Cited by 93Natural Antidiabetic Agents StudiesMedicinal Plant ResearchEthnobotanical and Medicinal Plants Studies

Some common medicinal plants with antidiabetic activity, known and available in Europe (A mini-review)

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Przeor, Monika·2022·Pharmaceuticals

Abstract

Diabetes is a metabolic disease that affected 9.3% of adults worldwide in 2019. Its co-occurrence is suspected to increase mortality from COVID-19. The treatment of diabetes is mainly based on the long-term use of pharmacological agents, often expensive and causing unpleasant side effects. There is an alarming increase in the number of pharmaceuticals taken in Europe. The aim of this paper is to concisely collect information concerning the few antidiabetic or hypoglycaemic raw plant materials that are present in the consciousness of Europeans and relatively easily accessible to them on the market and sometimes even grown on European plantations. The following raw materials are discussed in this mini-review: Morus alba L., Cinnamomum zeylanicum J.Presl, Trigonella foenum-graecum L., Phaseolus vulgaris L., Zingiber officinale Rosc., and Panax ginseng C.A.Meyer in terms of scientifically tested antidiabetic activity and the presence of characteristic biologically active compounds and their specific properties, including antioxidant properties. The characteristics of these raw materials are based on in vitro as well as in vivo studies: on animals and in clinical studies. In addition, for each plant, the possibility to use certain morphological elements in the light of EFSA legislation is given.

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  • Herbals/botanicals have demonstrated potent anti-diabetic effects via a variety of mechanisms, such as enhancing insulin sensitivity, stimulating insulin secretion, blocking carbohydrate absorption, and reducing oxidative stress.

    “Herbals/botanicals have demonstrated potent anti-diabetic effects via a variety of mechanisms, such as enhancing insulin sensitivity, stimulating insulin secretion, blocking the absorption of carbohydrates, and reducing OS; the inhibition of α-glucosidase enzyme and the generation of advanced glycation products, the transcription of GLUT-4 and PPAR, and the presence of antioxidants.”

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  1. [1]Alem Geberemeskel G. Godefa Debebe Y. Abraha Nguse N. Clinical study antidiabetic effect of fenugreek seed powder solution (Trigonella foenum-graecum L.) on hyperlipidemia in diabetic patients J. Diabetes Res. 2019 2019 8507453 10.1155/2019/8507453 31583253 PMC6748210 · DOI
  2. [3]Shaw J.E. Sicree R.A. Zimmet P.Z. Global estimates of the prevalence of diabetes for 2010 and 2030 Diabetes Res. Clin. Pract. 2010 87 4 14 10.1016/j.diabres.2009.10.007 19896746 · DOI · Paper page
  3. [4]Roglic G. Unwin N. Mortality attributable to diabetes: Estimates for the year 2010 Diabetes Res. Clin. Pract. 2010 87 15 19 10.1016/j.diabres.2009.10.006 19914728 · DOI
  4. [5]Wu Z. Tang Y. Cheng Q. Diabetes increases the mortality of patients with COVID-19: A meta-analysis Acta Diabetol. 2021 58 139 144 10.1007/s00592-020-01546-0 32583078 PMC7311595 · DOI
  5. [6]Szczepaniak O. Ligaj M. Kobus-Cisowska J. Tichoniuk M. Dziedziński M. Przeor M. Szulc P. The genoprotective role of naringin Biomolecules 2020 10 700 10.3390/biom10050700 32365989 PMC7277402 · DOI
  6. [7]Dziedzinski M. Kobus-Cisowska J. Szymanowska D. Stuper-Szablewska K. Baranowska M. Identification of polyphenols from coniferous shoots as natural antioxidants and antimicrobial compounds Molecules 2020 25 3527 10.3390/molecules25153527 32752298 PMC7435953 · DOI
  7. [8]Telichowska A. Kobus-Cisowska J. Szulc P. Phytopharmacological possibilities of bird cherry Prunus padus L. and Prunus serotina L. species and their bioactive phytochemicals Nutrients 2020 12 1966 10.3390/nu12071966 PMC7399899 32630652 · DOI
  8. [9]Kobus-Cisowska J. Szymanowska-Powałowska D. Szczepaniak O. Kmiecik D. Przeor M. Gramza-Michałowska A. Cielecka-Piontek J. Smuga-Kogut M. Szulc P. Composition and in vitro effects of cultivars of Humulus lupulus L. Hops on cholinesterase activity and microbial growth Nutrients 2019 11 1377 10.3390/nu11061377 31248112 PMC6627407 · DOI
  9. [10]Szczepaniak O.M. Kobus-Cisowska J. Kusek W. Przeor M. Functional properties of Cornelian cherry (Cornus mas L.): A comprehensive review Eur. Food Res. Technol. 2019 245 2071 2087 10.1007/s00217-019-03313-0 · DOI
  10. [11]Przeor M. Flaczyk E. Beszterda M. Szymandera-Buszka K.E. Piechocka J. Kmiecik D. Szczepaniak O. Kobus-Cisowska J. Jarzębski M. Tylewicz U. Air-drying temperature changes the content of the phenolic acids and flavonols in white mulberry (Morus alba L.) leaves Cienc. Rural 2019 49 10.1590/0103-8478cr20190489 · DOI
  11. [12]Tylewicz U. Oliveira G. Alminger M. Nohynek L. Dalla Rosa M. Romani S. Antioxidant and antimicrobial properties of organic fruits subjected to PEF-assisted osmotic dehydration Innov. Food Sci. Emerg. Technol. 2020 62 102341 10.1016/j.ifset.2020.102341 · DOI
  12. [13]Cavalcanti V.P. Aazza S. Bertolucci S.K.V. Pereira M.M.A. Cavalcanti P.P. Buttrós V.H.T. de Oliveira e Silva A.M. Pasqual M. Dória J. Plant, pathogen and biocontrol agent interaction effects on bioactive compounds and antioxidant activity in garlic Physiol. Mol. Plant Pathol. 2020 112 101550 10.1016/j.pmpp.2020.101550 · DOI
  13. [14]Tajner-Czopek A. Gertchen M. Rytel E. Kita A. Kucharska A.Z. Sokół-Łętowska A. Study of antioxidant activity of some medicinal plants having high content of caffeic acid derivatives Antioxidants 2020 9 412 10.3390/antiox9050412 32408518 PMC7278751 · DOI
  14. [15]Waśkiewicz A. Beszterda M. Bocianowski J. Goliński P. Natural occurrence of fumonisins and ochratoxin A in some herbs and spices commercialized in Poland analyzed by UPLC-MS/MS method Food Microbiol. 2013 36 426 431 10.1016/j.fm.2013.07.006 24010625 · DOI
