Cited by 11Medicinal Plant ResearchPhytochemistry and Biological ActivitiesPhytochemistry Medicinal Plant Applications

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Bridelia speciosa Müll.Arg. Stem bark Extracts as a Potential Biomedicine: From Tropical Western Africa to the Pharmacy Shelf

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Abstract

Bridelia species have been used in traditional African medicine for the management of diverse human ailments. In the current work, the detailed phytochemical profiles of the extracts of the stem bark of B. speciosa were evaluated and the antioxidant and enzyme inhibitory properties of the extracts were assessed. The anti-bacterial and anti-mycotic effects of the extracts were evaluated against selected pathogen strains. Additionally, the anti-proliferative effects were studied on the liver cancer HepG2 cell line. Finally, the putative protective effects were assessed on isolated rat liver that was challenged with lipopolysaccharide (LPS). The results revealed the presence of 36 compounds in the ethyl acetate extract, 44 in the methanol extract, and 38 in the water extract. Overall, the methanol extract showed the highest antioxidant activity, particularly in LPS-stimulated rat liver. Additionally, this extract exerted the highest antimycotic effect on C. albicans, whereas the water extract showed a promising anti-proliferative effect on liver cancer HepG2 cells. The methanol extract was also the most active as enzyme inhibitor, against acetylcholinesterase and butyrylcholinesterase. The current study appraises the antioxidant and enzyme inhibition properties of B. speciosa methanol extract and showed that this specie could be a promising source of biologically active phytochemicals, with potential health uses.

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  • The FRAP assay is a well-known, reliable approach that measures ferric reducing ability in a redox-linked colorimetric reaction that reduces Fe3+ to Fe2+.

    “The FRAP assay is a well-known, reliable approach that measures ferric reducing ability in a redox-linked colorimetric reaction that reduces Fe3+ to Fe2+ [78–81].”

    From Comparative and Correlational Evaluation of the Phytochemical Constituents and Antioxidant Activity of Musa sinensis L. and Musa paradisiaca L. Fruit Compartments (Musaceae) (2020) · cites this paper as [80]

    The Results and Discussion section calls FRAP a common in vitro method for measuring reducing power and says it assesses reduction of ferric iron (Fe3+) to ferrous iron (Fe2+). It does not specifically describe the reaction as colorimetric or establish that the assay is reliable. (LLM, conf=0.84)

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Research works printed but not linked: 56

