A novel KEAP1 inhibitor, tiliroside, activates NRF2 to protect against acetaminophen-induced oxidative stress and acute liver injury

Our study demonstrated that tiliroside could protect against AILI by activating the KEAP1/NRF2 pathway, which primarily inhibits the processing of oxidative stress and cell death. Our results suggest that tiliroside could serve as a potential agent for the clinical treatment of AILI.

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Publication Details

Journal
Hepatology Communications
Published
2025-02-26
DOI
https://doi.org/10.1097/hc9.0000000000000658
Citations
8
Primary Topic
Drug-Induced Hepatotoxicity and Protection
Type
article
Field-Weighted Citation Impact
12.46
Controls
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article

A novel KEAP1 inhibitor, tiliroside, activates NRF2 to protect against acetaminophen-induced oxidative stress and acute liver injury

Yunwen Yang, Fangfang Cai, Lei Liu, Peipei Wang et al.
8 citations
Hepatology Communications
Drug-Induced Hepatotoxicity and Protection
12.46
article

A novel KEAP1 inhibitor, tiliroside, activates NRF2 to protect against acetaminophen-induced oxidative stress and acute liver injury

Yunwen Yang, Fangfang Cai, Lei Liu, Peipei Wang, Wen Zhang, Kaiqian Zhou
article en
8 citations

Abstract

Our study demonstrated that tiliroside could protect against AILI by activating the KEAP1/NRF2 pathway, which primarily inhibits the processing of oxidative stress and cell death. Our results suggest that tiliroside could serve as a potential agent for the clinical treatment of AILI.

Hepatology CommunicationsVol. 9(3)
Nanjing University of Chinese Medicine (CN), Shanxi Medical University (CN), Second Affiliated Hospital of Nanjing Medical University (CN), Shanxi Provincial People’s Hospital (CN), Nanjing Medical University (CN)
Good health and well-being
Openalex Percentile: Top 1%
Drug-Induced Hepatotoxicity and Protection
12.46
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