• 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

PPAR 靶向药物治疗非酒精性脂肪性肝病的临床研究现状与展望。

Current Clinical Trial Status and Future Prospects of PPAR-Targeted Drugs for Treating Nonalcoholic Fatty Liver Disease.

机构信息

Department of Health Chemistry, Showa Pharmaceutical University, Machida, Tokyo 194-8543, Japan.

出版信息

Biomolecules. 2023 Aug 18;13(8):1264. doi: 10.3390/biom13081264.

DOI:10.3390/biom13081264
PMID:37627329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10452531/
Abstract

The number of patients with nonalcoholic fatty liver disease (NAFLD)/nonalcoholic steatohepatitis (NASH) is increasing globally and is raising serious concerns regarding the increasing medical and economic burden incurred for their treatment. The progression of NASH to more severe conditions such as cirrhosis and hepatocellular carcinoma requires liver transplantation to avoid death. Therefore, therapeutic intervention is required in the NASH stage, although no therapeutic drugs are currently available for this. Several anti-NASH candidate drugs have been developed that enable treatment via the modulation of distinct signaling cascades and include a series of drugs targeting peroxisome proliferator-activated receptor (PPAR) subtypes (PPARα/δ/γ) that are considered to be attractive because they can regulate both systemic lipid metabolism and inflammation. Multiple PPAR dual/pan agonists have been developed but only a few of them have been evaluated in clinical trials for NAFLD/NASH. Herein, we review the current clinical trial status and future prospects of PPAR-targeted drugs for treating NAFLD/NASH. In addition, we summarize our recent findings on the binding modes and the potencies/efficacies of several candidate PPAR dual/pan agonists to estimate their therapeutic potentials against NASH. Considering that the development of numerous PPAR dual/pan agonists has been abandoned because of their serious side effects, we also propose a repositioning of the already approved, safety-proven PPAR-targeted drugs against NAFLD/NASH.

摘要

全球范围内非酒精性脂肪性肝病(NAFLD)/非酒精性脂肪性肝炎(NASH)患者数量不断增加,这给治疗带来的日益增加的医疗和经济负担引起了严重关注。NASH 向肝硬化和肝细胞癌等更严重的情况进展需要进行肝移植以避免死亡。因此,需要在 NASH 阶段进行治疗,尽管目前尚无针对该病的治疗药物。已经开发出几种抗 NASH 的候选药物,这些药物通过调节不同的信号级联反应来进行治疗,包括一系列针对过氧化物酶体增殖物激活受体(PPAR)亚型(PPARα/δ/γ)的药物,这些药物被认为具有吸引力,因为它们可以调节全身脂质代谢和炎症。已经开发出多种 PPAR 双重/泛激动剂,但只有少数在临床试验中评估了其治疗 NAFLD/NASH 的效果。本文综述了目前针对 NAFLD/NASH 的 PPAR 靶向药物的临床试验现状和未来前景。此外,我们还总结了我们最近关于几种候选 PPAR 双重/泛激动剂的结合模式和效力/功效的发现,以评估它们对 NASH 的治疗潜力。考虑到许多 PPAR 双重/泛激动剂因严重副作用而被放弃开发,我们还提出了重新定位已经批准的、具有安全性的针对 NAFLD/NASH 的 PPAR 靶向药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80d/10452531/7dd5bf9e169a/biomolecules-13-01264-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80d/10452531/07f965185d03/biomolecules-13-01264-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80d/10452531/7dd5bf9e169a/biomolecules-13-01264-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80d/10452531/07f965185d03/biomolecules-13-01264-g001a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f80d/10452531/7dd5bf9e169a/biomolecules-13-01264-g002.jpg

