Wang Yi-Ran, Xie Na, Zhang Yan-Jing, Wang Lin, Sun Zhan, Zeng Tao
Institute of Toxicology, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.
Department of Gastroenterology, Jining Third People's Hospital, Jining, Shandong 272100, China.
Toxicol Res (Camb). 2023 May 15;12(3):480-492. doi: 10.1093/toxres/tfad033. eCollection 2023 Jun.
High-fat diet (HFD) and ethanol could synergistically induce liver damage, but the underlying mechanisms remain to be elucidated. M1-polarized macrophages have been demonstrated to be key players in ethanol-induced liver damage. The current study was designed to investigate whether hepatic steatosis could promote ethanol-induced liver injury by promoting liver macrophage M1 polarization. In the in vivo study, 12 weeks of HFD feeding induced a moderate increase in the F4/80 expression and protein levels of p-IKKα/β, p-IκBα, and p-p65, which was suppressed by single binge. In contrast, 8 weeks of HFD and multiple binges (two binges per week during the last 4 weeks) synergistically increased the F4/80 expression, mRNA levels of M1 polarization biomarkers including , , and , and protein levels of p65, p-p65, COX2, and Caspase 1. In the in vitro study, a nontoxic free fatty acids (FFAs) mixture (oleic acid/palmitic acid = 2: 1) induced a moderate increase of protein levels of p-p65 and NLRP3 in murine AML12 hepatocytes, which was inhibited by ethanol co-exposure. Ethanol alone induced proinflammatory polarization of murine J774A.1 macrophages evidenced by the enhanced secretion of TNF-α, increased mRNA levels of , , and , and upregulated protein levels of p65, p-p65, NLRP3, and Caspase 1, which was augmented by FFAs exposure. Collectively, these results suggest that HFD and multiple binges could synergistically induce liver damage by promoting the proinflammatory activation of macrophages in mice livers.
高脂饮食(HFD)和乙醇可协同诱导肝损伤,但其潜在机制仍有待阐明。M1极化的巨噬细胞已被证明是乙醇诱导肝损伤的关键因素。本研究旨在探讨肝脂肪变性是否通过促进肝巨噬细胞M1极化来加重乙醇诱导的肝损伤。在体内研究中,12周的高脂饮食喂养导致F4/80表达以及p-IKKα/β、p-IκBα和p-p65的蛋白水平适度增加,单次暴饮可抑制这种增加。相比之下,8周的高脂饮食和多次暴饮(在最后4周每周两次暴饮)协同增加了F4/80表达、M1极化生物标志物(包括 、 和 )的mRNA水平以及p65、p-p65、COX2和Caspase 1的蛋白水平。在体外研究中,无毒的游离脂肪酸(FFAs)混合物(油酸/棕榈酸 = 2:1)诱导小鼠AML12肝细胞中p-p65和NLRP3的蛋白水平适度增加,乙醇共同暴露可抑制这种增加。单独的乙醇诱导小鼠J774A.1巨噬细胞发生促炎极化,表现为TNF-α分泌增加、 、 和 的mRNA水平升高以及p65、p-p65、NLRP3和Caspase 1的蛋白水平上调,FFAs暴露可增强这种作用。总的来说,这些结果表明,高脂饮食和多次暴饮可通过促进小鼠肝脏中巨噬细胞的促炎激活来协同诱导肝损伤。