  1. Kebebew, 2017, Diversity, Knowledge and Use of Traditional Medicinal Plants in Guduru District, Horo Guduru Wollega Zone, Oromia Region of Ethiopia, J. Med. Plants Stud., 364, 364
  2. Ahmad Khan, M.S., Ahmad, I., and Chattopadhyay, D. (2019). Chapter 1-Herbal Medicine: Current Trends and Future Prospects. New Look to Phytomedicine, Academic Press. · DOI
  3. Feng, 2013, Valorization of bark for chemicals and materials: A review, Renew. Sustain. Energy Rev., 26, 560, 10.1016/j.rser.2013.06.024 · DOI
  4. Tanase, C., Coșarcă, S., and Muntean, D.-L. (2019). A Critical Review of Phenolic Compounds Extracted from the Bark of Woody Vascular Plants and Their Potential Biological Activity. Molecules, 24. · DOI
  5. Ferrante, 2019, Protective effects induced by alcoholic Phlomis fruticosa and Phlomis herba-venti extracts in isolated rat colon: Focus on antioxidant, anti-inflammatory, and antimicrobial activities in vitro, Phytother. Res., 33, 2387, 10.1002/ptr.6429 · DOI
  6. Orlando, G., Ferrante, C., Zengin, G., Sinan, K.I., Bene, K., Diuzheva, A., Jekő, J., Cziáky, Z., Di Simone, S., and Recinella, L. (2019). Qualitative Chemical Characterization and Multidirectional Biological Investigation of Leaves and Bark Extracts of Anogeissus leiocarpus (DC.) Guill. & Perr (Combretaceae). Antioxidants, 8. · DOI
  7. Tanase, C., Mocan, A., Coșarcă, S., Gavan, A., Nicolescu, A., Gheldiu, A.-M., Vodnar, D.C., Muntean, D.-L., and Crișan, O. (2019). Biological and chemical insights of beech (Fagus sylvatica L.) bark: A source of bioactive compounds with functional properties. Antioxidants, 8. · DOI
  8. Maroyi, A. (2017). Ethnopharmacology and therapeutic value of Bridelia micrantha (Hochst.) Baill. In tropical Africa: A comprehensive review. Molecules, 22. · DOI
  9. Ngueyem, 2009, The genus Bridelia: A phytochemical and ethnopharmacological review, J. Ethnopharmacol., 124, 339, 10.1016/j.jep.2009.05.019 · DOI
  10. Afolabi, 2018, Inhibitory potentials of phenolic-rich extracts from Bridelia ferruginea on two key carbohydrate-metabolizing enzymes and Fe2+-induced pancreatic oxidative stress, J. Integr. Med., 16, 192, 10.1016/j.joim.2018.04.006 · DOI
  11. Corallo, 1997, Cardiovascular pharmacology of aqueous extract of the leaves of Bridelia atroviridis Muell. Arg. (Euphorbiaceae) in the rat, J. Ethnopharmacol., 57, 189, 10.1016/S0378-8741(97)00071-8 · DOI
  12. Olajide, 2000, Studies on the anti-inflammatory and related pharmacological properties of the aqueous extract of Bridelia ferruginea stem bark, J. Ethnopharmacol., 71, 153, 10.1016/S0378-8741(99)00201-9 · DOI
  13. Ramesh, 2001, Antibacterial activity of luteoforol from Bridelia crenulata, Fitoterapia, 72, 409, 10.1016/S0367-326X(00)00317-8 · DOI
  14. Sokeng, 2005, Antihyperglycemic effect of Bridelia ndellensis ethanol extract and fractions in streptozotocin-induced diabetic rats, Afr. J. Tradit. Complement. Altern. Med., 2, 94, 10.4314/ajtcam.v2i2.31107 · DOI
  15. Tatiya, 2017, Evaluation of analgesic and anti-inflammatory activity of Bridelia retusa (Spreng) bark, J. Tradit. Complement. Med., 7, 441, 10.1016/j.jtcme.2016.12.009 · DOI
  16. Cimanga, 2001, Radical scavenging and xanthine oxidase inhibitory activity of phenolic compounds from Bridelia ferruginea stem bark, J. Pharm. Pharmacol., 53, 757, 10.1211/0022357011775893 · DOI
  17. Jayasinghe, 2003, Antifungal constituents of the stem bark of Bridelia retusa, Phytochemistry, 62, 637, 10.1016/S0031-9422(02)00623-4 · DOI
  18. Pegel, 1968, Constituents of Bridelia micrantha, Phytochemistry, 7, 655, 10.1016/S0031-9422(00)88243-6 · DOI
  19. Uysal, 2015, A phytochemical study on Potentilla anatolica: An endemic Turkish plant, Ind. Crop. Prod., 76, 1001, 10.1016/j.indcrop.2015.08.017 · DOI
  20. Blazekovic, 2011, Antioxidant activities and polyphenolic contents of three selected Micromeria species from Croatia, Molecules, 16, 1454, 10.3390/molecules16021454 · DOI · Paper page
  21. Zengin, 2014, Investigation of antioxidant potentials of solvent extracts from different anatomical parts of Asphodeline anatolica E. Tuzlaci: An endemic plant to Turkey, Afr. J. Tradit. Complement. Altern. Med., 11, 481, 10.4314/ajtcam.v11i2.37 · DOI
  22. Ferrante, 2019, Multiple pharmacological and toxicological investigations on Tanacetum parthenium and Salix alba extracts: Focus on potential application as anti-migraine agents, Food Chem. Toxicol., 133, 110783, 10.1016/j.fct.2019.110783 · DOI
  23. Grochowski, 2017, In vitro enzyme inhibitory properties, antioxidant activities, and phytochemical profile of Potentilla thuringiaca, Phytochem. Lett., 20, 365, 10.1016/j.phytol.2017.03.005 · DOI
  24. Zengin, 2019, Comprehensive approaches on the chemical constituents and pharmacological properties of flowers and leaves of American basil (Ocimum americanum L.), Food Res. Int., 125, 108610, 10.1016/j.foodres.2019.108610 · DOI
  25. Zengin, 2019, Chemical profiling and pharmaco-toxicological activity of Origanum sipyleum extracts: Exploring for novel sources for potential therapeutic agents, J. Food Biochem., 43, e13003, 10.1111/jfbc.13003 · DOI
  26. Veschi, 2018, Effects of repurposed drug candidates nitroxoline and nelfinavir as single agents or in combination with erlotinib in pancreatic cancer cells, J. Exp. Clin. Cancer Res., 37, 236, 10.1186/s13046-018-0904-2 · DOI
  27. Ferrante, 2017, Protective effects induced by microwave-assisted aqueous Harpagophytum extract on rat cortex synaptosomes challenged with amyloid β-peptide, Phytother. Res., 31, 1257, 10.1002/ptr.5850 · DOI
