Owumi Solomon, Olanlokun John O, Wu Bocheng, Duro-Ladipo Abiola Marian, Oyelere Sophia E, Khan Shabana I, Oyelere Adegboyega K
Cancer Research and Molecular Biology Laboratories, University of Ibadan, Ibadan 200005, Nigeria.
Laboratories for Biomembrane and Biotechnology Research, Department of Biochemistry, University of Ibadan, Ibadan 200005, Nigeria.
Molecules. 2024 Nov 29;29(23):5658. doi: 10.3390/molecules29235658.
Agunmu (ground herbal medicine) is a form of West African traditional medicine consisting of a cocktail of herbs. The goal of this study is to evaluate a formulation of Agunmu made from , , , , and , sold in the open market and commonly used for the treatment of malaria by the locals, for its antimalarial effects and to determine the active principles that may contribute to the antimalarial effect. The ethanolic extract obtained from this formulation (Ag-Iba) was analyzed, using TLC, LC-MS, and Tandem-MS techniques, to determine its phytochemical properties. The extract was tested in vitro against representative bacteria strains, cancer and normal human cell lines, and susceptible (D6) and resistant (W2) . In subsequent in vivo experiments, graded doses of the extract were used to treat mice infected with chloroquine-susceptible (NK-65) and chloroquine-resistant (ANKA) strains of . Bacteria growth was monitored with a disc diffusion assay, cancer cell viability was determined with MTS assay, and percentage parasitemia and parasite clearance were determined by microscopy. Bound heme content, host mitochondria permeability transition (mPT) pore opening, FF-ATPase, and lipid peroxidation were determined via spectrophotometry. Indices of oxidative stress, anti-oxidant activities, toxicity, cell death, and inflammatory responses were obtained using biochemical and ELISA techniques. The histology of the liver and spleen was performed using the standard method. We elucidated the structures of the critical active principles in the extract to be flavonoids: kaempferol, quercetin, myricetin, and their glycosides with little or no detectable levels of the toxic Aristolochic acids that are found in , one of the components of the formulation. The extract also showed anti-plasmodial activity in in vitro and in vivo models. Furthermore, the extract dose-dependently decreased mitochondrial dysfunction, cell death, and inflammatory and oxidative damage but increased antioxidant potentials. Presumably, the active principles in the extract work as a combinatorial therapy to elicit potent antimalarial activity. Overall, our study unraveled the active components from a commercial herbal formulation that could be reformulated for antimalarial therapy.
阿贡木(一种研磨的草药)是西非传统医学的一种形式,由多种草药混合而成。本研究的目的是评估一种在公开市场上出售且当地人常用于治疗疟疾的、由[草药名称1]、[草药名称2]、[草药名称3]、[草药名称4]和[草药名称5]制成的阿贡木制剂的抗疟效果,并确定可能有助于抗疟作用的活性成分。使用薄层色谱法(TLC)、液相色谱 - 质谱联用(LC - MS)和串联质谱技术对从该制剂(阿贡木 - 伊巴)中获得的乙醇提取物进行分析,以确定其植物化学性质。该提取物在体外针对代表性细菌菌株、癌细胞系和正常人类细胞系以及敏感(D6)和耐药(W2)[疟原虫名称]进行了测试。在随后的体内实验中,使用分级剂量的提取物治疗感染氯喹敏感(NK - 65)和氯喹耐药(ANKA)[疟原虫名称]菌株的小鼠。通过纸片扩散法监测细菌生长,用MTS法测定癌细胞活力,通过显微镜检查确定疟原虫血症百分比和寄生虫清除情况。通过分光光度法测定结合血红素含量、宿主线粒体通透性转换(mPT)孔开放、FF - ATP酶和脂质过氧化。使用生化和酶联免疫吸附测定(ELISA)技术获得氧化应激、抗氧化活性、毒性、细胞死亡和炎症反应的指标。采用标准方法对肝脏和脾脏进行组织学检查。我们阐明了提取物中关键活性成分的结构为黄酮类化合物:山奈酚、槲皮素、杨梅素及其糖苷,且制剂成分之一[植物名称]中几乎检测不到或未检测到有毒的马兜铃酸。该提取物在体外和体内模型中也显示出抗疟活性。此外,提取物剂量依赖性地降低线粒体功能障碍、细胞死亡以及炎症和氧化损伤,但增加抗氧化潜力。据推测,提取物中的活性成分作为一种联合疗法发挥强效抗疟活性。总体而言,我们的研究揭示了一种商业草药制剂中的活性成分,这些成分可重新配制用于抗疟治疗。