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Atorvastatin Upregulates the Expression of miR-126 in Apolipoprotein E-knockout Mice with Carotid Atherosclerotic Plaque

机译:阿托伐他汀将MiR-126在载脂蛋白E-kextout小鼠中提出miR-126的表达,颈动脉粥样硬化斑块

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摘要

Carotid atherosclerosis (AS) is a chronic inflammatory disease of the carotid arterial wall, which is very important in terms of the occurrence of cerebral vascular accidents. Studies have demonstrated that microRNAs (miRNAs) and their target genes are involved in the formation of atherosclerosis and that atorvastatin might reduce atherosclerotic plaques by regulating the expression of miRNAs. However, the related mechanism is not yet known. In this study, we first investigated the effects of atorvastatin on miR-126 and its target gene, i.e., vascular cell adhesion molecule-1 (VCAM-1) in apolipoprotein E-knockout (ApoE-/-) mice with carotid atherosclerotic plaque in vivo. We compared the expressions of miR-126 and VCAM-1 between the control, atherosclerotic model and atorvastatin treatment groups of ApoE-/- mice using RT-PCR and Western blot. We found the miR-126 expression was significantly down-regulated, and the VCAM-1 expression was significantly up-regulated in the atherosclerotic model group, which accelerated the progression of atherosclerosis in the ApoE-/- mice. These results following atorvastatin treatment indicated that miR-126 expression was significantly up-regulated, VCAM-1 expression was significantly down-regulated and atherosclerotic lesions were reduced. The present results might explain the mechanism by which miR-126 is involved in the formation of atherosclerosis in vivo. Our study first indicated that atorvastatin might exert its anti-inflammatory effects in atherosclerosis by regulating the expressions of miR-126 and VCAM-1 in vivo.
机译:颈动脉粥样硬化(AS)是颈动脉壁的慢性炎症疾病,在脑血管事故的发生方面非常重要。研究表明,微小RNA(miRNA)及其靶基因涉及动脉粥样硬化的形成,并且阿托伐他汀可以通过调节miRNA的表达来减少动脉粥样硬化斑块。但是,相关机制尚不清楚。在这项研究中,我们首先研究了用颈动脉动脉粥样硬化斑块的载脂蛋白e-kextout(apoe - / - )小鼠中阿托伐他汀对miR-126及其靶基因,即血管细胞粘附分子-1(Vcam-1)的影响体内。我们使用RT-PCR和Western印迹将MiR-126和VCAM-1与Apoe / - 小鼠的ApoE - / - 小鼠的阿托伐他汀治疗组之间的表达进行了比较。使用RT-PCR和Western印迹。我们发现miR-126表达显着下调,并且在动脉粥样硬化模型组中,VCAM-1表达显着上调,其加速了ApoE - / - 小鼠中动脉粥样硬化的进展。在阿托伐他汀治疗后的这些结果表明,MIR-126表达显着上调,VCAM-1表达显着下调,并且血栓性病变降低。目前的结果可能解释MIR-126参与体内动脉粥样硬化的机制。我们的研究首先表明,阿托伐他汀可以通过调节体内miR-126和Vcam-1的表达来发挥其在动脉粥样硬化中的抗炎作用。

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  • 作者单位

    Qingdao Univ Dept Neurol Affiliated Hosp 16 Jiangsu Rd Qingdao 266003 Shandong Peoples R China;

    Qingdao Univ Dept Neurol Affiliated Hiser Hosp Qingdao 266033 Peoples R China;

    Qingdao Univ Dept Neurol Affiliated Hosp 16 Jiangsu Rd Qingdao 266003 Shandong Peoples R China;

    Qingdao Univ Dept Neurol Affiliated Hosp 16 Jiangsu Rd Qingdao 266003 Shandong Peoples R China;

    Qingdao Univ Lab Human Micromorphol Coll Med Qingdao 266100 Peoples R China;

    Qingdao Univ Dept Crit Care Med Affiliated Hiser Hosp Qingdao 266033 Peoples R China;

    Qingdao Univ Dept Neurol Affiliated Hosp 16 Jiangsu Rd Qingdao 266003 Shandong Peoples R China;

    Qingdao Univ Dept Neurol Affiliated Hosp 16 Jiangsu Rd Qingdao 266003 Shandong Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子生物学;
  • 关键词

    Carotid atherosclerosis; miR-126; VCAM-1; Atorvastatin; Apolipoprotein E-knockout mice;

    机译:颈动脉粥样硬化;mir-126;vcam-1;阿托伐他汀;脂素蛋白e-敲除小鼠;

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