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桐花素对脂多糖和 D-半乳糖胺诱导的急性肝损伤的保护作用。

Protective effects of tenuigenin on lipopolysaccharide and d-galactosamine-induced acute liver injury.

机构信息

Department of Blood Transfusion, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150086, China.

Department of General Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150086, China.

出版信息

Microb Pathog. 2017 Nov;112:83-88. doi: 10.1016/j.micpath.2017.09.051. Epub 2017 Sep 25.

Abstract

Tenuigenin (TEN), a major active component of polygala tenuifolia root, has been reported to have a number of biological properties, such as anti-oxidative and anti-inflammatory activities. However, the protective effect of TEN on acute liver injury has not yet been reported. This research aims to detect the protective effect of TEN on lipopolysaccharide (LPS) and d-galactosamine (D-GalN)-induced acute liver injury in mice and to investigate the molecular mechanisms. TEN was administered intraperitoneally 1 h before LPS/D-GalN treatment. The levels of TNF-α, IL-1β, ALT, and AST were measured. The expression of NF-κB, ASK1, MAPKs, Nrf2, and HO-1 were detected by western blot analysis. The results showed that TEN significantly inhibited LPS/D-GalN-induced serum ALT and AST levels. TEN also inhibited LPS/D-GalN-induced TNF-α and IL-1β production. Furthermore, LPS/D-GalN-induced hepatic MDA and MPO activities were also inhibited by TEN. In addition, TEN was found to inhibit LPS/D-GalN-induced ASK1 expression, NF-κB and MAPKs activation and up-regulate the expression of Nrf2 and HO-1. In conclusion, TEN protected against LPS/GalN-induced acute liver injury by suppressing inflammatory and oxidative responses.

摘要

当归还(TEN)是远志根的主要活性成分之一,具有多种生物特性,如抗氧化和抗炎活性。然而,TEN 对急性肝损伤的保护作用尚未见报道。本研究旨在检测 TEN 对脂多糖(LPS)和 D-半乳糖胺(D-GalN)诱导的小鼠急性肝损伤的保护作用,并探讨其分子机制。TEN 在 LPS/D-GalN 处理前 1 小时腹腔注射给药。测定 TNF-α、IL-1β、ALT 和 AST 水平。Western blot 分析检测 NF-κB、ASK1、MAPKs、Nrf2 和 HO-1 的表达。结果表明,TEN 显著抑制 LPS/D-GalN 诱导的血清 ALT 和 AST 水平。TEN 还抑制了 LPS/D-GalN 诱导的 TNF-α和 IL-1β的产生。此外,TEN 还抑制了 LPS/D-GalN 诱导的肝 MDA 和 MPO 活性。此外,发现 TEN 抑制 LPS/D-GalN 诱导的 ASK1 表达、NF-κB 和 MAPKs 的激活,并上调 Nrf2 和 HO-1 的表达。总之,TEN 通过抑制炎症和氧化反应来防止 LPS/GalN 诱导的急性肝损伤。

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