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dc.contributor.authorKowalczyk, Tomasz
dc.contributor.authorSitarek, Przemysław
dc.contributor.authorSkała, Ewa
dc.contributor.authorRijo, Patrícia Dias de Mendonça
dc.contributor.authorAndrade, Joana
dc.contributor.authorSynowiec, Ewelina
dc.contributor.authorSzemraj, Janusz
dc.contributor.authorKrajewska, Urszula
dc.contributor.authorŚliwiński, Tomasz
dc.date.accessioned2019-12-12T07:52:47Z
dc.date.available2019-12-12T07:52:47Z
dc.date.issued2019-10-16
dc.identifier.issn1942-0994
dc.identifier.urihttp://hdl.handle.net/11089/31053
dc.description.abstractMenyanthes trifoliata L. is a valuable medical plant found in Europe, North America, and Asia, which grows on peat bogs and swamps. It has long been used in folk medicine as a remedy for various ailments. This is the first report to demonstrate the protective antioxidant and anti-inflammatory properties of aqueous methanolic extracts derived from the aerial parts (MtAPV) and roots (MtRV) of in vitro grown plants on human umbilical vein endothelial cells (HUVECs). It describes the influence of the tested extracts on the expression of antioxidant (HO-1, NQO1, NRF2, kEAP1, and GCLC) and inflammation-related genes (IL-1α, IL-1β, IL-6, TNF-α, and IFN-γ) in cells stimulated with H2O2 or LPS, respectively. In addition, M. trifoliata extracts were found to moderately affect the growth of certain bacterial and fungal pathogens, with the strongest antibacterial effect found against Pseudomonas aeruginosa and Enterococcus faecalis. M. trifoliata extracts demonstrated protective effects against mitochondrial DNA (mtDNA) and nuclear DNA (nDNA) damage caused by ROS, decreasing the numbers of mtDNA lesions in the ND1 and ND2 genes and nDNA damage in the TP53 and HPRT1 genes and reducing cleavage in PARP1- and γ-H2A.Xpositive cells. The root extract of in vitro M. trifoliata (MtRV) appears to have better anti-inflammatory, antioxidant, antimicrobial, and protective properties than the extract from the aerial part (MtAPV). These differences in biological properties may result from the higher content of selected phenolic compounds and betulinic acid in the MtRV than in the MtAPV extract. 1. Introduction Health-promoting properties of plants have been used in the prevention and therapy of many human diseases for thousands of years. Currently, it is estimated that 300,000 plant species exist worldwide [1]; however, relatively few have confirmed therapeutic or protective properties. Fortunately, modern methods and equipment allow much faster and Hindawi Oxidative Medicine and Cellular Longevity Volume 2019, Article ID 9165784, 13 pages https://doi.org/10.1155/2019/9165784pl_PL
dc.description.sponsorshipUniversity of Lodz Statutory Funding Grant Number B1711000000201.01.pl_PL
dc.language.isoenpl_PL
dc.publisherHindawipl_PL
dc.relation.ispartofseriesOxidative Medicine and Cellular Longevity;
dc.titleAn Evaluation of the DNA-Protective Effects of Extracts from Menyanthes trifoliata L. Plants Derived from In Vitro Culture Associated with Redox Balance and Other Biological Activitiespl_PL
dc.typeArticlepl_PL
dc.page.number1-13pl_PL
dc.contributor.authorAffiliationDepartment of Molecular Biotechnology and Genetics, University of Lodz, Banacha 12/16, 90-237 Lodz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Biology and Pharmaceutical Botany, Medical University of Lodz, Muszynskiego 1, 90-151 Lodz, Polandpl_PL
