首页> 外文期刊>Hepatology: Official Journal of the American Association for the Study of Liver Diseases >Short- or long-term high-fat diet feeding plus acute ethanol binge synergistically induce acute liver injury in mice: An important role for CXCL1
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Short- or long-term high-fat diet feeding plus acute ethanol binge synergistically induce acute liver injury in mice: An important role for CXCL1

机译:短期或长期的高脂饮食喂养加上急性乙醇暴饮可协同诱导小鼠急性肝损伤:CXCL1的重要作用

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摘要

Obesity and alcohol consumption often coexist and work synergistically to promote steatohepatitis; however, the underlying mechanisms remain obscure. Here, we demonstrate that feeding mice a high-fat diet (HFD) for as little as 3 days markedly exacerbated acute ethanol binge-induced liver neutrophil infiltration and injury. Feeding mice with an HFD for 3 months plus a single binge of ethanol induced much more severe steatohepatitis. Moreover, 3-day or 3-month HFD-plus-ethanol binge (3d-HFD+ethanol or 3m-HFD+ethanol) treatment markedly up-regulated the hepatic expression of several chemokines, including chemokine (C-X-C motif) ligand 1 (Cxcl1), which showed the highest fold (approximately 20-fold and 35-fold, respectively) induction. Serum CXCL1 protein levels were also markedly elevated after the HFD+ethanol treatment. Blockade of CXCL1 with a CXCL1 neutralizing antibody or genetic deletion of the Cxcl1 gene reduced the HFD+ethanol-induced hepatic neutrophil infiltration and injury, whereas overexpression of Cxcl1 exacerbated steatohepatitis in HFD-fed mice. Furthermore, expression of Cxcl1 messenger RNA was up-regulated in hepatocytes, hepatic stellate cells, and endothelial cells isolated from HFD+ethanol-fed mice compared to mice that were only given the HFD, with the highest fold induction observed in hepatocytes. In vitro stimulation of hepatocytes with palmitic acid up-regulated the expression of Cxcl1 messenger RNA, and this up-regulation was attenuated after treatment with an inhibitor of extracellular signal-regulated kinase 1/2, c-Jun N-terminal kinase, or nuclear factor B. In addition, hepatic or serum levels of free fatty acids were higher in HFD+ethanol-fed mice than in the control groups. Conclusion: An HFD combined with acute ethanol consumption synergistically induces acute liver inflammation and injury through the elevation of hepatic or serum free fatty acids and subsequent up-regulation of hepatic CXCL1 expression and promotion of hepatic neutrophil infiltration. (Hepatology 2015;62:1070-1085)
机译:肥胖和饮酒经常并存,并共同促进脂肪性肝炎。但是,基本机制仍然不清楚。在这里,我们证明以高脂饮食(HFD)喂养小鼠长达3天明显加剧了急性乙醇暴饮引起的肝中性粒细胞浸润和损伤。用HFD给小鼠喂食3个月,再加一小杯乙醇会诱发严重得多的脂肪性肝炎。此外,为期3天或3个月的HFD加乙醇暴饮(3d-HFD +乙醇或3m-HFD +乙醇)治疗显着上调了几种趋化因子的肝表达,包括趋化因子(CXC基序)配体1(Cxcl1 ),显示出最高的折叠率(分别约为20倍和35倍)。 HFD +乙醇处理后,血清CXCL1蛋白水平也明显升高。用CXCL1中和抗体阻断CXCL1或Cxcl1基因的基因缺失减少了HFD +乙醇诱导的肝中性粒细胞浸润和损伤,而Cxcl1的过表达加剧了由HFD喂养的小鼠的脂肪性肝炎。此外,与仅给予HFD的小鼠相比,从HFD +乙醇喂养的小鼠分离的肝细胞,肝星状细胞和内皮细胞中Cxcl1信使RNA的表达被上调,在肝细胞中观察到最高的诱导倍数。棕榈酸对肝细胞的体外刺激上调了Cxcl1信使RNA的表达,在用细胞外信号调节激酶1/2,c-Jun N端激酶或核仁抑制剂处理后,这种上调被减弱了。此外,HFD +乙醇喂养的小鼠的肝脏或血清中游离脂肪酸水平高于对照组。结论:HFD联合急性乙醇消耗可通过升高肝脏或血清游离脂肪酸并随后上调肝CXCL1表达并促进肝中性粒细胞浸润而协同诱导急性肝炎症和损伤。 (肝病2015; 62:1070-1085)

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