Euphorbia denticulata Lam.: A promising source of phyto-pharmaceuticals for the development of novel functional formulations

Biomedicine and Pharmacotherapy

Volumn 87, Issue , 2017, Pages 27-36

  Zengin, Gokhan ^a   Uysal, Ahmet ^a   Aktumsek, Abdurrahman ^a   Mocan, Andrei ^b   Mollica, Adriano ^c   Locatelli, Marcello ^c   Custodio, Luisa ^d   Neng, Nuno R ^e   Nogueira, José M F ^e   Aumeeruddy Elalfi, Zaahira ^f   Mahomoodally, M Fawzi ^f  

^a SELCUK UNIVERSITY   (Turkey)

^b IULIU HATIEGANU UNIVERSITY OF MEDICINE AND PHARMACY   (Romania)

^c UNIVERSITY OF CHIETI   (Italy)

^d UNIVERSITY OF ALGARVE   (Portugal)

^e UNIVERSITY OF LISBON   (Portugal)

^f UNIVERSITY OF MAURITIUS   (Mauritius)

Author keywords

Diabetes; Euphorbia denticulata; Molecular docking; Phyto pharmaceuticals; Polyphenols

Indexed keywords

4 HYDROXYBENZOIC ACID; AMYLASE; ANTIBIOTIC AGENT; ANTIOXIDANT; APIGENIN; BENZOIC ACID; CAFFEIC ACID; CATECHIN; CHOLINESTERASE; COUMARIC ACID; ENZYME INHIBITOR; EPICATECHIN; EPIGALLOCATECHIN GALLATE; EUPHORBIA DENTICULATA EXTRACT; FERULIC ACID; FLAVONE; FLAVONOID; GALLIC ACID; GENTAMICIN; MONOPHENOL MONOOXYGENASE; NARINGENIN; OXACILLIN; PHENOL DERIVATIVE; PLANT EXTRACT; QUERCETIN; ROSMARINIC ACID; SALICYLIC ACID; SYRINGIC ACID; TRIACYLGLYCEROL LIPASE; UNCLASSIFIED DRUG; VANILLIC ACID; ANTIINFECTIVE AGENT; PLANT MEDICINAL PRODUCT;

ANTIBACTERIAL ACTIVITY; ANTIOXIDANT ACTIVITY; ARTICLE; BIOLOGICAL ACTIVITY; CANDIDA ALBICANS; CHEMICAL COMPOSITION; COMPUTER MODEL; CONTROLLED STUDY; DEGENERATIVE DISEASE; DIABETES MELLITUS; EC50; ENZYME INHIBITION; ESCHERICHIA COLI; EUPHORBIA; EUPHORBIA DENTICULATA; FLOWER; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN TISSUE; HYDROGEN BOND; HYPERPIGMENTATION; KLEBSIELLA PNEUMONIAE; MICROCOCCUS LUTEUS; MINIMUM INHIBITORY CONCENTRATION; MOLECULAR DOCKING; MOLECULAR MODEL; NONHUMAN; OBESITY; OXIDATIVE STRESS; PHYTOCHEMISTRY; PLANT LEAF; PRIORITY JOURNAL; PSEUDOMONAS AERUGINOSA; SALMONELLA ENTERICA SEROVAR ENTERITIDIS; STAPHYLOCOCCUS AUREUS; CHEMISTRY; DRUG EFFECTS; DRUG FORMULATION; ISOLATION AND PURIFICATION; METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS; PHYSIOLOGY; PLANT STRUCTURES; PROCEDURES;

ANTI-BACTERIAL AGENTS; ANTIOXIDANTS; DRUG COMPOUNDING; EUPHORBIA; FLAVONOIDS; METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS; MOLECULAR DOCKING SIMULATION; PHENOLS; PHYTOCHEMICALS; PLANT COMPONENTS, AERIAL; PLANT EXTRACTS;

EID: 85007433729     PISSN: 07533322     EISSN: 19506007     Source Type: Journal    
DOI: 10.1016/j.biopha.2016.12.063     Document Type: Article

References (52)

