期刊论文详细信息
BMC Complementary and Alternative Medicine
Isolation and characterization of an antifungal compound 5-hydroxy-7,4’-dimethoxyflavone from Combretum zeyheri
Stanley Mukanganyama2  Jacob Midiwo1  Rumbidzai Mangoyi2 
[1] Department of Chemistry, University of Nairobi, Nairobi, Kenya;Department of Biochemistry, University of Zimbabwe, Harare, Mt. Pleasant, Zimbabwe
关键词: Isolation;    Chromatography;    4’-dimethoxyflavone;    5-hydroxy-7;    Antifungal;    Combretum zeyheri;   
Others  :  1233181
DOI  :  10.1186/s12906-015-0934-7
 received in 2015-05-15, accepted in 2015-11-10,  发布年份 2015
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【 摘 要 】

Background

Combretum zeyheri, belongs to the family Combretaceae and is one of the most popular herbal plants in tropical and subtropical countries. The leaves of Combretum zeyheri have been used as herbal medicine and have been reported to have pharmacological activity which includes anti-bacterial, anti-fungal, anticancer and antioxidant properties. The goal of this study was to isolate, identify and characterize compounds from C. zeyheri leaves which are responsible for its antifungal activity.

Methods

The preliminary isolation of C. zeyheri active compounds was carried out using chromatographic techniques which include sephadex gel column chromatography, silica gel column chromatography and thin-layer chromatography (TLC). The isolated compounds were then investigated for their antifungal activity using broth dilution assay. The combined effect of the most potent compound and an antifungal drug miconazole was investigated using the checkerboard assay. Time-kill assays were conducted for the combinations using the colony counting method. The mechanism of action of 5-hydroxy-7,4’-dimethoxyflavone as a potent antifungal agent was investigated by determining its inhibitory activity on Candida albicans drug efflux pumps using the ciprofloxacin assay. The ability of 5-hydroxy-7,4’-dimethoxyflavone to inhibit antioxidant enzymes as well as the biosynthesis of ergosterol were also investigated.

Results

A total of four pure compounds (A-D) were isolated from C. zeyheri leaf extract. Compound B (5-hydroxy-7,4’-dimethoxyflavone) was found to be active against Candida albicans using broth dilution method. This compound was also found to have synergistic activity on growth of C. albicans when combined with miconazole, completely inhibiting growth after only 4 hrs of incubation. Analysis of ergosterol content from Candida albicans showed a time-dependent decrease to 91 % and 63 % at 16 and 24 hrs respectively, in cells treated with ½ MIC of 5-hydroxy-7,4’-dimethoxyflavone. The compound 5-hydroxy-7,4’-dimethoxyflavone also showed inhibition of both the drug efflux pumps (with IC 50  = 51.64 μg/ml) and the antioxidant enzymes (at 5 μM).

Conclusion

The compound 5-hydroxy-7,4’-dimethoxyflavone may be partly responsible for the reported antifungal activity of C. zeyheri, and may serve as a potential source of lead compounds that can be developed as antifungal phytomedicines.

