• 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

动脉粥样硬化机制与降脂药物的新见解

A New Insight on Atherosclerosis Mechanism and Lipid-Lowering Drugs.

作者信息

Li Penghui, Jiang Wei

机构信息

Binhai New Area Hospital of TCM, 300000 Tianjin, China.

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, 300000 Tianjin, China.

出版信息

Rev Cardiovasc Med. 2025 Mar 5;26(3):25321. doi: 10.31083/RCM25321. eCollection 2025 Mar.

DOI:10.31083/RCM25321
PMID:40160588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11951287/
Abstract

Atherosclerosis (AS) is a chronic vascular disease primarily affecting large and medium-sized arteries, involving complex pathological mechanisms such as inflammatory responses, lipid metabolism disorders and vascular plaque formation. In recent years, several emerging research hotspots have appeared in the field of atherosclerosis, including gut microbiota, pyroptosis, ferroptosis, autophagy, cuproptosis, exosomes and non-coding RNA. Traditional lipid-lowering drugs play a crucial role in the treatment of AS but are not able to significantly reverse the pathological changes. This article aims to summarize the latest research progress in the pathogenesis of AS and the diagnosis and treatment of the disease by comprehensively analyzing relevant literature mainly from the past five years. Additionally, the mechanisms of action and research advances of statins, cholesterol absorption inhibitors, fibrates and novel lipid-lowering drugs are reviewed to provide new insights into the diagnosis and treatment of AS.

摘要

动脉粥样硬化(AS)是一种主要影响大中型动脉的慢性血管疾病,涉及炎症反应、脂质代谢紊乱和血管斑块形成等复杂病理机制。近年来,动脉粥样硬化领域出现了几个新兴研究热点,包括肠道微生物群、细胞焦亡、铁死亡、自噬、铜死亡、外泌体和非编码RNA。传统降脂药物在AS治疗中发挥着关键作用,但无法显著逆转病理变化。本文旨在通过全面分析主要来自过去五年的相关文献,总结AS发病机制及该疾病诊断与治疗的最新研究进展。此外,还综述了他汀类药物、胆固醇吸收抑制剂、贝特类药物及新型降脂药物的作用机制和研究进展,为AS的诊断与治疗提供新的见解。

相似文献

1
A New Insight on Atherosclerosis Mechanism and Lipid-Lowering Drugs.动脉粥样硬化机制与降脂药物的新见解
Rev Cardiovasc Med. 2025 Mar 5;26(3):25321. doi: 10.31083/RCM25321. eCollection 2025 Mar.
2
Lipid-Lowering Therapies for Atherosclerosis: Statins, Fibrates, Ezetimibe and PCSK9 Monoclonal Antibodies.动脉粥样硬化的降脂治疗:他汀类药物、贝特类药物、依折麦布和 PCSK9 单克隆抗体。
Curr Med Chem. 2021;28(36):7427-7445. doi: 10.2174/0929867328666210222092628.
3
Autophagy, Pyroptosis, and Ferroptosis: New Regulatory Mechanisms for Atherosclerosis.自噬、焦亡与铁死亡:动脉粥样硬化的新调控机制
Front Cell Dev Biol. 2022 Jan 13;9:809955. doi: 10.3389/fcell.2021.809955. eCollection 2021.
4
Targeting mitochondria by lipid-selenium conjugate drug results in malate/fumarate exhaustion and induces mitophagy-mediated necroptosis suppression.通过脂质-硒结合药物靶向线粒体可导致苹果酸/延胡索酸耗竭,并诱导依赖于线粒体自噬的坏死性凋亡抑制。
Int J Biol Sci. 2024 Oct 28;20(14):5793-5811. doi: 10.7150/ijbs.102424. eCollection 2024.
5
Macrophage Death as a Pharmacological Target in Atherosclerosis.巨噬细胞死亡作为动脉粥样硬化的一个药理学靶点
Front Pharmacol. 2019 Apr 4;10:306. doi: 10.3389/fphar.2019.00306. eCollection 2019.
6
Exosomes in Atherosclerosis: Role in the Pathogenesis and Targets for Therapy.动脉粥样硬化中的外泌体:在发病机制中的作用及治疗靶点
Curr Med Chem. 2024 May 3. doi: 10.2174/0109298673302220240430173404.
7
Low-density lipoprotein apheresis: an evidence-based analysis.低密度脂蛋白单采术:一项基于证据的分析。
Ont Health Technol Assess Ser. 2007;7(5):1-101. Epub 2006 Nov 1.
8
Cholesterol and Lipoprotein Metabolism and Atherosclerosis: Recent Advances In reverse Cholesterol Transport.胆固醇与脂蛋白代谢及动脉粥样硬化:胆固醇逆转运的最新进展。
Ann Hepatol. 2017 Nov;16(Suppl. 1: s3-105.):s27-s42. doi: 10.5604/01.3001.0010.5495.
9
Hyperlipidaemia in paediatric patients: the role of lipid-lowering therapy in clinical practice.儿科患者的高脂血症:降脂治疗在临床实践中的作用。
Drug Saf. 2010 Feb 1;33(2):115-25. doi: 10.2165/11319490-000000000-00000.
10
Optimal management of combined dyslipidemia: what have we behind statins monotherapy?混合性血脂异常的优化管理:他汀类药物单一疗法之后我们还有什么?
Adv Cardiol. 2008;45:127-153. doi: 10.1159/000115192.

