彗星试验
遗传毒性
DNA损伤
细胞毒性
活力测定
化学
芍药苷
MTT法
分子生物学
超氧化物
脂多糖
毒性
生物化学
细胞
生物
DNA
体外
免疫学
色谱法
酶
高效液相色谱法
有机化学
作者
In Deok Kim,Bae Jin Ha
标识
DOI:10.1016/j.tiv.2009.06.019
摘要
LPS is one of the major constituents of the outer membrane of Gram-negative bacteria. LPS-induced activation of macrophage results in the nitrite (NO) production and the secretion of a pro-inflammatory mediator such as PGE(2). Excessive NO reacts with the superoxide anion to generate a selective oxidant and nitrating agent, peroxynitrite, which interacts with biological molecules and damages the cell membranes of them, being able to result in the cell death. We evaluated the protective effects of paeoniflorin (PF) against LPS-induced toxicity by measuring its dose-dependent effects on cell viability in MTT assay, NO production in NO assay, PGE(2) production in prostaglandin E(2) (PGE(2)) assay, and DNA damage in comet assay in LPS-treated RAW 264.7 macrophages. In the comet assay, we also analyzed tail length, tail DNA, and tail moment as the markers of DNA strand breaks. PF-treatment significantly protected RAW 264.7 macrophages against LPS-induced toxicity with the increase of viable cells, the decrease of NO and PGE(2), and the repair of DNA damage.
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