Endoplasmic Reticulum Stress and Mitochondrial Stress in Drug-Induced Liver Injury

被引:27
|
作者
Pu, Sisi [1 ]
Pan, Yangyang [1 ]
Zhang, Qian [1 ]
You, Ting [1 ]
Yue, Tao [1 ]
Zhang, Yuxing [1 ]
Wang, Meng [1 ]
机构
[1] Gansu Agr Univ, Coll Vet Med, Lanzhou 730070, Peoples R China
来源
MOLECULES | 2023年 / 28卷 / 07期
基金
中国国家自然科学基金;
关键词
ERS; mitochondrial stress; drug-induced liver injury; UNFOLDED PROTEIN RESPONSE; N-TERMINAL KINASE; ER STRESS; KAPPA-B; VENOUS THROMBOEMBOLISM; SELECTIVE INHIBITORS; CROSSTALK UNDERLIES; ACETAMINOPHEN; HEPATOTOXICITY; ACTIVATION;
D O I
10.3390/molecules28073160
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Drug-induced liver injury (DILI) is a widespread and harmful disease closely linked to mitochondrial and endoplasmic reticulum stress (ERS). Globally, severe drug-induced hepatitis, cirrhosis, and liver cancer are the primary causes of liver-related morbidity and mortality. A hallmark of DILI is ERS and changes in mitochondrial morphology and function, which increase the production of reactive oxygen species (ROS) in a vicious cycle of mutually reinforcing stress responses. Several pathways are maladapted to maintain homeostasis during DILI. Here, we discuss the processes of liver injury caused by several types of drugs that induce hepatocyte stress, focusing primarily on DILI by ERS and mitochondrial stress. Importantly, both ERS and mitochondrial stress are mediated by the overproduction of ROS, destruction of Ca2+ homeostasis, and unfolded protein response (UPR). Additionally, we review new pathways and potential pharmacological targets for DILI to highlight new possibilities for DILI treatment and mitigation.
引用
收藏
页数:22
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