by positive control (acarbose) with 42.43% inhibition (IC50 66.07 μg/mL) at 50 μg/mL concentration. The fractions viz., hexane, diethyl ether, ethyl acetate and n-butanol obtained from an extract of Cornus capitata Wall. exhibited 98.98, 96.54, 98.55, 98.35% inhibitory activity at 200 μg/ml respectively (Table 2). It was observed that the inhibitory activity for α-glucosidase enzyme was maximum by ethyl acetate (IC50 50 μg/ml) followed by n-butanol (IC50 61.175 μg/mL), hexane (IC50 65.12 μg/mL) and diethyl ether fractions (IC50 71.85 μg/mL).
Enzyme kinetic study was carried out for the investigation of the type of inhibition by the crude methanolic extract of Cornus capitata Wall. The Lineweaver-Burk plot (Fig. 3) revealed that the extract showed a competitive type of inhibition. The y-intercept (1/Vmax) remains unaffected and slope (Km/Vmax) increased with the concentration of the inhibitor. The value of α, the degree of inhibition (constant for the degree of inhibition affecting the affinity of the enzyme to the substrate) was greater than 1. This confirms that the inhibitor preferentially binds to the free enzyme inhibiting the formation of the enzyme-substrate complex.
As the methanolic extract of Cornus capitata Wall. showed maximum inhibition potential against α-glucosidase enzyme, docking studies were performed to investigate the activity of some of its already reported chemical constituents (betulinic acid, epibetulin, arjunolic acid, lupeol, maslinic acid, and betulin) [6, 7]. Ligands were prepared using Chemsketch software, docked into the binding site of the 3WY1 protein (α-glucosidase enzyme) and found to fit well in the binding cavity of 3WY1 protein. Autodock 4 software was used to dock the ligands into the binding pocket. Docking conformations were visualized and analyzed for the number of H-bonds formed using Chimera software (Fig. 4). It revealed that the betulinic acid, epibetulin, arjunolic acid, betulin, lupeol, and maslinic acid possess good binding potential toward α-glucosidase enzyme (Table 3). Docking conformations analyzed for each ligand explicated the interactions through the formation of H-bonds with different amino acids residues of the protein 3WY1. Betulinic acid showed no H-bonds with amino acid residues but fits well in the binding cavity with the minimum free energy of binding as − 10.21 Kcal/mol and inhibition constant of 33.04 nM. Epibetulin showed two H-bonds with amino acid residues ARG 200 and HIS 332 with bond length 2.446 Å and 2.516 Å. Arjunolic acid showed the presence of two H-bonds with amino acid residues ASP 202 and ARG 200 with a bond length of 2.287 Å and 2.726 Å, respectively. Maslinic acid showing three H-bonds with amino acid residues ASP 202, ARG 200 and GLU 271 with bond length 2.296 Å, 2.731 Å, and 3.160 Å. Lupeol showed two H-bonds with amino acid residue ASP 62 with bond length 3.101 Å and 2.472 Å.
