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霍夫曼氏榕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特性评估。

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

作者信息

Djova Steve V, Nyegue Maximilienne A, Messi Angelique N, Afagnigni Alian D, Etoa François-X

机构信息

Department of Biochemistry, University of Yaounde I, PO Box 812, Yaounde, Cameroon.

Department of Microbiology, University of Yaounde I, PO Box 812, Yaounde, Cameroon.

出版信息

Evid Based Complement Alternat Med. 2019 Feb 18;2019:8908343. doi: 10.1155/2019/8908343. eCollection 2019.

Abstract

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 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 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 -D-fructofuranosyl--D-glucopyranoside (17). In the anti-inflammatory assay, aqueous extracts of the bark showed selective inhibition of 15-lipooxygenase with IC value of 32.2 ± 0.36  μg/mL and the result of the bovine serum albumin denaturation assay with IC value of 130± 5.78 g/mL showed moderate activity. The toxicity assay indicated that OSE are noncytotoxic on Vero cell line with LC value of 50 mg/mL and nongenotoxic toward 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.

摘要

它已被用于传统医学中治疗疼痛、炎症和关节炎。它是黄酮类复杂二聚体的丰富来源,具有作为治疗药物开发模板的潜在用途。因此,本研究的目的是研究树皮水提取物(OSE)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。植物化学研究按照液相色谱 - 质谱法进行,分离则使用薄层色谱法和柱色谱法。细胞毒性通过线粒体活力[3 - (4,5 - 二甲基噻唑 - 2 - 基) - 2,5 - 二苯基四氮唑溴盐](MTT)法进行研究,而提取物的遗传毒性潜力则使用测试菌株TA98和TA100来确定。OSE的抗炎作用通过体外抑制15 - 脂氧合酶和牛血清白蛋白变性(BSA)试验进行评估。对从OSE中提取的化合物的研究导致鉴定和分离出六种已知化合物,即hemerocallone(9)、6,7 - 二甲氧基 - 3' - 4' - 二甲氧基异黄酮(10)、紫草酸苷(13)、穗花杉双黄酮(14)、贝壳杉黄酮(15)和β - D - 呋喃果糖基 - α - D - 吡喃葡萄糖苷(17)。在抗炎试验中,树皮的水提取物对15 - 脂氧合酶表现出选择性抑制,IC值为32.2±0.36μg/mL,牛血清白蛋白变性试验结果的IC值为130±5.78μg/mL,显示出中等活性。毒性试验表明,OSE对Vero细胞系无细胞毒性,LC值为50mg/mL,对测试菌株TA98和TA100无遗传毒性。本研究结果支持喀麦隆选定药用植物在治疗炎症方面的传统用途。OSE的无细胞毒性和无遗传毒性表明该植物使用安全。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4895/6398047/41524f05b50b/ECAM2019-8908343.001.jpg

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