首页> 外文期刊>Journal of Surgical Research: Clinical and Laboratory Investigation >Early increased MT1-MMP expression and late MMP-2 and MMP-9 activity during Angiotensin II induced aneurysm formation.
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Early increased MT1-MMP expression and late MMP-2 and MMP-9 activity during Angiotensin II induced aneurysm formation.

机译:在血管紧张素II诱导动脉瘤形成过程中,早期MT1-MMP表达增加,而后期MMP-2和MMP-9活性升高。

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BACKGROUND: Angiotensin II (Ang II) is associated with a variety of cardiovascular diseases including aneurysm formation. The aim of this study was to evaluate the temporal changes in MT1-matrix metalloproteinase (MMP) and MMP-2 and -9 expression and activity during the course of Ang II induced experimental aneurysm formation. METHODS: Apolipoprotein E knockout mice (ApoE null) were infused with either 1000 ng/kg/min of Ang II (n = 20) or saline (n = 20) and then sacrificed at 7, 14, 21, and 28 days of infusion (n = 5/group/strain). Aortic diameters were measured by digital microscopy. Systolic blood pressure (SBP) was measured in the rodent tail. Suprarenal abdominal aortas had MT1-MMP mRNA levels and MMP-2 and MMP-9 mRNA levels and activity quantitated using reverse transcriptase-polymerase chain reaction (rt-PCR) and gelatin zymography, respectively. Statistical analyses included nonpaired t-test, Fisher's exact test, and analysis of variance (ANOVA). RESULTS: Aneurysms occurred in 40, 40, 20, and 80% of ApoE null-Ang II mice at 7, 14, 21, and 28 days, respectively. An early and significant rise in MT1-MMP mRNA occurred in ApoE null mice infused with Ang II mice, while there was no significant change in MMP-2 or MMP-9 mRNA levels. Total MMP-2 and MMP-9 activity increased over time in ApoE null mice infused with Ang II, peaking at 28 days (ANOVA, P < 0.01). SBP was significantly elevated by 7 days in ApoE null mice infused with Ang II compared to ApoE null mice infused with saline (123 +/- 16 versus 102 +/- 6 mm Hg, P < 0.05). CONCLUSIONS: Angiotensin II induces an early increase in aortic MT1-MMP expression with a subsequent increase in MMP-2 and MMP-9 activity. The process by which these changes cause aneurysm formation warrants further investigation.
机译:背景:血管紧张素II(Ang II)与多种心血管疾病(包括动脉瘤形成)相关。这项研究的目的是评估在Ang II诱导的实验性动脉瘤形成过程中MT1-基质金属蛋白酶(MMP)和MMP-2和-9表达以及活性的时间变化。方法:用1000 ng / kg / min的Ang II(n = 20)或生理盐水(n = 20)注射载脂蛋白E基因敲除小鼠(ApoE null),然后在输注第7、14、21和28天处死(n = 5 /组/株)。通过数字显微镜测量主动脉直径。在啮齿动物尾巴中测量收缩压(SBP)。肾上腹主动脉的MT1-MMP mRNA水平,MMP-2和MMP-9 mRNA水平及活性分别通过逆转录聚合酶链反应(rt-PCR)和明胶酶法定量。统计分析包括非配对t检验,Fisher精确检验和方差分析(ANOVA)。结果:40、40、20和80%的ApoE null-Ang II小鼠分别在第7、14、21和28天出现动脉瘤。在注入Ang II小鼠的ApoE无效小鼠中,MT1-MMP mRNA的早期显着升高,而MMP-2或MMP-9 mRNA水平没有显着变化。在注入Ang II的ApoE无效小鼠中,总MMP-2和MMP-9活性随时间增加,在28天达到峰值(ANOVA,P <0.01)。与注入盐水的ApoE缺失小鼠相比,注入Ang II的ApoE缺失小鼠的SBP显着升高了7天(123 +/- 16对102 +/- 6 mm Hg,P <0.05)。结论:血管紧张素II诱导主动脉MT1-MMP表达的早期增加,随后MMP-2和MMP-9活性增加。这些变化导致动脉瘤形成的过程值得进一步研究。

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