In the present study, solvent selection for extraction purpose was done on the basis of already available literature . Previous studies suggest that methanol and hot water are the ideal solvents for extraction of antioxidants and other endogenous compounds present in a plant . Thus, the extraction of plant material was done by a maceration process in absolute methanol to obtain the maximum content of chemical constituents. Various studies have suggested the role of plant extracts as α-glucosidase inhibitors clearly indicating the potential of these extracts to manage hyperglycemia . The activity of these plant extracts can be attributed to phytoconstituents present in them, such as flavonoids, alkaloids, terpenoids, anthocyanins, glycosides, phenolic compounds. In the present study, among all the methanolic plant extracts, Cornus capitata Wall. extract explicated a remarkable inhibition potential (98.37% at 50 μg/mL) against the α-glucosidase enzyme. The other methanolic extracts were found to be less effective against the α-glucosidase enzyme. On the basis of activity shown by the crude methanolic extract of Cornus capitata Wall., it was further fractionated successively in different polar and non-polar solvents . Among its fractions, ethyl acetate fraction showed the maximum inhibitory activity. Extraction of a type of compound depends upon the selection of the solvent. Ethyl acetate fraction is known to be rich in flavonoids [17, 21]. Thus, enzyme inhibitory activity shown by ethyl acetate fraction can be attributed to its rich flavonoid contents. Critical analysis of the results obtained suggested that the methanolic crude extract of leaves of Cornus capitata Wall. showed better activity than its all fractionates. The decrease in the enzyme inhibitory activity shown by different fractions may be due to the synergistic effect of the chemical constituents present in the crude methanolic extract. This suggests that the activity of crude methanolic extract of Cornus capitata Wall. was due to the synergistic potential of chemical constituents present in it. Due to limited literature regarding the evaluation of antidiabetic activity of Cornus capitata Wall., the information was gathered about other species of Cornus. Various species of Cornus have been reported in the literature for showing remarkable antidiabetic activity. Cornus officinalis has been categorized as an important plant by the ministry of health of the People’s Republic of China and also declared as a valuable food supplement for the management of diabetes . Nearly 90% of the ancient Chinese herbal medicines contain Cornus officinalis as an ingredient . It has been reported to contain iridoid glycoside and several other constituents in its crude extract responsible for showing remarkable α-glucosidase inhibitory effects in vitro and in vivo models . Similarly, Cornus mas (L.) also known as Cornelian cherry, is used in the preparation of beverages in European regions and used as an effective medicine for the treatment of Diabetes in Asia . Thus, Cornus capitata leaves can also provide a possible medication for the better management of diabetes which has not been investigated yet.
To obtain further information regarding the type of inhibition, kinetic studies were carried out using a crude methanolic extract of Cornus capitata Wall. It was observed that the slope and Km increased with the increasing concentration of the extract (inhibitor) but Vmax remained unaffected which indicated that Cornus capitata Wall. methanolic extract inhibited the reaction to proceed through competitive interaction with the substrate. The mechanism involved in this type of inhibition includes either strong affinity or structural similarity to the substrate [25, 26]. It can facilitate its binding with the active site of the enzyme, thus inhibiting the reaction to proceed forward. Therefore, to obtain useful information about the α-glucosidase enzyme inhibitory activity by methanolic extract of Cornus capitata Wall., the lead regarding the chemical constituents present in it was taken from available literature [6, 7]. However, very little attention has been paid to this plant. The literature was further explored to find the evidence supporting the antidiabetic activities of the constituents present in the crude methanolic extract of Cornus capitata Wall. It was found that the pentacyclic triterpenoids such as arjunolic acid, betulinic acid, betulin, epibetulin, maslinic acid, and lupeol may be responsible for its antidiabetic activity [27, 28]. Consequently, in order to understand the interactions between the protein 3WY1 (α-glucosidase enzyme homolog) and the constituents present in Cornus capitata Wall. methanolic extract, docking studies were carried out. It revealed the significant binding efficiencies of the chemical constituents present in Cornus capitata Wall., with binding pocket of protein (PDB ID: 3WY1) showing the consistent result with the in vitro findings, thus strengthening the basis of the remarkable α-glucosidase inhibitory potential of Cornus capitata Wall. (Additional file 2: Figures S1-S7). Triterpenoids can act as lead molecules in the treatment of diabetes and its complications. Pentacyclic triterpenes such as betulinic acid, betulin, lupeol, maslinic acid etc. have been studied in both in vivo and in vitro models suggesting their potential in the treatment of diabetes and its complications [28, 29]. Stability of a ligand in the binding pocket is calculated as minimum binding energy. Betulinic acid showed minimum binding energy i.e. 10.21 Kcal/mol followed by epibetulin, arjunolic acid, maslinic acid, lupeol, and betulin. Their significant α-glucosidase inhibitory effect may be due to the main triterpene nucleus and hydroxyl groups at R1 and R2 positions (Additional file 2: Figure S8). It favors hydrogen bonding and electrostatic interactions between the binding pocket of enzyme and hydroxyl groups. Carboxyl group at R3 position favors activity potential in pentacyclic triterpenes . Several studies support the potential of betulinic acid as an effective α-glucosidase inhibitor with IC50 varying from 7.6–14.9 μM [31, 32]. This activity can be due to hydroxyl group attached at R2 position (electron-donating group) and a carboxyl group attached. Further, replacement of hydroxyl group with carbonyl groups directly affect the inhibitory potential of pentacyclic triterpenes as in case of epibetulin. Additional hydroxyl group present other than R1 and R2 position in case of arjunolic acid decreased its inhibitory potential based on structure-activity relationship . Low inhibitory potential of betulin, when compared to its derivative, betulinic acid indicated the importance of carboxylic group [33, 34]. Decreased activity of lupeol and absence of carboxylic acid in its structure can also be co-related. Maslinic acid is hydrophobic in nature with a rigid skeleton which results in its decreased bioavailability. However, its glycosylation at R2 and R3 position increase its inhibitory potential . Also, molecular shape and size of a compound decide easy penetration in the binding pockets followed by its interactions. Substituent groups and their positions in case of pentacyclic triterpenoids plays a very crucial role. Thus, Cornus capitata Wall. can be used as an effective drug for the treatment and prevention of diabetes.
