ISSN 2097-5724 CN 61-1535/R 主管·主办:陕西省疾病预防控制中心
疾病预防与控制 Disease Prevention and Control 医学学术期刊 双月刊
2026-03-005 综述 2026, 2(03): 17-20

拮抗马兜铃酸肝毒性的策略:从基础研究到临床应用进展

兰州大学第一医院,兰州大学,甘肃省普通外科临床医学研究中心

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摘要

马兜铃酸(AA)是一类存在于马兜铃科植物中的硝基菲羧酸化合物,具有显著的肾毒性和肝毒性,可诱发脱氧核糖核酸(DNA)加合物形成,导致肝细胞损伤、纤维化甚至肝癌。近年来,针对AA肝毒性的拮抗策略研究取得重要进展。基础研究表明,抗氧化剂、抗炎药物及调控CYP450代谢酶和转运蛋白等干预手段可有效减轻AA诱导的氧化应激与线粒体功能障碍。此外,天然产物如小檗碱、葡萄籽原花青素、水飞蓟宾等显示出良好保护作用。在临床层面,早期识别AA暴露史、结合生物标志物监测及个体化保肝治疗已逐步应用于高风险人群管理。未来,基于多组学技术的机制解析与靶向干预策略有望推动AA肝毒性防治从实验室向精准临床转化。

Abstract

Aristolochic acid(AA), a nitro-phenanthrene carboxylic acid compound present in Aristolochiaceae plants, exhibits significant nephrotoxicity and hepatotoxicity. It can induce DNA adduct formation, leading to hepatocyte damage, fibrosis, and even hepatocellular carcinoma. In recent years, substantial progress has been made in developing antagonistic strategies against AA-induced hepatotoxicity. Fundamental studies indicate that interventions such as antioxidants, anti-inflammatory agents, and modulation of CYP450 metabolic enzymes and transporters can effectively mitigate AA-induced oxidative stress and mitochondrial dysfunction. Additionally, natural products including berberine, grape seed proanthocyanidins, and silibinin have demonstrated notable protective effects. Clinically, early identification of AA exposure history, combined with biomarker monitoring and individualized hepatoprotective therapies, has been progressively implemented in the management of high-risk populations. Future research, leveraging multiomics technologies for mechanistic elucidation and targeted intervention strategies, holds promise for translating AA hepatotoxicity prevention and treatment from laboratory settings to precision clinical applications.

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[1]芮少珍,周燕.拮抗马兜铃酸肝毒性的策略:从基础研究到临床应用进展[J].疾病预防与控制,2026,2(03):17-20.