dc.contributor.authorAffiliationCenter for Research in Biosciences and Health Technologies (CBIOS), Universidade Lusófona de Humanidades e Tecnologias, 1749-024 Lisbon, Portugalpl_PL
dc.contributor.authorAffiliationInstituto de Investigação do Medicamento (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa, 1649-003 Lisbon, Portugalpl_PL
dc.contributor.authorAffiliationLaboratory of Medical Genetics, Faculty of Biology and Environmental Protection, University of Lodz, Pomorska 141/143, 90-236 Lodz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Medical Biochemistry, Medical University of Lodz, Mazowiecka 6/8, 92-215 Lodz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Pharmaceutical Biochemistry, Molecular Biology Laboratory, Medical University of Lodz, Muszynskiego 1, 90-151 Lodz, Polandpl_PL
dc.identifier.eissn1942-0994
dc.referencesC. Mora, D. P. Tittensor, S. Adl, A. G. B. Simpson, and B. Worm, “How many species are there on earth and in the ocean?,” PLoS Biology, vol. 9, no. 8, article e1001127, 2011.pl_PL
dc.referencesX. Liu, K. Vrieling, and P. G. L. Klinkhamer, “Interactions between plant metabolites affect herbivores: a study with pyrrolizidine alkaloids and chlorogenic acid,” Frontiers in Plant Science, vol. 8, p. 903, 2017.pl_PL
dc.referencesS. Latif, G. Chiapusio, and L. A. Weston, “Allelopathy and the role of allelochemicals in plant defence,” Advances in Botanical Research, vol. 82, pp. 19–54, 2017.pl_PL
dc.referencesJ. Reichling, “Plant-Microbe Interactions and Secondary Metabolites with Antibacterial, Antifungal and Antiviral Properties,” in Functions and biotechnology of plant secondary metabolites, vol. 39, pp. 214–347, Blackwell, Oxford, UK, 2nd edition, 2010.pl_PL
dc.referencesA. G. Atanasov, B. Waltenberger, E. M. Pferschy-Wenzig et al., “Discovery and resupply of pharmacologically active plantderived natural products: a review,” Biotechnology Advances, vol. 33, no. 8, pp. 1582–1614, 2015.pl_PL
dc.referencesH. Yang, T. Tian, D. Wu, D. Guo, and J. Lu, “Prevention and treatment effects of edible berries for three deadly diseases: cardiovascular disease, cancer and diabetes,” Critical Reviews in Food Science and Nutrition, vol. 59, no. 12, pp. 1903–1912, 2019.pl_PL
dc.referencesF. L. Thompson, L. A. Hermanutz, and D. J. Innes, “The reproductive ecology of island populations of distylous Menyanthes trifoliata (Menyanthaceae),” Canadian Journal of Botany, vol. 76, no. 5, pp. 818–828, 1998.pl_PL
dc.referencesT. Kowalczyk, P. Sitarek, E. Skała et al., “Induction of apoptosis by in vitro and in vivo plant extracts derived from Menyanthes trifoliata L. in human cancer cells,” Cytotechnology, vol. 71, no. 1, pp. 165–180, 2019.pl_PL
dc.referencesJ. Kuduk-Jaworska, J. Szpunar, K. Gąsiorowski, and B. Brokos, “Immunomodulating polysaccharide fractions of Menyanthes trifoliata L.,” Zeitschrift für Naturforschung C, vol. 59, no. 7-8, pp. 485–493, 2004.pl_PL
dc.referencesH. Tunón, L. Bohlin, and G. Öjteg, “The effect of Menyanthes trifoliata L. on acute renal failure might be due to PAF-inhibition,” Phytomedicine, vol. 1, no. 1, pp. 39–45, 1994.pl_PL
dc.referencesF. Martz, M. Turunen, R. Julkunen-Tiitto, K. Lakkala, and M. L. Sutinen, “Effect of the temperature and the exclusion of UVB radiation on the phenolics and iridoids in Menyanthes trifoliata L. leaves in the subarctic,” Environmental Pollution, vol. 157, no. 12, pp. 3471–3478, 2009.pl_PL
