Inhibitory effects of herbal monomers on ferroptosis in renal fibrosis: a review and mechanistic study.

2025-07-22
Frontiers in pharmacology 16
- Kaixiang Liu
- Min Yu
- Yangyang He
- Ting Wang
- Guisen Li
- Li Wang
- Xiang Zhong

PubMed: 40766752
DOI: 10.3389/fphar.2025.1610573

Study Design

Type: Review
Methods: Using the keywords "ferroptosis", "chronic kidney disease", "renal fibrosis", "Chinese herbal medicine", "natural products", "bioactive components", and "herb", we conducted an extensive literature search of several databases, including PubMed, Web of Science, CNKI, and Wanfang database, to identify studies reporting the role of CHM monomers in inhibiting ferroptosis and improving renal fibrosis.

Background and purpose

Renal fibrosis is a common characteristic of chronic kidney disease (CKD). Studies have confirmed the role of ferroptosis in the pathogenesis of various kidney diseases, making it a new research hotspot in the field of renal fibrosis. Monomers of Chinese herbal medicines (CHMs) can improve renal fibrosis by multi-target inhibition of ferroptosis. This review aimed to explore the roles and mechanisms of CHMs in renal fibrosis.

Methods

Using the keywords "ferroptosis", "chronic kidney disease", "renal fibrosis", "Chinese herbal medicine", "natural products", "bioactive components", and "herb", we conducted an extensive literature search of several databases, including PubMed, Web of Science, CNKI, and Wanfang database, to identify studies reporting the role of CHM monomers in inhibiting ferroptosis and improving renal fibrosis. The names of the plants covered in the review have been checked through MPNS (http://mpns.kew.org). All monomers of CHMs were identified in the Pharmacopoeia of the People's Republic of China.

Results

In total, 21 monomers of CHMs were identified in this study, most of which were flavonoids, followed by terpenoids and coumarins. This review showed that monomers of CHMs inhibited ferroptosis and improved renal fibrosis through multi-target mechanisms. They maintained iron homeostasis by acting on NCOA4 and Nrf2 to reduce ferritinophagy. They also inhibited lipid peroxidation and regulated the antioxidant system by modulating ACSL4, NOX4, Nrf2, FSP1, and GPX4 and inhibiting Smad3 to improve renal fibrosis.

Conclusion

Monomers of CHMs effectively inhibited ferroptosis and prevented renal fibrosis in various animal models and cell models of CKD. However, further in-depth studies with better designs are needed to identify the exact targets of monomers of CHMs and improve the treatment of renal fibrosis and CKD.