In conclusion, our study demonstrated the potent α-glucosidase inhibitory potential of methanolic extract of leaves of Cornus capitata Wall. among different plant extracts and its fractions, suggesting that the activity was due to the synergistic potential of chemical constituents present in it. It can interfere or delay the absorption process of dietary carbohydrates leading to suppression of increase in levels of glucose after a meal. The study provided partial evidence for pharmacological basis regarding clinical applications of Cornus capitata in the treatment of diabetes. Further, kinetic analysis and docking studies supported the substantially strong inhibitory activity shown by the crude methanolic extract of Cornus capitata Wall. (leaves). However, further research including in vivo studies and isolation of the active constituents will be interesting to explore to confirm the efficacy of Cornus capitata Wall. leaves extract before its extensive use in suppressing hyperglycemia in diabetic patients.
- IC50 :
50% inhibitory concentration
- PDB ID:
Protein data bank ID
Joshi SR, Standl E, Tong N, Shah P, Kalra S, Rathod R. Therapeutic potential of α-glucosidase inhibitors in type 2 diabetes mellitus: an evidence-based review. Expert Opin Pharmacother. 2015;16(13):1959–81.
AG HB. Pharmacology of α-glucosidase inhibition. Eur J Clin Investig. 1994;S3:3–10.
Van de Laar FA, Lucassen PL, Akkermans RP, Van de Lisdonk EH, De Grauw WJ. Alpha-glucosidase inhibitors for people with impaired glucose tolerance or impaired fasting blood glucose. Cochrane Libr. 2006;4:CD005061-CD005061.
DiNicolantonio JJ, Bhutani J, O'Keefe JH. Acarbose: safe and effective for lowering postprandial hyperglycaemia and improving cardiovascular outcomes. Open heart. 2015;2(1):e000327.
Kapoor LD. Handbook of Ayurvedic medicinal plants: herbal reference library. Newyork: Routledge; 2017.
Bhakuni RS, Shukla YN, Thakur RS. Constituents of Cornus capitata. J Nat Prod. 1986;49(4):714.
Bhakuni RS, Shukla YN, Thakur RS. Triterpenoids from Cornus capitata. Phytochemistry. 1987;26(9):2607–10.
Pant S, Samant SS. Ethnobotanical observations in the Mornaula reserve forest of Komoun, west Himalaya. India Ethnobot Leaflets. 2010;2010(2):8.
Sidhu MC, Thakur S. Documentation of antidiabetic medicinal plants in district Mandi of Himachal Pradesh (India). Int J PharmaTech Res. 2015;8:164–9.
Amjad MS. Ethnobotanical profiling and floristic diversity of Bana Valley, Kotli (Azad Jammu and Kashmir), Pakistan. Asian Pac J Trop Biomed. 2015;5(4):292–9.
Abbasi AM, Khan MA, Ahmad M, Zafar M, Jahan S, Sultana S. Ethnopharmacological application of medicinal plants to cure skin diseases and in folk cosmetics among the tribal communities of North-West Frontier Province, Pakistan. J Ethnopharmacol. 2010;128(2):322–35.
