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非洲药用植物 Ximenia caffra 的提取物的植物化学分析及抗炎活性。

Phytochemical Analysis and Anti-Inflammatory Activity of the Extracts of the African Medicinal Plant Ximenia caffra.

机构信息

New Use Agriculture and Natural Plant Products Program, Department of Plant Biology and Pathology, Rutgers University, 59 Dudley Road, New Brunswick, NJ 08901, USA ; Department of Medicinal Chemistry, Ernest Mario School of Pharmacy, Rutgers University, 160 Frelinghuysen Road, Piscataway, NJ 08854, USA.

Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers University, 160 Frelinghuysen Road, Piscataway, NJ 08854, USA.

出版信息

J Anal Methods Chem. 2015;2015:948262. doi: 10.1155/2015/948262. Epub 2015 Feb 17.

Abstract

A method was developed for identification and quantification of polyphenols in the leaves of Ximenia caffra using HPLC/UV/MS. Based on analyzing the MS and UV data and in comparison to the authentic standards, a total of 10 polyphenols were identified and quantified, including gallic acid, catechin, quercetin, kaempferol, and their derivatives. The total content of these compounds was found to be approximately 19.45 mg/g in the leaf and the most abundant is quercetin-rutinoside (9.08 mg/g). The total phenolic content as measured by Folin-Ciocalteu assay was 261.87 ± 7.11 mg GAE/g and the total antioxidant capacity as measured in vitro was 1.46 ± 0.01 mmol Trolox/g. The antiproliferative effect of the leaf extract was measured by MTS assay with IC50 value of 239.0 ± 44.5 μg/mL. Cell-based assays show that the leaf extract inhibits the mRNA expression of proinflammatory genes (IL-6, iNOS, and TNF-α) by using RT-qPCR, implying its anti-inflammatory effects. It was further demonstrated that the underlying therapeutic mechanism involves the suppression of NF-κB, a shared pathway between cell death and inflammation.

摘要

采用高效液相色谱/紫外/质谱联用(HPLC/UV/MS)法对 Ximenia caffra 叶中的多酚进行了鉴定和定量分析。基于对 MS 和 UV 数据的分析,并与标准品进行比较,共鉴定和定量了 10 种多酚,包括没食子酸、儿茶素、槲皮素、山奈酚及其衍生物。叶中这些化合物的总含量约为 19.45mg/g,其中含量最丰富的是槲皮素-芸香糖苷(9.08mg/g)。Folin-Ciocalteu 法测定的总酚含量为 261.87±7.11mgGAE/g,体外测定的总抗氧化能力为 1.46±0.01mmolTrolox/g。采用 MTS 法测定叶提取物的增殖抑制活性,IC50 值为 239.0±44.5μg/mL。细胞实验表明,叶提取物通过 RT-qPCR 抑制促炎基因(IL-6、iNOS 和 TNF-α)的 mRNA 表达,表明其具有抗炎作用。进一步研究表明,其潜在的治疗机制涉及抑制 NF-κB,这是细胞死亡和炎症之间的共同途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c9f/4346700/c1800cf73b59/JAMC2015-948262.001.jpg

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