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Interleukin‐1 inhibition facilitates recovery from liver injury and promotes regeneration of hepatocytes in alcoholic hepatitis in mice

机译:白细胞介素-1抑制有助于从肝损伤中恢复,促进小鼠酒精肝炎中肝细胞的再生

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Abstract Background & Aims Inflammation and impaired hepatocyte regeneration contribute to liver failure in alcoholic hepatitis ( AH ). Interleukin ( IL )‐1 is a key inflammatory cytokine in the pathobiology of AH . The role of IL ‐1 in liver regeneration in the recovery phase of alcohol‐induced liver injury is unknown. Methods In this study, we tested IL ‐1 receptor antagonist to block IL ‐1 signalling in a mouse model of acute‐on‐chronic liver injury on liver inflammation and hepatocyte regeneration in AH . Results We observed that inhibition of IL ‐1 signalling decreased liver inflammation and neutrophil infiltration, and resulted in enhanced regeneration of hepatocytes and increased rate of recovery from liver injury in AH . Conclusion Our novel findings suggest that IL ‐1 drives sustained liver inflammation and impaired hepatocyte regeneration even after cessation of ethanol exposure.
机译:抽象背景& 目的炎症和肝细胞再生受损有助于酒精肝炎(AH)的肝脏衰竭。 白细胞介素(IL)-1是αh病理学中的关键炎症细胞因子。 IL -1在醇诱导的肝损伤的回收阶段肝再生的作用是未知的。 本研究的方法,我们测试了IL -1受体拮抗剂在肝脏炎症和肝细胞再生的急性慢性肝损伤的小鼠模型中阻断IL -1信号传导。 结果我们观察到抑制IL -1信号传导降低肝脏炎症和中性粒细胞渗透,导致肝细胞再生增强,从肝损伤中增加恢复速率均α。 结论我们的新发现表明,即使在停止乙醇暴露后,IL -1甚至肝细胞炎症也受损,肝细胞再生受损。

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