相似文献

1
Current Clinical Trial Status and Future Prospects of PPAR-Targeted Drugs for Treating Nonalcoholic Fatty Liver Disease.PPAR 靶向药物治疗非酒精性脂肪性肝病的临床研究现状与展望。
Biomolecules. 2023 Aug 18;13(8):1264. doi: 10.3390/biom13081264.
2
[The Perspective of PPAR Dual/Pan Agonists as Therapeutic Drugs against NAFLD].[过氧化物酶体增殖物激活受体双重/泛激动剂作为抗非酒精性脂肪性肝病治疗药物的前景]
Yakugaku Zasshi. 2022;142(12):1335-1343. doi: 10.1248/yakushi.22-00159-1.
3
Functional and Structural Insights into the Human PPARα/δ/γ Targeting Preferences of Anti-NASH Investigational Drugs, Lanifibranor, Seladelpar, and Elafibranor.抗非酒精性脂肪性肝炎(NASH)研究药物拉尼贝特、塞拉地帕和依拉贝特对人过氧化物酶体增殖物激活受体α/δ/γ靶向偏好的功能和结构见解
Antioxidants (Basel). 2023 Jul 29;12(8):1523. doi: 10.3390/antiox12081523.
4
Anti-NASH Drug Development Hitches a Lift on PPAR Agonism.抗 NASH 药物研发因 PPAR 激动剂而受阻。
Cells. 2019 Dec 21;9(1):37. doi: 10.3390/cells9010037.
5
Functional and Structural Insights into Human PPARα/δ/γ Subtype Selectivity of Bezafibrate, Fenofibric Acid, and Pemafibrate.贝扎贝特、非诺贝特和帕玛贝特对人 PPARα/δ/γ 亚型选择性的功能和结构见解。
Int J Mol Sci. 2022 Apr 25;23(9):4726. doi: 10.3390/ijms23094726.
6
Structural Basis for Anti-non-alcoholic Fatty Liver Disease and Diabetic Dyslipidemia Drug Saroglitazar as a PPAR α/γ Dual Agonist.作为一种 PPARα/γ双重激动剂,用于治疗非酒精性脂肪性肝病和糖尿病血脂异常的药物沙格列汀的结构基础。
Biol Pharm Bull. 2021;44(9):1210-1219. doi: 10.1248/bpb.b21-00232.
7
Roles of the peroxisome proliferator-activated receptors (PPARs) in the pathogenesis of nonalcoholic fatty liver disease (NAFLD).过氧化物酶体增殖物激活受体(PPARs)在非酒精性脂肪性肝病(NAFLD)发病机制中的作用。
Pharmacol Res. 2023 Jun;192:106786. doi: 10.1016/j.phrs.2023.106786. Epub 2023 May 3.
8
Elafibranor: a potential drug for the treatment of nonalcoholic steatohepatitis (NASH).Elafibranor:一种有潜力用于治疗非酒精性脂肪性肝炎(NASH)的药物。
Expert Opin Investig Drugs. 2020 Feb;29(2):117-123. doi: 10.1080/13543784.2020.1668375. Epub 2019 Sep 25.
9
A Phase 2 Double Blinded, Randomized Controlled Trial of Saroglitazar in Patients With Nonalcoholic Steatohepatitis.一项沙格列汀治疗非酒精性脂肪性肝炎患者的 2 期双盲、随机对照临床试验。
Clin Gastroenterol Hepatol. 2021 Dec;19(12):2670-2672. doi: 10.1016/j.cgh.2020.10.051. Epub 2020 Nov 2.
10
Human hepatic in vitro models reveal distinct anti-NASH potencies of PPAR agonists.人类肝脏体外模型揭示了 PPAR 激动剂对非酒精性脂肪性肝炎的不同治疗潜力。
Cell Biol Toxicol. 2021 Apr;37(2):293-311. doi: 10.1007/s10565-020-09544-2. Epub 2020 Jul 1.

引用本文的文献

1
A Plant-Based Strategy for MASLD: (Thunb.) DC. Extract Reduces Hepatic Lipid Accumulation and Improves Glycogen Storage In Vitro and In Vivo.一种用于代谢相关脂肪性肝病的植物性策略:(拇指)DC提取物可减少肝脏脂质积累并在体外和体内改善糖原储存
Int J Mol Sci. 2025 Aug 30;26(17):8442. doi: 10.3390/ijms26178442.
2
Nuclear receptors in metabolic, inflammatory, and oncologic diseases: mechanisms, therapeutic advances, and future directions.代谢、炎症和肿瘤疾病中的核受体:作用机制、治疗进展及未来方向
Eur J Med Res. 2025 Sep 9;30(1):843. doi: 10.1186/s40001-025-03073-6.
3
Pharmacological inhibition of Peroxisome Proliferation-Activated Receptor Delta (PPARδ) imparts selective leukemia cell death.

