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Icariside Ⅱ Contributes to Epimedii folium-Induced Hepatotoxicity Through Enhancing NLRP3 Inflammasome Activation

28 Pages Posted: 27 Aug 2019

See all articles by Zhilei Wang

Zhilei Wang

Government of the People's Republic of China - China Military Institute of Chinese Materia

Guang Xu

Government of the People's Republic of China - China Military Institute of Chinese Materia

Hongbo Wang

Government of the People's Republic of China - Fifth Medical Center

Xiaoyan Zhan

Government of the People's Republic of China - China Military Institute of Chinese Materia

Yuan Gao

Capital Medical University

Nian Chen

Chengdu University of Traditional Chinese Medicine

Ruisheng Li

Government of the People's Republic of China - Fifth Medical Center

Xueai Song

Government of the People's Republic of China - Fifth Medical Center

Yuming Guo

Government of the People's Republic of China - Fifth Medical Center

Ming Niu

Government of the People's Republic of China - China Military Institute of Chinese Materia

Jiabo Wang

Government of the People's Republic of China - China Military Institute of Chinese Materia

Youping Liu

Chengdu University of Traditional Chinese Medicine

Xiaohe Xiao

Government of the People's Republic of China - Senior Department of Hepatology

Zhaofang Bai

Government of the People's Republic of China - Senior Department of Hepatology; Government of the People's Republic of China - Military Patient Management Department

More...

Abstract

Idiosyncratic drug-induced liver injury (IDILI) continues to be a leading cause of failures in drug development and the main reason for post-marketing safety warnings and withdrawals of drugs. Epimedii folium (EF), an herbal medicine widely used in China, Japan, and Korea, has been shown to cause idiosyncratic liver injury, but the underlying mechanisms are poorly understood. Increasing evidences have indicated that most cases of IDILI are immune mediated. Here, we report that icariside Ⅱ (ICS Ⅱ), the major active and metabolic constituent of EF, causes idiosyncratic liver injury by promoting NLRP3 inflammasome activation. ICS Ⅱ enhances NLRP3 inflammasome activation triggered by adenosine triphosphate (ATP) and nigericin, but not silicon dioxide (SiO2), monosodium urate crystal (MSU) or cytosolic lipopolysaccharide (LPS). Moreover, the activation of NLRC4 and AIM2 inflammasomes is not affected by ICS Ⅱ. Mechanistically, synergistic induction of mitochondrial reactive oxygen species (mtROS) is a crucial contributor to the enhancing effect of ICS Ⅱ on ATP- or nigericin-induced NLRP3 inflammasome activation. Importantly, in vivo data show that a combination of nonhepatotoxic doses of LPS and ICS Ⅱ causes liver injury in wild-type mice but not NLRP3-knockout mice. In conclusion, ICS Ⅱ acts as a specific promoter to increase ATP- and nigericin-induced NLRP3 inflammasome activation, which is responsible for EF-induced liver injury. Our findings also suggest that ICS Ⅱ or EF should be avoided in cases of diseases that are associated with ATP/nigericin-induced NLRP3 inflammasome activation, which may be risk factors for EF-induced liver injury.

Funding Statement: This work has been supported by National Natural Science Foundation of China (81874368, 81630100), Beijing Nova Program (Z181100006218001), National Science & Technology Major Project “Key New Drug Creation and Manufacturing Program” (2017ZX09301022, 2018ZX09101002).

Declaration of Interests: The authors declare no conflict of interest.

Ethics Approval Statement: All experimental procedures in this study were performed according to the guidelines of laboratory animals care and use and approved by the animal ethics committee of the Fifth Medical Centre, Chinese PLA (People’s Liberation Army) General Hospital.

Keywords: Epimedii folium; icariside Ⅱ; idiosyncratic drug-induced liver injury; NLRP3 inflammasome

Suggested Citation

Wang, Zhilei and Xu, Guang and Wang, Hongbo and Zhan, Xiaoyan and Gao, Yuan and Chen, Nian and Li, Ruisheng and Song, Xueai and Guo, Yuming and Niu, Ming and Wang, Jiabo and Liu, Youping and Xiao, Xiaohe and Bai, Zhaofang, Icariside Ⅱ Contributes to Epimedii folium-Induced Hepatotoxicity Through Enhancing NLRP3 Inflammasome Activation (August 23, 2019). Available at SSRN: https://ssrn.com/abstract=3441808 or http://dx.doi.org/10.2139/ssrn.3441808

Zhilei Wang

Government of the People's Republic of China - China Military Institute of Chinese Materia

Beijing
China

Guang Xu

Government of the People's Republic of China - China Military Institute of Chinese Materia

Beijing
China

Hongbo Wang

Government of the People's Republic of China - Fifth Medical Center

China

Xiaoyan Zhan

Government of the People's Republic of China - China Military Institute of Chinese Materia

Beijing
China

Yuan Gao

Capital Medical University

Beijing
China

Nian Chen

Chengdu University of Traditional Chinese Medicine

China

Ruisheng Li

Government of the People's Republic of China - Fifth Medical Center

China

Xueai Song

Government of the People's Republic of China - Fifth Medical Center

China

Yuming Guo

Government of the People's Republic of China - Fifth Medical Center

China

Ming Niu

Government of the People's Republic of China - China Military Institute of Chinese Materia

Beijing
China

Jiabo Wang

Government of the People's Republic of China - China Military Institute of Chinese Materia

Beijing
China

Youping Liu

Chengdu University of Traditional Chinese Medicine ( email )

China

Xiaohe Xiao

Government of the People's Republic of China - Senior Department of Hepatology ( email )

Zhaofang Bai (Contact Author)

Government of the People's Republic of China - Senior Department of Hepatology ( email )

Government of the People's Republic of China - Military Patient Management Department ( email )