1. [1] Bouriche, H., Moussaoui, S., Meziti, H., Senator, A., Anti-inflammatory activity of methanolic extract of santolina chamaecyparissus. Int. Symp. Med. Plants Nat. Prod. 1098 (2013), 23–30.
2. [2] Balunas, M.J., Kinghorn, A.D., Drug discovery from medicinal plants. Life Sci. 78:5 (2005), 431–441.
3. [3] Hamilton, A.C., Medicinal plants, conservation and livelihoods. Biodivers. Conserv. 13:8 (2004), 1477–1517.
4. [4] Betteridge, D.J., What is oxidative stress?. Metabolism 49:2 (2000), 3–8.
5. [5] Maritim, A., Sanders, A., Watkins, R.J., Diabetes, oxidative stress, and antioxidants: a review. J. Biochem. Mol. Toxicol. 17:1 (2003), 24–38.
6. [6] Gonzalez, R., Ballester, I., Lopez-Posadas, R., Suarez, M., Zarzuelo, A., Martinez-Augustin, O., Medina, F.S.D., Effects of flavonoids and other polyphenols on inflammation. Crit. Rev. Food Sci. Nutr. 51:4 (2011), 331–362.
7. [7] Yao, L.H., Jiang, Y., SHI, J., Tomas-Barberan, F., Datta, N., Singanusong, R., Chen, S., Flavonoids in food and their health benefits. Plant Foods Hum. Nutr. 59:3 (2004), 113–122.
8. [8] Slinkard, K., Singleton, V.L., Total phenol analysis: automation and comparison with manual methods. Am. J. Enol. Viticult. 28:1 (1977), 49–55.
9. [9] Mocan, A., Zengin, G., Uysal, A., Gunes, E., Mollica, A., Degirmenci, N.S., Alpsoy, L., Aktumsek, A., Biological and chemical insights of Morina persica L.: a source of bioactive compounds with multifunctional properties. J. Funct. Foods 25 (2016), 94–109.
10. [10] Roh, C., Jung, U., Screening of crude plant extracts with anti-obesity activity. Int. J. Mol. Sci. 13:2 (2012), 1710–1719.
11. [11] Zengin, G., Uysal, A., Gunes, E., Aktumsek, A., Survey of phytochemical composition and biological effects of three extracts from a wild plant (Cotoneaster nummularia Fisch et Mey.): a potential source for functional food ingredients and drug formulations. PLoS One, 9(11), 2014, e113527.
12. [12] Berman, H.M., Westbrook, J., Feng, Z., Gilliland, G., Bhat, T.N., Weissig, H., Shindyalov, I.N., Bourne, P.E., The protein data bank. Nucleic Acids Res. 28:1 (2000), 235–242.
13. [13] Pesaresi, A., Lamba, D., Torpedo Californica acetylcholinesterase in complex with a tacrine-nicotinamide hybrid inhibitor. 2016 http://www.rcsb.org/pdb/explore/explore do?structureId=4X3C.
14. [14] Nachon, F., Carletti, E., Ronco, C., Trovaslet, M., Nicolet, Y., Jean, L., Renard, P.-Y., Crystal structures of human cholinesterases in complex with huprine W and tacrine: elements of specificity for anti-Alzheimer's drugs targeting acetyl-and butyryl-cholinesterase. Biochem. J 453:3 (2013), 393–399.
15. [15] Zhuo, H., Payan, F., Qian, M., Crystal structure of the pig pancreatic α-amylase complexed with ρ-nitrophenyl-α-d-maltoside-flexibility in the active site. Protein J. 23:6 (2004), 379–387.
16. [16] Yamamoto, K., Miyake, H., Kusunoki, M., Osaki, S., Steric hindrance by 2 amino acid residues determines the substrate specificity of isomaltase from Saccharomyces cerevisiae. J. Biosci. Bioeng. 112:6 (2011), 545–550.
17. [17] Egloff, M.-P., Marguet, F., Buono, G., Verger, R., Cambillau, C., van Tilbeurgh, H., The 2.46. ANG. Resolution structure of the pancreatic lipase-colipase complex inhibited by a C11 alkyl phosphonate. Biochemistry 34:9 (1995), 2751–2762.
18. [18] Ismaya, W.T., Rozeboom, H.J., Weijn, A., Mes, J.J., Fusetti, F., Wichers, H.J., Dijkstra, B.W., Crystal structure of Agaricus bisporus mushroom tyrosinase: identity of the tetramer subunits and interaction with tropolone. Biochemistry 50:24 (2011), 5477–5486.
