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乌那酸与脂多糖在人肝癌 HepG2 细胞中的交互毒性作用

Interactive toxicity of usnic acid and lipopolysaccharides in human liver HepG2 cells.

机构信息

Division of Toxicology, Office of Applied Research and Safety Assessment, Center for Food Safety and Applied Nutrition, U. S. Food and Drug Administration, Laurel, MD 20708, USA.

出版信息

J Appl Toxicol. 2012 Sep;32(9):739-49. doi: 10.1002/jat.2768. Epub 2012 Jul 9.

Abstract

Usnic acid (UA), a natural botanical product, is a constituent of some dietary supplements used for weight loss. It has been associated with clinical hepatotoxicity leading to liver failure in humans. The present study was undertaken to evaluate the interactive toxicity, if any, of UA with lipopolysaccarides (LPS), a potential contaminant of food, at low non-toxic concentrations. The human hepatoblastoma HepG2 cells were treated with the vehicle control and test agents, separately and in a binary mixture, for 24 h at 37°C in 5% CO2. After the treatment period, the cells were evaluated by the traditional biochemical endpoints of toxicity in combination with the toxicogenomic endpoints that included cytotoxicity, oxidative stress, mitochondrial injury and changes in pathway-focused gene expression profiles. Compared with the controls, low non-toxic concentrations of UA and LPS separately showed no effect on the cells as determined by the biochemical endpoints. However, the simultaneous mixed exposure of the cells to their binary mixture resulted in increased cytotoxicity, oxidative stress and mitochondrial injury. The pathway-focused gene expression analysis resulted in the altered expression of several genes out of 84 genes examined. Most altered gene expressions induced by the binary mixture of UA and LPS were different from those induced by the individual constituents. The genes affected by the mixture were not modulated by either UA or LPS. The results of the present study suggest that the interactions of low nontoxic concentrations of UA and LPS produce toxicity in HepG2 cells.

摘要

乌头酸(UA)是一种天然植物产物,是一些用于减肥的膳食补充剂的成分。它已被认为与导致人类肝功能衰竭的临床肝毒性有关。本研究旨在评估 UA 与脂多糖(LPS)在低非毒性浓度下是否存在相互毒性,LPS 是食物的潜在污染物。用人肝癌 HepG2 细胞分别用载体对照和测试剂处理,在 37°C 和 5%CO2 下处理 24 小时。处理期后,通过毒性的传统生化终点和毒理基因组终点评估细胞,包括细胞毒性、氧化应激、线粒体损伤和途径重点基因表达谱的变化。与对照相比,低非毒性浓度的 UA 和 LPS 单独使用时通过生化终点确定对细胞没有影响。然而,细胞同时混合暴露于两者的混合物中会导致细胞毒性、氧化应激和线粒体损伤增加。通路重点基因表达分析导致 84 个检测基因中的几个基因的表达发生改变。UA 和 LPS 混合物诱导的大多数基因表达改变与单个成分诱导的改变不同。混合物影响的基因不受 UA 或 LPS 的调节。本研究的结果表明,低非毒性浓度的 UA 和 LPS 的相互作用会在 HepG2 细胞中产生毒性。

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