  28. Feng, H., Nemzer, B., and DeVries, J.W. (2019). 9-Bioactive compounds and beneficial functions of sprouted grains. Sprouted Grains, Elsevier.
  29. Panche, 2016, Flavonoids: An overview, J. Nutr. Sci., 5, e47, 10.1017/jns.2016.41 · DOI
  30. Watson, R.R., Preedy, V.R., and Zibadi, S. (2018). Chapter 24—Analyzing Ingredients in Dietary Supplements and Their Metabolites. Polyphenols: Mechanisms of Action in Human Health and Disease, Academic Press. [2nd ed.].
  31. Melton, L., Shahidi, F., and Varelis, P. (2019). Phenolic Acids. Encyclopedia of Food Chemistry, Academic Press.
  32. Henry, 2016, Chapter One-Oats—From Farm to Fork, Advances in Food and Nutrition Research, Volume 77, 1, 10.1016/bs.afnr.2015.12.001 · DOI
  33. Nabeelah Bibi, S., Fawzi, M.M., Gokhan, Z., Rajesh, J., Nadeem, N., Kannan, R.R., RDDG, A., and Pandian, S.K. (2019). Ethnopharmacology, Phytochemistry, and Global Distribution of Mangroves—A Comprehensive Review. Mar. Drugs, 17. · DOI
  34. Mahomoodally, 2018, Volatile components, pharmacological profile, and computational studies of essential oil from Aegle marmelos (Bael) leaves: A functional approach, Ind. Crop. Prod., 126, 13, 10.1016/j.indcrop.2018.09.054 · DOI
  35. McDonald, 2001, Phenolic content and antioxidant activity of olive extracts, Food Chem., 73, 73, 10.1016/S0308-8146(00)00288-0 · DOI
  36. Reddy, N.S., Navanesan, S., Sinniah, S.K., Wahab, N.A., and Sim, K.S. (2012). Phenolic content, antioxidant effect and cytotoxic activity of Leea indica leaves. BMC Complement. Altern. Med., 12. · DOI
  37. Lobo, 2010, Free radicals, antioxidants and functional foods: Impact on human health, Pharmacol. Rev., 4, 118, 10.4103/0973-7847.70902 · DOI · Paper page
  38. Baloglu, 2019, Multidirectional insights on Chrysophyllum perpulchrum leaves and stem bark extracts: HPLC-ESI-MSn profiles, antioxidant, enzyme inhibitory, antimicrobial and cytotoxic properties, Ind. Crop. Prod., 134, 33, 10.1016/j.indcrop.2019.03.066 · DOI
  39. Mahomoodally, 2019, Multi-targeted potential of Pittosporum senacia Putt.: HPLC-ESI-MSn analysis, in silico docking, DNA protection, antimicrobial, enzyme inhibition, anti-cancer and apoptotic activity, Comput. Biol. Chem., 83, 107114, 10.1016/j.compbiolchem.2019.107114 · DOI
  40. Yurt, 2017, Effects of electromagnetic fields exposure on the antioxidant defense system, J. Microsc. Ultrastruct., 5, 167, 10.1016/j.jmau.2017.07.003 · DOI
  41. Bhagavan, N.V., and Ha, C.-E. (2011). Chapter 6-Enzymes and Enzyme Regulation. Essentials of Medical Biochemistry, Academic Press. · DOI
  42. Klimova, 2018, Global View on Alzheimer’s Disease and Diabetes Mellitus: Threats, Risks and Treatment Alzheimer’s Disease and Diabetes Mellitus, Curr. Alzheimer Res., 15, 1277, 10.2174/1567205015666180925110222 · DOI
  43. Lee, 2018, Diabetes and Alzheimer’s Disease: Mechanisms and Nutritional Aspects, Clin. Nutr. Res., 7, 229, 10.7762/cnr.2018.7.4.229 · DOI
  44. Femminella, 2019, Evaluating the effects of the novel GLP-1 analogue liraglutide in Alzheimer’s disease: Study protocol for a randomised controlled trial (ELAD study), Trials, 20, 191, 10.1186/s13063-019-3259-x · DOI
  45. Picot, 2017, In vitro and in silico studies of mangiferin from Aphloia theiformis on key enzymes linked to diabetes type 2 and associated complications, Med. Chem., 13, 633, 10.2174/1573406413666170307163929 · DOI
  46. Fang, 2016, Ferulic acid—Carbazole hybrid compounds: Combination of cholinesterase inhibition, antioxidant and neuroprotection as multifunctional anti-Alzheimer agents, Bioorgan. Med. Chem., 24, 886, 10.1016/j.bmc.2016.01.010 · DOI
  47. Mo, 2019, Design, synthesis, biological evaluation, and molecular modeling studies of quinoline-ferulic acid hybrids as cholinesterase inhibitors, Bioorgan. Chem., 93, 103310, 10.1016/j.bioorg.2019.103310 · DOI
  48. Li, 2018, Corilagin from longan seed: Identification, quantification, and synergistic cytotoxicity on SKOv3ip and hey cells with ginsenoside Rh2 and 5-fluorouracil, Food Chem. Toxicol., 119, 133, 10.1016/j.fct.2018.05.018 · DOI
  49. Shi, 2017, In Vitro and In Vivo Effects of Norathyriol and Mangiferin on α-Glucosidase, Biochem. Res. Int., 2017, 1206015, 10.1155/2017/1206015 · DOI
  50. Chu, H., Duan, Y., Lang, S., Jiang, L., Wang, Y., Llorente, C., Liu, J., Mogavero, S., Bosques-Padilla, F., and Abraldes, J.G. (2019). The Candida albicans exotoxin Candidalysin promotes alcohol-associated liver disease. J. Hepatol. · DOI
  51. Khiewkamrop, 2018, Epistructured catechins, EGCG and EC facilitate apoptosis induction through targeting de novo lipogenesis pathway in HepG2 cells, Cancer Cell Int., 18, 46, 10.1186/s12935-018-0539-6 · DOI
  52. Abnosi, 2018, The toxic effect of gallic acid on biochemical factors, viability and proliferation of rat bone marrow mesenchymal stem cells was compensated by boric acid, J. Trace Elem. Med. Biol., 48, 246, 10.1016/j.jtemb.2018.04.016 · DOI
  53. Mole, 2008, Tryptophan catabolites in mesenteric lymph may contribute to pancreatitis-associated organ failure, Br. J. Surg. Inc. Eur. J. Surg. Swiss Surg., 95, 855
  54. Nakagami, 1996, 3-Hydroxykynurenine toxicity on the rat striatum in vivo, Jpn. J. Pharmacol., 71, 183, 10.1254/jjp.71.183 · DOI
  55. Han, 2017, Dopamine D2 receptor signalling controls inflammation in acute pancreatitis via a PP2A-dependent Akt/NF-κB signalling pathway, Br. J. Pharmacol., 174, 4751, 10.1111/bph.14057 · DOI
  56. Zhou, 2018, Dopamine alleviated acute liver injury induced by lipopolysaccharide/d-galactosamine in mice, Int. Immunopharmacol., 61, 249, 10.1016/j.intimp.2018.06.004 · DOI

