• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

非酒精性脂肪性肝病的新靶点

New targets for NAFLD.

作者信息

Parlati Lucia, Régnier Marion, Guillou Hervé, Postic Catherine

机构信息

Université de Paris, Institut Cochin, CNRS, INSERM, F- 75014 Paris, France.

Hôpital Cochin, 24, rue du Faubourg Saint Jacques, 75014 Paris, France.

出版信息

JHEP Rep. 2021 Aug 8;3(6):100346. doi: 10.1016/j.jhepr.2021.100346. eCollection 2021 Dec.

DOI:10.1016/j.jhepr.2021.100346
PMID:34667947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8507191/
Abstract

Non-alcoholic fatty liver disease (NAFLD) is a growing cause of chronic liver disease worldwide. It is characterised by steatosis, liver inflammation, hepatocellular injury and progressive fibrosis. Several preclinical models (dietary and genetic animal models) of NAFLD have deepened our understanding of its aetiology and pathophysiology. Despite the progress made, there are currently no effective treatments for NAFLD. In this review, we will provide an update on the known molecular pathways involved in the pathophysiology of NAFLD and on ongoing studies of new therapeutic targets.

摘要

非酒精性脂肪性肝病(NAFLD)是全球慢性肝病日益增多的一个病因。其特征为脂肪变性、肝脏炎症、肝细胞损伤和进行性纤维化。NAFLD的几种临床前模型(饮食和基因动物模型)加深了我们对其病因学和病理生理学的理解。尽管取得了进展,但目前尚无针对NAFLD的有效治疗方法。在本综述中,我们将提供有关NAFLD病理生理学中已知分子途径以及新治疗靶点正在进行的研究的最新信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03bf/8507191/13d5dea83c39/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03bf/8507191/a61edd3265d6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03bf/8507191/13d5dea83c39/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03bf/8507191/a61edd3265d6/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03bf/8507191/13d5dea83c39/gr2.jpg

相似文献

1
New targets for NAFLD.非酒精性脂肪性肝病的新靶点
JHEP Rep. 2021 Aug 8;3(6):100346. doi: 10.1016/j.jhepr.2021.100346. eCollection 2021 Dec.
2
The ménage à trois of autophagy, lipid droplets and liver disease.自噬、脂滴与肝脏疾病的三者关系。
Autophagy. 2022 Jan;18(1):50-72. doi: 10.1080/15548627.2021.1895658. Epub 2021 Apr 2.
3
n-3 Polyunsaturated fatty acids for the management of alcoholic liver disease: A critical review.n-3 多不饱和脂肪酸治疗酒精性肝病:批判性评价。
Crit Rev Food Sci Nutr. 2019;59(sup1):S116-S129. doi: 10.1080/10408398.2018.1544542. Epub 2018 Dec 22.
4
Experimental Nonalcoholic Steatohepatitis and Liver Fibrosis Are Ameliorated by Pharmacologic Activation of Nrf2 (NF-E2 p45-Related Factor 2).通过Nrf2(NF-E2 p45相关因子2)的药理学激活可改善实验性非酒精性脂肪性肝炎和肝纤维化。
Cell Mol Gastroenterol Hepatol. 2017 Dec 13;5(3):367-398. doi: 10.1016/j.jcmgh.2017.11.016. eCollection 2018 Mar.
5
Monascin and ankaflavin act as natural AMPK activators with PPARα agonist activity to down-regulate nonalcoholic steatohepatitis in high-fat diet-fed C57BL/6 mice.虾青素和安卡黄素作为天然 AMPK 激活剂,具有 PPARα 激动剂活性,可下调高脂饮食喂养的 C57BL/6 小鼠的非酒精性脂肪性肝炎。
Food Chem Toxicol. 2014 Feb;64:94-103. doi: 10.1016/j.fct.2013.11.015. Epub 2013 Nov 22.
6
Methionine restriction prevents the progression of hepatic steatosis in leptin-deficient obese mice.限制蛋氨酸摄入可防止瘦素缺乏型肥胖小鼠的肝脂肪变性进展。
Metabolism. 2013 Nov;62(11):1651-61. doi: 10.1016/j.metabol.2013.06.012. Epub 2013 Aug 5.
7
Free radical biology for medicine: learning from nonalcoholic fatty liver disease.医学中的自由基生物学:从非酒精性脂肪性肝病中学习。
Free Radic Biol Med. 2013 Dec;65:952-968. doi: 10.1016/j.freeradbiomed.2013.08.174. Epub 2013 Aug 29.
8
Nonalcoholic Fatty Liver Disease and Staging of Hepatic Fibrosis.非酒精性脂肪性肝病与肝纤维化分期。
Adv Exp Med Biol. 2024;1460:539-574. doi: 10.1007/978-3-031-63657-8_18.
9
Metabolic dysregulation and emerging therapeutical targets for hepatocellular carcinoma.肝细胞癌的代谢失调与新兴治疗靶点
Acta Pharm Sin B. 2022 Feb;12(2):558-580. doi: 10.1016/j.apsb.2021.09.019. Epub 2021 Sep 25.
10
Novel insights of dietary polyphenols and obesity.膳食多酚与肥胖的新认识。
J Nutr Biochem. 2014 Jan;25(1):1-18. doi: 10.1016/j.jnutbio.2013.09.001.