  15. [16]Sowa P. Marcinčáková D. Miłek M. Sidor E. Legáth J. Dżugan M. Analysis of cytotoxicity of selected asteraceae plant extracts in real time, their antioxidant properties and polyphenolic profile Molecules 2020 25 5517 10.3390/molecules25235517 PMC7728153 33255596 · DOI
  16. [17]Kozlowska M. Zbikowska A. Marciniak-Lukasiak K. Kowalska M. Herbal extracts incorporated into shortbread cookies: Impact on color and fat quality of the cookies Biomolecules 2019 9 858 10.3390/biom9120858 PMC6995587 31835857 · DOI
  17. [18]Przeor M. Flaczyk E. Kmiecik D. Kobus-Cisowska J. Bueschke M. Kulczyński B. Polish consumers’ awareness and knowledge about functional food Univ. Technol. Stetin. Agric. Aliment. Pisc. Zootech 2018 341 59 68 10.21005/AAPZ2018.46.2.07 · DOI
  18. [19]Musabayane C.T. Bwititi P.T. Ojewole J.A.O. Effects of oral administration of some herbal extracts on food consumption and blood glucose levels in normal and streptozotocin-treated diabetic rats Methods Find. Exp. Clin. Pharmacol. 2006 28 223 228 10.1358/mf.2006.28.4.990202 16801983 · DOI
  19. [20]Baset M. Ali T. Elshamy H. El Sadek A. Sami D. Badawy M. Abou-Zekry S. Heiba H. Saadeldin M. Abdellatif A. Anti-diabetic effects of fenugreek (Trigonella foenum-graecum): A comparison between oral and intraperitoneal—An animal study Int. J. Funct. Nutr. 2020 1 2 10.3892/ijfn.2020.2 · DOI
  20. [21]Salehi B. Ata A. Anil Kumar N.V. Sharopov F. Ramírez-Alarcón K. Ruiz-Ortega A. Abdulmajid Ayatollahi S. Tsouh Fokou P.V. Kobarfard F. Amiruddin Zakaria Z. Antidiabetic potential of medicinal plants and their active components Biomolecules 2019 9 551 10.3390/biom9100551 PMC6843349 31575072 · DOI
  21. [22]Singab A.N. Youssef F.S. Ashour M.L. Medicinal plants with potential antidiabetic activity and their assessment Med. Aromat. Plants 2014 3 151 10.4172/2167-0412.1000151 · DOI
  22. [23]Arumugam G. Manjula P. Paari N. A review: Anti diabetic medicinal plants used for diabetes mellitus J. Acute Dis. 2013 2 196 200 10.1016/S2221-6189(13)60126-2 · DOI
  23. [24]Chhetri D.R. Parajuli P. Subba G.C. Antidiabetic plants used by Sikkim and Darjeeling Himalayan tribes, India J. Ethnopharmacol. 2005 99 199 202 10.1016/j.jep.2005.01.058 15894127 · DOI
  24. [25]Przeor M. Flaczyk E. Kmiecik D. Buchowski M.S. Staniek H. Tomczak-Graczyk A. Kobus-Cisowska J. Gramza-Michałowska A. Foksowicz-Flaczyk J. Functional properties and antioxidant activity of Morus alba L. leaves var. Zolwinska Wielkolistna (WML-P)—the effect of controlled conditioning process Antioxidants 2020 9 668 10.3390/antiox9080668 PMC7463858 32722613 · DOI
  25. [26]Chinsembu K.C. Diabetes mellitus and nature’s pharmacy of putative antidiabetic plants J. Herb. Med. 2019 15 100230 10.1016/j.hermed.2018.09.001 · DOI
  26. [27]Durazzo A. D’Addezio L. Camilli E. Piccinelli R. Turrini A. Marletta L. Marconi S. Lucarini M. Lisciani S. Gabrielli P. From plant compounds to botanicals and back: A current snapshot Molecules 2018 23 1844 10.3390/molecules23081844 30042375 PMC6222869 · DOI
  27. [28]Chan C.H. Ngoh G.C. Yusoff R. A brief review on anti diabetic plants: Global distribution, active ingredients, extraction techniques and acting mechanisms Pharmacogn. Rev. 2012 6 22 28 10.4103/0973-7847.95854 22654401 PMC3358964 · DOI
  28. [29]Eddouks M. Maghrani M. Lemhadri A. Ouahidi M.L. Jouad H. Ethnopharmacological survey of medicinal plants used for the treatment of diabetes mellitus, hypertension and cardiac diseases in the south-east region of Morocco (Tafilalet) J. Ethnopharmacol. 2002 82 97 103 10.1016/S0378-8741(02)00164-2 12241983 · DOI
  29. [30]Gholap S. Kar A. Hypoglycaemic effects of some plant extracts are possibly mediated through inhibition in corticosteroid concentration Pharmazie 2004 59 876 878 15587591
  30. [31]Heidari R. Zareae S. Heidarizadeh M. Extraction, purification, and inhibitory effect of alpha-amylase inhibitor from wheat (Triticum aestivum Var. Zarrin) Pakistan J. Nutr. 2005 4 101 105 10.3923/pjn.2005.101.105 · DOI
  31. [32]Miura T. Itoh C. Iwamoto N. Kato M. Kawai M. Park S.R. Suzuki I. Hypoglycemic activity of the fruit of the Momordica charantia in type 2 diabetic mice J. Nutr. Sci. Vitaminol. 2001 47 340 344 10.3177/jnsv.47.340 11814149 · DOI
  32. [33]Crespy V. Williamson G. A review of the health effects of green tea catechins in in vivo animal models J. Nutr. 2004 134 10.1093/jn/134.12.3431S 15570050 · DOI
  33. [34]Bnouham M. Ziyyat A. Mekhfi H. Tahri A. Legssyer A. Medicinal plants with potential antidiabetic activity-A review of ten years of herbal medicine research (1990–2000) Int J Diabetes Metab. 2006 14 1 25 10.1159/000497588 · DOI
  34. [35]Kim M.J. Ryu G.R. Chung J.S. Sim S.S. Rhie D.J. Yoon S.H. Hahn S.J. Kim M.S. Jo Y.H. Protective effects of epicatechin against the toxic effects of streptozotocin on rat pancreatic islets: In vivo and in vitro Pancreas 2003 26 292 299 10.1097/00006676-200304000-00014 12657957 · DOI
  35. [36]Mukherjee P.K. Maiti K. Mukherjee K. Houghton P.J. Leads from Indian medicinal plants with hypoglycemic potentials J. Ethnopharmacol. 2006 106 1 28 10.1016/j.jep.2006.03.021 16678368 · DOI
  36. [37]Esmaeili M.A. Yazdanparast R. Hypoglycaemic effect of Teucrium polium: Studies with rat pancreatic islets J. Ethnopharmacol. 2004 95 27 30 10.1016/j.jep.2004.06.023 15374603 · DOI
  37. [38]Kaneto H. Matsuoka T. Nakatani Y. Kawamori D. Matsuhisa M. Yamasaki Y. Oxidative stress and the JNK pathway in diabetes Curr. Diabetes Rev. 2005 1 65 72 10.2174/1573399052952613 18220583 · DOI
  38. [39]Shin A.H. Oh C.J. Park J.-P. Glycation-induced inactivation of antioxidant enzymes and modulation of cellular redox status in lens cells Arch. Pharmacal Res. 2006 29 577 581 10.1007/BF02969268 16903078 · DOI
  39. [40]Suryavanshi S.V. Kulkarni Y.A. NF-κβ: A potential target in the management of vascular complications of diabetes Front. Pharmacol. 2017 8 798 10.3389/fphar.2017.00798 29163178 PMC5681994 · DOI
  40. [41]Herrera T. Navarro del Hierro J. Fornari T. Reglero G. Martin D. Inhibitory effect of quinoa and fenugreek extracts on pancreatic lipase and α-amylase under in vitro traditional conditions or intestinal simulated conditions Food Chem. 2019 270 509 517 10.1016/j.foodchem.2018.07.145 30174080 · DOI