Metadata

Authors
Mahomoodally, M. F., Sinan, K. I., Bene, K., Zengin, G., Orlando, G., Menghini, L., Veschi, S., Chiavaroli, A., Recinella, L., Brunetti, L., Leone, S., Angelini, P., Hubka, V., Covino, S., Venanzoni, R., Picot-Allain, M. C. N., De Lellis, L., Cama, A., Cziáky, Z., Jekő, J., & Ferrante, C.
Affiliations
  • Duy Tan University (VN)
  • Selçuk University (TR)
  • Laboratoire de Botanique et Phytothérapie, Unité de Formation et de Recherche Sciences de la Nature, 02 BP 801 Abidjan 02, Université Nangui Abrogoua, 00225 Abidjan, Cote D’Ivoire
  • Department of Biology, Science Faculty, Selcuk Universtiy, Campus, 42130 Konya, Turkey
  • University of Chieti-Pescara (IT)
  • University of Perugia (IT)
  • Laboratory of Fungal Genetics and Metabolism, Institute of Microbiology of the Czech Academy of Sciences, 14220 Prague, Czech Republic
  • University of Mauritius (MU)
  • Department of Pharmacy, “G. d’Annunzio” University Chieti-Pescara, 66100 Chieti, Italy
  • University of Nyíregyháza (HU)
Corresponding author
Orlando, Giustino
Venue
Antioxidants
Publisher
MDPI AG
Published
2020-02-02
Volume
9
Issue
2
Pages
128
ISSN
2076-3921 (ISSN-L)
OpenAlex
W3004396451
Cited by
11
References
0
Citations by year
2026: 1 · 2024: 2 · 2023: 2 · 2022: 1 · 2021: 2 · 2020: 2
FWCI
1.13
Type
journal article
Language
en
Open access
Locations
  • Antioxidants (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Topics
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Medicinal Plant Research
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Phytochemistry and Biological Activities
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Phytochemistry Medicinal Plant Applications
Keywords
stem bark extract, phytochemical profiling, antioxidant activity, acetylcholinesterase inhibition, butyrylcholinesterase inhibition, antibacterial activity, antifungal activity, Candida albicans, HepG2 cells, antiproliferative activity, liver cancer, hepatoprotection, lipopolysaccharide-induced liver injury, African traditional medicine, medicinal plants

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