人参及其生物活性成分治疗非酒精性脂肪肝的研究进展

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-01-08 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S500719
Liyuan Hao, Shenghao Li, Caige Li, Zhiqin Zhang, Xiaoyu Hu, Huimin Yan
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引用次数: 0

摘要

非酒精性脂肪肝(NAFLD)是全球慢性肝病的主要病因,目前还没有公认的有效治疗方法。近年来,人参及其主要活性成分(如人参皂苷)在治疗这些肝病方面显示出潜在的保护作用。对于非酒精性脂肪肝,研究表明,人参可改善肝脏脂质代谢,减轻炎症反应,抑制氧化应激和纤维化,从而减轻非酒精性脂肪肝的进展。此外,人参还能通过清除自由基和增强抗氧化酶活性来抑制氧化应激,并能通过干扰纤维化信号通路来阻碍纤维化。这些综合效应有助于减轻非酒精性脂肪肝的进展。这些发现凸显了人参作为治疗非酒精性脂肪肝潜在候选疗法的前景。然而,尽管人参在治疗人类非酒精性脂肪肝方面疗效显著,但临床研究的数量和质量仍然有限,缺乏大规模、多中心的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服用的安全性也需要进一步研究。本综述总结了人参及其活性成分在人类非酒精性脂肪肝中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,以便为临床应用提供更有力的科学支持。此外,我们还对人参与非酒精性脂肪肝的关系进行了网络药理学分析,以确定和研究人参治疗非酒精性脂肪肝的潜在靶点。这项分析旨在为开发以人参为基础的药物防治非酒精性脂肪肝提供理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Review of the Therapeutic Potential of Ginseng and Its Bioactive Components in Nonalcoholic Fatty Liver Disease.

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.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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