本文引用的文献

1
Functional and Structural Insights into the Human PPARα/δ/γ Targeting Preferences of Anti-NASH Investigational Drugs, Lanifibranor, Seladelpar, and Elafibranor.抗非酒精性脂肪性肝炎(NASH)研究药物拉尼贝特、塞拉地帕和依拉贝特对人过氧化物酶体增殖物激活受体α/δ/γ靶向偏好的功能和结构见解
Antioxidants (Basel). 2023 Jul 29;12(8):1523. doi: 10.3390/antiox12081523.
2
Treating NASH by targeting peroxisome proliferator-activated receptors.通过靶向过氧化物酶体增殖物激活受体治疗非酒精性脂肪性肝炎。
J Hepatol. 2023 Nov;79(5):1302-1316. doi: 10.1016/j.jhep.2023.07.004. Epub 2023 Jul 17.
3
Effects of saroglitazar in the treatment of non-alcoholic fatty liver disease or non-alcoholic steatohepatitis: A systematic review and meta-analysis.
过氧化物酶体增殖物激活受体δ(PPARδ)的药理学抑制可导致选择性白血病细胞死亡。
Cancer Metab. 2025 Jul 25;13(1):36. doi: 10.1186/s40170-025-00402-5.
4
Pathogenesis and Clinical Management of Metabolic Dysfunction-Associated Steatotic Liver Disease.代谢功能障碍相关脂肪性肝病的发病机制与临床管理
Int J Mol Sci. 2025 Jun 14;26(12):5717. doi: 10.3390/ijms26125717.
5
Predicting peroxisome proliferator-activated receptor gamma potency of small molecules: a synergistic consensus model and deep learning binding affinity approach powered by Enalos Cloud Platform.预测小分子的过氧化物酶体增殖物激活受体γ活性:一种由Enalos云平台驱动的协同共识模型和深度学习结合亲和力方法
Mol Divers. 2025 Jun 14. doi: 10.1007/s11030-025-11230-6.
6
Targeting the Liver Serine Protease TMPRSS6 Ameliorates Steatosis and Attenuates Fibrosis in Experimental MASLD.靶向肝脏丝氨酸蛋白酶TMPRSS6可改善实验性代谢相关脂肪性肝病的脂肪变性并减轻纤维化。
Liver Int. 2025 Jul;45(7):e70163. doi: 10.1111/liv.70163.
7
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.
8
Competitive Ligand-Induced Recruitment of Coactivators to Specific PPARα/δ/γ Ligand-Binding Domains Revealed by Dual-Emission FRET and X-Ray Diffraction of Cocrystals.通过双发射荧光共振能量转移和共晶体X射线衍射揭示竞争性配体诱导共激活因子募集至特定PPARα/δ/γ配体结合结构域
Antioxidants (Basel). 2025 Apr 20;14(4):494. doi: 10.3390/antiox14040494.
9
Current Therapeutic Landscape for Metabolic Dysfunction-Associated Steatohepatitis.代谢功能障碍相关脂肪性肝炎的当前治疗现状
Int J Mol Sci. 2025 Feb 19;26(4):1778. doi: 10.3390/ijms26041778.
10
Proteomics Profiling Reveals Pharmaceutical Excipient PEG400 Induces Nuclear-Receptor-Activation-Affected Lipid Metabolism and Metabolic Enzyme Expression.蛋白质组学分析揭示药用辅料聚乙二醇400诱导核受体激活影响脂质代谢和代谢酶表达
Int J Mol Sci. 2025 Feb 18;26(4):1732. doi: 10.3390/ijms26041732.
沙格列汀治疗非酒精性脂肪性肝病或非酒精性脂肪性肝炎的疗效:系统评价和荟萃分析。
Clin Res Hepatol Gastroenterol. 2023 Aug;47(7):102174. doi: 10.1016/j.clinre.2023.102174. Epub 2023 Jun 26.
4
PPAR-alpha/gamma agonists, glucagon-like peptide-1 receptor agonists and metformin for non-alcoholic fatty liver disease: A network meta-analysis.过氧化物酶体增殖物激活受体-α/γ 激动剂、胰高血糖素样肽-1 受体激动剂和二甲双胍治疗非酒精性脂肪性肝病的网状 Meta 分析。
J Int Med Res. 2023 Jun;51(6):3000605231177191. doi: 10.1177/03000605231177191.
5
Gamma-glutamyl transferase predicts pemafibrate treatment response in non-alcoholic fatty liver disease.γ-谷氨酰转移酶可预测非酒精性脂肪性肝病患者对 pemafibrate 的治疗反应。
J Gastroenterol Hepatol. 2023 Oct;38(10):1743-1749. doi: 10.1111/jgh.16222. Epub 2023 May 23.
6
Efficacy and safety of saroglitazar in real-world patients of non-alcoholic fatty liver disease with or without diabetes including compensated cirrhosis: A tertiary care center experience.沙罗格列扎在合并或不合并糖尿病(包括代偿期肝硬化)的非酒精性脂肪性肝病真实世界患者中的疗效和安全性:一家三级医疗中心的经验
JGH Open. 2023 Feb 20;7(3):215-220. doi: 10.1002/jgh3.12878. eCollection 2023 Mar.
7
Effect of pemafibrate on liver enzymes and shear wave velocity in non-alcoholic fatty liver disease patients.佩马贝特对非酒精性脂肪性肝病患者肝酶和剪切波速度的影响。
Front Med (Lausanne). 2023 Feb 7;10:1073025. doi: 10.3389/fmed.2023.1073025. eCollection 2023.
8
MAFLD: a multisystem disease.代谢相关脂肪性肝病:一种多系统疾病。
Ther Adv Endocrinol Metab. 2023 Jan 28;14:20420188221145549. doi: 10.1177/20420188221145549. eCollection 2023.
9
Saroglitazar suppresses the hepatocellular carcinoma induced by intraperitoneal injection of diethylnitrosamine in C57BL/6 mice fed on choline deficient, l-amino acid- defined, high-fat diet.沙格列汀抑制胆碱缺乏、必需氨基酸定义、高脂肪饮食喂养的 C57BL/6 小鼠腹腔注射二乙基亚硝胺诱导的肝细胞癌。
BMC Cancer. 2023 Jan 17;23(1):59. doi: 10.1186/s12885-023-10530-0.
10
Pemafibrate improves liver dysfunction and non-invasive surrogates for liver fibrosis in patients with non-alcoholic fatty liver disease with hypertriglyceridemia: a multicenter study.非诺贝特改善伴有高三酰甘油血症的非酒精性脂肪性肝病患者的肝功能障碍和肝纤维化的非侵入性替代标志物:一项多中心研究。
Hepatol Int. 2023 Jun;17(3):606-614. doi: 10.1007/s12072-022-10453-1. Epub 2022 Dec 30.