Suppr超能文献

慢性肝病中的抗氧化剂和抗炎剂:分子机制与治疗

Antioxidant and anti-inflammatory agents in chronic liver diseases: Molecular mechanisms and therapy.

作者信息

Zhang Chun-Ye, Liu Shuai, Yang Ming

机构信息

Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, United States.

The First Affiliated Hospital, Zhejiang University, Hangzhou 310006, Zhejiang Province, China.

出版信息

World J Hepatol. 2023 Feb 27;15(2):180-200. doi: 10.4254/wjh.v15.i2.180.

Abstract

Chronic liver disease (CLD) is a continuous process that causes a reduction of liver function lasting more than six months. CLD includes alcoholic liver disease (ALD), non-alcoholic fatty liver disease (NAFLD), chronic viral infection, and autoimmune hepatitis, which can lead to liver fibrosis, cirrhosis, and cancer. Liver inflammation and oxidative stress are commonly associated with the development and progression of CLD. Molecular signaling pathways such as AMP-activated protein kinase (AMPK), C-Jun N-terminal kinase, and peroxisome proliferator-activated receptors (PPARs) are implicated in the pathogenesis of CLD. Therefore, antioxidant and anti-inflammatory agents from natural products are new potent therapies for ALD, NAFLD, and hepatocellular carcinoma (HCC). In this review, we summarize some powerful products that can be potential applied in all the stages of CLD, from ALD/NAFLD to HCC. The selected agents such as β-sitosterol, curcumin, genistein, and silymarin can regulate the activation of several important molecules, including AMPK, Farnesoid X receptor, nuclear factor erythroid 2-related factor-2, PPARs, phosphatidylinositol-3-kinase, and lysyl oxidase-like proteins. In addition, clinical trials are undergoing to evaluate their efficacy and safety.

摘要

慢性肝病(CLD)是一个持续的过程,会导致肝功能下降持续超过六个月。CLD包括酒精性肝病(ALD)、非酒精性脂肪性肝病(NAFLD)、慢性病毒感染和自身免疫性肝炎,这些可导致肝纤维化、肝硬化和癌症。肝脏炎症和氧化应激通常与CLD的发生和发展相关。分子信号通路如AMP激活的蛋白激酶(AMPK)、C-Jun氨基末端激酶和过氧化物酶体增殖物激活受体(PPARs)与CLD的发病机制有关。因此,来自天然产物的抗氧化剂和抗炎剂是治疗ALD、NAFLD和肝细胞癌(HCC)的新型有效疗法。在本综述中,我们总结了一些可潜在应用于CLD各个阶段(从ALD/NAFLD到HCC)的强效产物。所选药物如β-谷甾醇、姜黄素、染料木黄酮和水飞蓟宾可调节包括AMPK、法尼酯X受体、核因子红细胞2相关因子2、PPARs、磷脂酰肌醇-3-激酶和赖氨酰氧化酶样蛋白等几种重要分子的激活。此外,正在进行临床试验以评估它们的疗效和安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68ec/10011909/901970e90208/WJH-15-180-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验