19. [19] Pettersen, E.F., Goddard, T.D., Huang, C.C., Couch, G.S., Greenblatt, D.M., Meng, E.C., Ferrin, T.E., UCSF Chimera—a visualization system for exploratory research and analysis. J. Comput. Chem. 25:13 (2004), 1605–1612.
20. [20] Release, S., 4: Maestro, Version 10.4. 2015, Schrödinger, LLC, New York, NY.
21. [21] Irwin, J.J., Sterling, T., Mysinger, M.M., Bolstad, E.S., Coleman, R.G., ZINC: a free tool to discover chemistry for biology. J. Chem. Inf. Model. 52:7 (2012), 1757–1768.
22. [22] Ashraf, A., Sarfraz, R.A., Rashid, M.A., Shahid, M., Antioxidant, antimicrobial, antitumor, and cytotoxic activities of an important medicinal plant (Euphorbia royleana) from Pakistan. J. Food Drug Anal. 23:1 (2015), 109–115.
23. [23] Basma, A.A., Zakaria, Z., Latha, L.Y., Sasidharan, S., Antioxidant activity and phytochemical screening of the methanol extracts of Euphorbia hirta L. Asian Pac. J. Trop. Med. 4:5 (2011), 386–390.
24. [24] Ertas, A., Yilmaz, M.A., Firat, M., Chemical profile by LC-MS/MS, GC/MS and antioxidant activities of the essential oils and crude extracts of two Euphorbia species. Nat. Prod. Res. 29:6 (2015), 529–534.
25. [25] Scalbert, A., Johnson, I.T., Saltmarsh, M., Polyphenols: antioxidants and beyond. Am. J. Clin. Nutr. 81:1 (2005), 215S–217S.
26. [26] Scalbert, A., Manach, C., Morand, C., Rémésy, C., Jiménez, L., Dietary polyphenols and the prevention of diseases. Crit. Rev. Food Sci. Nutr. 45:4 (2005), 287–306.
27. [27] Petersen, M., Simmonds, M.S., Rosmarinic acid. Phytochemistry 62:2 (2003), 121–125.
28. [28] Heo, H.J., Kim, M.-J., Lee, J.-M., Choi, S.J., Cho, H.-Y., Hong, B., Kim, H.-K., Kim, E., Shin, D.-H., Naringenin from Citrus junos has an inhibitory effect on acetylcholinesterase and a mitigating effect on amnesia. Dement. Geriatr. Cogn. Disord. 17:3 (2004), 151–157.
29. [29] Senol, F.S., Ślusarczyk, S., Matkowski, A., Pérez-Garrido, A., Girón-Rodríguez, F., Cerón-Carrasco, J.P., den-Haan, H., Peña-García, J., Pérez-Sánchez, H., Domaradzki, K., Selective in vitro and in silico butyrylcholinesterase inhibitory activity of diterpenes and rosmarinic acid isolated from Perovskia atriplicifolia Benth. and Salvia glutinosa L. Phytochemistry 133 (2017), 33–44.
30. [30] Okello, E.J., Leylabi, R., McDougall, G.J., Inhibition of acetylcholinesterase by green and white tea and their simulated intestinal metabolites. Food Funct. 3:6 (2012), 651–661.
31. [31] Suganthy, N., Pandima Devi, K., In vitro antioxidant and anti-cholinesterase activities of Rhizophora mucronata. Pharm. Biol. 54:1 (2016), 118–129.
32. [32] Şenol, F., Orhan, I., Yilmaz, G., Cicek, M., Şener, B., Acetylcholinesterase, butyrylcholinesterase, and tyrosinase inhibition studies and antioxidant activities of 33 Scutellaria L. taxa from Turkey. Food Chem. Toxicol. 48:3 (2010), 781–788.
33. [33] Srividhya, R., Gayathri, R., Kalaiselvi, P., Impact of epigallo catechin-3-gallate on acetylcholine-acetylcholine esterase cycle in aged rat brain. Neurochem. Int. 60:5 (2012), 517–522.
34. [34] Kubo, I., Kinst-Hori, I., Kubo, Y., Yamagiwa, Y., Kamikawa, T., Haraguchi, H., Molecular design of antibrowning agents. J. Agric. Food Chem. 48:4 (2000), 1393–1399.
35. [35] Apostolidis, E., Karayannakidis, P.D., Kwon, Y.-I., Lee, C.M., Seeram, N.P., Seasonal variation of phenolic antioxidant-mediated α-glucosidase inhibition of Ascophyllum nodosum. Plant Foods Hum. Nutr. 66:4 (2011), 313–319.
36. [36] You, Q., Chen, F., Wang, X., Jiang, Y., Lin, S., Anti-diabetic activities of phenolic compounds in muscadine against alpha-glucosidase and pancreatic lipase. LWT Food Sci. Technol. 46:1 (2012), 164–168.
