NEFA公司
SIRT3
内分泌学
内科学
兴奋剂
脂肪肝
锡尔图因
化学
脂肪酸
生物
奶牛
平衡
信号转导
脂质过氧化
脂解
非诺贝特
氧化应激
作者
Ding Li,Jiajun Liu,Lei Tian,Renxu Chang,Le Zhang,Hang Yu,Hayley Pitts,Loor Juan,Siqing Mao,Yanqiong Wen,Tao Peng,Fachun Wan,Weijun Shen,Zuo Wang,Chuang Xu,Lei Liu
标识
DOI:10.1021/acs.jafc.5c13831
摘要
Elevated nonesterified fatty acid (NEFA) levels, resulting from excessive fat mobilization, are recognized as the pathological basis for fatty liver in dairy cows. Hepatotoxicity of high NEFA is antagonized by the activity of Sirtuin 3 (SIRT3). However, it is unclear whether SIRT3 antagonizes ferroptosis in bovine hepatocytes. Hence, we aimed to investigate the interplay between NEFA and SIRT3 on ferroptosis. High NEFA caused ferroptosis in cultured bovine hepatocytes, as validated by lipid peroxidation measurement, ultrastructure observation, and key gene expression. SIRT3 overexpression alleviated high NEFA-induced ferroptosis. RNA-seq revealed that NEFA-induced ferroptosis was inhibited by SIRT3 through the JNK signaling pathway, and this was further confirmed by the JNK signaling agonist assay. Dairy cows with fatty liver showed reduced hepatic SIRT3 protein levels alongside heightened JNK signaling activity. These results highlight the potential for targeting the SIRT3-JNK axis to prevent or alleviate NEFA-induced hepatotoxicity during the periparturient period.
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