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固醇调节元件结合蛋白-1c 的下调与燃烧性 NASH 的发展有关。

Down-regulation of SREBP-1c is associated with the development of burned-out NASH.

机构信息

Department of Gastroenterology, Shinshu University School of Medicine, Japan.

出版信息

J Hepatol. 2010 Oct;53(4):724-31. doi: 10.1016/j.jhep.2010.04.033. Epub 2010 Jul 1.

Abstract

BACKGROUND & AIMS: It is well-known that hepatic triglycerides (TG) diminish with the progression of non-alcoholic steatohepatitis (NASH), which has been designated as burned-out NASH, but its mechanism remains unclear. We aimed to explore the changes in hepatic fatty acid (FA) and TG metabolism with disease progression.

METHODS

Hepatic expression of key genes in healthy individuals (n=6) and patients with simple steatosis (SS, n=10), mild NASH (fibrosis stage 1-2, n=20), and advanced NASH (fibrosis stage 3-4, n=20) were assessed by quantitative polymerase chain reaction.

RESULTS

Hepatic expression of genes related to FA uptake and oxidation and very-low-density lipoprotein synthesis/export did not differ among the groups. However, the mRNA levels of sterol regulatory element-binding protein (SREBP)-1c and its downstream genes FA synthase, acetyl-coenzyme A carboxylase 1, and diacylglycerol acyltransferase 1 were inversely correlated with fibrosis stage. Immunoblot analysis revealed a remarkable reduction in mature SREBP-1c levels in advanced NASH. Furthermore, hepatic expression of tumor necrosis factor-alpha increased in accordance with fibrosis progression, which was possibly related to the decrease in hepatic SREBP-1c expression.

CONCLUSIONS

Down-regulation of SREBP-1c and lipogenic enzymes may be associated with the development of burned-out NASH.

摘要

背景与目的

众所周知,非酒精性脂肪性肝炎(NASH)的进展会导致肝甘油三酯(TG)减少,这种情况被称为“枯竭性 NASH”,但其机制尚不清楚。本研究旨在探讨疾病进展过程中肝脂肪酸(FA)和 TG 代谢的变化。

方法

通过定量聚合酶链反应评估健康个体(n=6)和单纯性脂肪变性(SS,n=10)、轻度 NASH(纤维化分期 1-2,n=20)和进展性 NASH(纤维化分期 3-4,n=20)患者肝内关键基因的表达。

结果

各组间 FA 摄取和氧化以及极低密度脂蛋白合成/输出相关基因的肝表达无差异。然而,固醇调节元件结合蛋白-1c(SREBP-1c)及其下游基因脂肪酸合酶、乙酰辅酶 A 羧化酶 1 和二酰基甘油酰基转移酶 1 的 mRNA 水平与纤维化分期呈负相关。免疫印迹分析显示,进展性 NASH 中成熟 SREBP-1c 水平显著降低。此外,肿瘤坏死因子-α的肝表达随着纤维化的进展而增加,这可能与肝 SREBP-1c 表达的减少有关。

结论

SREBP-1c 和生脂酶的下调可能与枯竭性 NASH 的发生有关。

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