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膳食氧化固醇 7-酮胆固醇加速肥胖小鼠肝脏脂质蓄积和巨噬细胞浸润。

Dietary Oxysterol, 7-Ketocholesterol Accelerates Hepatic Lipid Accumulation and Macrophage Infiltration in Obese Mice.

机构信息

Department of Cardiovascular Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.

Genome Information Research Center, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.

出版信息

Front Endocrinol (Lausanne). 2021 Mar 10;11:614692. doi: 10.3389/fendo.2020.614692. eCollection 2020.

Abstract

Non-alcoholic fatty liver disease is strongly associated with obese and type 2 diabetes. It has been reported that an oxidized cholesterol, 7-ketocholesterol (7KC), might cause inflammatory response in macrophages and plasma 7KC concentration were higher in patients with cardiovascular diseases or diabetes. Therefore, we have decided to test whether small amount of 7KC in diet might induce hepatic steatosis and inflammation in two types of obese models. We found that addition of 0.01% 7KC either in chow diet (CD, regular chow diet with 1% cholesterol) or western type diet (WD, high fat diet with 1% cholesterol) accelerated hepatic neutral lipid accumulation by Oil Red O staining. Importantly, by lipid extraction analysis, it has been recognized that triglyceride rather than cholesterol species was significantly accumulated in CD+7KC compared to CD as well as in WD+7KC compared to WD. Immunostaining revealed that macrophages infiltration was increased in CD+7KC compared to CD, and also in WD+7KC compared to WD. These phenotypes were accompanied by inducing inflammatory response and downregulating fatty acid oxidation. Furthermore, RNA sequence analysis demonstrated that 7KC reduced expression of genes which related to autophagy process. Levels of LC3-II protein were decreased in WD+7KC compared to WD. Similarly, we have confirmed the effect of 7KC on acceleration of steatohepatitis in db/db mice model. Collectively, our study has demonstrated that small amount of dietary 7KC contributed to accelerate hepatic steatosis and inflammation in obese mice models.

摘要

非酒精性脂肪性肝病与肥胖和 2 型糖尿病密切相关。据报道,一种氧化胆固醇 7-酮胆固醇(7KC)可能在巨噬细胞中引起炎症反应,并且心血管疾病或糖尿病患者的血浆 7KC 浓度较高。因此,我们决定测试饮食中少量的 7KC 是否会在两种肥胖模型中引起肝脂肪变性和炎症。我们发现,在 chow 饮食(CD,含 1%胆固醇的常规 chow 饮食)或西式饮食(WD,含 1%胆固醇的高脂肪饮食)中添加 0.01%的 7KC 均可通过油红 O 染色加速肝中性脂质的积累。重要的是,通过脂质提取分析,已经认识到与 CD 相比,CD+7KC 中甘油三酯而不是胆固醇种类明显积累,与 WD 相比,WD+7KC 中也是如此。免疫染色显示,与 CD 相比,CD+7KC 中巨噬细胞浸润增加,与 WD 相比,WD+7KC 中也是如此。这些表型伴随着诱导炎症反应和下调脂肪酸氧化。此外,RNA 序列分析表明,7KC 降低了与自噬过程相关的基因的表达。与 WD 相比,WD+7KC 中的 LC3-II 蛋白水平降低。同样,我们已经证实了 7KC 对 db/db 小鼠模型加速脂肪性肝炎的作用。总之,我们的研究表明,饮食中少量的 7KC 有助于加速肥胖小鼠模型中的肝脂肪变性和炎症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ae3/7989701/9c8282b99df8/fendo-11-614692-g001.jpg

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