dc.referencesS. H. Lim, E. S. Jeon, J. Lee, S. Y. Han, and H. Chae, “Pharmacognostic outlooks on medical herbs of Sasang typology,” Integrative Medicine Research, vol. 6, no. 3, pp. 231–239, 2017.pl_PL
dc.referencesR. Gautam, M. Singh, S. Gautam, J. K. Rawat, S. A. Saraf, and G. Kaithwas, “Rutin attenuates intestinal toxicity induced by methotrexate linked with anti-oxidative and antiinflammatory effects,” BMC Complementary and Alternative Medicine, vol. 16, no. 1, p. 99, 2016.pl_PL
dc.referencesL. Wang, H. L. Wu, X. L. Yin, Y. Hu, H. W. Gu, and R. Q. Yu, “Simultaneous determination of umbelliferone and scopoletin in Tibetan medicine Saussurea laniceps and traditional Chinese medicine Radix angelicae pubescentis using excitationemission matrix fluorescence coupled with second-order calibration method,” Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, vol. 170, pp. 104–110, 2017.pl_PL
dc.referencesP. Sitarek, E. Skała, M. Toma et al., “Transformed root extract of Leonurus sibiricus induces apoptosis through intrinsic and extrinsic pathways in various grades of human glioma cells,” Pathology Oncology Research, vol. 23, no. 3, pp. 679–687, 2017.pl_PL
dc.referencesT. D. Schmittgen and K. J. Livak, “Analyzing real-time PCR data by the comparative CT method,” Nature Protocols, vol. 3, no. 6, pp. 1101–1108, 2008.pl_PL
dc.referencesO. Rothfuss, T. Gasser, and N. Patenge, “Analysis of differential DNA damage in the mitochondrial genome employing a semi-long run real-time PCR approach,” Nucleic Acids Research, vol. 38, no. 4, article e24, 2010.pl_PL
dc.referencesP. Sitarek, E. Synowiec, T. Kowalczyk, T. Śliwiński, and E. Skała, “An in vitro estimation of the cytotoxicity and genotoxicity of root extract from Leonurus sibiricus L. overexpressing AtPAP1 against different cancer cell lines,” Molecules, vol. 23, no. 8, article 2049, 2018.pl_PL
dc.referencesP. Sitarek, P. Rijo, C. Garcia et al., “Antibacterial, anti-inflammatory, antioxidant, and antiproliferative properties of essential oils from hairy and normal roots of Leonurus sibiricus L. and their chemical composition,” Oxidative Medicine and Cellular Longevity, vol. 2017, Article ID 7384061, 12 pages, 2017.pl_PL
dc.referencesH. Tunón, C. Olavsdotter, and L. Bohlin, “Evaluation of antiinflammatory activity of some Swedish medicinal plants. Inhibition of prostaglandin biosynthesis and PAF-induced exocytosis,” Journal of Ethnopharmacology, vol. 48, no. 2, pp. 61– 76, 1995.pl_PL
dc.referencesJ. D. Rosenblat, D. S. Cha, R. B. Mansur, and R. S. McIntyre, “Inflamed moods: a review of the interactions between inflammation and mood disorders,” Progress in NeuroPsychopharmacology & Biological Psychiatry, vol. 53, pp. 23–34, 2014.pl_PL
dc.referencesN.P.Babu,P.Pandikumar,andS.Ignacimuthu,“Anti-inflammatory activity of Albizia lebbeck Benth., an ethnomedicinal plant, in acute and chronic animal models of inflammation,” Journal of Ethnopharmacology, vol. 125, no. 2, pp. 356–360, 2009.pl_PL
dc.referencesA. U. Ahmed, “An overview of inflammation: mechanism and consequences,” Frontiers of Biology in China, vol. 6, p. 274, 2011.pl_PL
dc.referencesA.’a. Al-Bakheit, S. Abu-Romman, A. Sharab, and M. Al Shhab, “Anti-inflammatory effect of Varthemia iphionoides extracts against prostate cancer in vitro,” European Journal of Inflammation, vol. 15, no. 1, pp. 8–14, 2017.pl_PL
