Fomogne-Fodjo M C Y, Ndinteh D T, Olivier D K, Kempgens P, van Vuuren S, Krause R W M
Department of Chemistry, Rhodes University, PO Box 94, Grahamstown 6140, South Africa.
Department of Applied Chemistry, University of Johannesburg, PO Box 17011, Doornfontein, Johannesburg 2028, South Africa.
J Ethnopharmacol. 2017 Jan 4;195:238-245. doi: 10.1016/j.jep.2016.11.027. Epub 2016 Nov 15.
Tetracera potatoria Afzel. Exg. Don (Dilleniaceae) is a medicinal plant used traditionally in Africa for the treatment of tuberculosis related ailments and respiratory infections. The antibacterial activity of the medium polar extracts of T. potatoria leaves and stem bark was recently reported against Mycobacterium smegmatis (MIC 25µg/mL) and M. aurum (65µg/mL), two fast-growing Mycobacterium strains used as model micro-organisms for the more pathogenic strain Mycobacterium tuberculosis (Fomogne-Fodjo et al., 2014). The aim of this study was consequently to isolate the compounds possibly contributing to this activity, and which may therefore be promising precursors to be used for the development of novel anti-TB drugs.
T. potatoria medium polar extract [MeOH/DCM (1:1, v/v)] was fractionated sequentially with petroleum ether to which EtOAC and MeOH were gradually added to increase the polarity. The examination of T. potatoria extract and its fractions was guided by bioassays for anti-mycobacterial activity against M. smegmatis (ATCC 23246) and M. aurum (NCTC 10437) using the minimum inhibitory concentration (MIC) method. All the isolated compounds were structurally elucidated using spectroscopic techniques and evaluated for their anti-mycobacterial activity.
Two novel secondary metabolites (1, 2) named tetraceranoate and N-hydroxy imidate-tetracerane, together with five known compounds [β-stigmasterol (3), stigmast-5-en-3β-yl acetate (4), betulinic acid (5), betulin (6) and lupeol (7)] were isolated and identified. Tetraceranoate exhibited the best activity against M. smegmatis with a minimum inhibitory concentration (MIC) of 7.8µg/mL, while β-stigmasterol, betulinic acid and betulin showed appreciable anti-mycobacterial activity against both strains (MIC 15µg/mL).
Seven compounds were isolated from the medium polar extract [MeOH/DCM (1:1, v/v)] of T. potatoria stem bark. Only tetraceranoate one of the isolated compounds showed antibacterial activity against M. smegmatis having efficacy as high as rifampicin (one of a three drug regimen recommended in the initial phase short-course anti-tuberculosis therapy). Thus, tetraceranoate might be an interesting target for systematic testing of anti-TB treatment and management. This research supports the use of T. potatoria in African traditional medicine for the treatment of tuberculosis related symptoms.
波叶锡叶藤(Tetracera potatoria Afzel. Exg. Don,五桠果科)是一种药用植物,在非洲传统上用于治疗与结核病相关的疾病和呼吸道感染。最近有报道称,波叶锡叶藤叶和茎皮的中等极性提取物对耻垢分枝杆菌(MIC 25µg/mL)和金色分枝杆菌(65µg/mL)具有抗菌活性,这两种快速生长的分枝杆菌菌株被用作致病性更强的结核分枝杆菌的模型微生物(Fomogne-Fodjo等人,2014年)。因此,本研究的目的是分离可能有助于这种活性的化合物,这些化合物可能是用于开发新型抗结核药物的有前景的前体。
波叶锡叶藤中等极性提取物[甲醇/二氯甲烷(1:1,v/v)]先用石油醚依次分级,然后逐渐加入乙酸乙酯和甲醇以增加极性。通过使用最低抑菌浓度(MIC)法对耻垢分枝杆菌(ATCC 23246)和金色分枝杆菌(NCTC 10437)的抗分枝杆菌活性进行生物测定,来指导对波叶锡叶藤提取物及其馏分的检测。所有分离出的化合物均采用光谱技术进行结构鉴定,并评估其抗分枝杆菌活性。
分离并鉴定出两种新型次生代谢产物(1, 2),分别命名为波叶锡叶藤酸酯和N-羟基亚胺酸-波叶锡叶藤烷,以及五种已知化合物[β-谷甾醇(3)、豆甾-5-烯-3β-基乙酸酯(4)、桦木酸(5)、桦木醇(6)和羽扇豆醇(7)]。波叶锡叶藤酸酯对耻垢分枝杆菌表现出最佳活性,最低抑菌浓度(MIC)为7.8µg/mL,而β-谷甾醇、桦木酸和桦木醇对两种菌株均表现出明显的抗分枝杆菌活性(MIC 15µg/mL)。
从波叶锡叶藤茎皮的中等极性提取物[甲醇/二氯甲烷(1:1,v/v)]中分离出七种化合物。只有分离出的化合物之一波叶锡叶藤酸酯对耻垢分枝杆菌具有抗菌活性,其效力高达利福平(初始阶段短程抗结核治疗推荐的三联药物方案之一)。因此,波叶锡叶藤酸酯可能是系统测试抗结核治疗和管理的一个有趣靶点。本研究支持波叶锡叶藤在非洲传统医学中用于治疗与结核病相关症状的应用。