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Phytochemical Study of Aqueous Extract of Ochna schweinfurthiana F. Hoffm Powder Bark and Evaluation of Their Anti-Inflammatory Cytotoxic and Genotoxic Properties

机译:ch草叶树皮水提取物的植物化学研究及其抗炎细胞毒性和遗传毒性的评价

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摘要

Ochna schweinfurthiana has been used in traditional medicine to treat pain, inflammation, and arthritis. It is a rich source of complex dimers of flavonoids with potential use as templates for the development of therapeutic drugs. Hence, the aim of this study was to study the phytochemical content and evaluate the in vitro cytotoxic, genotoxic, and anti-inflammatory activities of the aqueous extract of Ochna schweinfurthiana bark (OSE). Phytochemical study was carried out according to LC-MS procedures, while isolation was carried out using thin layer and column chromatographies. Cytotoxicity was investigated by the mitochondrial viability [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] (MTT) method while genotoxicity potential of the extract was ascertained using the Salmonella typhimurium test strains TA98 and TA100. The anti-inflammatory effect of OSE was evaluated by the in vitro inhibition of 15-lipooxygenase enzyme and bovine serum albumin denaturation (BSA) assays. The investigation of compounds extracted from OSE led to the identification and isolation of six known compounds, namely, hemerocallone (9), 6,7-dimethoxy-3'-4'-dimethoxyisoflavone (10), lithospermoside (13), amentoflavone (14), agathisflavone (15), and β-D-fructofuranosyl-α-D-glucopyranoside (17). In the anti-inflammatory assay, aqueous extracts of the bark showed selective inhibition of 15-lipooxygenase with IC50 value of 32.2 ± 0.36  μg/mL and the result of the bovine serum albumin denaturation assay with IC50 value of 130± 5.78 μg/mL showed moderate activity. The toxicity assay indicated that OSE are noncytotoxic on Vero cell line with LC50 value of 50 mg/mL and nongenotoxic toward Salmonella typhimurium tester strain TA98 and TA100. Result from this study supports the traditional use of the selected medicinal plants in Cameroon for the treatment of inflammatory conditions. Noncytotoxicity and nongenotoxicity of OSE suggest that this plant is safe for use.
机译:Ochna schweinfurthiana已在传统医学中用于治疗疼痛,炎症和关节炎。它是类黄酮的复杂二聚体的丰富来源,可潜在地用作开发治疗药物的模板。因此,本研究的目的是研究植物化学成分Ochna schweinfurthiana树皮(OSE)的水提物的植物化学成分并评估其体外细胞毒性,遗传毒性和抗炎活性。根据LC-MS程序进行植物化学研究,同时使用薄层色谱和柱色谱进行分离。通过线粒体生存力[3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四溴甲烷](MTT)方法研究了细胞毒性,同时使用鼠伤寒沙门氏菌测试菌株TA98和TA100确定了提取物的遗传毒性潜力。 。通过体外抑制15-脂氧合酶和牛血清白蛋白变性(BSA)分析评估了OSE的抗炎作用。对从OSE提取的化合物的研究导致了六种已知化合物的鉴定和分离,分别是半call草酮(9),6,7-二甲氧基-3'-4'-二甲氧基异黄酮(10),紫草苷(13),黄酮(14) ),agathisflavone(15)和β-D-果糖呋喃糖基-α-D-吡喃葡萄糖苷(17)。在抗炎试验中,树皮的水提物显示选择性抑制15-脂氧合酶,IC50值为32.2±0.36μg/ mL,牛血清白蛋白变性试验的IC50值为130±5.78μg/ mL。适度的活动。毒性试验表明,OSE对Vero细胞系无细胞毒性,LC50值为50 mg / mL,对鼠伤寒沙门氏菌测试株TA98和TA100无遗传毒性。这项研究的结果支持喀麦隆传统药用植物用于炎症性疾病的治疗。 OSE的非细胞毒性和非遗传毒性表明该植物可以安全使用。

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