Terpenoids in the management of MASLD: Multi-target mechanisms, therapeutic potential, and future perspectives
Chengzi Huang1, Rong Zhang2, Caizhi Liu2
1Chengdu University of Traditional Chinese Medicine, Chengdu 610075, China; Department of Anorectal, The Affiliated Hospital, Southwest Medical University, Luzhou 646000, China; Department of Endocrinology and Metabolism, Shanghai Diabetes Institute, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200233, China.
Abstract:
Metabolic dysfunction-associated steatotic liver disease (MASLD) is a highly prevalent chronic liver disorder characterized by a complex interplay of pathogenic factors, including excessive energy intake, insulin resistance, and genetic susceptibility. Given its multifactorial pathogenesis, therapeutic strategies targeting multiple pathways are particularly desirable. Terpenoids, a structurally diverse class of natural compounds derived from medicinal plants, have attracted increasing attention as potential therapeutic agents for MASLD because of their multi-target pharmacological properties. This review summarizes recent advances in the therapeutic potential and molecular mechanisms of representative terpenoids-including monoterpenoids, sesquiterpenoids, diterpenoids, triterpenoids, and tetraterpenoids-in the context of MASLD. These compounds exert therapeutic effects mainly by improving lipid metabolism, oxidative stress, inflammation, autophagy, fibrosis, and gut-liver axis dysfunction. We also summarize the limited clinical evidence and the major challenges for translation. Although terpenoids show considerable promise, more rigorous clinical validation is required.
Related Concept Videos
Anthelminthic Agents
Clinical Significance of Antibiotic Resistance
Therapeutic Drug Monitoring: Affecting Factors
Inflammatory Bowel Disease IV: Pharmacological Management
Pharmacologic...
Pharmacogenomics: Identification of New Drug Targets
MALDI-TOF Mass Spectrometry