Sati OP, Uniyal SK, Bahuguna S, Kikuchi T. Clematoside-S, a triterpenoid saponin from the roots of Clematis grata. Phytochemistry. 1990;29(11):3676–8.
Rawat R, Vashistha DP. Roylea cinerea (D. Don) Baillon: a traditional curative of diabetes, its cultivation prospects in Srinagar Valley of Uttarakhand. Int J Adv Pharm Biol Chem. 2013;2(2):372–5.
Kumari KL, Abeysinghe DC, Dharmadasa RM. Distribution of phytochemicals and bioactivity in different parts and leaf positions of Stevia Rebaudiana (Bertoni) Bertoni-a non-caloric, natural sweetener. World. 2016;4(6):162–5.
Khan S, Khan T, Shah AJ. Total phenolic and flavonoid contents and antihypertensive effect of the crude extract and fractions of Calamintha vulgaris. Phytomedicine. 2018;47:174–83.
Nureye D, Assefa S, Nedi T, Engidawork E. In vivo antimalarial activity of the 80 Methanolic root bark extract and solvent fractions of Gardenia ternifolia Schumach. & Thonn.(Rubiaceae) against Plasmodium berghei. Evid Based Complement Alternat Med. 2018;2018.
Pistia-Brueggeman G, Hollingsworth RI. A preparation and screening strategy for glycosidase inhibitors. Tetrahedron. 2001;57(42):8773–8.
Murugan R, Parimelazhagan T. Comparative evaluation of different extraction methods for antioxidant and anti-inflammatory properties from Osbeckia parvifolia Arn.–an in vitro approach. JKSUS. 2014;26(4):267–75.
Sultana B, Anwar F, Przybylski R. Antioxidant activity of phenolic components present in barks of Azadirachta indica, Terminalia arjuna, Acacia nilotica, and Eugenia jambolana lam. Trees. Food Chem. 2007;104(3):1106–14.
Nair SS, Kavrekar V, Mishra A. In vitro studies on alpha amylase and alpha glucosidase inhibitory activities of selected plant extracts. Euro J Exp Bio. 2013;3(1):128–32.
Sobreira F, Hernandes LS, Vetore-Neto A, Díaz IE, Santana FC, Mancini-Filho J, Bacchi EM. Gastroprotective activity of the hydroethanolic extract and ethyl acetate fraction from Kalanchoe pinnata (lam.) Pers. Braz J Pharm Sci. 2017;53(1).
He K, Song S, Zou Z, Feng M, Wang D, Wang Y, Li X, Ye X. The hypoglycemic and synergistic effect of Loganin, Morroniside, and Ursolic acid isolated from the fruits of Cornus officinalis. Phytother Res. 2016;30(2):283–91.
He LH. Comparative study for α-glucosidase inhibitory effects of total iridoid glycosides in the crude products and the wine-processed products from Cornus officinalis. Yakugaku Zasshi. 2011;131(12):1801–5.
JX W, Wu XH, Li CQ, NF C, WY K. Study on inhibitive effect of extracts from Cornus officinalis on α-glucosidase [J]. Chinese J Exper Trad Med Form. 2011;5:024.
Jayaprakasam B, Olson LK, Schutzki RE, Tai MH, Nair MG. Amelioration of obesity and glucose intolerance in high-fat-fed C57BL/6 mice by anthocyanins and ursolic acid in cornelian cherry (Cornus mas). J Agric Food Chem. 2006;54(1):243–8.
Chiba S. Molecular mechanism in α-glucosidase and glucoamylase. Biosci Biotechnol Biochem. 1997;61(8):1233–9.
Khatun MH, Nesa ML, Islam R, Ripa FA, Kadir S. Antidiabetic and antidiarrheal effects of the methanolic extract of Phyllanthus reticulatus leaves in mice. Asian Pac J Reprod. 2014;3(2):121–7.