dc.referencesC. Ma, L. Zhu, J. Wang et al., “Anti-inflammatory effects of water extract of Taraxacum mongolicum hand.-Mazz on lipopolysaccharide-induced inflammation in acute lung injury by suppressing PI3K/Akt/mTOR signaling pathway,” Journal of Ethnopharmacology, vol. 168, pp. 349–355, 2015.pl_PL
dc.referencesS. A. Adebayo, J. P. Dzoyem, L. J. Shai, and J. N. Eloff, “The anti-inflammatory and antioxidant activity of 25 plant species used traditionally to treat pain in southern African,” BMC Complementary and Alternative Medicine, vol. 15, no. 1, p. 159, 2015.pl_PL
dc.referencesH. Fang, R. A. Pengal, X. Cao et al., “Lipopolysaccharideinduced macrophage inflammatory response is regulated by SHIP,” Journal of Immunology, vol. 173, no. 1, pp. 360–366, 2004.pl_PL
dc.referencesP. Mizgier, A. Z. Kucharska, A. Sokół-Łętowska, J. KolniakOstek, M. Kidoń, and I. Fecka, “Characterization of phenolic compoundsandantioxidantandanti-inflammatoryproperties of red cabbage and purple carrot extracts,” Journal of Functional Foods, vol. 21, pp. 133–146, 2016.pl_PL
dc.referencesM. J. Rodrigues, V. Neves, A. Martins et al., “In vitro antioxidant and anti-inflammatory properties of Limonium algarvense flowers’ infusions and decoctions: a comparison with green tea (Camellia sinensis),” Food Chemistry, vol. 200, pp. 322–329, 2016.pl_PL
dc.referencesM. H. Grace, D. Esposito, M. A. Timmers et al., “Chemical composition, antioxidant and anti-inflammatory properties of pistachio hull extracts,” Food Chemistry, vol. 210, pp. 85– 95, 2016.pl_PL
dc.referencesJ. J. Yoon, Y. J. Lee, J. S. Kim, D. G. Kang, and H. S. Lee, “Protective role of betulinic acid on TNF-α-induced cell adhesion molecules in vascular endothelial cells,” Biochemical and Biophysical Research Communications, vol. 391, no. 1, pp. 96–101, 2010.pl_PL
dc.referencesW. T. Wu, M. C. Mong, Y. C. Yang, Z. H. Wang, and M. C. Yin, “Aqueous andethanol extracts of daylily flower (Hemerocallis fulva L.) protect HUVE cells against high glucose,” Journal of Food Science, vol. 83, no. 5, pp. 1463–1469, 2018.pl_PL
dc.referencesB.Zdzisińska,W.Rzeski,R.Paduchetal.,“Differentialeffectof betulin and betulinic acid on cytokine production in human whole blood cell cultures,” Polish Journal of Pharmacology, vol. 55, no. 2, pp. 235–238, 2003.pl_PL
dc.referencesK. S. Kim, D. S. Lee, D. C. Kim et al., “Anti-inflammatory effects and mechanisms of action of coussaric and betulinic acids isolated from diospyros kaki in lipopolysaccharidestimulated RAW 264.7 macrophages,” Molecules, vol. 21, no. 9, article 1206, 2016.pl_PL
dc.referencesX. Huang, Q. Pan, Z. Mao et al., “Sinapic acid inhibits the IL1β-induced inflammation via MAPK downregulation in rat chondrocytes,” Inflammation, vol. 41, no. 2, pp. 562–568, 2018.pl_PL
dc.referencesK. J. Yun, D. J. Koh, S. H. Kim et al., “Anti-inflammatory effects of sinapic acid through the suppression of inducible nitric oxide synthase, cyclooxygase-2, and proinflammatory cytokines expressions via nuclear factor-κB inactivation,” Journal of Agricultural and Food Chemistry, vol. 56, no. 21, pp. 10265–10272, 2008.pl_PL
dc.referencesM.Jayachandran,R.Vinayagam,R.R.Ambati,B.Xu,andS.S. M. Chung, “Guava leaf extract diminishes hyperglycemia and oxidative stress, prevents β-cell death, inhibits inflammation, and regulates NF-κB signaling pathway in STZ induceddiabetic rats,” BioMed Research International, vol. 2018, Article ID 4601649, 14 pages, 2018.pl_PL
