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DOI 10.3390/biom16060815

Медицинская библиотека · Biomolecules · 2026

Natural Alkaloids Against Liver Injury: Mechanistic Insights and Multi-Target Therapeutic Potential.

Xiao Yating, Tian Zhirui, Cui Jie, Yang Xia, Wang Dong, Cai Yangyang, Wu Qian, Jin Yaxin, Chen Hua, Ji Kai

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Аннотация

Liver injury is a complex pathological condition with increasing incidence due to diverse etiologies, including drug-induced liver injury, metabolic dysfunction-associated steatotic liver disease, alcoholic liver disease, viral hepatitis, and autoimmune disorders. Its progression is characterized by persistent hepatic damage and gradual loss of liver function, which may ultimately lead to fibrosis, cirrhosis, and liver failure. However, currently available hepatoprotective drugs still present several limitations, such as insufficient target specificity, limited therapeutic efficacy, and potential adverse effects, highlighting the need for safer and more effective alternatives. Based on a comprehensive search of databases including PubMed, Web of Science, China National Knowledge Infrastructure and Google Scholar, this review summarizes the pathogenic mechanisms of major liver injury types and the therapeutic potential of natural alkaloids. As key secondary metabolites of medicinal plants, alkaloids exhibit structural diversity, potent bioactivities, and favorable safety profiles. Increasing evidence suggests that natural alkaloids exert hepatoprotective effects through multi-target and multi-pathway mechanisms, including the regulation of oxidative stress, inflammation, lipid metabolism, and cell death. These findings highlight their promising potential for the prevention and treatment of liver injury and provide a theoretical basis for the development of novel hepatoprotective agents.

Для цитирования: Xiao Yating, Tian Zhirui, Cui Jie, Yang Xia, Wang Dong, Cai Yangyang, Wu Qian, Jin Yaxin, Chen Hua, Ji Kai. Natural Alkaloids Against Liver Injury: Mechanistic Insights and Multi-Target Therapeutic Potential.. Biomolecules. 2026. DOI: 10.3390/biom16060815.

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