Transcriptomic profile analysis of the left atrium in spontaneously hypertensive rats in the early stage

内科学 心房颤动 纤维化 内分泌学 中庭(建筑) 医学 肌肉肥大 转录组 左心房 血管紧张素受体 血管紧张素II 心脏病学 受体 基因表达 生物 基因 生物化学
作者
Qinghua Fang,Jing Wang,Jiangjun Wei,Xianglin Long,Yao Wang,Jiacheng He,Xin Yuan,Jianlin Du
出处
期刊:Frontiers in Pharmacology [Frontiers Media]
卷期号:13 被引量:5
标识
DOI:10.3389/fphar.2022.989636
摘要

Left atrial remodeling, characterized by enlargement and hypertrophy of the left atrium and increased fibrosis, was accompanied by an increased incidence of atrial fibrillation. While before morphological changes at the early stage of hypertension, how overloaded hypertension influences the transcriptomic profile of the left atrium remains unclear. Therefore, RNA-sequencing was performed to define the RNA expressing profiles of left atrium in spontaneously hypertensive rats (SHRs) and normotensive Wistar-Kyoto (WKY) rats as a control group. We also compared the changes in the RNA expression profiles in SHRs treated with an angiotensin receptor blocker (ARB) and angiotensin receptor-neprilysin inhibitor (ARNI) to assess the distinct effects on the left atrium. In total, 1,558 differentially expressed genes were found in the left atrium between WKY rats and SHRs. Bioinformatics analysis showed that these mRNAs could regulate upstream pathways in atrial remodeling through atrial fibrosis, inflammation, electrical remodeling, and cardiac metabolism. The regulated transcripts detected in the left atrial tissue in both the ARB-treated and ARNI-treated groups were related to metabolism. In contrast to the ARB-treated rates, the transcripts in ARNI-treated rats were mapped to the cyclic guanosine monophosphate-protein kinase G signaling pathway.
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