dc.referencesJ. H. Lee, J. H. Won, J. M. Choi et al., “Protective effect of ellagic acid on concanavalin A-induced hepatitis via toll-like receptor and mitogen-activated protein kinase/nuclear factor κb signaling pathways,” Journal of Agricultural and Food Chemistry, vol. 62, no. 41, pp. 10110–10117, 2014.pl_PL
dc.referencesS. J. Hwang, Y. W. Kim, Y. Park, H. J. Lee, and K. W. Kim, “Anti-inflammatory effects of chlorogenic acid in lipopolysaccharide-stimulated RAW 264.7 cells,” Inflammation Research, vol. 63, no. 1, pp. 81–90, 2014.pl_PL
dc.referencesV. A. Kostyuk, A. I. Potapovich, T. O. Suhan, C. De Luca, and L. G. Korkina, “Antioxidant and signal modulation properties of plant polyphenols in controlling vascular inflammation,” European Journal of Pharmacology, vol. 658, no. 2-3, pp. 248–256, 2011.pl_PL
dc.referencesM. De La Luz Cádiz-Gurrea, I. Borrás-Linares, J. LozanoSánchez, J. Joven, S. Fernández-Arroyo, and A. SeguraCarretero, “Cocoa and grape seed byproducts as a source of antioxidant and anti-inflammatory proanthocyanidins,” International Journal of Molecular Sciences, vol. 18, no. 2, p. 376, 2017.pl_PL
dc.referencesM. S. Karimian, M. Pirro, M. Majeed, and A. Sahebkar, “Curcumin as a natural regulator of monocyte chemoattractant protein-1,” Cytokine and Growth Factor Reviews, vol. 33, pp. 55–63, 2017.pl_PL
dc.referencesP. Pullikotil, H. Chen, R. Muniyappa et al., “Epigallocatechin gallate induces expression of heme oxygenase-1 in endothelial cells via p38 MAPK and Nrf-2 that suppresses proinflammatory actions of TNF-α,” The Journal of Nutritional Biochemistry, vol. 23, no. 9, pp. 1134–1145, 2012.pl_PL
dc.referencesV. K. Bajpai, M. B. Alam, M. K. Ju et al., “Antioxidant mechanism of polyphenol-rich Nymphaea nouchali leaf extract protecting DNA damage and attenuating oxidative stress-induced cell death via Nrf2-mediated heme-oxygenase1 induction coupled with ERK/p38 signaling pathway,” Biomedicine & Pharmacotherapy, vol. 103, pp. 1397–1407, 2018.pl_PL
dc.referencesA. I. Casas, V. T. V. Dao, A. Daiber et al., “Reactive oxygenrelateddiseases:therapeutictargetsandemergingclinicalindications,” Antioxidants & Redox Signaling, vol. 23, no. 14, pp. 1171–1185, 2015.pl_PL
dc.referencesM. Mittal, M. R. Siddiqui, K. Tran, S. P. Reddy, and A. B. Malik, “Reactive oxygen species in inflammation and tissue injury,” Antioxidants & Redox Signaling, vol. 20, no. 7, pp. 1126–1167, 2014.pl_PL
dc.referencesS. Manoharan, G. J. Guillemin, R. S. Abiramasundari, M. M. Essa, M.Akbar, andM. D.Akbar, “Theroleof reactive oxygen species in thepathogenesisof Alzheimer’sdisease, Parkinson’s disease, and Huntington’s disease: a mini review,” Oxidative Medicine and Cellular Longevity, vol. 2016, Article ID 8590578, 15 pages, 2016.pl_PL
dc.referencesF. Festa, T. Aglitti, G. Duranti, R. Ricordy, P. Perticone, and R. Cozzi, “Strong antioxidant activity of ellagic acid in mammalian cells in vitro revealed by the comet assay,” Anticancer Research, vol. 21, no. 6A, pp. 3903–3908, 2001.pl_PL
dc.referencesK. Sevgi, B. Tepe, and C. Sarikurkcu, “Antioxidant and DNA damage protection potentials of selected phenolic acids,” Food and Chemical Toxicology, vol. 77, pp. 12–21, 2015.pl_PL
dc.referencesS.R.Abbas,S.M.Sabir,S.D.Ahmad,A.A.Boligon, andM.L. Athayde, “Phenolic profile, antioxidant potential and DNA damage protecting activity of sugarcane (Saccharum officinarum),” Food Chemistry, vol. 147, pp. 10–16, 2014.pl_PL