  41. [42]Xiao J. Ni X. Kai G. Chen X. A review on structure-activity relationship of dietary polyphenols inhibiting α-amylase Crit. Rev. Food Sci. Nutr. 2013 53 497 506 10.1080/10408398.2010.548108 23391016 · DOI
  42. [43]Ali H. Houghton P.J. Soumyanath A. α-Amylase inhibitory activity of some Malaysian plants used to treat diabetes; with particular reference to Phyllanthus amarus J. Ethnopharmacol. 2006 107 449 455 10.1016/j.jep.2006.04.004 16678367 · DOI
  43. [44]Ozkan G. Kamiloglu S. Ozdal T. Boyacioglu D. Capanoglu E. Potential use of Turkish medicinal plants in the treatment of various diseases Molecules 2016 21 257 10.3390/molecules21030257 26927038 PMC6273156 · DOI
  44. [45]Kumari R. Srivastava S. Srivastava R.P. Nutritional evaluation of fresh leaves of mulberry genotypes Agric. Sci. Dig. 2009 29 198 201 10.1080/09637480600801837 · DOI
  45. [48]Kobus-Cisowska J. Gramza-Michalowska A. Kmiecik D. Flaczyk E. Korczak J. Mulberry fruit as an antioxidant component in muesli Agric. Sci. 2013 4 130 135 10.4236/as.2013.45B024 · DOI
  46. [49]Kobus-Cisowska J. Dziedziński M. Szymanowska D. Szczepaniak O. Byczkiewicz S. Telichowska A. Szulc P. The effects of Morus alba L. fortification on the quality, functional properties and sensory attributes of bread stored under refrigerated conditions Sustainability 2020 12 6691 10.3390/su12166691 · DOI
  47. [50]Przeor M. Flaczyk E. Morwa biała—Nieocenione znaczenie zdrowotne Przem. Spożywczy 2016 5 33 35 10.15199/65.2016.5.7 · DOI
  48. [52]Butt M.S. Nazir A. Sultan M.T. Schroën K. Morus alba L. nature’s functional tonic Trends Food Sci. Technol. 2008 19 505 512 10.1016/j.tifs.2008.06.002 · DOI
  49. [53]Kwon H.J. Chung J.Y. Kim J.Y. Kwon O. Comparison of 1-deoxynojirimycin and aqueous mulberry leaf extract with emphasis on postprandial hypoglycemic effects: In vivo and in vitro studies J. Agric. Food Chem. 2011 59 3014 3019 10.1021/jf103463f 21370820 · DOI
  50. [54]Yin Z. Zhang W. Feng F. Zhang Y. Kang W. α-Glucosidase inhibitors isolated from medicinal plants Food Sci. Hum. Wellness 2014 3 136 174 10.1016/j.fshw.2014.11.003 · DOI
  51. [55]Liu Q. Li X. Li C. Zheng Y. Peng G. 1-Deoxynojirimycin alleviates insulin resistance via activation of insulin signaling PI3K/AKT pathway in skeletal muscle of db/db mice Molecules 2015 20 21700 21714 10.3390/molecules201219794 26690098 PMC6331926 · DOI
  52. [56]Pandey V.K. Mathur A. Khan M.F. Kakkar P. Activation of PERK-eIF2α-ATF4 pathway contributes to diabetic hepatotoxicity: Attenuation of ER stress by Morin Cell. Signal. 2019 59 41 52 10.1016/j.cellsig.2019.03.008 30877037 · DOI
  53. [57]Shane-McWhorter L. Biological complementary therapies: A focus on botanical products in diabetes Diabetes Spectr. 2001 14 199 208 10.2337/diaspect.14.4.199 · DOI
  54. [58]Broca C. Gross R. Petit P. Sauvaire Y. Manteghetti M. Tournier M. Masiello P. Gomis R. Ribes G. 4-hydroxyisoleucine: Experimental evidence of its insulinotropic and antidiabetic properties Am. J. Physiol.-Endocrinol. Metab. 1999 277 E617 E623 10.1152/ajpendo.1999.277.4.E617 10516120 · DOI
  55. [59]Sanlier N. Gencer F. Role of spices in the treatment of diabetes mellitus: A minireview Trends Food Sci. Technol. 2020 99 441 449 10.1016/j.tifs.2020.03.018 · DOI
  56. [63]Santos H.O. da Silva G.A.R. To what extent does cinnamon administration improve the glycemic and lipid profiles? Clin. Nutr. ESPEN 2018 27 1 9 10.1016/j.clnesp.2018.07.011 30144878 · DOI
  57. [64]Singh P. Jayaramaiah R.H. Agawane S.B. Vannuruswamy G. Korwar A.M. Anand A. Dhaygude V.S. Shaikh M.L. Joshi R.S. Boppana R. Potential dual role of eugenol in inhibiting advanced glycation end products in diabetes: Proteomic and mechanistic insights Sci. Rep. 2016 6 18798 10.1038/srep18798 26739611 PMC4704049 · DOI
  58. [65]Ali B.H. Blunden G. Tanira M.O. Nemmar A. Some phytochemical, pharmacological and toxicological properties of ginger (Zingiber officinale Roscoe): A review of recent research Food Chem. Toxicol. 2008 46 409 420 10.1016/j.fct.2007.09.085 17950516 · DOI
  59. [66]Ezzat S.M. Ezzat M.I. Okba M.M. Menze E.T. Abdel-Naim A.B. The hidden mechanism beyond ginger (Zingiber officinale Rosc.) potent in vivo and in vitro anti-inflammatory activity J. Ethnopharmacol. 2018 214 113 123 10.1016/j.jep.2017.12.019 29253614 · DOI
  60. [67]Chavan J.J. Kshirsagar P.R. Pai S.R. Pawar N.V. Micropropagation, metabolite profiling, antioxidant activities and chromatographic determination of bioactive molecules across in vitro conditions and subsequent field cultivation stages of ‘Shampoo Ginger’ (Zingiber zerumbet L. Roscoe ex Sm) Biocatal. Agric. Biotechnol. 2018 16 79 89 10.1016/j.bcab.2018.07.015 · DOI
  61. [68]Tran N. Pham B. Le L. Bioactive compounds in anti-diabetic plants: From herbal medicine to modern drug discovery Biology 2020 9 252 10.3390/biology9090252 32872226 PMC7563488 · DOI · Paper page
  62. [69]Huang Y.-C. Lin C.-Y. Huang S.-F. Lin H.-C. Chang W.-L. Chang T.-C. Effect and mechanism of ginsenosides CK and Rg1 on stimulation of glucose uptake in 3T3-L1 adipocytes J. Agric. Food Chem. 2010 58 6039 6047 10.1021/jf9034755 20441170 · DOI
  63. [70]Kim K.-S. Yang H.J. Lee I.-S. Kim K.-H. Park J. Jeong H.-S. Kim Y. Ahn K.S. Na Y.-C. Jang H.-J. The aglycone of ginsenoside Rg3 enables glucagon-like peptide-1 secretion in enteroendocrine cells and alleviates hyperglycemia in type 2 diabetic mice OPEN Sci. Rep. 2015 5 18325 10.1038/srep18325 26675132 PMC4682129 · DOI
  64. [71]Tian W. Chen L. Zhang L. Wang B. Li X. Fan K. Ai C. Xia X. Li S. Li Y. Effects of ginsenoside Rg1 on glucose metabolism and liver injury in streptozotocin-induced type 2 diabetic rats Genet. Mol. Res. 2017 16 16019463 10.4238/gmr16019463 28362999 · DOI
  65. [73]Yuan Q. Xie Y. Wang W. Yan Y. Ye H. Jabbar S. Zeng X. Extraction optimization, characterization and antioxidant activity in vitro of polysaccharides from mulberry (Morus alba L.) leaves Carbohydr. Polym. 2015 128 52 62 10.1016/j.carbpol.2015.04.028 26005139 · DOI
