Anti-fibrosis effect of astragaloside IV in animal models of cardiovascular diseases and its mechanisms: a systematic review.

IF 3.9 3区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY
Pharmaceutical Biology Pub Date : 2025-12-01 Epub Date: 2025-04-22 DOI:10.1080/13880209.2025.2488994
Shiyu Zhang, Shijie Li, Xue Li, Chen Wan, Lin Cui, Youping Wang
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引用次数: 0

Abstract

Context: Myocardial fibrosis is a common manifestation of end-stage cardiovascular disease, but there is a lack of means to reverse fibrosis. Astragaloside IV (AS-IV), the major active component of Astragalus membranaceus Fisch. ex Bunge Fabaceae, possesses diverse biological activities that have beneficial effects against cardiovascular disease.

Objective: This systematic review aims to summarize the anti-fibrosis effect of AS-IV in animal models (rats or mice only) and its underlying mechanisms, and provide potential directions for the clinical use of AS-IV.

Methods: PubMed, EMBASE, Web of Science, CNKI, Wanfang database, and SinoMed were searched from inception to 31 December 2024. The following characteristics of the included studies were extracted and summarized: animal model, route of administration, dose/concentration, measurement indicators, and potential mechanisms. The quality of the included studies was assessed used a 10-item scale from SYRCLE.

Results and conclusion: AS-IV represents a promising multi-target candidate for myocardial fibrosis treatment in the 24 eligible studies included in the analysis. This systematic review is the first to comprehensively evaluate the anti-fibrosis mechanisms of AS-IV across heterogeneous cardiovascular disease animal models, including myocardial infarction, hypertension, ischemia-reperfusion injury, and myocarditis. The underlying mechanisms of the anti-fibrosis effects of AS-IV may include collagen metabolism, anti-apoptosis, anti-inflammation and, pyroptosis, antioxidants, improving mitochondrial function, regulating senescence, etc. Current evidence remains preclinical, with critical gaps in toxicological profiles, human safety thresholds, and clinical adverse reaction data. Future research must integrate robust toxicological evaluations, optimized combination therapies, and adaptive clinical trials to validate translational potential.

黄芪甲苷在心血管疾病动物模型中的抗纤维化作用及其机制综述
背景:心肌纤维化是终末期心血管疾病的常见表现,但缺乏逆转纤维化的手段。黄芪甲苷(Astragaloside IV, AS-IV)是黄芪的主要活性成分。蚕豆科植物,具有多种生物活性,对心血管疾病有有益作用。目的:本系统综述旨在总结AS-IV在动物模型(大鼠或小鼠)中的抗纤维化作用及其机制,为AS-IV的临床应用提供可能的方向。方法:检索PubMed、EMBASE、Web of Science、中国知网(CNKI)、万方数据库、中国医学信息网(sinmed)自建库至2024年12月31日。提取并总结纳入研究的以下特点:动物模型、给药途径、剂量/浓度、测量指标及可能机制。纳入研究的质量采用sycle的10项量表进行评估。结果和结论:在纳入分析的24项符合条件的研究中,AS-IV是一种有希望的多靶点心肌纤维化治疗候选药物。本系统综述首次全面评价AS-IV在异质心血管疾病动物模型中的抗纤维化机制,包括心肌梗死、高血压、缺血再灌注损伤和心肌炎。AS-IV抗纤维化作用的机制可能包括胶原代谢、抗凋亡、抗炎、抗焦亡、抗氧化、改善线粒体功能、调节衰老等。目前的证据仍然是临床前的,在毒理学概况、人体安全阈值和临床不良反应数据方面存在重大差距。未来的研究必须整合强有力的毒理学评估、优化的联合疗法和适应性临床试验,以验证转化潜力。
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来源期刊
Pharmaceutical Biology
Pharmaceutical Biology 医学-药学
CiteScore
6.70
自引率
2.60%
发文量
191
审稿时长
1 months
期刊介绍: Pharmaceutical Biology will publish manuscripts describing the discovery, methods for discovery, description, analysis characterization, and production/isolation (including sources and surveys) of biologically-active chemicals or other substances, drugs, pharmaceutical products, or preparations utilized in systems of traditional medicine. Topics may generally encompass any facet of natural product research related to pharmaceutical biology. Papers dealing with agents or topics related to natural product drugs are also appropriate (e.g., semi-synthetic derivatives). Manuscripts will be published as reviews, perspectives, regular research articles, and short communications. The primary criteria for acceptance and publication are scientific rigor and potential to advance the field.
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