Huangqi-Danshen Decoction Alleviates Cardiac Fibrosis Following Myocardial Infarction by Inhibiting USP22 to Enhance the Ubiquitination of BRD4.

IF 11.3 1区 医学 Q1 CHEMISTRY, MEDICINAL
Phytomedicine Pub Date : 2026-09-01 Epub Date: 2026-07-21 DOI:10.1016/j.phymed.2026.158618
Jiaqi Hao, Mengkai Lu, Muxin Zhang, Lin Lin, Yuanlong Hu, Lei Zhang, Chao Li
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引用次数: 0

Abstract

Background: Myocardial fibrosis is a critical pathological process in the development of heart failure following myocardial infarction (MI). The Huangqi-Danshen decoction (HDD) has shown cardioprotective effects in clinical practice. Nonetheless, the precise molecular mechanisms underlying its antifibrotic effects remain to be elucidated.

Objective: This study aimed to systematically investigate the therapeutic effects of HDD on myocardial fibrosis post-MI and to determine the underlying molecular mechanisms.

Methods: An MI model was established in mice by ligating the left anterior descending coronary artery. Cardiac function and morphology were evaluated using echocardiography and histological analysis. In in vitro experiments, TGF-β1-stimulated human cardiac fibroblasts were treated with HDD-containing serum. The underlying mechanism of HDD was investigated using proteomic screening and molecular biology techniques.

Results: HDD markedly improved cardiac function and attenuated myocardial fibrosis in MI mice. Proteomic analysis identified BRD4 as a key epigenetic target of HDD. HDD reduced BRD4 expression and H3K27ac levels, accompanied by decreased fibrosis-related marker expression. BRD4 overexpression or TSA treatment counteracted the inhibitory effects of HDD on H3K27ac and fibrotic markers, supporting the involvement of the BRD4/H3K27ac axis. Mechanistically, HDD promoted ubiquitin-proteasome-dependent BRD4 degradation by disrupting the interaction between BRD4 and the deubiquitinase USP22. USP22 overexpression reversed, whereas USP22 knockdown largely phenocopied, the antifibrotic effects of HDD.

Conclusion: HDD ameliorates myocardial fibrosis by targeting the USP22-BRD4 axis, promoting BRD4 degradation and inhibiting H3K27ac-mediated profibrotic transcription, offering a novel epigenetic therapeutic strategy.

黄芪丹参汤通过抑制USP22增强BRD4泛素化减轻心肌梗死后心肌纤维化。
背景:心肌纤维化是心肌梗死(MI)后心力衰竭发展的关键病理过程。黄芪丹参汤在临床上已显示出保护心脏的作用。尽管如此,其抗纤维化作用的确切分子机制仍有待阐明。目的:本研究旨在系统探讨HDD对心肌梗死后心肌纤维化的治疗作用,并探讨其分子机制。方法:结扎左冠状动脉前降支,建立小鼠心肌梗死模型。采用超声心动图和组织学分析评价心功能和形态。体外实验中,用含hdd的血清处理TGF-β1刺激的人心脏成纤维细胞。利用蛋白质组学筛选和分子生物学技术对HDD的潜在机制进行了研究。结果:HDD能明显改善心肌梗死小鼠心功能,减轻心肌纤维化。蛋白质组学分析发现BRD4是HDD的关键表观遗传靶点。HDD降低BRD4表达和H3K27ac水平,并伴有纤维化相关标志物表达降低。BRD4过表达或TSA治疗抵消了HDD对H3K27ac和纤维化标志物的抑制作用,支持BRD4/H3K27ac轴的参与。从机制上讲,HDD通过破坏BRD4和去泛素酶USP22之间的相互作用,促进泛素蛋白酶体依赖性BRD4降解。USP22过表达逆转,而USP22敲低在很大程度上复制了HDD的抗纤维化作用。结论:HDD通过靶向USP22-BRD4轴,促进BRD4降解和抑制h3k27ac介导的纤维化转录来改善心肌纤维化,提供了一种新的表观遗传治疗策略。
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来源期刊
Phytomedicine
Phytomedicine 医学-药学
CiteScore
10.30
自引率
5.10%
发文量
670
审稿时长
91 days
期刊介绍: Phytomedicine is a therapy-oriented journal that publishes innovative studies on the efficacy, safety, quality, and mechanisms of action of specified plant extracts, phytopharmaceuticals, and their isolated constituents. This includes clinical, pharmacological, pharmacokinetic, and toxicological studies of herbal medicinal products, preparations, and purified compounds with defined and consistent quality, ensuring reproducible pharmacological activity. Founded in 1994, Phytomedicine aims to focus and stimulate research in this field and establish internationally accepted scientific standards for pharmacological studies, proof of clinical efficacy, and safety of phytomedicines.
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