Xu Tiantian, Song Qing, Zhou Li, Yang Wenwen, Wu Xiangyao, Qian Qianyu, Chai Hui, Han Qiang, Pan Hongzhi, Dou Xiaobing, Li Songtao
College of Basic Medicine and Public Health, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
College of Life Science, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Nutr Metab (Lond). 2021 Jan 19;18(1):13. doi: 10.1186/s12986-021-00540-9.
Lipotoxicity-induced cell death plays a detrimental role in the pathogenesis of metabolic diseases. Ferulic acid, widespread in plant-based food, is a radical scavenger with multiple bioactivities. However, the benefits of ferulic acid against hepatic lipotoxicity are largely unclear. Here, we investigated the protective effect of ferulic acid against palmitate-induced lipotoxicity and clarified its potential mechanisms in AML-12 hepatocytes.
AML-12 mouse hepatocytes were exposed to palmitate to mimic lipotoxicity. Different doses (25, 50, and 100 μM) of ferulic acid were added 2 h before palmitate treatment. Cell viability was detected by measuring lactate dehydrogenase release, nuclear staining, and the expression of cleaved-caspase-3. Intracellular reactive oxygen species content and mitochondrial membrane potential were analysed by fluorescent probes. The potential mechanisms were explored by molecular biological methods, including Western blotting and quantitative real-time PCR, and were further verified by siRNA interference.
Our data showed that ferulic acid significantly inhibited palmitate-induced cell death, rescued mitochondrial membrane potential, reduced reactive oxygen species accumulation, and decreased inflammatory factor activation, including IL-6 and IL-1beta. Ferulic acid significantly stimulated autophagy in hepatocytes, whereas autophagy suppression blocked the protective effect of ferulic acid against lipotoxicity. Ferulic acid-activated autophagy, which was triggered by SIRT1 upregulation, was mechanistically involved in its anti-lipotoxicity effects. SIRT1 silencing blocked most beneficial changes induced by ferulic acid.
We demonstrated that the phytochemical ferulic acid, which is found in plant-based food, protected against hepatic lipotoxicity, through the SIRT1/autophagy pathway. Increased intake of ferulic acid-enriched food is a potential strategy to prevent and/or improve metabolic diseases with lipotoxicity as a typical pathological feature.
脂毒性诱导的细胞死亡在代谢性疾病的发病机制中起有害作用。阿魏酸广泛存在于植物性食物中,是一种具有多种生物活性的自由基清除剂。然而,阿魏酸对肝脏脂毒性的益处尚不清楚。在此,我们研究了阿魏酸对棕榈酸诱导的脂毒性的保护作用,并阐明了其在AML-12肝细胞中的潜在机制。
将AML-12小鼠肝细胞暴露于棕榈酸以模拟脂毒性。在棕榈酸处理前2小时加入不同剂量(25、50和100μM)的阿魏酸。通过测量乳酸脱氢酶释放、细胞核染色和裂解的半胱天冬酶-3的表达来检测细胞活力。用荧光探针分析细胞内活性氧含量和线粒体膜电位。通过蛋白质免疫印迹和定量实时PCR等分子生物学方法探索潜在机制,并通过小干扰RNA进行进一步验证。
我们的数据表明,阿魏酸显著抑制棕榈酸诱导的细胞死亡,挽救线粒体膜电位,减少活性氧积累,并降低炎症因子激活,包括白细胞介素-6和白细胞介素-1β。阿魏酸显著刺激肝细胞中的自噬,而自噬抑制则阻断了阿魏酸对脂毒性的保护作用。阿魏酸激活的自噬由沉默信息调节因子1上调触发,其机制参与了其抗脂毒性作用。沉默信息调节因子1沉默阻断了阿魏酸诱导的大多数有益变化。
我们证明,植物性食物中含有的植物化学物质阿魏酸通过沉默信息调节因子1/自噬途径预防肝脏脂毒性。增加富含阿魏酸食物的摄入量是预防和/或改善以脂毒性为典型病理特征的代谢性疾病的潜在策略。