Article

Chlorogenic acid promotes liver regeneration after partial hepatectomy through activating Nrf2 via directly targeting Keap1

Hao-yu Xue1,2, Xin-nan Gu1, Zhuang Huang3, Ze Zhang1, Kun-yu Zhang1, Zhen-lin Huang1, Bin Lu1, Jian-gao Fan2, Meng-juan Wei1,4, Li-li Ji1
1 The MOE Key Laboratory for Standardization of Chinese Medicines, Shanghai Key Laboratory of Compound Chinese Medicines and The SATCM Key Laboratory for New Resources and Quality Evaluation of Chinese Medicines, Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China
2 Department of Gastroenterology, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China
3 School of Pharmacy, Hubei University of Chinese Medicine, Wuhan 430065, China
4 Shanghai Academy of International Standardization for Traditional Chinese Medicine, Shanghai 201203, China
Correspondence to: Meng-juan Wei: wmj_aijia@163.com, Li-li Ji: jilili@shutcm.edu.cn,
DOI: 10.1038/s41401-026-01770-4
Received: 30 July 2025
Accepted: 29 January 2026
Advance online: 20 March 2026

Abstract

Liver regeneration (LR) is crucial for liver function recovery, but there is still no effective treatment to promote LR. Chlorogenic acid (CGA) is the main active compound of Eucommia ulmoides Oliv., which is traditionally recorded to possess liver tonifying function. Our results revealed that CGA promoted LR in mice performed with 90% and 70% partial hepatectomy (PHx). CGA activated nuclear factor erythroid 2-related factor 2 (Nrf2) through interacting with kelch-like ECH-associated protein 1 (Keap1) during LR process. Nrf2 activation initiated the mRNA expression of E2 promoter binding factor 1 (E2F1) to accelerate cell cycle progression. Moreover, Nrf2 activation also initiated the mRNA expression of peroxisome proliferative-activated receptor, gamma, coactivator 1-alpha (PGC-1α) to promote ATP production, which supplied the sufficient energy to support LR. The importance of Nrf2 was further validated in Nrf2 knockout and liver specific Keap1 genetic depletion mice. Moreover, Arg415 residue in the kelch domain of Keap1 was proved to be pivotal for the binding of CGA with Keap1. Our findings not only highlighted the critical role of Nrf2 during LR process, but also provided a solid research foundation for exploring CGA as a promising therapeutic candidate to promote LR.

Keywords: liver regeneration; chlorogenic acid; partial hepatectomy; nuclear factor erythroid 2-related factor 2; Kelch-like ECH- associated protein 1

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