  66. [74]Flaczyk E. Kobus-Cisowska J. Przeor M. Korczak J. Remiszewski M. Korbas E. Buchowski M. Chemical characterization and antioxidative properties of Polish variety of Morus alba L. leaf aqueous extracts from the laboratory and pilot-scale processes Agric. Sci. 2013 4 141 147 10.4236/as.2013.45B026 · DOI
  67. [75]Zhang D.-Y. Wan Y. Hao J.-Y. Hu R.-Z. Chen C. Yao X.-H. Zhao W.-G. Liu Z.-Y. Li L. Evaluation of the alkaloid, polyphenols, and antioxidant contents of various mulberry cultivars from different planting areas in eastern China Ind. Crop. 2018 122 298 307 10.1016/j.indcrop.2018.05.065 · DOI
  68. [76]Cheng K.C. Wang C.J. Chang Y.C. Hung T.W. Lai C.J. Kuo C.W. Huang H.P. Mulberry fruits extracts induce apoptosis and autophagy of liver cancer cell and prevent hepatocarcinogenesis in vivo J. Food Drug Anal. 2020 28 84 93 10.1016/j.jfda.2019.06.002 31883611 PMC13521059 · DOI
  69. [77]Riche D.M. Riche K.D. East H.E. Barrett E.K. May W.L. Impact of mulberry leaf extract on type 2 diabetes (Mul-DM): A randomized, placebo-controlled pilot study Complement. Ther. Med. 2017 32 105 108 10.1016/j.ctim.2017.04.006 28619294 · DOI
  70. [78]Li F. Zhang B. Chen G. Fu X. The novel contributors of anti-diabetic potential in mulberry polyphenols revealed by UHPLC-HR-ESI-TOF-MS/MS Food Res. Int. 2017 100 873 884 10.1016/j.foodres.2017.06.052 28873762 · DOI
  71. [79]Ranjan B. Kumar R. Verma N. Mittal S. Pakrasi P.L. Venkatesh Kumar R. Evaluation of the antidiabetic properties of S-1708 mulberry variety Pharmacogn. Mag. 2017 13 S280 S288 10.4103/pm.pm_490_16 28808393 PMC5538167 · DOI
  72. [80]Gryn-Rynko A. Bazylak G. Olszewska-Slonina D. New potential phytotherapeutics obtained from white mulberry (Morus alba L.) leaves Biomed. Pharmacother. 2016 84 628 636 10.1016/j.biopha.2016.09.081 27694008 · DOI
  73. [81]Harauma A. Murayama T. Ikeyama K. Sano H. Arai H. Takano R. Kita T. Hara S. Kamei K. Yokode M. Mulberry leaf powder prevents atherosclerosis in apolipoprotein E-deficient mice Biochem. Biophys. Res. Commun. 2007 358 751 756 10.1016/j.bbrc.2007.04.170 17506985 · DOI
  74. [82]Rodrigues E.L. Marcelino G. Silva G.T. Figueiredo P.S. Garcez W.S. Corsino J. Guimarães R.D.C.A. Freitas K.D.C. Nutraceutical and medicinal potential of the Morus species in metabolic dysfunctions Int. J. Mol. Sci. 2019 20 301 10.3390/ijms20020301 30646503 PMC6358891 · DOI
  75. [83]Hwang J.Y. Sung W.C. Shyu Y.S. Effect of mulberry lees addition on dough mixing characteristics and the quality of mulberry toast J. Mar. Sci. Technol. 2008 16 103 108 10.51400/2709-6998.2021 · DOI
  76. [84]Wen P. Hu T.-G. Linhardt R.J. Liao S.-T. Wu H. Zou Y.-X. Mulberry: A review of bioactive compounds and advanced processing technology Trends Food Sci. Technol. 2019 83 138 158 10.1016/j.tifs.2018.11.017 · DOI
  77. [87]Adisakwattana S. Ruengsamran T. Kampa P. Sompong W. In vitro inhibitory effects of plant-based foods and their combinations on intestinal α-glucosidase and pancreatic α-amylase BMC Complement. Altern. Med. 2012 12 110 10.1186/1472-6882-12-110 22849553 PMC3522002 · DOI
  78. [88]Lim H.H. Yang S.J. Kim Y. Lee M. Lim Y. Combined treatment of mulberry leaf and fruit extract ameliorates obesity-related inflammation and oxidative stress in high fat diet-induced obese mice J. Med. Food 2013 16 673 680 10.1089/jmf.2012.2582 23957352 PMC3751316 · DOI
  79. [89]Mahboubi M. Morus alba (mulberry), a natural potent compound in management of obesity Pharmacol. Res. 2019 146 104341 10.1016/j.phrs.2019.104341 31276774 · DOI
  80. [90]Peng C.H. Liu L.K. Chuang C.M. Chyau C.C. Huang C.N. Wang C.J. Mulberry water extracts possess an anti-obesity effect and ability to inhibit hepatic lipogenesis and promote lipolysis J. Agric. Food Chem. 2011 59 2663 2671 10.1021/jf1043508 21361295 · DOI
  81. [91]Tond S.B. Fallah S. Salemi Z. Seifi M. Influence of mulberry leaf extract on serum adiponectin, visfatin and lipid profile levels in type 2 diabetic rats Brazilian Arch. Biol. Technol. 2016 59 16160297 10.1590/1678-4324-2016160297 · DOI
  82. [92]Ann J.Y. Eo H. Lim Y. Mulberry leaves (Morus alba L.) ameliorate obesity-induced hepatic lipogenesis, fibrosis, and oxidative stress in high-fat diet-fed mice Genes Nutr. 2015 10 46 10.1007/s12263-015-0495-x 26463593 PMC4604156 · DOI
  83. [93]Liu L.K. Lee H.J. Shih Y.W. Chyau C.C. Wang C.J. Mulberry anthocyanin extracts inhibit LDL oxidation and macrophage-derived foam cell formation induced by oxidative LDL J. Food Sci. 2008 73 H113 H121 10.1111/j.1750-3841.2008.00801.x 19241587 · DOI · Paper page
  84. [94]Katsube T. Yamasaki M. Shiwaku K. Ishijima T. Matsumoto I. Abe K. Yamasaki Y. Effect of flavonol glycoside in mulberry (Morus alba L.) leaf on glucose metabolism and oxidative stress in liver in diet-induced obese mice J. Sci. Food Agric. 2010 90 2386 2392 10.1002/jsfa.4096 20648552 · DOI
  85. [95]Metwally F.M. Ahmed H.H. Rashad H. Zaazaa A.M. Insights into the role of Morus alba in reversing obesity-associated hepatic steatosis and related metabolic disorder in rats Asian J. Pharm. Clin. Res. 2016 9 231 238 10.22159/ajpcr.2016.v9s2.13674 · DOI
  86. [96]Ren C. Zhang Y. Cui W. Lu G. Wang Y. Gao H. Huang L. Mu Z. A polysaccharide extract of mulberry leaf ameliorates hepatic glucose metabolism and insulin signaling in rats with type 2 diabetes induced by high fat-diet and streptozotocin Int. J. Biol. Macromol. 2015 72 951 959 10.1016/j.ijbiomac.2014.09.060 25316427 · DOI
  87. [97]Cai S. Sun W. Fan Y. Guo X. Xu G. Xu T. Hou Y. Zhao B. Feng X. Liu T. Effect of mulberry leaf (Folium Mori) on insulin resistance via IRS-1/PI3K/Glut-4 signalling pathway in type 2 diabetes mellitus rats Pharm. Biol. 2016 54 2685 2691 10.1080/13880209.2016.1178779 27158744 · DOI
  88. [98]Sudha P. Zinjarde S.S. Bhargava S.Y. Kumar A.R. Potent a-amylase inhibitory activity of Indian Ayurvedic medicinal plants BMC Complement. Altern. Med. 2011 11 5 10.1186/1472-6882-11-5 21251279 PMC3037352 · DOI
