The Active Components of Traditional Chinese Medicines Regulate the Multi-Target Signaling Pathways of Metabolic Dysfunction-Associated Fatty Liver Disease.

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-04-09 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S514498
Zhicong Song, Shuai Bu, Suzhen Sang, Jie Li, Xihai Zhang, Xu Song, Yuqin Ran
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Abstract

Metabolic dysfunction-associated fatty liver disease (MAFLD), which is characterized by hepatocyte lipid accumulation driven by systemic metabolic dysregulation, represents a critical therapeutic challenge in the context of the global metabolic syndrome epidemic. The clinically recommended drugs for MAFLD mainly include antioxidants, hepatoprotective anti-inflammatory drugs, and weight-loss drugs. However, the mechanisms underlying the progression of MAFLD is characterized by nonlinearity, highlighting the urgent need for safer multi-target alternative therapies. Although existing single-target pharmacological interventions often show limited efficacy and adverse effects, the multi-component and multi-target nature of the active ingredients in traditional Chinese medicine (TCM) formulations represent new opportunities for systemic metabolic regulation. In this study, by searching PubMed and Web of Science, we identified 108 experimental studies. By evaluating multiple mechanisms, such as improving lipid metabolism and insulin resistance, alleviating oxidative stress damage, inhibiting liver inflammation, suppressing liver fibrosis, reducing endoplasmic reticulum stress, regulating hepatocyte autophagy, inhibiting hepatocyte apoptosis, improving mitochondrial dysfunction, and regulating the intestinal flora, we constructed a cross-scale regulatory network for the treatment of MAFLD by the active components of TCM. Subsequently, the dynamic target groups were screened, and a new paradigm of "mechanism-oriented and spatiotemporal-optimized" design for TCM compound prescriptions was proposed, providing a theoretical framework for the development of precise therapies that can improve liver lipid metabolism, block inflammation and fibrosis, and restore intestinal homeostasis.

中药有效成分调控代谢功能障碍相关脂肪肝多靶点信号通路
代谢功能障碍相关脂肪性肝病(MAFLD)的特征是由全身代谢失调驱动的肝细胞脂质积累,在全球代谢综合征流行的背景下,这是一个关键的治疗挑战。临床上推荐的治疗MAFLD的药物主要有抗氧化剂、保肝抗炎药和减肥药。然而,MAFLD的发展机制具有非线性的特点,因此迫切需要更安全的多靶点替代疗法。尽管现有的单靶点药物干预往往显示出有限的疗效和不良反应,但中药制剂中有效成分的多组分和多靶点性质为全身代谢调节提供了新的机会。在本研究中,通过检索PubMed和Web of Science,我们确定了108项实验研究。通过评价其改善脂质代谢和胰岛素抵抗、减轻氧化应激损伤、抑制肝脏炎症、抑制肝纤维化、减轻内质网应激、调节肝细胞自噬、抑制肝细胞凋亡、改善线粒体功能障碍、调节肠道菌群等多种机制,构建了中药活性成分治疗MAFLD的跨尺度调控网络。随后,筛选动态靶点群体,提出“机制导向、时空优化”的中药复方设计新范式,为开发改善肝脏脂质代谢、阻断炎症和纤维化、恢复肠道稳态的精准疗法提供理论框架。
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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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