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黄芪多糖对非酒精性脂肪性肝病的药理作用及分子保护机制

Pharmacological Effects and Molecular Protective Mechanisms of Astragalus Polysaccharides on Nonalcoholic Fatty Liver Disease.

作者信息

Zhang Jing, Feng Quansheng

机构信息

College of Basic Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Front Pharmacol. 2022 Mar 3;13:854674. doi: 10.3389/fphar.2022.854674. eCollection 2022.

DOI:10.3389/fphar.2022.854674
PMID:35308224
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8929346/
Abstract

Nonalcoholic fatty liver disease (NAFLD) has been renamed metabolic dysfunction-associated fatty liver disease (MAFLD), a condition for which there is now no authorized treatment. The search for new medications to treat MAFLD made from natural substances is gaining traction. The function of anti-oxidant, anti-inflammation, hypoglycaemic, antiviral, hypolipidemic, and immunomodulatory actions of Astragalus polysaccharides (APS), a chemical molecule isolated from Astragalus membranaceus, has become the focus of therapeutic attention. We have a large number of papers on the pharmacological effects of APS on NAFLD that have never been systematically reviewed before. According to our findings, APS may help to slow the progression of non-alcoholic fatty liver disease (NAFL) to non-alcoholic steatohepatitis (NASH). Lipid metabolism, insulin resistance (IR), oxidative stress (OS), endoplasmic reticulum stress (ERS), inflammation, fibrosis, autophagy, and apoptosis are some of the pathogenic pathways involved. SIRT1/PPARα/FGF21, PI3K/AKT/IRS-1, AMPK/ACC, mTOR/4EBP-1/S6K1, GRP78/IRE-1/JNK, AMPK/PGC-1/NRF1, TLR4/MyD88/NF-κB, and TGF-β/Smad pathways were the most common molecular protective mechanisms. All of the information presented in this review suggests that APS is a natural medication with a lot of promise for NAFLD, but more study, bioavailability studies, medicine type and dosage, and clinical proof are needed. This review could be useful for basic research, pharmacological development, and therapeutic applications of APS in the management of MAFLD.

摘要

非酒精性脂肪性肝病(NAFLD)已更名为代谢功能障碍相关脂肪性肝病(MAFLD),目前尚无针对该病症的获批治疗方法。寻找由天然物质制成的治疗MAFLD的新药物正越来越受到关注。从黄芪中分离出的化学分子黄芪多糖(APS)的抗氧化、抗炎、降血糖、抗病毒、降血脂和免疫调节作用已成为治疗关注的焦点。我们有大量关于APS对NAFLD药理作用的论文,此前从未进行过系统综述。根据我们的研究结果,APS可能有助于减缓非酒精性脂肪肝(NAFL)向非酒精性脂肪性肝炎(NASH)的进展。脂质代谢、胰岛素抵抗(IR)、氧化应激(OS)、内质网应激(ERS)、炎症、纤维化、自噬和凋亡是其中一些涉及的致病途径。SIRT1/PPARα/FGF21、PI3K/AKT/IRS-1、AMPK/ACC、mTOR/4EBP-1/S6K1、GRP78/IRE-1/JNK、AMPK/PGC-1/NRF1、TLR4/MyD88/NF-κB和TGF-β/Smad途径是最常见的分子保护机制。本综述中呈现的所有信息表明,APS是一种对NAFLD有很大前景的天然药物,但还需要更多的研究、生物利用度研究、药物类型和剂量以及临床证据。本综述可能对APS在MAFLD管理中的基础研究、药理开发和治疗应用有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f01/8929346/92a563ab70ee/fphar-13-854674-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f01/8929346/4a8d7690ea16/fphar-13-854674-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f01/8929346/4c8c114a212e/fphar-13-854674-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f01/8929346/92a563ab70ee/fphar-13-854674-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f01/8929346/4a8d7690ea16/fphar-13-854674-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f01/8929346/4c8c114a212e/fphar-13-854674-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f01/8929346/92a563ab70ee/fphar-13-854674-g003.jpg

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