【 授权许可】

   
2015 Mangoyi et al.

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【 参考文献 】
  • [1]Vandeputte P, Ferrari S, Coste AT. Antifungal Resistance and New Strategies to Control Fungal Infections. Int J Microbiol. 2012; 2012(713687):1-26.
  • [2]Perlin DS. Antifungal drug resistance: do molecular methods provide a way forward? Curr Opin Infect Dis. 2009; 22:568-573.
  • [3]Badiee P, Hashemizadeh Z. Opportunistic invasive fungal infections: diagnosis & clinical management. Indian J Med Res. 2014; 139:195-204.
  • [4]Carrillo-Muñoz J, Finquelievich J, Tur-Tur C, Eraso E, Jauregizar N, Quindós G, Giusiano G. Combination antifungal therapy: A strategy for the management of invasive fungal infections. Rev Esp Quimioter. 2014; 27:141-158.
  • [5]Paramythiotou E, Frantzeskaki F, Flevari A, Armaganidis A, Dimopoulos G. Invasive Fungal Infections in the ICU: How to Approach, How to Treat. Molecules. 2014; 19:1085-1119.
  • [6]Jothy S, Zakaria Z, Chen Y, Lau YL, Latha LY, Shin L, Sasidharan S. Bioassay-Directed Isolation of Active Compounds with Antiyeast Activity from a Cassia fistula Seed Extract. Molecules. 2011; 16:7583-7592.
  • [7]Avila E, Serna A, Aguilar F, Lezama R. Cytotoxic Activity of Four Mexican Medicinal Plants. Proc West Pharmacol Soc. 2009; 52:78-82.
  • [8]Maroyi A. Traditional use of medicinal plants in south-central Zimbabwe: review and perspectives. J Ethnobiol Ethnomed. 2013; 9:31. BioMed Central Full Text
  • [9]Fyhrquist P, Mwasumbi L, Haeggstrom CA, Vuorela H, Hiltunen R, Vuorela P. Ethnobotanical and antimicrobial investigation of some species of Terminalia and Combretum (Combretaceae) growing in Tanzania. J Ethnopharmacol. 2002; 79:169-177.
  • [10]Mangoyi R, Mukanganyama S (2011) In Vitro Antifungal Activities of Selected Medicinal Plants from Zimbabwe against Candida albicans and Candida krusei. The African Journal of Plant Science and Biotechnology 5:1–7
  • [11]Mangoyi R, Mafukidze W, Marobela K, Mukanganyama S. Antifungal Activities and Preliminary Phytochemical Investigation of Combretum Species from Zimbabwe. Microbial and Biochemical Technology. 2012; 4:037-044.
  • [12]Masoko P, Eloff JN. Bioautography indicates the multiplicity of antifungal compounds from twenty-four southern African Combretum species (Combretaceae). Afr J Biotechnol. 2006; 5:1625-1647.
  • [13]Spjut RW: World Botanical Associates Plant Collections for Antitumor Screening: Review of plants collected for antitumor screening. 2010, 1: 48
  • [14]Boora F, Chirisa E, Mukanganyama S: Evaluation of nitrite radical scavenging properties of selected Zimbabwean plant extracts and implications for anti-oxidative uses in food preservation. 2014
  • [15]Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951; 193:265.
  • [16]Habig W, Pabst MJ, Jakoby WB. The first enzymatic step in mercapturic acid formation. Glutathione-S-transferase. J Biol Chem. 1974; 249:7130-7139.
  • [17]Luck H: Catalase. pp. in H.U. Bergmeyer (Ed): Verlag Chemie and academic pres. Weinheim, New York. 1963, 885–888
  • [18]Misra, HP: Handbook of Methods for Oxygen Radical Research, ed. Greenwald, R. A. (CRC, Boca Raton, FL), 1985, 237–241
  • [19]Carlberg I, Mannervik B. Glutathione reductase. Methods Enzymol. 1985; 113:484-490.
  • [20]Mohandas J, Marshall JJ, Duggin GG, Horvath JS, Tiller DJ. Low activities of glutathione-related enzymes as factors in the genesis of urinary bladder cancer. Cancer Res. 1984; 44:5086-5091.
  • [21]Zaheer N, Tewari KK, Krishnan PS. Mitochondrial forms of glucose-6-phosphate dehydrogenase 6-phosphogluconic acid dehydrogenase in rat liver. Arch Biochem Biophys. 1967; 120:22-34.
  • [22]Campbell BC, Chan KL, Kim JH. Chemosensitization as a Means to Augment Commercial Antifungal Agents. Front Microbiol. 2012; 3:79.
  • [23]Kolak U, Hacibekiroglu I, Ozturk M, Ozgokce F, Ulubelen A. Antioxidant and anticholinesterase constituents of Salvia poculata. Turk J Chem. 2009; 33:813-823.
  • [24]Martini ND, Katerere DRP, Eloff JN. Biological activity of five antibacterial flavonoids from Combretum erythrophyllum (Combretaceae). J of Ethno. 2004; 93:207-212.
  • [25]Kummee S, Tewtraku S, Subhadhirasaku S, Songklanakarin J. Antimicrobial activity of the ethanol extract and compounds from the rhizomes of Kaempferia parviflora. Sci Technol. 2008; 30:463-466.
  • [26]Lomovskaya O, Watkins W. Inhibition of Efflux Pumps as a Novel Approach to Combat Drug Resistance in Bacteria. J Mol Microbiol Biotechnol. 2001; 2:225-236.
  • [27]Alcazar-Fuoli L, Mellado E. Ergosterol biosynthesis in Aspergillus fumigatus: its relevance as an antifungal target and role in antifungal drug resistance. Frontiers in Microbiology, Fungi and Their Interactions. 2013; 3:1-6.
  • [28]Krauss J, Gratzl C, Sturm V, Müller C, Staudacher V, Schmidt CQ, Bracher F. Synthesis and Biological Evaluation of Novel Alkyl-Imidazolyl Carbinols and their Esters: Potent Antimycotics. Sci Pharm. 2013; 81:641-650.
  • [29]Rajput SB, Karuppayil SM. Small molecules inhibit growth, viability and ergosterol biosynthesis in Candida albicans. Springerplus. 2013; 2:26. BioMed Central Full Text
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