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高脂饮食诱导肥胖大鼠心肌中的微小RNA表达谱

microRNA Expression Profiles in Myocardium of High-Fat Diet-Induced Obesity Rat.

作者信息

Yang Huimin, Xin Xin, Yu Hang, Bao Yandong, Jia Pengyu, Wu Nan, Jia Dalin

机构信息

Department of Cardiology, The Central Laboratory, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, People's Republic of China.

出版信息

Diabetes Metab Syndr Obes. 2020 Apr 15;13:1147-1159. doi: 10.2147/DMSO.S248948. eCollection 2020.

DOI:10.2147/DMSO.S248948
PMID:32346302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7167270/
Abstract

PURPOSE

A high-fat diet (HFD) can lead to cardiac dysfunction, hypertrophy, and fibrosis. This study aimed to explore microRNA expression profiles in the myocardium of HFD-induced obesity rat.

MATERIALS AND METHODS

Wistar rats were randomly divided into two groups, and fed with normal chow diet (NCD) or HFD for 20 weeks. Cardiac function was evaluated by echocardiography. Left ventricular myocardium was harvested to assess the extent of myocardial morphology alteration. MicroRNA expression was analyzed using Agilent miRNA microarray and quantitative real-time PCR (qRT-PCR) was used to validate the microarray data. The mirdbV6 database was used to forecast the miRNA target genes. The role of microRNAs in palmitate-induced cardiac hypertrophy and fibrosis in primary neonatal rat cardiomyocytes was evaluated by loss- and gain-of-function experiments.

RESULTS

Significant changes in cardiac function, hypertrophy, fibrosis, and apoptosis were found in HFD rats as compared with NCD rats. miR-141-3p and miR-144-3p were also significantly upregulated in the myocardium of HFD-induced obesity rat. A series of genes involved in essential biological processes, including anatomical structure development and metabolic process, was targeted by these two miRNAs. These target genes were also implicated in signaling pathways involved in the PI3K-Akt signaling pathway, Wnt signaling pathway, autophagy, and protein processing in the endoplasmic reticulum. Inhibition of miR-141 or overexpression of miR-144 attenuated palmitate-induced cardiac hypertrophy and fibrosis. In contrast, overexpression of miR-141 or inhibition of miR-144 aggravated palmitate-induced cardiac hypertrophy and fibrosis.

CONCLUSION

This study identifies that miR-141 and miR-144 are candidate miRNAs associated with the development of HFD-induced cardiac dysfunction and structure alteration.

摘要

目的

高脂饮食(HFD)可导致心脏功能障碍、肥大和纤维化。本研究旨在探讨高脂饮食诱导的肥胖大鼠心肌中微小RNA的表达谱。

材料与方法

将Wistar大鼠随机分为两组,分别给予正常饲料(NCD)或高脂饮食20周。通过超声心动图评估心脏功能。采集左心室心肌以评估心肌形态改变的程度。使用安捷伦miRNA微阵列分析微小RNA表达,并采用定量实时聚合酶链反应(qRT-PCR)验证微阵列数据。使用mirdbV6数据库预测miRNA靶基因。通过功能丧失和功能获得实验评估微小RNA在原代新生大鼠心肌细胞中棕榈酸诱导的心脏肥大和纤维化中的作用。

结果

与NCD大鼠相比,HFD大鼠在心脏功能、肥大、纤维化和凋亡方面有显著变化。在高脂饮食诱导的肥胖大鼠心肌中,miR-141-3p和miR-144-3p也显著上调。这两种微小RNA靶向了一系列参与基本生物学过程的基因,包括解剖结构发育和代谢过程。这些靶基因还涉及PI3K-Akt信号通路、Wnt信号通路、自噬和内质网中的蛋白质加工等信号通路。抑制miR-141或过表达miR-144可减轻棕榈酸诱导的心脏肥大和纤维化。相反,过表达miR-141或抑制miR-144会加重棕榈酸诱导的心脏肥大和纤维化。

结论

本研究确定miR-141和miR-144是与高脂饮食诱导的心脏功能障碍和结构改变相关的候选微小RNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/8464b309cdb4/DMSO-13-1147-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/cf34db47124c/DMSO-13-1147-g0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/8b02744cabd4/DMSO-13-1147-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/5b416d4e50dd/DMSO-13-1147-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/0eb171985ecf/DMSO-13-1147-g0007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/8464b309cdb4/DMSO-13-1147-g0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/cf34db47124c/DMSO-13-1147-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/ca89361d5b25/DMSO-13-1147-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/674108a6cfac/DMSO-13-1147-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/9c55fd84ebb4/DMSO-13-1147-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/8b02744cabd4/DMSO-13-1147-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/5b416d4e50dd/DMSO-13-1147-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/0eb171985ecf/DMSO-13-1147-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/5db8032bbd72/DMSO-13-1147-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e3a/7167270/8464b309cdb4/DMSO-13-1147-g0009.jpg

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