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茵陈蒿热水和乙醇水提物对乙酰氨基酚诱导的小鼠急性肝损伤的保护作用。

Protective effect of hot-water and ethanol-aqueous extracts from Anneslea fragrans against acetaminophen-induced acute liver injury in mice.

机构信息

Faculty of Food Science and Engineering, Kunming University of Science and Technology, Kunming, 650500, China.

Department of Chemistry, Liaocheng University, Liaocheng, 252059, China.

出版信息

Food Chem Toxicol. 2023 Sep;179:113973. doi: 10.1016/j.fct.2023.113973. Epub 2023 Jul 27.

Abstract

Anneslea fragrans Wall. (AF) is an important medicinal and edible plant in China. The principal objectives of this study are to explore the hepatoprotective effect of ethanol-aqueous (AFE) and hot-water (AFW) extracts in vitro and in vivo. UPLC-ESI-MS/MS analysis showed that AFW and AFE are rich in dihydrochalcones. Both AFW and AFE significantly up-regulated the expressions of SOD, CAT and GSH, reduced the MDA content in acetaminophen (APAP)-induced HepG2 cells, and suppressed the expressions of NO, TNF-α, IL-1β, and IL-6 in LPS-induced RAW246.7 cells. In APAP-induced mice, AFW and AFE administration significantly decreased the plasma levels of AST and ALT, and improved liver tissue damage, the collagen deposition and fibrosis formation. Moreover, AFW and AFE decreased the MDA and ROS accumulations via activating Nrf2 pathway to increase the hepatic GSH contents and activities of SOD, CAT, HO-1, and NQO-1, reduced the levels of NO, TNF-α, IL-1β, and IL-6 by suppressing the JNK/p38/ERK/NF-κB pathways, and alleviated apoptosis via regulating Bcl-2, Bax, caspase-3/9 protein expressions. This study provides a new sight that AFW and AFE may have a potential natural resource for the treatment of liver injury.

摘要

安妮香桃木(AF)是中国一种重要的药用和食用植物。本研究的主要目的是探索其水提物(AFW)和醇提物(AFE)的体外和体内肝保护作用。UPLC-ESI-MS/MS 分析表明,AFW 和 AFE 富含二氢查耳酮。AFW 和 AFE 均能显著上调 SOD、CAT 和 GSH 的表达,降低对乙酰氨基酚(APAP)诱导的 HepG2 细胞中 MDA 含量,并抑制 LPS 诱导的 RAW246.7 细胞中 NO、TNF-α、IL-1β 和 IL-6 的表达。在 APAP 诱导的小鼠中,AFW 和 AFE 给药可显著降低血浆中 AST 和 ALT 水平,改善肝组织损伤、胶原沉积和纤维化形成。此外,AFW 和 AFE 通过激活 Nrf2 通路减少 MDA 和 ROS 积累,增加肝 GSH 含量和 SOD、CAT、HO-1 和 NQO-1 的活性,通过抑制 JNK/p38/ERK/NF-κB 通路降低 NO、TNF-α、IL-1β 和 IL-6 水平,并通过调节 Bcl-2、Bax、caspase-3/9 蛋白表达减轻细胞凋亡。本研究为 AFW 和 AFE 可能成为治疗肝损伤的天然资源提供了新的视角。

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