Involvement of P450s and nuclear receptors in the hepatoprotective effect of quercetin on liver injury by bacterial lipopolysaccharide

CYP2E1 CYP1A2 脂多糖 肝损伤 氧化应激 药理学 受体 槲皮素 化学 细胞色素P450 孕烷X受体 细胞因子 肝功能 抗氧化剂 核受体 生物化学 医学 免疫学 内科学 转录因子 基因
作者
Ling Zhao,Fang Chen,Yuanli Zhang,Ling Yue,Hongrui Guo,Gang Ye,Fei Shi,Cheng Lv,Bo Jing,Huaqiao Tang,Zhongqiong Yin,Hualin Fu,Jvchun Lin,Yinglun Li,Xun Wang
出处
期刊:Immunopharmacology and Immunotoxicology [Informa]
卷期号:42 (3): 211-220 被引量:6
标识
DOI:10.1080/08923973.2020.1742154
摘要

Objective: Quercetin (Que), a flavonoid, possesses anti-inflammatory and antioxidant properties. It has been shown to protect against liver injury induced by various factors. This study was designed to investigate the underlying mechanism of its protective effect against lipopolysaccharide (LPS)- induced liver damage.Methods: Mice were pretreated with Que for 7 consecutive days and then exposed to LPS. To study the hepatoprotective effect of Que, oxidative stress parameters, inflammatory cytokine levels in liver and serum liver function indexes were examined. Protein and mRNA expression of nuclear orphan receptors and cytochrome P450 enzymes were measured by Western Blotting and qPCR, respectively.Results: Que significantly reduced circulating ALT, AST, ALP, and ameliorated LPS-induced histological alterations. In addition, Que obviously decreased markers of oxidative stress and pro-inflammatory cytokines. Furthermore, Que carried out the hepatoprotective effect via regulation of the expression of nuclear orphan receptors (CAR, PXR) and cytochrome P450 enzymes (CYP1A2, CYP2E1, CYP2D22, CYP3A11).Conclusions: Our findings suggested that Que pretreatment could ameliorate LPS-induced liver injury.
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