Targeting atherosclerotic inflammation: Advances in NLRP3 inflammasome inhibitors beyond LDL-C.

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Acta Pharmaceutica Pub Date : 2026-06-30 Print Date: 2026-06-01 DOI:10.2478/acph-2026-0019
Ligang Bao, Xialing Dai
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引用次数: 0

Abstract

Atherosclerosis, the main pathological background of cardiovascular diseases, is not only characterized by lipid metabolism disorders but also chronic inflammation as a major driver of disease progression. As a key regulator of inflammatory immune responses, the NLRP3 inflamma-some is involved in the development and instability of atherosclerotic plaques. Although reducing low-density lipoprotein cholesterol (LDL-C) confers benefits, residual cardiovascular risk persists, necessitating novel anti-inflammatory therapies. This review provides a comprehensive overview of NLRP3 inflammasome activation mechanisms and its role in plaque inflammation. We systematically summarize current NLRP3 inhibitors under preclinical and clinical development, including small molecules and biologics, with emphasis on design strategies, structural characteristics and pharmacological activities. Challenges in clinical translation, such as tissue targeting and safety, are also discussed. By integrating recent advances in molecular mechanisms and medicinal chemistry, this article aims to provide a theoretical basis for targeted anti-inflammatory therapies beyond lipid lowering.

靶向动脉粥样硬化炎症:NLRP3炎性体抑制剂的研究进展
动脉粥样硬化是心血管疾病的主要病理背景,不仅以脂质代谢紊乱为特征,而且慢性炎症是疾病进展的主要驱动因素。作为炎症免疫反应的关键调节因子,NLRP3炎性蛋白参与动脉粥样硬化斑块的发展和不稳定。尽管降低低密度脂蛋白胆固醇(LDL-C)会带来益处,但残留的心血管风险仍然存在,因此需要新的抗炎疗法。本文综述了NLRP3炎症小体的激活机制及其在斑块炎症中的作用。我们系统地总结了目前临床前和临床开发的NLRP3抑制剂,包括小分子和生物制剂,重点介绍了设计策略、结构特征和药理活性。在临床翻译的挑战,如组织靶向和安全性,也进行了讨论。本文旨在结合分子机制和药物化学方面的最新进展,为除降脂外的靶向抗炎治疗提供理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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