Antimicrobial action of α-arbutin, β-arbutin and hydroquinone: truth and fiction
DOI:
https://doi.org/10.5281/zenodo.13820076Keywords:
hydroquinone, hydroquinone glycosides, structure-action relationship, comparative analysis, molecular dockingAbstract
Introduction. The leaves of lingonberry and bearberry are used in medicine for the treatment and prevention of urological infectious diseases due to the presence of diuretic and uroseptic action. This pharmacological activity is associated with the action of β-arbutin and hydroquinone. However, until now there has been no study of the relationship between the structure and antimicrobial action of β-arbutin and hydroquinone. The purpose of study was to estimate the antimicrobial action in vitro, in silico of α- and β-arbutin, hydroquinone, and also to conduct a comparative analysis of the antimicrobial properties of these compounds and to refute the theory of the presence of the antimicrobial action of arbutin only due to the action of hydroquinone.Materials and methods. Molecular docking was performed using AutoDockTools 1.5.6, antimicrobial activity was assessed using the "well" and "dilution" methods. Results and discussion. Theoretical studies have shown that α- and β-arbutin are highly selective inhibitors against gram-negative targets such as deoxyribonucleic acid (DNA) gyrase, dihydrofolate reductase (DHFR), deacetylase, and fungal targets such as 14α-demethylase, beta-1,3-glucanase, thymidylate kinase, whereas hydroquinone had low selectivity against all targets. The "well" assay showed that hydroquinone inhibits gram-positive bacteria more actively than β- and α-arbutin, and in the case of gram-negative bacteria, α-arbutin had a higher inhibitory effect than β-arbutin and hydroquinone, while β-arbutin inhibits fungal growth more actively than α-arbutin and hydroquinone. The minimum inhibitory concentration (MIC) values of hydroquinone for gram-positive, gram-negative and fungal microorganisms were almost 2-3 times higher than MIC of β- and α-arbutin. Meanwhile, MIC of α-arbutin was lower for E. coli, P. vulgaris than β-arbutin, and the results were the same in other cases. Conclusions. The antimicrobial effect of α- and β-arbutin, hydroquinone against strains of S. aureus, B. subtilis, E. coli, P. vulgaris, P. aeruginosa and C. albicans was studied in vitro and in silico. Theoretical results showed that it is impossible to create a "panacea" from one compound that would suppress the growth of both bacteria and fungi. According to theoretical and practical results, the antimicrobial effect of α- and β-arbutin is 2-3 times higher than that of hydroquinone. It has been experimentally confirmed that α-arbutin suppresses the growth of gram-negative strains much more strongly than β-arbutin. The theory that arbutin has an antimicrobial effect only due to the action of hydroquinone has been theoretically and practically refuted.
Keywords: hydroquinone, hydroquinone glycosides, structure-action relationship, comparative analysis, molecular docking
References
Xu KX, Xue MG, Li Z, Ye BC, Zhang B. Recent Progress on Feasible Strategies for Arbutin Production. Front Bioeng Biotechnol. 2022;10:1-10. DOI: https://doi.org/10.3389/fbioe.2022.914280
Asensio E, Vitales D, Pérez I, Peralba L, Viruel J, Montaner C, Vallès J, Garnatje T, Sales E. Phenolic Compounds Content and Genetic Diversity at Population Level across the Natural Distribution Range of Bearberry (Arctostaphylos uva-ursi, Ericaceae) in the Iberian Peninsula. Plants. 2020;9(9):1250. DOI: https://doi.org/10.3390/plants9091250
Zhou H, Zhao J, Li A, Reetz MT. Chemical and Biocatalytic Routes to Arbutin †. Molecules. 2019;24(18):3303. DOI: https://doi.org/10.3390/molecules24183303
Lee HJ, Kim KW. Anti-inflammatory effects of arbutin in lipopolysaccharide-stimulated BV2 microglial cells. Inflamm Res. 2012;61(8):817-25. DOI: https://doi.org/10.1007/s00011-012-0474-2
Yu X, Jin H, Liu W, Wang Q, Qi Q. Engineering Corynebacterium glutamicum to produce 5-aminolevulinic acid from glucose. Microb Cell Fact. 2015;14(1):1-23. DOI: https://doi.org/10.1186/s12934-015-0364-8
Su Y, Sun X, Wu R, Zhang X, Tu Y. Molecular spectroscopic behaviors of beta-arbutin in anti-skin cancer. Spectrosc Lett. 2020;53(3):172-83. DOI: https://doi.org/10.1080/00387010.2020.1715441
Liu L, Duan X, Wu J. Modulating the direction of carbon flow in Escherichia coli to improve l -tryptophan production by inactivating the global regulator FruR. J Biotechnol. 2016;231:141-8. DOI: https://doi.org/10.1016/j.jbiotec.2016.06.008
Funayama M, Arakawa H, Yamamoto R, Nishino T, Shin T, Murao S. Effects ofα- andβ-Arbutin on Activity of Tyrosinases from Mushroom and Mouse Melanoma. Biosci Biotechnol Biochem. 1995;59(1):143-4. DOI: https://doi.org/10.1271/bbb.59.143
Ryyti R, Hämäläinen M, Peltola R, Moilanen E. Beneficial effects of lingonberry (Vaccinium vitis-idaea L.) supplementation on metabolic and inflammatory adverse effects induced by high-fat diet in a mouse model of obesity. PLOS ONE. 2020;15(5):e0232605. DOI: https://doi.org/10.1371/journal.pone.0232605
Ștefănescu BE, Szabo K, Mocan A, Crişan G. Phenolic Compounds from Five Ericaceae Species Leaves and Their Related Bioavailability and Health Benefits. Molecules. 2019;24(11):2046. DOI: https://doi.org/10.3390/molecules24112046
Golikova S, editor. First Aid for Acute Poisoning. Handbook of Toxicology [Neotlozhnaya pomoshch' pri ostrykh otravleniyakh. Spravochnik po toksikologii]. Moscow: Medicines; 1977.
