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小柴胡汤通过激活 Nrf2 通路减轻大鼠肝纤维化。

Xiaochaihutang attenuates liver fibrosis by activation of Nrf2 pathway in rats.

机构信息

Research Center for Medicine & Biology, Zunyi Medical University, Zunyi, Guizhou, 563003, PR China.

Research Center for Medicine & Biology, Zunyi Medical University, Zunyi, Guizhou, 563003, PR China.

出版信息

Biomed Pharmacother. 2017 Dec;96:847-853. doi: 10.1016/j.biopha.2017.10.065. Epub 2017 Nov 6.

Abstract

Xiaochaihutang (XCHT) is a decoction of seven botanical extracts used for liver diseases traditionally in East Asia. However, few studies have investigated its anti-hepatic fibrosis effects and the mechanisms of action. Oxidative stress is one of the key factors responsible for occurrence and development of hepatic fibrosis and nuclear factor erythroid 2-related factor 2 (Nrf2) serves as a major regulator of the cellular defense system against oxidative stress. The aim of the present study was to investigate the effect of XCHT on liver fibrosis and focuse on the Nrf2 pathway in the protection of XCHT against CCl-induced oxidative stress. Liver fibrosis was induced by repeated injection of CCl over a period of 9 weeks. Starting from the 6th week, rats in treatment groups were given the appropriate doses of XCHT granules and Silybin. We discovered that CCl caused significant fibrosis damage in rat liver, and XCHT (5g/kg and 10g/kg, po for 4 weeks) significantly improved the liver functions and fibrosis degree. XCHT treatment significantly decreased the number of α-SMA positive stained cells, indicating suppression of activated hepatic stellate cells (HSCs). Compared with the CCl treatment, administration of XCHT significantly increased the hepatic levels of Nqo1, HO-1, GCLC and GCLM, the major components of the Nrf2 pathway. These studies demonstrated that XCHT is an effective therapeutic agent for treatment of hepatic fibrosis and the mechanism of action might be due to up-regulation of the Nrf2 pathway against oxidative stress, making further inhibition of activated HSCs.

摘要

小柴胡汤(XCHT)是一种由七种植物提取物组成的方剂,传统上用于东亚的肝脏疾病。然而,很少有研究调查其抗肝纤维化作用及其作用机制。氧化应激是导致肝纤维化发生和发展的关键因素之一,核因子红细胞 2 相关因子 2(Nrf2)是细胞抗氧化应激防御系统的主要调节剂。本研究旨在探讨 XCHT 对肝纤维化的影响,并聚焦于 Nrf2 通路在 XCHT 对抗 CCl 诱导的氧化应激中的保护作用。通过反复注射 CCl 9 周的时间诱导肝纤维化。从第 6 周开始,治疗组大鼠给予适当剂量的 XCHT 颗粒和水飞蓟素。我们发现 CCl 导致大鼠肝纤维化严重损伤,而 XCHT(5g/kg 和 10g/kg,po 给药 4 周)显著改善了肝功能和纤维化程度。XCHT 治疗显著减少了α-SMA 阳性染色细胞的数量,表明对活化的肝星状细胞(HSCs)的抑制作用。与 CCl 处理相比,XCHT 的给药显著增加了肝组织中 Nqo1、HO-1、GCLC 和 GCLM 的水平,这些都是 Nrf2 通路的主要组成部分。这些研究表明,XCHT 是治疗肝纤维化的有效治疗药物,其作用机制可能是通过上调 Nrf2 通路对抗氧化应激,从而进一步抑制活化的 HSCs。

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