  89. [99]Kimura T. Nakagawa K. Kubota H. Kojima Y. Goto Y. Yamgishi K. Oita S. Oikawa S. Miyazawa T. Food-grade mulberry powder enriched with 1-deoxynojirimycin suppresses the elevation of postprandial blood glucose in humans J. Agric. Food Chem. 2007 55 5869 5874 10.1021/jf062680g 17555327 · DOI
  90. [100]Hansawasdi C. Kawabata J. α-Glucosidase inhibitory effect of mulberry (Morus alba) leaves on Caco-2 Fitoterapia 2006 77 568 573 10.1016/j.fitote.2006.09.003 17071014 · DOI
  91. [101]Jiao Y. Wang X. Jiang X. Kong F. Wang S. Yan C. Antidiabetic effects of Morus alba fruit polysaccharides on high-fat diet- and streptozotocin-induced type 2 diabetes in rats J. Ethnopharmacol. 2017 199 119 127 10.1016/j.jep.2017.02.003 28163112 · DOI
  92. [102]Hu T.G. Wen P. Liu J. Long X.S. Liao S.T. Wu H. Zou Y.X. Combination of mulberry leaf and oat bran possessed greater hypoglycemic effect on diabetic mice than mulberry leaf or oat bran alone J. Funct. Foods 2019 61 103503 10.1016/j.jff.2019.103503 · DOI
  93. [103]Li Y. Zhang X. Liang C. Hu J. Yu Z. Safety evaluation of mulberry leaf extract: Acute, subacute toxicity and genotoxicity studies Regul. Toxicol. Pharmacol. 2018 95 220 226 10.1016/j.yrtph.2018.03.007 29530616 · DOI
  94. [105]Wani S.A. Kumar P. Fenugreek: A review on its nutraceutical properties and utilization in various food products J. Saudi Soc. Agric. Sci. 2018 17 97 106 10.1016/j.jssas.2016.01.007 · DOI
  95. [106]Ahmad A. Alghamdi S.S. Mahmood K. Afzal M. Fenugreek a multipurpose crop: Potentialities and improvements Saudi J. Biol. Sci. 2016 23 300 310 10.1016/j.sjbs.2015.09.015 27307778 PMC4894452 · DOI
  96. [107]El Nasri N.A. El Tinay A.H. Functional properties of fenugreek (Trigonella foenum graecum) protein concentrate Food Chem. 2007 103 582 589 10.1016/j.foodchem.2006.09.003 · DOI
  97. [109]He Y. Ding C. Wang X. Wang H. Suo Y. Using response surface methodology to optimize countercurrent chromatographic separation of polyphenol compounds from fenugreek (Trigonella foenum-graecum L.) seeds J. Liq. Chromatogr. Relat. Technol. 2015 38 29 35 10.1080/10826076.2013.864981 · DOI
  98. [110]Gaur V. Bodhankar S.L. Mohan V. Thakurdesai P.A. Neurobehavioral assessment of hydroalcoholic extract of Trigonella foenum-graecum seeds in rodent models of Parkinson’s disease Pharm. Biol. 2013 51 550 557 10.3109/13880209.2012.747547 23368940 · DOI
  99. [112]Kumar P. Bhandari U. Jamadagni S. Fenugreek seed extract inhibit fat accumulation and ameliorates dyslipidemia in high fat diet-induced obese rats Biomed. Res. Int. 2014 2014 606021 10.1155/2014/606021 24868532 PMC4020548 · DOI
  100. [113]Kaviarasan S. Naik G.H. Gangabhagirathi R. Anuradha C.V. Priyadarsini K.I. In vitro studies on antiradical and antioxidant activities of fenugreek (Trigonella foenum graecum) seeds Food Chem. 2007 103 31 37 10.1016/j.foodchem.2006.05.064 · DOI
  101. [115]Rao M.U. Sreenivasulu M. Chengaiah B. Reddy K.J. Chetty C.M. Herbal medicines for diabetes mellitus: A review Int. J. PharmTech Res. 2010 2 1883 1892
  102. [117]Arivalagan M. Gangopadhyay K.K. Kumar G. Determination of steroidal saponins and fixed oil content in fenugreek (Trigonella foenum-graecum) genotypes Indian J. Pharm. Sci. 2013 75 110 113 10.4103/0250-474X.113542 23901171 PMC3719140 · DOI
  103. [118]Eidi A. Eidi M. Sokhteh M. Effect of fenugreek (Trigonella foenum-graecum L) seeds on serum parameters in normal and streptozotocin-induced diabetic rats Nutr. Res. 2007 27 728 733 10.1016/j.nutres.2007.09.006 · DOI
  104. [119]Verma N. Usman K. Patel N. Jain A. Dhakre S. Swaroop A. Bagchi M. Kumar P. Preuss H.G. Bagchi D. A multicenter clinical study to determine the efficacy of a novel fenugreek seed (Trigonella foenum-graecum) extract (FenfuroTM) in patients with type 2 diabetes Food Nutr. Res. 2016 60 32382 10.3402/fnr.v60.32382 27733237 PMC5061863 · DOI
  105. [120]Singh A. Rai J. Mahajan D.S. Comparative evaluation of glipizide and fenugreek (Trigonella foenum-graecum) seeds as monotherapy and combination therapy on glycaemic control and lipid profile in patients with type 2 diabetes mellitus Int. J. Basic Clin. Pharmacol. 2016 3 942 950 10.18203/2319-2003.ijbcp20161549 · DOI
  106. [121]Fæste C.K. Namork E. Lindvik H. Allergenicity and antigenicity of fenugreek (Trigonella foenum-graecum) proteins in foods J. Allergy Clin. Immunol. 2009 123 187 194 10.1016/j.jaci.2008.09.012 18930518 · DOI
  107. [122]Ouzir M. El Bairi K. Amzazi S. Toxicological properties of fenugreek (Trigonella foenum graecum) Food Chem. Toxicol. 2016 96 145 154 10.1016/j.fct.2016.08.003 27498339 · DOI
  108. [123]Momtaz S. Hassani S. Khan F. Ziaee M. Abdollahi M. Cinnamon, a promising prospect towards Alzheimer’s disease Pharmacol. Res. 2018 130 241 258 10.1016/j.phrs.2017.12.011 29258915 · DOI
  109. [124]Tapsell L.C. Hemphill I. Cobiac L. Patch C.S. Sullivan D.R. Fenech M. Roodenrys S. Keogh J.B. Clifton P.M. Williams P.G. Health benefits of herbs and spices: The past, the present, the future Med. J. Aust. 2006 185 1 24 10.5694/j.1326-5377.2006.tb00548.x 17022438 · DOI
  110. [125]Vasconcelos N.G. Croda J. Simionatto S. Antibacterial mechanisms of cinnamon and its constituents: A review Microb. Pathog. 2018 120 198 203 10.1016/j.micpath.2018.04.036 29702210 · DOI
  111. [126]Chanotiya C.S. Yadav A. Enantioenriched (3s)-(+)-linalool in the leaf oil of cinnamomum tamala nees et eberm. From Kumaon J. Essent. Oil Res. 2010 22 593 596 10.1080/10412905.2010.9700407 · DOI
  112. [127]Wang Y. Zhang Y. Shi Y. Pan X. Lu Y. Cao P. Antibacterial effects of cinnamon (Cinnamomum zeylanicum) bark essential oil on Porphyromonas gingivalis Microb. Pathog. 2018 116 26 32 10.1016/j.micpath.2018.01.009 29325862 · DOI
  113. [128]Lu M. Yuan B. Zeng M. Chen J. Antioxidant capacity and major phenolic compounds of spices commonly consumed in China Food Res. Int. 2011 44 530 536 10.1016/j.foodres.2010.10.055 · DOI
  114. [129]Sharafeldin K. Rizvi M.R. Effect of traditional plant medicines (Cinnamomum zeylanicum and Syzygium cumini) on oxidative stress and insulin resistance in streptozotocin-induced diabetic rats J. Basic Appl. Zool. 2015 72 126 134 10.1016/j.jobaz.2015.09.002 · DOI
