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Review | Open Access

Research progress on regulation of mitochondrial function by traditional Chinese medicine in alleviating acetaminophen-induced liver injury

Shuang Xiaa,c,d,1Rong Caoa,b,c,d,1Zhiyu Hua,c,dJiayi Liua,c,dXiaoxiang Fana,c,dZhichao Jiangb,eHui Gonga,c,d( )Miao Yana,c,d( )
Department of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha 410011, China
Hunan University of Chinese Medicine, Changsha 410208, China
International Research Center for Precision Medicine, Transformative Technology and Software Services, Changsha 410011, China
Toxicology Counseling Center of Hunan Province, Changsha 410011, China
The Second People's Hospital of Hunan Province/Brain Hospital of Hunan Province, Changsha 410007, China

1 Contributed equally.

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Abstract

Drug-induced liver injury is a significant contributor to cases of acute liver failure and the primary reason for drug withdrawal due to safety concerns. Acetaminophen (N-acetyl-para-aminophenol, APAP) is a widely used antipyretic and analgesic drug worldwide. It has been reported that APAP-induced hepatotoxicity accounts for approximately 50 % of acute liver failure cases in Europe and the United States. Currently, N-acetylcysteine is still the only drug approved for the treatment of APAP-induced hepatotoxicity. Nevertheless, its restricted therapeutic window constrains its clinical utility. There is an urgent need to find new drugs for the prevention and treatment of APAP-induced liver failure. Mitochondria are the main toxic targets of APAP, playing important roles in the injury, progression, and recovery stages of its hepatotoxicity. Excessive poisonous metabolites of APAP, such as N-acetyl-benzoquinone imine (NAPQI), can bind to mitochondrial proteins, inducing mitochondrial oxidative stress and changes in membrane permeability, leading to the release of pro-apoptotic factors into the nucleus and causing hepatocyte death. Mitochondrial fusion and fission, autophagy, and biogenesis collectively constitute the mitochondrial quality control system, which plays an important role in maintaining mitochondrial homeostasis and resisting APAP hepatotoxicity. Traditional Chinese medicine (TCM) is a treasure of the Chinese nation, with many herbal medicines used clinically for liver protection. Previous reviews summarized that TCM exerted its protective effects by reducing oxidative stress, combating inflammation and anti-apoptotic pathways. However, few reviews highlighted the regulating effects of TCM on mitochondrial function. This review focuses on elucidating the effects of TCM on regulating mitochondrial oxidative stress and mitochondrial quality control system and preventing APAP-induced liver failure, providing a theoretical basis for developing preventive and therapeutic drugs for APAP-induced liver failure from TCM in the future.

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Cite this article:
Xia S, Cao R, Hu Z, et al. Research progress on regulation of mitochondrial function by traditional Chinese medicine in alleviating acetaminophen-induced liver injury. Precision Medication, 2024, 1(1). https://doi.org/10.1016/j.prmedi.2024.10.008

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Received: 19 August 2024
Accepted: 07 September 2024
Published: 04 December 2024
© 2024 Chinese General Practice Publishing House Co., Ltd.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).