dc.referencesP. Singh, S. P. Vishwakarma, and R. L. Singh, “Antioxidant, oxidative DNA damage protective and antimicrobial activities of the plant Trigonella foenum-graecum,” Journal of the Science of Food and Agriculture, vol. 94, no. 12, pp. 2497– 2504, 2014.pl_PL
dc.referencesK. Kozics, V. Klusová, A. Srančíková et al., “Effects of Salvia officinalis and Thymus vulgaris on oxidant-induced DNA damage and antioxidant status in HepG2 cells,” Food Chemistry, vol. 141, no. 3, pp. 2198–2206, 2013.pl_PL
dc.referencesA. C. Dametto, D. Agustoni, T. F. Moreira et al., “Chemical composition and in vitro chemoprevention assessment of Eugenia jambolana Lam. (Myrtaceae) fruits and leaves,” Journal of Functional Foods, vol. 36, pp. 490–502, 2017.pl_PL
dc.referencesS. Schaefer, M. Baum, G. Eisenbrand, H. Dietrich, F. Will, and C. Janzowski, “Polyphenolic apple juice extracts and their major constituents reduce oxidative damage in human colon cell lines,” Molecular Nutrition & Food Research, vol. 50, no. 1, pp. 24–33, 2006.pl_PL
dc.referencesS. Schaefer, M. Baum, G. Eisenbrand, H. Dietrich, F. Will, and C. Janzowski, “Polyphenolic apple juice extracts and their major constituents reduce oxidative damage in human colon cell lines,” Molecular Nutrition & Food Research, vol. 50, no. 1, pp. 24–33, 2006.pl_PL
dc.referencesF. Guglielmi, C. Luceri, L. Giovannelli, P. Dolara, and M. Lodovici, “Effect of 4-coumaric and 3,4-dihydroxybenzoic acid on oxidative DNA damage in rat colonic mucosa,” The British Journal of Nutrition, vol. 89, no. 5, pp. 581–587, 2003.pl_PL
dc.referencesC. H. Tsai, S. F. Tzeng, S. C. Hsieh et al., “A standardized Wedelia chinensis extract overcomes the feedback activation of HER2/3 signaling upon androgen-ablation in prostate cancer,” Frontiers in Pharmacology, vol. 8, p. 721, 2017.pl_PL
dc.referencesC.SoldaniandA.I.Scovassi,“Poly(ADP-ribose)polymerase-1 cleavage during apoptosis: an update,” Apoptosis, vol. 7, no. 4, pp. 321–328, 2002.pl_PL
dc.referencesH. Wei and X. Yu, “Functions of PARylation in DNA damage repair pathways,” Genomics, Proteomics & Bioinformatics, vol. 14, no. 3, pp. 131–139, 2016.pl_PL
dc.referencesL. J. Kuo and L. X. Yang, “Gamma-H2AX - a novel biomarker for DNA double-strand breaks,” In Vivo, vol. 22, no. 3, pp. 305–309, 2008.pl_PL
dc.referencesM. Hausmann, E. Wagner, J. H. Lee et al., “Super-resolution localization microscopy of radiation-induced histone H2AXphosphorylation in relation to H3K9-trimethylation in HeLa cells,” Nanoscale, vol. 10, no. 9, pp. 4320–4331, 2018.pl_PL
dc.referencesC.Y.Lin, P.N.Chen, Y.S.Hsieh, andS. C.Chu, “Koelreuteria formosana extract impedes in vitro human LDL and prevents oxidised LDL-induced apoptosis in human umbilical vein endothelialcells,”FoodChemistry,vol.146,pp.299–307,2014.pl_PL
dc.referencesH. Chang, W. Yuan, H. Wu, X. Yin, and H. Xuan, “Bioactive components and mechanisms of Chinese poplar propolis alleviates oxidized low-density lipoprotein-induced endothelial cells injury,” BMC Complementary and Alternative Medicine, vol. 18, no. 1, p. 142, 2018.pl_PL
dc.referencesS. He, R. Ou, W. Wang et al., “Camptosorus sibiricus rupr aqueous extract prevents lung tumorigenesis via dual effects against ROS and DNA damage,” Journal of Ethnopharmacology, vol. 220, pp. 44–56, 2018.pl_PL