  115. [130]Mirfeizi M. Mehdizadeh Tourzani Z. Mirfeizi S.Z. Asghari Jafarabadi M. Rezvani H.R. Afzali M. Controlling type 2 diabetes mellitus with herbal medicines: A triple-blind randomized clinical trial of efficacy and safety J. Diabetes 2016 8 647 656 10.1111/1753-0407.12342 26362826 · DOI
  116. [131]Vafa M. Mohammadi F. Shidfar F. Sormaghi M.S. Heidari I. Golestan B. Amiri F. Effects of cinnamon consumption on glycemic status, lipid profile and body composition in type 2 diabetic patients Int. J. Prev. Med. 2012 3 531 536 22973482 PMC3429799
  117. [132]Unlu M. Ergene E. Unlu G.V. Zeytinoglu H.S. Vural N. Composition, antimicrobial activity and in vitro cytotoxicity of essential oil from Cinnamomum zeylanicum Blume (Lauraceae) Food Chem. Toxicol. 2010 48 3274 3280 10.1016/j.fct.2010.09.001 20828600 · DOI
  118. [133]Qadir M.M.F. Bhatti A. Ashraf M.U. Sandhu M.A. Anjum S. John P. Immunomodulatory and therapeutic role of Cinnamomum verum extracts in collagen-induced arthritic BALB/c mice Inflammopharmacology 2018 26 157 170 10.1007/s10787-017-0349-9 28429097 · DOI
  119. [134]Kamath J.V. Rana A.C. Roy Chowdhury A. Pro-healing effect of Cinnamomum zeylanicum bark Phyther. Res. 2003 17 970 972 10.1002/ptr.1293 13680838 · DOI
  120. [135]Jamali N. Jalali M. Saffari-Chaleshtori J. Samare-Najaf M. Samareh A. Effect of cinnamon supplementation on blood pressure and anthropometric parameters in patients with type 2 diabetes: A systematic review and meta-analysis of clinical trials Diabetes Metab. Syndr. Clin. Res. Rev. 2020 14 119 125 10.1016/j.dsx.2020.01.009 32032898 · DOI
  121. [137]An K. Zhao D. Wang Z. Wu J. Xu Y. Xiao G. Comparison of different drying methods on Chinese ginger (Zingiber officinale Roscoe): Changes in volatiles, chemical profile, antioxidant properties, and microstructure Food Chem. 2016 197 1292 1300 10.1016/j.foodchem.2015.11.033 26675871 · DOI
  122. [139]Shanmugam K.R. Mallikarjuna K. Nishanth K. Kuo C.H. Reddy K.S. Protective effect of dietary ginger on antioxidant enzymes and oxidative damage in experimental diabetic rat tissues Food Chem. 2011 124 1436 1442 10.1016/j.foodchem.2010.07.104 · DOI
  123. [140]Young H.Y. Luo Y.L. Cheng H.Y. Hsieh W.C. Liao J.C. Peng W.H. Analgesic and anti-inflammatory activities of [6]-gingerol J. Ethnopharmacol. 2005 96 207 210 10.1016/j.jep.2004.09.009 15588672 · DOI
  124. [141]Elshater A.-E.A. Salman M.M.A. Moussa M.M.A. Effect of Ginger Extract Consumption on levels of blood Glucose, Lipid Profile and Kidney Functions in Alloxan Induced-Diabetic Rats Egypt. Acad. J. Biol. Sci 2009 2 153 162 10.21608/eajbsa.2009.15515 · DOI
  125. [143]Bhandari U. Sharma J.N. Zafar R. The protective action of ethanolic ginger (Zingiber officinale) extract in cholesterol fed rabbits J. Ethnopharmacol. 1998 61 167 171 10.1016/S0378-8741(98)00026-9 9683348 · DOI
  126. [144]Funk J.L. Frye J.B. Oyarzo J.N. Chen J. Zhang H. Timmermann B.N. Anti-inflammatory effects of the essential oils of ginger (Zingiber officinale Roscoe) in experimental rheumatoid arthritis PharmaNutrition 2016 4 123 131 10.1016/j.phanu.2016.02.004 27872812 PMC5115784 · DOI
  127. [145]Jafarzadeh A. Nemati M. Therapeutic potentials of ginger for treatment of Multiple sclerosis: A review with emphasis on its immunomodulatory, anti-inflammatory and anti-oxidative properties J. Neuroimmunol. 2018 324 54 75 10.1016/j.jneuroim.2018.09.003 30243185 · DOI · Paper page
  128. [146]Haksar A. Sharma A. Chawla R. Kumar R. Arora R. Singh S. Prasad J. Gupta M. Tripathi R.P. Arora M.P. Zingiber officinale exhibits behavioral radioprotection against radiation-induced CTA in a gender-specific manner Pharmacol. Biochem. Behav. 2006 84 179 188 10.1016/j.pbb.2006.04.008 16797061 · DOI
  129. [147]Ryan J.L. Morrow G.R. Ginger Oncol. Nurse Ed. 2010 24 46 27595143 PMC5008850
  130. [148]Akhani S.P. Vishwakarma S.L. Goyal R.K. Anti-diabetic activity of Zingiber officinale in streptozotocin-induced type I diabetic rats J. Pharm. Pharmacol. 2004 56 101 105 10.1211/0022357022403 14980006 · DOI
  131. [149]Abdulrazaq N.B. Cho M. Win N.N. Zaman R. Rahman M.T. Beneficial effects of ginger (Zingiber officinale) on carbohydrate metabolism in streptozotocin-induced diabetic rats Br. J. Nutr. 2012 108 1194 1201 10.1017/S0007114511006635 22152092 · DOI
  132. [150]Ramudu S.K. Korivi M. Kesireddy N. Lee L.-C. Cheng I.-S. Kuo C.-H. Kesireddy S.R. Nephro-protective effects of a ginger extract on cytosolic and mitochondrial enzymes against streptozotocin (STZ)-induced diabetic complications in rats Chin. J. Physiol. 2011 54 79 86 10.4077/CJP.2011.AMM006 21789888 · DOI
  133. [151]Akash M.S.H. Rehman K. Tariq M. Chen S. Zingiber officinale and type 2 diabetes mellitus: Evidence from experimental studies Crit. Rev. Eukaryot. Gene Expr. 2015 25 91 112 10.1615/CritRevEukaryotGeneExpr.2015013358 26080605 · DOI
  134. [152]Rani M.P. Krishna M.S. Padmakumari K.P. Raghu K.G. Sundaresan A. Zingiber officinale extract exhibits antidiabetic potential via modulating glucose uptake, protein glycation and inhibiting adipocyte differentiation: An in vitro study J. Sci. Food Agric. 2012 92 1948 1955 10.1002/jsfa.5567 22261727 · DOI
  135. [153]Li Y. Tran V.H. Duke C.C. Roufogalis B.D. Gingerols of Zingiber officinale enhance glucose uptake by increasing cell surface GLUT4 in cultured L6 myotubes Planta Med. 2012 78 1549 1555 10.1055/s-0032-1315041 22828920 · DOI
  136. [154]El Gayar M.H. Aboromia M.M.M. Ibrahim N.A. Abdel Hafiz M.H. Effects of ginger powder supplementation on glycemic status and lipid profile in newly diagnosed obese patients with type 2 diabetes mellitus Obes. Med. 2019 14 100094 10.1016/j.obmed.2019.100094 · DOI
  137. [155]Khandouzi N. Shidfar F. Rajab A. Rahideh T. Hosseini P. Taheri M.M. The effects of Ginger on fasting blood sugar, hemoglobin A1c, apolipoprotein B, apolipoprotein A-I and malondialdehyde in type 2 diabetic patients Iran. J. Pharm. Res. 2015 14 131 140 PMC4277626 25561919
