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泽泻提取物通过 FXR 介导的基因抑制改善 MAFLD 小鼠肝脏铁失调。

Alisma Orientalis Extract Ameliorates Hepatic Iron Deregulation in MAFLD Mice via FXR-Mediated Gene Repression.

机构信息

MOE Joint International Research Laboratory of Animal Health & Food Safety, Nanjing Agricultural University, Nanjing 210095, China.

Key Laboratory of Animal Physiology & Biochemistry, College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, China.

出版信息

Nutrients. 2024 Jul 15;16(14):2272. doi: 10.3390/nu16142272.

Abstract

Iron is a vital trace element for our bodies and its imbalance can lead to various diseases. The progression of metabolic-associated fatty liver disease (MAFLD) is often accompanied by disturbances in iron metabolism. Alisma orientale extract (AOE) has been reported to alleviate MAFLD. However, research on its specific lipid metabolism targets and its potential impact on iron metabolism during the progression of MAFLD remains limited. To establish a model of MAFLD, mice were fed either a standard diet (CON) or a high-fat diet (HFD) for 9 weeks. The mice nourished on the HFD were then randomly assigned to the HF group and the HFA group, with the HFA group receiving AOE by gavage on a daily basis for 13 weeks. Supplementation with AOE remarkably reduced overabundant lipid accumulation in the liver and restored the iron content of the liver. AOE partially but significantly reversed dysregulated lipid metabolizing genes (SCD1, PPAR γ, and CD36) and iron metabolism genes (TFR1, FPN, and HAMP) induced by HFD. Chromatin immunoprecipitation assays indicated that the reduced enrichment of FXR on the promoters of SCD1 and FPN genes induced by HFD was significantly reversed by AOE. These findings suggest that AOE may alleviate HFD-induced disturbances in liver lipid and iron metabolism through FXR-mediated gene repression.

摘要

铁是我们身体必需的微量元素,其失衡可导致各种疾病。代谢相关脂肪性肝病(MAFLD)的进展常伴有铁代谢紊乱。泽泻提取物(AOE)已被报道可缓解 MAFLD。然而,其对 MAFLD 进展中铁代谢的具体脂质代谢靶点及其潜在影响的研究仍很有限。为建立 MAFLD 模型,将小鼠分别用标准饮食(CON)或高脂肪饮食(HFD)喂养 9 周。然后,用 HFD 喂养的小鼠被随机分为 HF 组和 HFA 组,HFA 组每天通过灌胃接受 AOE 治疗 13 周。AOE 补充可显著减少肝脏中过多的脂质堆积,并恢复肝脏的铁含量。AOE 部分但显著逆转了 HFD 诱导的脂质代谢基因(SCD1、PPARγ和 CD36)和铁代谢基因(TFR1、FPN 和 HAMP)的失调。染色质免疫沉淀分析表明,AOE 显著逆转了 HFD 诱导的 SCD1 和 FPN 基因启动子上 FXR 富集的减少。这些发现表明,AOE 可能通过 FXR 介导的基因抑制缓解 HFD 诱导的肝脏脂质和铁代谢紊乱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/840e/11279993/fced0b044004/nutrients-16-02272-g001.jpg

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