Amoussa Abdou Madjid O, Lagnika Latifou, Bourjot Mélanie, Vonthron-Senecheau Cathérine, Sanni Ambaliou
Unité de Biochimie et Biologie Moléculaire, Equipe de Biochimie et Substances Naturelles Bioactives, Faculté des Sciences et Techniques, Université d'Abomey-Calavi, Cotonou, 04 BP 0320, Bénin.
Laboratoire d'Innovation Thérapeutique, Faculté de Pharmacie, UMR CNRS-Unistra 7200, Illkirch, France.
BMC Complement Altern Med. 2016 Aug 12;16(1):284. doi: 10.1186/s12906-016-1266-y.
Acacia ataxacantha is a medicinal specie used extensively in traditional medicine of Benin republic to treat infectious diseases. Our previous study showed interesting antibacterial and antifungal activities against six strains of bacteria and six strains of fungi. The aim of this study was to investigate the antimicrobial and antioxidant activities of compounds isolated from A. ataxacantha.
Chromatographic and spectroscopic methods were used to isolate and identify three compounds (1-3) from the bark of A. ataxacantha. Phytochemical investigation of A. ataxacantha (Fabaceae) led to the isolation of three triterpenoids (1-3). The structure of isolated compounds was established by differents spectroscopic methods such as UV, (1)H NMR, (13)C NMR, 2D NMR and Mass. All isolated compounds were tested for antimicrobial activity using agar disc-diffusion and microdilution methods. The radical scavenging activity of isolated compounds was assessed using 2,2-diphenyl-1-picrylhydrazyl (DPPH) method.
Phytochemical investigation led to the isolation and identification of lupeol (1), betulinic acid (2) and betulinic acid-3-trans-caffeate (3). Moderate antimicrobial activity was obtained with compound 3 against methicillin-resitant Staphylococcus aureus, Enterococcus feacalis and Pseudomonas aeruginosa with MIC value of 25 μg/ml and Staphylococcus aureus (MIC of 50 μg/ml). Compounds 3 was more active against Staphylococcus epidermidis and Candida albicans with a MIC value of 12.5 μg/ml in boths cases. Compounds 3 had also interesting antioxidant activity with an IC50 of 3.57 μg/ml compared to quercetin (1.04 μg/ml).
The overall results of this study provide evidence that the compound 3, isolated from A. ataxacantha, exhibit antimicrobial activity against Gram-positive and Gram-negative bacteria and yeast, especially against C. albicans.
无刺金合欢是贝宁共和国传统医学中广泛用于治疗传染病的药用植物。我们之前的研究表明,其对六种细菌菌株和六种真菌菌株具有有趣的抗菌和抗真菌活性。本研究的目的是调查从无刺金合欢中分离出的化合物的抗菌和抗氧化活性。
采用色谱和光谱方法从无刺金合欢树皮中分离并鉴定出三种化合物(1-3)。对无刺金合欢(豆科)进行植物化学研究,分离出三种三萜类化合物(1-3)。通过紫外光谱、氢核磁共振、碳核磁共振、二维核磁共振和质谱等不同光谱方法确定分离出的化合物的结构。使用琼脂纸片扩散法和微量稀释法对所有分离出的化合物进行抗菌活性测试。使用2,2-二苯基-1-苦基肼(DPPH)法评估分离出的化合物的自由基清除活性。
植物化学研究导致分离并鉴定出羽扇豆醇(1)、桦木酸(2)和桦木酸-3-反式咖啡酸酯(3)。化合物3对耐甲氧西林金黄色葡萄球菌、粪肠球菌和铜绿假单胞菌具有中等抗菌活性,最低抑菌浓度(MIC)值为25μg/ml,对金黄色葡萄球菌的MIC值为50μg/ml。化合物3对表皮葡萄球菌和白色念珠菌更具活性,在这两种情况下MIC值均为12.5μg/ml。化合物3还具有有趣的抗氧化活性,与槲皮素(1.04μg/ml)相比,其半数抑制浓度(IC50)为3.57μg/ml。
本研究的总体结果提供了证据,表明从无刺金合欢中分离出的化合物3对革兰氏阳性菌、革兰氏阴性菌和酵母菌具有抗菌活性,尤其是对白色念珠菌。