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Role of MicroRNAs in Renin-Angiotensin-Aldosterone System-Mediated Cardiovascular Inflammation and Remodeling

机译:MicroRNA在肾素 - 血管紧张素 - 醛固酮系统介导的心血管炎症和重塑中的作用

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摘要

MicroRNAs are endogenous regulators of gene expression either by inhibiting translation or protein degradation. Recent studies indicate that microRNAs play a role in cardiovascular disease and renin-angiotensin-aldosterone system- (RAAS-) mediated cardiovascular inflammation, either as mediators or being targeted by RAAS pharmacological inhibitors. The exact role(s) of microRNAs in RAAS-mediated cardiovascular inflammation and remodeling is/are still in early stage of investigation. However, few microRNAs have been shown to play a role in RAAS signaling, particularly miR-155, miR-146a/b, miR-132/122, and miR-483-3p. Identification of specific microRNAs and their targets and elucidating microRNA-regulated mechanisms associated RAS-mediated cardiovascular inflammation and remodeling might lead to the development of novel pharmacological strategies to target RAAS-mediated vascular pathologies. This paper reviews microRNAs role in inflammatory factors mediating cardiovascular inflammation and RAAS genes and the effect of RAAS pharmacological inhibition on microRNAs and the resolution of RAAS-mediated cardiovascular inflammation and remodeling. Also, this paper discusses the advances on microRNAs-based therapeutic approaches that may be important in targeting RAAS signaling.
机译:微小RNA是基因表达内源性调节剂或者通过抑制翻译或蛋白质的降解。最近的研究表明,微RNA发挥心血管疾病和肾素 - 血管紧张素 - 醛固酮系统 - (RAAS-)介导的心血管炎症中的作用,无论是作为调停人或RAAS抑制剂药物作为目标。微RNA在RAAS介导的炎症心血管疾病和重塑的确切作用(S)/仍处于调查的初步阶段。然而,很少微小RNA已被显示出在RAAS信令,特别的miR-155,的miR-146a的/ B的作用,的miR-132/122和miR-483-3p。具体microRNA和他们的目标和相关阐明微小RNA调控机制的鉴定RAS介导的炎症心血管疾病和重塑可能导致的新药理战略为发展目标RAAS介导的血管病变。在介导炎症心血管和RAAS基因和药理学RAAS抑制对微RNA的作用和RAAS介导的炎症心血管疾病和重塑的分辨率炎性因子本文回顾了微RNA的作用。此外,本文讨论基于微小RNA-了可用于靶向RAAS信令重要的治疗方法的进步。

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