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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Phytochemical Study of Aqueous Extract of Ochna schweinfurthiana F. Hoffm Powder Bark and Evaluation of Their Anti-Inflammatory, Cytotoxic, and Genotoxic Properties
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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:Ochna Schweinfurthiana F. Hoffm粉树皮和抗炎,细胞毒性和基因毒性特性的植物化学植物研究

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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:OchnaSchweinfurthiana已被用于传统医学以治疗疼痛,炎症和关节炎。它是一种丰富的黄酮类化合物来源,具有潜在的用途,作为治疗药物的发展模板。因此,本研究的目的是研究植物化学含量,并评估Ochna Schweinfurthiana树皮(OSE)水提取物的体外细胞毒性,遗传毒性和抗炎活性。根据LC-MS程序进行植物化学研究,同时使用薄层和色谱分离进行分离。通过线粒体活力研究了细胞毒性[3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑粒溴化物](MTT)方法,而使用沙门氏菌毛刺试管TA98和TA100确定提取物的遗传毒性潜力。通过对15-脂氧合酶和牛血清白蛋白变性(BSA)测定的体外抑制来评价OSE的抗炎作用。从OSE中提取的化合物的研究导致六种已知化合物的鉴定和分离,即血拨中藻体(9),6,7-二甲氧基-3'-4'-二甲氧基氨基甲酰伐(10),岩藻糖苷(13),Amentoflavone(14 ),agathisflavone(15)和β-D-Fructofuranosyl-α-D-吡喃葡萄糖(17)。在抗炎测定中,树皮的水性提取物显示出15-脂氧合酶的选择性抑制,IC50值为32.2±0.36Ω·0μg/ mL,牛血清白蛋白变性测定的结果为130±5.78μg/ ML显示中度活动。毒性测定表明,OSE在VERO细胞系上是非胞间毒性,LC50值为50mg / ml和NongeNotoxic朝向沙门氏菌毒蕈氏菌菌株TA98和TA100。本研究的结果支持喀麦隆所选药用植物的传统用途,用于治疗炎症病症。 OSE的非胞性毒性和非肝毒性表明这种植物使用安全。

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