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限时进食可改善蛋氨酸胆碱缺乏饮食诱导的小鼠脂肪性肝炎。

Time-restricted feeding ameliorates MCDD-induced steatohepatitis in mice.

作者信息

Jung Ik-Rak, Ahima Rexford S, Kim Sangwon F

机构信息

Department of Medicine, Division of Endocrinology, Diabetes and Metabolism, Johns Hopkins University, Baltimore, Maryland, USA.

出版信息

bioRxiv. 2023 Nov 17:2023.11.15.567214. doi: 10.1101/2023.11.15.567214.

Abstract

Non-Alcoholic Steatohepatitis (NASH) is an inflammatory form of Non-Alcoholic Fatty Liver Disease (NAFLD), closely associated with disease progression, cirrhosis, liver failure, and hepatocellular carcinoma. Time-restricted feeding (TRF) has been shown to decrease body weight and adiposity and improve metabolic outcomes, however, the effect of TRF on NASH has not yet been fully understood. We had previously reported that inositol polyphosphate multikinase (IPMK) mediates hepatic insulin signaling. Importantly, we have found that TRF increases hepatic IPMK levels. Therefore, we investigated whether there is a causal link between TRF and IPMK in a mouse model of NASH, i.e., methionine and choline deficient diet (MCDD)-induced steatohepatitis. Here, we show that TRF alleviated markers of NASH, i.e., reduced hepatic steatosis, liver triglycerides (TG), serum alanine transaminase (ALT) and aspartate aminotransferase (AST), inflammation and fibrosis in MCDD mice. Interestingly, MCDD led to a significant reduction in IPMK levels, and the deletion of hepatic IPMK exacerbates the NASH phenotype induced by MCDD, accompanied by increased gene expression of pro-inflammatory chemokines. Conversely, TRF restored IPMK levels and significantly reduced gene expression of proinflammatory cytokines and chemokines. Our results demonstrate that TRF attenuates MCDD-induced NASH via IPMK-mediated changes in hepatic steatosis and inflammation.

摘要

非酒精性脂肪性肝炎(NASH)是一种非酒精性脂肪性肝病(NAFLD)的炎症形式,与疾病进展、肝硬化、肝衰竭和肝细胞癌密切相关。限时进食(TRF)已被证明可减轻体重和肥胖并改善代谢结果,然而,TRF对NASH的影响尚未完全了解。我们之前曾报道过肌醇多磷酸多激酶(IPMK)介导肝脏胰岛素信号传导。重要的是,我们发现TRF可提高肝脏IPMK水平。因此,我们在NASH小鼠模型即蛋氨酸和胆碱缺乏饮食(MCDD)诱导的脂肪性肝炎中研究了TRF与IPMK之间是否存在因果关系。在此,我们表明TRF减轻了NASH的标志物,即减少了MCDD小鼠的肝脏脂肪变性、肝脏甘油三酯(TG)、血清丙氨酸转氨酶(ALT)和天冬氨酸转氨酶(AST)、炎症和纤维化。有趣的是,MCDD导致IPMK水平显著降低,而肝脏IPMK的缺失加剧了MCDD诱导的NASH表型,同时促炎趋化因子的基因表达增加。相反,TRF恢复了IPMK水平并显著降低了促炎细胞因子和趋化因子的基因表达。我们的结果表明,TRF通过IPMK介导的肝脏脂肪变性和炎症变化减轻了MCDD诱导的NASH。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8fc/10680721/7748122f2d84/nihpp-2023.11.15.567214v1-f0001.jpg

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