  138. [156]Shidfar F. Rajab A. Rahideh T. Khandouzi N. Hosseini S. Shidfar S. The effect of ginger (Zingiber officinale) on glycemic markers in patients with type 2 diabetes J. Complement. Integr. Med. 2015 12 165 170 10.1515/jcim-2014-0021 25719344 · DOI
  139. [157]Mahluji S. Attari V.E. Mobasseri M. Payahoo L. Ostadrahimi A. Golzari S.E. Effects of ginger (Zingiber officinale) on plasma glucose level, HbA1c and insulin sensitivity in type 2 diabetic patients Int. J. Food Sci. Nutr. 2013 64 682 686 10.3109/09637486.2013.775223 23496212 · DOI · Paper page
  140. [158]Li Y. Tran V.H. Duke C.C. Roufogalis B.D. Preventive and protective properties of Zingiber officinale (Ginger) in diabetes mellitus, diabetic complications, and associated lipid and other metabolic disorders: A brief review Evid.-Based Complement. Altern. Med. 2012 2012 516870 10.1155/2012/516870 PMC3519348 23243452 · DOI
  141. [159]Popowski D. Pawłowska K.A. Deipenbrock M. Hensel A. Kruk A. Melzig M.F. Piwowarski J.P. Granica S. Antiadhesive activity of hydroethanolic extract from bean pods of Phaseolus vulgaris (common bean) against uropathogenic E. coli and permeability of its constituents through Caco-2 cells monolayer J. Ethnopharmacol. 2021 274 114053 10.1016/j.jep.2021.114053 33746003 · DOI
  142. [160]Madrera R.R. Negrillo A.C. Valles B.S. Fernández J.J.F. Phenolic content and antioxidant activity in seeds of common bean (Phaseolus vulgaris L.) Foods 2021 10 864 10.3390/foods10040864 33921060 PMC8071416 · DOI
  143. [161]Bljajić K. Brajković A. Čačić A. Vujić L. Jablan J. Carvalho I.S.D. Končić M.Z. Chemical composition, antioxidant, and α-glucosidase-inhibiting activity of aqueous and hydroethanolic extracts of traditional antidiabetics from Croatian ethnomedicine Horticulturae 2021 7 15 10.3390/horticulturae7020015 · DOI
  144. [162]Damián-Medina K. Salinas-Moreno Y. Milenkovic D. Figueroa-Yáñez L. Marino-Marmolejo E. Higuera-Ciapara I. Vallejo-Cardona A. Lugo-Cervantes E. In silico analysis of antidiabetic potential of phenolic compounds from blue corn (Zea mays L.) and black bean (Phaseolus vulgaris L.) Heliyon 2020 6 e03632 10.1016/j.heliyon.2020.e03632 32258479 PMC7110303 · DOI
  145. [163]Lomas-Soria C. Pérez-Ramírez I.F. Caballero-Pérez J. Guevara-Gonzalez R.G. Guevara-Olvera L. Loarca-Piña G. Guzman-Maldonado H.S. Reynoso-Camacho R. Cooked common beans (Phaseolus vulgaris L.) modulate renal genes in streptozotocin-induced diabetic rats J. Nutr. Biochem. 2015 26 761 768 10.1016/j.jnutbio.2015.02.006 25863648 · DOI
  146. [164]Halenova T. Raksha N. Kravchenko O. Vovk T. Yurchenko A. Vareniuk I. Savchuk O. Ostapchenko L. Hypoglycemic activity of Phaseolus vulgaris (L.) aqueous extract in type 1 diabetic rats Curr. Issues Pharm. Med. Sci. 2019 32 210 218 10.2478/cipms-2019-0036 · DOI
  147. [165]Almuaigel M.F. Seif M.A. Albuali H.W. Alharbi O. Alhawash A. Hypoglycemic and hypolipidemic effects of aqueous extract of Phaseolus vulgaris pods in streptozotocin-diabetic rats Biomed. Pharmacother. 2017 94 742 746 10.1016/j.biopha.2017.07.135 28800543 · DOI
  148. [166]Ocho-Anin Atchibri A.L. Brou K.D. Kouakou T.H. Kouadio Y.J. Gnakri D. Screening for antidiabetic activity and phytochemical constituents of common bean (Phaseolus vulgaris L.) seeds J. Med. Plants Res. 2010 4 1757 1761 10.5897/JMPR10.280 · DOI
  149. [167]Shi Z. Zhang X. Zhu Y. Yao Y. Ren G. Natural extracts from white common bean (Phaseolus vulgaris L.) inhibit 3T3-L1 adipocytes differentiation Appl. Sci. 2020 11 167 10.3390/app11010167 · DOI
  150. [170]Park H.J. Kim D.H. Park S.J. Kim J.M. Ryu J.H. Ginseng in traditional herbal prescriptions J. Ginseng Res. 2012 36 225 241 10.5142/jgr.2012.36.3.225 23717123 PMC3659587 · DOI
  151. [171]Lee J.H. Kim S.C. Lee H.Y. Cho D.Y. Jung J.G. Kang D. Kang S.S. Cho K.M. Changes in nutritional compositions of processed mountain-cultivated ginseng sprouts (Panax ginseng) and screening for their antioxidant and anti-inflammatory properties J. Funct. Foods 2021 86 104668 10.1016/j.jff.2021.104668 · DOI
  152. [172]Guo N. Yang Y. Yang X. Guan Y. Yang J. Quan J. Yan H. Hou W. Zhang G. Growth age of mountain cultivated ginseng affects its chemical composition Ind. Crops Prod. 2021 167 113531 10.1016/j.indcrop.2021.113531 · DOI
  153. [173]Qi H. Zhang Z. Liu J. Chen Z. Huang Q. Li J. Chen J. Wang M. Zhao D. Wang Z. Comparisons of isolation methods, structural features, and bioactivities of the polysaccharides from three common Panax species: A review of recent progress Molecules 2021 26 4997 10.3390/molecules26164997 34443587 PMC8400370 · DOI
  154. [174]Liu L. Xu F.R. Wang Y.Z. Traditional uses, chemical diversity and biological activities of Panax L. (Araliaceae): A review J. Ethnopharmacol. 2020 263 112792 10.1016/j.jep.2020.112792 32311488 · DOI
  155. [175]Szczuka D. Nowak A. Zakłos-Szyda M. Kochan E. Szymańska G. Motyl I. Blasiak J. American ginseng (Panax quinquefolium L.) as a source of bioactive phytochemicals with pro-health properties Nutrients 2019 11 1041 10.3390/nu11051041 PMC6567205 31075951 · DOI
  156. [176]Fan S. Zhang Z. Su H. Xu P. Qi H. Zhao D. Li X. Panax ginseng clinical trials: Current status and future perspectives Biomed. Pharmacother. 2020 132 110832 10.1016/j.biopha.2020.110832 33059260 · DOI
  157. [177]Dzimitrowicz A. Cyganowski P. Pohl P. Milkowska W. Jermakowicz-Bartkowiak D. Jamroz P. Plant extracts activated by cold atmospheric pressure plasmas as suitable tools for synthesis of gold nanostructures with catalytic uses Nanomaterials 2020 10 1088 10.3390/nano10061088 32492774 PMC7353295 · DOI
  158. [178]Panossian A. Abdelfatah S. Efferth T. Network pharmacology of ginseng (Part II): The differential effects of red ginseng and ginsenoside Rg5 in cancer and heart diseases as determined by transcriptomics Pharmaceuticals 2021 14 1010 10.3390/ph14101010 34681234 PMC8540751 · DOI
  159. [179]Chou C.-K. Huang Y.-S. Lin P.-Y. Imai K. Chen S.-M. Lee J.-A. The ginsenoside Rg1 rescues mitochondrial disorders in aristolochic acid-induced nephropathic mice Life 2021 11 1018 10.3390/life11101018 34685389 PMC8539135 · DOI
