Antibacterial effects of Alchornea cordifolia (Schumach. and Thonn.) Müll. Arg extracts and compounds on gastrointestinal, skin, respiratory and urinary tract pathogens

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• 作者：X. Siwe Noundou^a ; ^{xavsiw@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; R.W.M. Krause^a ; S.F. van Vuuren^b ; D. Tantoh Ndinteh^c ; D.K. Olivier^b
• 关键词：ATCC ; American type culture collection ; CC ; column chromatography ; CFU ; colony forming units ; CHCl3 ; chloroform ; COSY ; correlation spectroscopy ; DCM ; dichloromethane ; DEPT ; distortionless enhancement by polarisation transfer ; DMSO ; dimethyl sulfoxide ; EtOH ; ethanol ; EtOAc ; ethyl acetate ; FTIR ; Fourier transform infrared spectroscopy ; H2O ; water ; HMBC ; heteronuclear multiple bond correlation ; HNC ; Herbier National du Cameroun (i.e. National Herbarium of Cameroon) ; HSQC ; heteronuclear single quant
• 刊名：Journal of Ethnopharmacology
• 出版年：2016
• 出版时间：17 February 2016
• 年：2016
• 卷：179
• 期：Complete
• 页码：76-82
• 全文大小：376 K

文摘

The leaves, stems and roots of Alchornea cordifolia (Schumach. and Thonn.) Müll. Arg. are used as traditional medicine in many African countries for the management of gastrointestinal, respiratory and urinary tract infections as well as for the treatment of wounds.

Aim of the study

To determine the in vitro antibacterial activity of the crude extracts of leaves and stems of A. cordifolia on gastrointestinal, skin, respiratory and urinary tract pathogens and to identify the compounds in the extracts that may be responsible for this activity.

Materials and methods

The antibacterial activities of crude extracts [hexane, chloroform (CHCl₃), ethyl acetate (EtOAc), ethanol (EtOH), methanol (MeOH) and water (H₂O)] as well as pure compounds isolated from these extracts were evaluated by means of the micro-dilution assay against four Gram-positive bacteria, i.e. Bacillus cereus ATCC 11778, Enterococcus faecalis ATCC 29212, Staphylococcus aureus ATCC 25923 and S. saprophyticus ATCC 15305, as well as four Gram-negative bacterial strains, i.e. Escherichia coli ATCC 25922, Klebsiella pneumoniae ATCC 13883, Moraxella catarrhalis ATCC 23246 and Proteus mirabilis ATCC 43071. The isolation of the active constituents was undertaken by bio-autographic assays in conjunction with chromatographic techniques. The identification and characterisation of the isolated compounds were done using mass spectrometry (MS) and Fourier transformed infrared spectrometry (FTIR) as well as 1D- and 2D- nuclear magnetic resonance (NMR) analyses.

Results

The leaves and stems of A. cordifolia exhibited varied antibacterial activity against all eight pathogens. Most of the MIC values ranged between 63 and 2000 µg/ml. The highest activities for the crude extracts (63 µg/ml) were observed against S. saprophyticus [stem (EtOAc, CHCl₃ and hexane), leaves (MeOH, EtOH, EtOAc and CHCl₃)], E. coli [stem (MeOH and EtOH), leaves (MeOH, EtOH, EtOAc and CHCl₃)], M. catarrhalis [leaves (EtOAc and CHCl₃)], K. pneumoniae [stem (CHCl₃), leaves (CHCl₃)] and S. aureus [leaves (CHCl₃)]. Seven constituents [stigmasterol (1), stigmasta-4,22-dien-3-one (2), friedelin (3), friedelane-3-one-28-al (4), 3-O-acetyl-aleuritolic acid (5), 3-O-acetyl-erythrodiol (6) and methyl-3,4,5-trihydroxybenzoate (methyl gallate) (7)] were isolated from the stem MeOH extract. All these compounds displayed some antibacterial activity against the eight pathogens with highest activity against S. saprophyticus (2 µg/ml). Furthermore, this is the first report of compounds 1, 2, 3, 4, 6 and 7 isolated from A. cordifolia and where a complete set of 2D-NMR data for fridelane-3-one-28-al (4) is presented.

Conclusion

The study demonstrated that the antibacterial activities of A. cordifolia extracts may be due to the presence of the seven isolated compounds, where compounds 3–6 showed the best activity. The observed activity against gastrointestinal, skin, respiratory and urinary tract pathogens supports the traditional use for the treatment of such ailments.