Mashkovsky М. Medicines [Lekarstvennyye sredstva]. 16th ed. Mashkovsky S, editor. Moscow: New Wave; 2012. 1216 p.
Maslov O, Komisarenko M, Ponomarenko S, Horopashna D, Osolodchenko T, Kolisnyk S, Derymedvid L, Shovkova Z, Akhmedov E. Investigation the influence of biologically active compounds on the antioxidant, antibacterial and anti-inflammatory activities of red raspberry (Rubus idaeous l.) leaf extract. Curr Issues Pharm Med Sci. 2022;35(4):229-35. DOI: https://doi.org/10.2478/cipms-2022-0040
Volyanskiy Y, Gritsenko I, Shyrokobokov V. The study of the specific activity of antimicrobial drugs: a method recommendation. Kiev: StEntScPhC Ministry of Helthcare of Ukraine; 2004. 38 p.
Mbarga MJ, Podoprigora IV, Volina EG, Ermolaev AV, Smolyakova LA. Evaluation of Changes Induced in the Probiotic Escherichia coli M17 Following Recurrent Exposure to Antimicrobials. J Pharm Res Int. 2021:158-67. DOI: https://doi.org/10.9734/jpri/2021/v33i29b31601
Morris GM, Huey R, Olson AJ. Using AutoDock for Ligand‐Receptor Docking. Curr Protoc Bioinform. 2008;24(1):1-10. DOI: https://doi.org/10.1002/0471250953.bi0814s24
RCSB PDB: Homepage. RCSB PDB: Homepage. Available from: https://www.rcsb.org/.
PubChem. PubChem;. Available from: https://pubchem.ncbi.nlm.nih.gov/.
CASTp 3.0: Computed Atlas of Surface Topography of proteins;. Available from: http://sts.bioe.uic.edu/castp/index.html?201l
Kondža M, Brizić I, Jokić S. Flavonoids as CYP3A4 Inhibitors In Vitro. Biomedicines. 2024;12(3):644. DOI: https://doi.org/10.3390/biomedicines12030644
Jadhav AK, Karuppayil SM. Molecular docking studies on thirteen fluoroquinolines with human topoisomerase II a and b. Silico Pharmacol. 2017;5(1):22-3. DOI: https://doi.org/10.1007/s40203-017-0024-2
Mbarga MJ, Podoprigora IV, Volina EG, Ermolaev AV, Smolyakova LA. Evaluation of Changes Induced in the Probiotic Escherichia coli M17 Following Recurrent Exposure to Antimicrobials. J Pharm Res Int. 2021:158-67. DOI: https://doi.org/10.9734/jpri/2021/v33i29b31601
Rahman M, Browne JJ, Van Crugten J, Hasan MF, Liu L, Barkla BJ. In Silico, Molecular Docking and In Vitro Antimicrobial Activity of the Major Rapeseed Seed Storage Proteins. Front Pharmacol. 2020;11:22-40. DOI: https://doi.org/10.3389/fphar.2020.01340
Zuo K, Liang L, Du W, Sun X, Liu W, Gou X, Wan H, Hu J. 3D-QSAR, Molecular Docking and Molecular Dynamics Simulation of Pseudomonas aeruginosa LpxC Inhibitors. Int J Mol Sci. 2017;18(5):761. DOI: https://doi.org/10.3390/ijms18050761
Bertonha AF, Silva CC, Shirakawa KT, Trindade DM, Dessen A. Penicillin-binding protein (PBP) inhibitor development: A 10-year chemical perspective. Exp Biol Med. 2023. DOI: https://doi.org/10.1177/15353702231208407
Prajapati J, Goswami D, Dabhi M, Acharya D, Rawal RM. Potential dual inhibition of SE and CYP51 by eugenol conferring inhibition of Candida albicans: Computationally curated study with experimental validation. Comput Biol Med. 2022:106237. DOI: https://doi.org/10.1016/j.compbiomed.2022.106237
Ruiz-Herrera J, Ortiz-Castellanos L. Cell wall glucans of fungi. A review. Cell Surf. 2019;5:100022. DOI: https://doi.org/10.1016/j.tcsw.2019.100022
da Nóbrega Alves D, Monteiro AF, Andrade PN, Lazarini JG, Abílio GM, Guerra FQ, Scotti MT, Scotti L, Rosalen PL, Castro RD. Docking Prediction, Antifungal Activity, Anti-Biofilm Effects on Candida spp., and Toxicity against Human Cells of Cinnamaldehyde. Molecules. 2020;25(24):5969. DOI: https://doi.org/10.3390/molecules25245969
Gritsenko IS, Bolotov VV, Klimenko LY, Kostina TA, Mykytenko OY, Kolisnyk SV. Analytical chemistry: textbook [the textbook for students of higher school]. Gritsenko IS, editor. Kharkiv: NUPh: Golden Pages; 2019. 600 p.
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