引用本文的文献

1
Thermoneutral housing worsens MASLD and reveals defective brown adipose tissue response to β3-adrenergic stimulation.热中性环境会使代谢相关脂肪性肝病恶化,并揭示棕色脂肪组织对β3-肾上腺素能刺激的反应存在缺陷。
iScience. 2025 Jul 26;28(9):113221. doi: 10.1016/j.isci.2025.113221. eCollection 2025 Sep 19.
2
Immune Microenvironment on the Molecular Mechanisms and Therapeutic Targets of MAFLD.免疫微环境对MAFLD分子机制及治疗靶点的影响
Immunotargets Ther. 2025 Jul 11;14:719-733. doi: 10.2147/ITT.S530451. eCollection 2025.
3
New drug therapies for metabolic dysfunction-associated steatohepatitis.

本文引用的文献

1
Saroglitazar for the Treatment of NASH: The Peroxisome Proliferator-Activated Receptor Story Goes On!司美格鲁肽治疗非酒精性脂肪性肝炎:过氧化物酶体增殖物激活受体的故事仍在继续!
Hepatology. 2021 Oct;74(4):1730-1733. doi: 10.1002/hep.32024. Epub 2021 Aug 30.
2
Integrative study of diet-induced mouse models of NAFLD identifies PPARα as a sexually dimorphic drug target.饮食诱导的非酒精性脂肪性肝病(NAFLD)小鼠模型的综合研究鉴定 PPARα 为一种性别二态性药物靶点。
Gut. 2022 Apr;71(4):807-821. doi: 10.1136/gutjnl-2020-323323. Epub 2021 Apr 26.
3
Liver-targeting drugs and their effect on blood glucose and hepatic lipids.
用于代谢功能障碍相关脂肪性肝炎的新型药物疗法。
Liver Res. 2025 Jan 17;9(2):94-103. doi: 10.1016/j.livres.2025.01.001. eCollection 2025 Jun.
4
Unraveling the Gut-Liver-Brain Axis: Microbiome, Inflammation, and Emerging Therapeutic Approaches.解析肠-肝-脑轴:微生物群、炎症及新兴治疗方法
Mediators Inflamm. 2025 Jun 18;2025:6733477. doi: 10.1155/mi/6733477. eCollection 2025.
5
Daytime-restricted feeding induces lean MAFLD in high-fat diet-fed mice by upregulating CD36-mediated lipid accumulation.限时进食通过上调CD36介导的脂质积累在高脂饮食喂养的小鼠中诱导出瘦型MAFLD。
J Lipid Res. 2025 Jun 23;66(8):100853. doi: 10.1016/j.jlr.2025.100853.
6
Targeting the gut microbiota and lipid metabolism: potential mechanisms of natural products for the treatment of non-alcoholic fatty liver disease.靶向肠道微生物群与脂质代谢:天然产物治疗非酒精性脂肪性肝病的潜在机制
Front Pharmacol. 2025 Jun 9;16:1610498. doi: 10.3389/fphar.2025.1610498. eCollection 2025.
7
Macrophage Signaling Pathways in Health and Disease: From Bench to Bedside Applications.健康与疾病中的巨噬细胞信号通路:从实验室到临床应用
MedComm (2020). 2025 Jun 16;6(7):e70256. doi: 10.1002/mco2.70256. eCollection 2025 Jul.
8
In vitro antioxidant effects and in vivo hepatoprotective effects of Osbeckia octandra, Vernonia cinerea and Atalantia ceylanica on a high fat diet induced metabolic dysfunction-associated steatotic liver disease mouse model.八蕊野牡丹、伤寒草和锡兰叶下珠对高脂饮食诱导的代谢功能障碍相关脂肪性肝病小鼠模型的体外抗氧化作用和体内肝脏保护作用
