Hao Liyuan, Li Shenghao, Li Caige, Zhang Zhiqin, Hu Xiaoyu, Yan Huimin
School of Clinical Medicine, Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, People's Republic of China.
Department of Infectious Diseases, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, People's Republic of China.
Drug Des Devel Ther. 2025 Jan 8;19:83-96. doi: 10.2147/DDDT.S500719. eCollection 2025.
Non-alcoholic fatty liver disease (NAFLD) is the major cause of chronic liver disease worldwide, with no universally recognized effective treatments currently available. In recent years, ginseng and its principal active components, such as ginsenosides, have shown potential protective effects in the treatment of these liver diseases. In NAFLD, studies have demonstrated that ginseng can improve hepatic lipid metabolism, reduce inflammatory responses, and inhibit oxidative stress and fibrosis, thereby attenuating the progression of NAFLD. Additionally, ginseng inhibits oxidative stress by scavenging free radicals and enhancing antioxidant enzyme activities, and it can impede fibrosis by interfering with the fibrotic signaling pathways. These combined effects contribute to attenuating the progression of NAFLD. These findings highlight the promise of ginseng as a potential therapeutic candidate for the treatment of NAFLD. However, despite the significant efficacy of ginseng in human NAFLD treatment, the number and quality of clinical studies remain limited, with a lack of large-scale, multicenter clinical trials to confirm these effects. Moreover, the pharmacokinetic properties of different ginsenosides, optimal therapeutic dosages, and the safety of long-term use require further investigation. This review summarizes the existing evidence on the mechanisms of action of ginseng and its active components in human NAFLD, assesses their potential as therapeutic options, and proposes future research directions to provide stronger scientific support for clinical application. Additionally, we performed a network pharmacology analysis of ginseng in relation to NAFLD to identify and investigate potential targets of ginseng in the treatment of NAFLD. This analysis aims to provide a theoretical foundation for the development of ginseng -based drugs for combating NAFLD.
非酒精性脂肪性肝病(NAFLD)是全球慢性肝病的主要病因,目前尚无普遍认可的有效治疗方法。近年来,人参及其主要活性成分,如人参皂苷,在这些肝病的治疗中显示出潜在的保护作用。在NAFLD中,研究表明人参可以改善肝脏脂质代谢,减少炎症反应,抑制氧化应激和纤维化,从而减缓NAFLD的进展。此外,人参通过清除自由基和增强抗氧化酶活性来抑制氧化应激,并且可以通过干扰纤维化信号通路来阻止纤维化。这些综合作用有助于减缓NAFLD的进展。这些发现突出了人参作为NAFLD潜在治疗候选药物的前景。然而,尽管人参在人类NAFLD治疗中具有显著疗效,但临床研究的数量和质量仍然有限,缺乏大规模、多中心临床试验来证实这些效果。此外,不同人参皂苷的药代动力学特性、最佳治疗剂量以及长期使用的安全性需要进一步研究。本综述总结了人参及其活性成分在人类NAFLD作用机制的现有证据,评估了它们作为治疗选择的潜力,并提出了未来的研究方向,以为临床应用提供更强有力的科学支持。此外,我们对人参与NAFLD进行了网络药理学分析,以确定和研究人参在NAFLD治疗中的潜在靶点。该分析旨在为开发抗NAFLD的人参基药物提供理论基础。