dc.referencesR. S. Carvalho, C. A. Carollo, J. C. de Magalhães et al., “Antibacterial and antifungal activities of phenolic compoundenriched ethyl acetate fraction from Cochlospermum regium (mart. Et. Schr.) Pilger roots: mechanisms of action and synergism with tannin and gallic acid,” South African Journal of Botany, vol. 114, pp. 181–187, 2018.pl_PL
dc.referencesR. R. Chand, A. D. Jokhan, R. D. Gopalan, and T. Osborne, “Antibacterial and antifungal activities of essential oils from medicinalplantsfound intheSouthPacific,” TheSouthPacificJournal of Natural and Applied Sciences, vol. 35, no. 1, pp. 10– 19, 2017.pl_PL
dc.referencesK. Bashir Dar, A. Hussain Bhat, S. Amin et al., “Evaluation of antibacterial, antifungal and phytochemical screening of Solanum nigrum,” Biochemistry & Analytical Biochemistry, vol. 6, no. 1, p. 309, 2017.pl_PL
dc.referencesE. Ivanišová, T. Krajčovič, M. Tokár, Š. Dráb, A. Kántor, and M.Kačániová,“Potentialofwildplantsasasourceofbioactive compounds,” Animal Science & Biotechnologies, vol. 50, pp. 109–114, 2017.pl_PL
dc.referencesB. Paudel, H. D. Bhattarai, I. C. Kim et al., “Estimation of antioxidant, antimicrobial activity and brine shrimp toxicity of plants collected from Oymyakon region of the republic of Sakha (Yakutia), Russia,” Biological Research, vol. 47, no. 1, p. 10, 2014.pl_PL
dc.referencesC. S. Rempe, K. P. Burris, S. C. Lenaghan, and C. N. Stewart, “The potential of systems biology to discover antibacterial mechanisms of plant phenolics,” Frontiers in Microbiology, vol. 8, p. 422, 2017.pl_PL
dc.referencesH. O. B. Oloyede, H. O. Ajiboye, M. O. Salawu, and T. O. Ajiboye, “Influence of oxidative stress on the antibacterial activity of betulin, betulinic acid and ursolic acid,” Microbial Pathogenesis, vol. 111, pp. 338–344, 2017.pl_PL
dc.referencesG. M. Woldemichael, M. P. Singh, W. M. Maiese, and B. N. Timmermann,“ConstituentsofantibacterialextractofCaesalpinia paraguariensis Burk,” Zeitschrift für Naturforschung C, vol. 58, no. 1-2, pp. 70–75, 2003.pl_PL
dc.referencesC. Chandramu, R. D. Manohar, D. G. L. Krupadanam, and R. V. Dashavantha, “Isolation, characterization and biological activity of betulinic acid and ursolic acid from Vitex negundo L,” Phytotherapy Research, vol. 17, no. 2, pp. 129–134, 2003.pl_PL
dc.referencesL. Catteau, L. Zhu, F. Van Bambeke, and J. Quetin-Leclercq, “Naturalandhemi-syntheticpentacyclictriterpenesasantimicrobials and resistance modifying agents against Staphylococcus aureus: a review,” Phytochemistry Reviews, vol. 17, no. 5, pp. 1129–1163, 2018.pl_PL
dc.referencesT. Wu, X. Zang, M. He, S. Pan, and X. Xu, “Structure–activity relationship of flavonoids on their anti-Escherichia coli activity and inhibition of DNA gyrase,” Journal of Agricultural and Food Chemistry, vol. 61, no. 34, pp. 8185–8190, 2013.pl_PL
dc.referencesS. Khan, T. Ur-Rehman, B. Mirza, I. Ul-Haq, and M. Zia, “Antioxidant, antimicrobial, cytotoxic and protein kinase inhibitionactivitiesof fifteentraditionalmedicinalplantsfrom Pakistan,” Pharmaceutical Chemistry Journal, vol. 51, no. 5, pp. 391–398, 2017.pl_PL
dc.referencesC.Willyard,“Thedrug-resistantbacteriathatposethegreatest health threats,” Nature, vol. 543, no. 7643, p. 15, 2017.pl_PL
dc.contributor.authorEmailtomasz.kowalczyk@biol.uni.lodz.plpl_PL
dc.identifier.doi10.1155/2019/9165784
dc.relation.volume2019pl_PL
dc.disciplinenauki biologicznepl_PL


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