本文引用的文献

1
Copper's dual role: unravelling the link between copper homeostasis, cuproptosis, and cardiovascular diseases.铜的双重角色:揭示铜稳态、铜死亡和心血管疾病之间的联系。
Hypertens Res. 2024 May;47(5):1440-1442. doi: 10.1038/s41440-024-01636-4. Epub 2024 Mar 11.
2
Copper homeostasis and cuproptosis in atherosclerosis: metabolism, mechanisms and potential therapeutic strategies.动脉粥样硬化中的铜稳态与铜死亡:代谢、机制及潜在治疗策略
Cell Death Discov. 2024 Jan 13;10(1):25. doi: 10.1038/s41420-023-01796-1.
3
Epitranscriptomic Modification of MicroRNA Increases Atherosclerosis Susceptibility.微小RNA的表观转录组修饰增加动脉粥样硬化易感性。
Circulation. 2023 Nov 28;148(22):1819-1822. doi: 10.1161/CIRCULATIONAHA.123.065455. Epub 2023 Nov 27.
4
Inflammatory Cell-Derived MYDGF Attenuates Endothelial LDL Transcytosis to Protect Against Atherogenesis.炎性细胞衍生的 MYDGF 减弱内皮细胞 LDL 转胞吞作用,从而防止动脉粥样硬化形成。
Arterioscler Thromb Vasc Biol. 2023 Nov;43(11):e443-e467. doi: 10.1161/ATVBAHA.123.319905. Epub 2023 Sep 28.
5
Different stimuli induce endothelial dysfunction and promote atherosclerosis through the Piezo1/YAP signaling axis.不同的刺激通过 Piezo1/YAP 信号轴诱导内皮功能障碍并促进动脉粥样硬化。
Arch Biochem Biophys. 2023 Oct 1;747:109755. doi: 10.1016/j.abb.2023.109755. Epub 2023 Sep 14.
6
Adrenomedullin, transcriptionally regulated by vitamin D receptors, alleviates atherosclerosis in mice through suppressing AMPK-mediated endothelial ferroptosis.维生素 D 受体转录调控的肾上腺髓质素通过抑制 AMPK 介导的内皮细胞铁死亡缓解小鼠动脉粥样硬化。
Environ Toxicol. 2024 Jan;39(1):199-211. doi: 10.1002/tox.23958. Epub 2023 Sep 9.
7
Phosphatidylethanolamine alleviates OX-LDL-induced macrophage inflammation by upregulating autophagy and inhibiting NLRP1 inflammasome activation.磷脂酰乙醇胺通过上调自噬和抑制 NLRP1 炎性小体激活缓解 OX-LDL 诱导的巨噬细胞炎症。
Free Radic Biol Med. 2023 Nov 1;208:402-417. doi: 10.1016/j.freeradbiomed.2023.08.031. Epub 2023 Sep 1.
8
IQGAP1 promotes mitochondrial damage and activation of the mtDNA sensor cGAS-STING pathway to induce endothelial cell pyroptosis leading to atherosclerosis.IQGAP1 促进线粒体损伤和 mtDNA 传感器 cGAS-STING 通路的激活,诱导内皮细胞发生细胞焦亡,从而导致动脉粥样硬化。
Int Immunopharmacol. 2023 Oct;123:110795. doi: 10.1016/j.intimp.2023.110795. Epub 2023 Aug 17.
9
NPRC deletion mitigated atherosclerosis by inhibiting oxidative stress, inflammation and apoptosis in ApoE knockout mice.NPRC 缺失通过抑制载脂蛋白 E 基因敲除小鼠的氧化应激、炎症和细胞凋亡来减轻动脉粥样硬化。
Signal Transduct Target Ther. 2023 Aug 9;8(1):290. doi: 10.1038/s41392-023-01560-y.
10
Apigenin inhibits macrophage pyroptosis through regulation of oxidative stress and the NF-κB pathway and ameliorates atherosclerosis.芹菜素通过调节氧化应激和 NF-κB 通路抑制巨噬细胞焦亡,改善动脉粥样硬化。
Phytother Res. 2023 Nov;37(11):5300-5314. doi: 10.1002/ptr.7962. Epub 2023 Aug 1.