BMC Complement Med Ther. 2025 May 23;25(1):186. doi: 10.1186/s12906-025-04918-7.
9
Development of SOCS1 mimetics as novel approach to harmonize inflammation, oxidative stress, and fibrogenesis in metabolic dysfunction-associated steatotic liver disease.开发SOCS1模拟物作为协调代谢功能障碍相关脂肪性肝病中炎症、氧化应激和纤维化形成的新方法。
Redox Biol. 2025 Jul;84:103670. doi: 10.1016/j.redox.2025.103670. Epub 2025 May 11.
10
Targeting Metabolism: Innovative Therapies for MASLD Unveiled.靶向代谢:非酒精性脂肪性肝炎的创新疗法揭秘。
Int J Mol Sci. 2025 Apr 25;26(9):4077. doi: 10.3390/ijms26094077.
肝靶向药物及其对血糖和肝脂的影响。
Diabetologia. 2021 Jul;64(7):1461-1479. doi: 10.1007/s00125-021-05442-2. Epub 2021 Apr 20.
4
Saroglitazar, a PPAR-α/γ Agonist, for Treatment of NAFLD: A Randomized Controlled Double-Blind Phase 2 Trial.沙格列汀,一种 PPAR-α/γ 激动剂,用于治疗非酒精性脂肪性肝病:一项随机对照、双盲 2 期试验。
Hepatology. 2021 Oct;74(4):1809-1824. doi: 10.1002/hep.31843. Epub 2021 Jul 19.
5
Fructose- and sucrose- but not glucose-sweetened beverages promote hepatic de novo lipogenesis: A randomized controlled trial.果糖和蔗糖饮料而非葡萄糖饮料会促进肝脏从头合成脂肪:一项随机对照试验。
J Hepatol. 2021 Jul;75(1):46-54. doi: 10.1016/j.jhep.2021.02.027. Epub 2021 Mar 6.
6
Lipid and glucose metabolism in white adipocytes: pathways, dysfunction and therapeutics.白色脂肪细胞中的脂类和糖代谢:途径、功能障碍与治疗学。
Nat Rev Endocrinol. 2021 May;17(5):276-295. doi: 10.1038/s41574-021-00471-8. Epub 2021 Feb 24.
7
Nonalcoholic steatohepatitis: the role of peroxisome proliferator-activated receptors.非酒精性脂肪性肝炎:过氧化物酶体增殖物激活受体的作用。
Nat Rev Gastroenterol Hepatol. 2021 Jan;18(1):24-39. doi: 10.1038/s41575-020-00366-5. Epub 2020 Oct 22.
8
Dysregulated lipid metabolism links NAFLD to cardiovascular disease.脂质代谢失调将非酒精性脂肪性肝病与心血管疾病联系起来。
Mol Metab. 2020 Dec;42:101092. doi: 10.1016/j.molmet.2020.101092. Epub 2020 Oct 1.
9
Peroxisome Proliferator-Activated Receptors and Their Novel Ligands as Candidates for the Treatment of Non-Alcoholic Fatty Liver Disease.过氧化物酶体增殖物激活受体及其新型配体作为非酒精性脂肪性肝病治疗的候选药物。
Cells. 2020 Jul 8;9(7):1638. doi: 10.3390/cells9071638.
10
Hepatocyte-specific deletion of Pparα promotes NAFLD in the context of obesity.肝实质细胞特异性敲除 Pparα 在肥胖背景下促进非酒精性脂肪肝病。
Sci Rep. 2020 Apr 16;10(1):6489. doi: 10.1038/s41598-020-63579-3.