Apigenin alleviated PA-induced pyroptosis by activating autophagy in hepatocytes

上睑下垂 炎症体 芹菜素 自噬 化学 NALP3 细胞生物学 程序性细胞死亡 药理学 生物化学 受体 生物 类黄酮 细胞凋亡 抗氧化剂
作者
Zhuoqun Meng,Beiwei Zhu,Min Gao,Guang Wang,Hongjiang Zhou,Jing Lu,Shuang Guan
出处
期刊:Food & Function [Royal Society of Chemistry]
卷期号:13 (10): 5559-5570 被引量:21
标识
DOI:10.1039/d1fo03771d
摘要

Apigenin is a kind of natural flavonoid that abundantly exists in fruits and vegetables. Pyroptosis is a new, pro-inflammatory type of programmed necrosis cell death, and the NOD-like receptor family pyrin domain containing 3 (NLRP3) inflammasome is the key molecule to induce pyroptosis. Excessive hepatic pyroptosis results in liver injury. In the study, we found for the first time that apigenin could alleviate palmitic acid (PA)-induced NLRP3 inflammasome activation and pyroptosis in HepG2 cells and primary mouse hepatic cells. Meanwhile, apigenin could promote the autophagy of hepatocytes. When the autophagy inhibitor chloroquine (CQ) was added, the data showed that the recovery effect of apigenin on PA-induced pyroptosis was weakened, indicating that apigenin could alleviate PA-induced pyroptosis by activating autophagy. Further mechanistic studies showed that apigenin regulated the NLRP3 inflammasome through two ways, so as to alleviate PA-induced pyroptosis. On the one hand, apigenin eliminated damaged mitochondria by activating autophagy, thereby clearing reactive oxygen species (ROS) production and inhibiting the activation of the NLRP3 inflammasome, and on the other hand, activation of autophagy could directly degrade the NLRP3 inflammasome. Our study provides a new idea and target for the use of functional factors in food to alleviate liver injury.
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