Alqahtani A, Hamid K, Kam A, Wong KH, Abdelhak Z, Razmovski-Naumovski V, Chan K, Li KM, Groundwater PW, Li GQ. The pentacyclic triterpenoids in herbal medicines and their pharmacological activities in diabetes and diabetic complications. Curr Med Chem. 2013;20(7):908–31.
Kumar S, Narwal S, Kumar V, Prakash O. α-Glucosidase inhibitors from plants: a natural approach to treat diabetes. Pharmacogn Rev. 2011;5(9):19.
Uddin G, Rauf A, Al-Othman AM, Collina S, Arfan M, Ali G, Khan I. Pistagremic acid, a glucosidase inhibitor from Pistacia integerrima. Fitoterapia. 2012;83(8):1648–52.
Mbaze LM, Poumale HM, Wansi JD, Lado JA, Khan SN, Iqbal MC, Ngadjui BT, Laatsch H. α-Glucosidase inhibitory pentacyclic triterpenes from the stem bark of Fagara tessmannii (Rutaceae). Phytochemistry. 2007;68(5):591–5.
Zhang BW, Xing Y, Wen C, Yu XX, Sun WL, Xiu ZL, Dong YS. Pentacyclic triterpenes as α-glucosidase and α-amylase inhibitors: structure-activity relationships and the synergism with acarbose. Bioorganic Med Chem lett. 2017;27(22):5065–70.
Matsuda H, Li Y, Murakami T, Matsumura N, Yamahara J, Yoshikawa M. Antidiabetic principles of natural medicines. III. Structure-related inhibitory activity and action mode of oleanolic acid glycosides on hypoglycemic activity. Chem Pharm Bull. 1998;46(9):1399–403.
Yoshikawa M, Matsuda H, Harada E, Murakami T, Wariishi N, Yamahara J, Murakami N. Elatoside E, a new hypoglycemic principle from the root cortex of Aralia elata seem.: structure-related hypoglycemic activity of oleanolic acid glycosides. Chem Pharm Bull. 1994;42(6):1354–6.
Xu J, Nie X, Hong Y, Jiang Y, Wu G, Yin X, Wang C, Wang X. Synthesis of water soluble glycosides of pentacyclic dihydroxytriterpene carboxylic acids as inhibitors of α-glucosidase. Carbohydr Res. 2016;424:42–53.
The authors duly acknowledge the financial assistance granted by the University Grants Commission (UGC), New Delhi for instrumentation facility under UGC CPEPA and UPE program. The authors are thankful to Head, Department of Botanical and Environmental Sciences, Guru Nanak Dev University, Amritsar for providing research facilities.
The present study was supported by the University Grants Commission (UGC), New Delhi under the Rajiv Gandhi National Fellowship scheme to the first author (vide grant no. 201415-RGNF-2014-15-SC-PUN-68052).
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Table S1. Plants used in study with their parts, family with accession numbers. Table S2. Chemical structures of Reported chemical constituents from Cornus capitata prepared via Chemsketch for Docking a) Arjunolic acid b) Betulin c) Betulinic acid d) Epibetulin e) Lupeol f) Maslinic acid. (DOCX 86 kb)
Figure S1. Docking conformation showing binding of 3WY1 protein with Betulinic acid. Figure S2. Docking conformation showing binding of 3WY1 protein with Epibetulin. Figure S3. Docking conformation showing binding of 3WY1 protein with Arjunolic acid. Figure S4. Docking conformation showing binding of 3WY1 protein with Maslinic acid. Figure S5. Docking conformation showing binding of 3WY1 protein with Lupeol. Figure S6. Docking conformation showing binding of 3WY1 protein with Betulin. Figure S7. Docking conformation showing binding of 3WY1 protein with Acarbose. Figure S8. Main structure of penta-cyclic triterpenoid. (DOCX 6269 kb)
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Bhatia, A., Singh, B., Arora, R. et al. In vitro evaluation of the α-glucosidase inhibitory potential of methanolic extracts of traditionally used antidiabetic plants. BMC Complement Altern Med 19, 74 (2019). https://doi.org/10.1186/s12906-019-2482-z
- Clematis grata wall.
- Cornus capitata wall.
- Roylea cinerea (D. Don) Baill