37. [37] Mahomoodally, F.M., Ramcharun, S., In vitro kinetic of inhibition of lipase, antioxidant activity, glucose entrapment and polyphenolic content of Solanum linnaeanum. J. Biol. Active Prod. Nat. 5:6 (2015), 383–396.
38. [38] Friesner, R.A., Banks, J.L., Murphy, R.B., Halgren, T.A., Klicic, J.J., Mainz, D.T., Repasky, M.P., Knoll, E.H., Shelley, M., Perry, J.K., Glide: a new approach for rapid, accurate docking and scoring. 1. Method and assessment of docking accuracy. J. Med. Chem. 47:7 (2004), 1739–1749.
39. [39] Mocan, A., Zengin, G., Crişan, G., Mollica, A., Enzymatic assays and molecular modeling studies of Schisandra chinensis lignans and phenolics from fruit and leaf extracts. J. Enzyme Inhib. Med. Chem. 31:S4 (2016), 200–2010.
40. [40] Tiwari, V., Kuhad, A., Chopra, K., Epigallocatechin-3-gallate ameliorates alcohol-induced cognitive dysfunctions and apoptotic neurodegeneration in the developing rat brain. Int. J. Neuropsychopharmacol. 13:8 (2010), 1053–1066.
41. [41] Matsui, T., Tanaka, T., Tamura, S., Toshima, A., Tamaya, K., Miyata, Y., Tanaka, K., Matsumoto, K., α-Glucosidase inhibitory profile of catechins and theaflavins. J. Agric. Food Chem. 55:1 (2007), 99–105.
42. [42] Gao, J., Xu, P., Wang, Y., Wang, Y., Hochstetter, D., Combined effects of green tea extracts, green tea polyphenols or epigallocatechin gallate with acarbose on inhibition against α-amylase and α-glucosidase in vitro. Molecules 18:9 (2013), 11614–11623.
43. [43] Grove, K.A., Sae-Tan, S., Kennett, M.J., Lambert, J.D., (−)- epigallocatechin-3-gallate inhibits pancreatic lipase and reduces body weight gain in high fat-fed obese mice. Obesity 20:11 (2012), 2311–2313.
44. [44] Lunagariya, N.A., Patel, N.K., Jagtap, S.C., Bhutani, K.K., Inhibitors of pancreatic lipase: state of the art and clinical perspectives. EXCLI J., 13, 2014, 897.
45. [45] No, J.K., Kim, Y.J., Shim, K.H., Jun, Y.S., Rhee, S.H., Yokozawa, T., Chung, H.Y., Inhibition of tyrosinase by green tea components. Life Sci. 65:21 (1999), PL241–PL246.
46. [46] Zhu, F., Asada, T., Sato, A., Koi, Y., Nishiwaki, H., Tamura, H., Rosmarinic acid extract for antioxidant, antiallergic, and α-glucosidase inhibitory activities, isolated by supramolecular technique and solvent extraction from Perilla leaves. J. Agric. Food Chem. 62:4 (2014), 885–892.
47. [47] Vladimir-Knežević, S., Blažeković, B., Kindl, M., Vladić, J., Lower-Nedza, A.D., Brantner, A.H., Acetylcholinesterase inhibitory, antioxidant and phytochemical properties of selected medicinal plants of the Lamiaceae family. Molecules 19:1 (2014), 767–782.
48. [48] Bustanji, Y., Issa, A., Mohammad, M., Hudaib, M., Tawah, K., Alkhatib, H., Almasri, I., Al-Khalidi, B., Inhibition of hormone sensitive lipase and pancreatic lipase by Rosmarinus officinalis extract and selected phenolic constituents. J. Med. Plants Res. 4:21 (2010), 2235–2242.
49. [49] Lin, L., Dong, Y., Zhao, H., Wen, L., Yang, B., Zhao, M., Comparative evaluation of rosmarinic acid, methyl rosmarinate and pedalitin isolated from Rabdosia serra (MAXIM.) HARA as inhibitors of tyrosinase and α-glucosidase. Food Chem. 129:3 (2011), 884–889.
50. [50] Jain, D.P., Pancholi, S.S., Patel, R., Synergistic antioxidant activity of green tea with some herbs. J. Adv. Pharm. Technol. Res., 2(3), 2011, 177.
51. [51] Barber, M.S., McConnell, V.S., DeCaux, B.S., Antimicrobial intermediates of the general phenylpropanoid and lignin specific pathways. Phytochemistry 54:1 (2000), 53–56.
52. [52] Dixon, R.A., Natural products and plant disease resistance. Nature 411:6839 (2001), 843–847.