  160. [180]Kim H.J. Park K.H. Kim D.H. Chae H.J. Sung G.H. Kim Y.O. In vitro assessments of bone microcomputed tomography in an aged male rat model supplemented with Panax ginseng Saudi J. Biol. Sci. 2018 25 1135 1139 10.1016/j.sjbs.2018.04.006 30174513 PMC6117371 · DOI
  161. [181]Hwang J.H. Park S.H. Choi E.K. Jung S.J. Pyo M.K. Chae S.W. A randomized, double-blind, placebo-controlled pilot study to assess the effects of protopanaxadiol saponin–enriched ginseng extract and pectinase-processed ginseng extract on the prevention of acute respiratory illness in healthy people J. Ginseng Res. 2020 44 697 703 10.1016/j.jgr.2019.01.002 32913399 PMC7471208 · DOI
  162. [182]Lee S.T. Chu K. Sim J.Y. Heo J.H. Kim M. Panax ginseng enhances cognitive performance in Alzheimer disease Alzheimer Dis. Assoc. Disord. 2008 22 222 226 10.1097/WAD.0b013e31816c92e6 18580589 · DOI
  163. [183]Cui Y. Shu X.-O. Gao Y.-T. Cai H. Tao M.-H. Zheng W. Association of ginseng use with survival and quality of life among breast cancer patients Am. J. Epidemiol. 2006 163 645 653 10.1093/aje/kwj087 16484447 · DOI
  164. [184]Jung S.J. Hwang J.H. Park S.H. Choi E.K. Ha K.C. Baek H.I. Shin D.G. Seo J.H. Chae S.W. A 12-week, randomized, double-blind study to evaluate the efficacy and safety of liver function after using fermented ginseng powder (GBCK25) Food Nutr. Res. 2020 64 10.29219/fnr.v64.3517 PMC7217291 32425736 · DOI
  165. [185]Kochan E. Nowak A. Zakłos-Szyda M. Szczuka D. Szymańska G. Motyl I. Panax quinquefolium L. ginsenosides from hairy root cultures and their clones exert cytotoxic, genotoxic and pro-apoptotic activity towards human colon adenocarcinoma cell line Caco-2 Molecules 2020 25 2262 10.3390/molecules25092262 PMC7249024 32403328 · DOI
  166. [186]Tardy A.L. De Fer B.B. Cañigueral S. Kennedy D. Scholey A. Hitier S. Aran A. Pouteau E. Reduced self-perception of fatigue after intake of Panax ginseng root extract (G115®) formulated with vitamins and minerals—an open-label study Int. J. Environ. Res. Public Health 2021 18 6257 10.3390/ijerph18126257 34207838 PMC8296094 · DOI
  167. [187]Yoon J.W. Kang S.M. Vassy J.L. Shin H. Lee Y.H. Ahn H.Y. Choi S.H. Park K.S. Jang H.C. Lim S. Efficacy and safety of ginsam, a vinegar extract from Panax ginseng, in type 2 diabetic patients: Results of a double-blind, placebo-controlled study J. Diabetes Investig. 2012 3 309 317 10.1111/j.2040-1124.2011.00185.x PMC4014955 24843582 · DOI
  168. [188]Park S.H. Oh M.R. Choi E.K. Kim M.G. Ha K.C. Lee S.K. Kim Y.G. Park B.H. Kim D.S. Soo-Wan C. An 8-wk, randomized, double-blind, placebo-controlled clinical trial for the antidiabetic effects of hydrolyzed ginseng extract J. Ginseng Res. 2014 38 239 243 10.1016/j.jgr.2014.05.006 25379002 PMC4213818 · DOI
  169. [189]Oh M.-R. Park S.-H. Kim S.-Y. Back H.-I. Kim M.-G. Jeon J.-Y. Ha K.-C. Na W.-T. Cha Y.-S. Park B.-H. Postprandial glucose-lowering effects of fermented red ginseng in subjects with impaired fasting glucose or type 2 diabetes: A randomized, double-blind, placebo-controlled clinical trial BMC Complement. Altern. Med. 2014 14 237 10.1186/1472-6882-14-237 25015735 PMC4227112 · DOI
  170. [190]Hye Cho Y. Cheol Ahn S. Yeoup Lee S. Wook Jeong D. Jung Choi E. Jin Kim Y. Gyu Lee J. Lee Y.-H. Shin OMD B.-C. Effect of Korean red ginseng on insulin sensitivity in non-diabetic healthy overweight and obese adults Asia Pac. J. Clin. Nutr. 2013 22 365 371 10.6133/apjcn.2013.22.3.04 23945406 · DOI
  171. [191]Kwon D.H. Bose S. Song M.Y. Lee M.J. Lim C.Y. Kwon B.S. Kim H.J. Efficacy of Korean red ginseng by single nucleotide polymorphism in obese women: Randomized, double-blind, placebo-controlled trial J. Ginseng Res. 2012 36 176 10.5142/jgr.2012.36.2.176 23717118 PMC3659576 · DOI
  172. [192]Zhu J. Chen H. Song Z. Wang X. Sun Z. Effects of ginger (Zingiber officinale Roscoe) on type 2 diabetes mellitus and components of the metabolic syndrome: A systematic review and meta-analysis of randomized controlled trials Evid.-Based Complement. Altern. Med. 2018 2018 5692962 10.1155/2018/5692962 PMC5818945 29541142 · DOI
  173. [193]Jeon W.J. Oh J.S. Park M.S. Ji G.E. Anti-hyperglycemic effect of fermented ginseng in type 2 diabetes mellitus mouse model Phyther. Res. 2013 27 166 172 10.1002/ptr.4706 22511336 · DOI
  174. [194]Kim S.T. Kim H.B. Lee K.H. Choi Y.R. Kim H.J. Shin I.S. Gyoung Y.S. Joo S.S. Steam-dried ginseng berry fermented with Lactobacillus plantarum controls the increase of blood glucose and body weight in type 2 obese diabetic db/db mice J. Agric. Food Chem. 2012 60 5438 5445 10.1021/jf300460g 22563735 · DOI
  175. [195]Raposo A. Saraiva A. Ramos F. Carrascosa C. Raheem D. Bárbara R. Silva H. The role of food supplementation in microcirculation—A comprehensive review Biology 2021 10 616 10.3390/biology10070616 34356471 PMC8301032 · DOI

Cited by

Sorted by citations

Authors
Przeor, M.
Affiliations
Poznań University of Life Sciences (PL)
Corresponding author
Przeor, Monika
Venue
Pharmaceuticals
Publisher
MDPI AG
Published
2022-01-04
Volume
15
Issue
1
Pages
65
ISSN
1424-8247 (ISSN-L)
OpenAlex
W4206815251
Cited by
93
References
4
Citations by year
2026: 14 · 2025: 24 · 2024: 26 · 2023: 18 · 2022: 11
FWCI
2.81
Type
journal article
Language
en
Open access
Locations
  • Pharmaceuticals (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • CeON Repository (Centre for Evaluation in Education and Science) (submittedVersion, other-oa)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
Polish Ministry of Science and Higher Education (005/RID/2018/19)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Natural Antidiabetic Agents Studies
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Medicinal Plant Research
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Ethnobotanical and Medicinal Plants Studies
Keywords
medicinal plants, antidiabetic activity, hypoglycemic activity, diabetes mellitus, Morus alba, Cinnamomum zeylanicum, fenugreek, Phaseolus vulgaris, ginger, Panax ginseng, antioxidant activity, bioactive compounds, medicinal plant raw materials

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