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首页> 外文期刊>European review for medical and pharmacological sciences. >Changes in expressions of miR-22-3p and MMP-9 in rats with thoracic aortic aneurysm and their significance
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Changes in expressions of miR-22-3p and MMP-9 in rats with thoracic aortic aneurysm and their significance

机译:胸主动脉瘤大鼠MiR-22-3P和MMP-9表达的变化及其意义

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OBJECTIVE: The purpose of this study was to explore the changes in the expressions of micro ribonucleic acid (miR)-22-3p and matrix metalloproteinase-9 (MMP-9) in rats with thoracic aortic aneurysm (TAA) and their significance. MATERIALS AND METHODS: A total of 16 specific pathogen-free Sprague-Dawley female rats were randomly divided into normal group (n=8) and angiotensin II (Ang II) group (n=8). Ang II was perfused using the micro pump in Ang II group, while the same amount of normal saline was perfused in the normal group. After continuous intervention, the tumor formation rate in the thoracic aorta was observed, and the expression of miR-22-3p was detected via Reverse Transcription-Polymerase Chain Reaction (RT-PCR) in both groups. Other 16 rats were selected and randomly divided into agomiR-22-3p group (n=8) and control group (n=8). In the agomiR-22-3p group, agomiR-22 and Ang II were continuously injected via angular vein. In the control group, agomiR negative control was injected, and Ang II was continuously perfused. After intervention for 4 weeks, the tumor formation rate in the thoracic aorta was observed, and the expression of MMP-9 was determined via immunofluorescence and immunohistochemistry in both groups. RESULTS: After intervention for 4 weeks, the expression of miR-22-3p in Ang II group was significantly lower than that in normal group (p0.05). After drug administration for 4 weeks, agomiR-22-3p group had a lower tumor formation rate (p0.05) and a lower expression of MMP-9 than the control group (p0.05). CONCLUSIONS: The expression of miR-22-3p declines in TAA rats, and miR-22-3p can inhibit the expression of MMP-9, thus suppressing the formation of TAA in rats.
机译:目的:本研究的目的是探讨具有胸主动脉瘤(TAA)的大鼠的微核糖核酸(MIR)-22-3P和基质金属蛋白酶-9(MMP-9)的表达的变化及其意义。材料和方法:将总共16种特异性病原体Sprague-Dawley雌性大鼠随机分为正常组(n = 8)和血管紧张素II(Ang II)基团(n = 8)。使用Ang II组中的微泵灌注Ang II,而在正常组中灌注相同量的正常盐水。在连续干预之后,观察到胸主动脉中的肿瘤形成速率,并通过两组中的逆转录聚合酶链反应(RT-PCR)检测miR-22-3p的表达。选择其他16只大鼠并随机分为AgomiR-22-3P组(n = 8)和对照组(n = 8)。在AgomiR-22-3P组中,通过角静脉连续注射Agomir-22和Ang II。在对照组中,注射了Agomir阴性对照,并且昂然常规。干预4周后,观察到胸主动脉中的肿瘤形成速率,并且通过两组的免疫荧光和免疫组织化学测定MMP-9的表达。结果:干预4周后,Ang II组miR-22-3p的表达明显低于正常组(P <0.05)。药物施用4周后,Agomir-22-3P组肿瘤形成率较低(P <0.05),比对照组的MMP-9的较低表达(P <0.05)。结论:TaA大鼠MiR-22-3P的表达,MIR-22-3P可以抑制MMP-9的表达,从而抑制大鼠TAA的形成。

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