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尖瓣猪殃殃中的黄酮苷及其对肝脂质蓄积的抑制作用。

Flavone glycosides from Sicyos angulatus and their inhibitory effects on hepatic lipid accumulation.

机构信息

Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul, 151-742, Republic of Korea.

Laboratory Animal Resource Center, Korea Research Institute of Bioscience and Biotechnology, Republic of Korea.

出版信息

Phytochemistry. 2019 Jan;157:53-63. doi: 10.1016/j.phytochem.2018.10.013. Epub 2018 Oct 24.

Abstract

A library of extracted natural materials (Korea Bioactive Natural Material Bank) have been screened to discover candidates for the treatment of non-alcoholic liver disease (NAFLD), and the 70% ethanol extract of Sicyos angulatus was found to inhibit hepatic lipid accumulation. Bioassay-guided fractionation of this bioactive extract yielded five previously undescribed flavonoid glycosides and one previously undescribed flavonolignan glycoside along with seven known flavonoid glycosides. The chemical structures of these compounds were elucidated by a combination of extensive spectroscopic analysis, including MS, NMR and UV techniques. Eight compounds of all isolated compounds showed inhibitory effects on the lipid accumulation induced by high concentrations of palmitic acid and glucose in HepG2 cells. Four selected compounds were tested for lipid content in a dose-dependent manner (10, 20 and 40 μM), and among those compounds, kaempferol 3-O-β-d-glucopyranosyl-7-O-α-l-rhamnopyranoside showed the strongest inhibition of hepatic lipid production in HepG2 cells. In an oil-red O staining assay, five compounds were shown to reduce hepatic lipid accumulation better than what was observed in the vehicle control group. The present study suggests a new class of chemical entities for developing bioactive agents for the treatment of diseases caused by fat accumulation in the liver.

摘要

已从提取的天然物质库(韩国生物活性天然物质库)中筛选出候选物质,用于治疗非酒精性肝病(NAFLD),发现朝鲜蓟的 70%乙醇提取物可抑制肝脂质蓄积。对这种具有生物活性的提取物进行生物测定指导的分段分离,得到了五个以前未描述的类黄酮糖苷和一个以前未描述的类黄酮木脂素糖苷,以及七个已知的类黄酮糖苷。这些化合物的化学结构通过广泛的光谱分析(包括 MS、NMR 和 UV 技术)来阐明。所有分离化合物中的八种化合物均显示出对 HepG2 细胞中高浓度棕榈酸和葡萄糖诱导的脂质积累的抑制作用。对四种选定的化合物进行了剂量依赖性的脂质含量测试(10、20 和 40μM),其中,山柰酚 3-O-β-d-吡喃葡萄糖基-7-O-α-l-鼠李吡喃糖苷在 HepG2 细胞中显示出最强的抑制肝脂质生成作用。在油红 O 染色试验中,五种化合物显示出比在载体对照组中观察到的更好的肝脂质蓄积减少作用。本研究为开发用于治疗因肝脏脂肪堆积引起的疾病的生物活性药物提供了一类新的化学实体。

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