拓步雄, 李超民, 彭利静, 刘 薇, 李 慧. 血管紧张素Ⅱ在正常和高血压条件下上调心肌细胞中基质金属酶蛋白-2和组织金属酶蛋白抑制物-1的表达[J]. 心脏杂志, 2014, 26(5): 508-513.
    引用本文: 拓步雄, 李超民, 彭利静, 刘 薇, 李 慧. 血管紧张素Ⅱ在正常和高血压条件下上调心肌细胞中基质金属酶蛋白-2和组织金属酶蛋白抑制物-1的表达[J]. 心脏杂志, 2014, 26(5): 508-513.
    Angiotensin II upregulates expressions of matrix metaIloproteinase-2 and tissue inhibitors of metalloproteinase-1 in cardiomyocytes[J]. Chinese Heart Journal, 2014, 26(5): 508-513.
    Citation: Angiotensin II upregulates expressions of matrix metaIloproteinase-2 and tissue inhibitors of metalloproteinase-1 in cardiomyocytes[J]. Chinese Heart Journal, 2014, 26(5): 508-513.

    血管紧张素Ⅱ在正常和高血压条件下上调心肌细胞中基质金属酶蛋白-2和组织金属酶蛋白抑制物-1的表达

    Angiotensin II upregulates expressions of matrix metaIloproteinase-2 and tissue inhibitors of metalloproteinase-1 in cardiomyocytes

    • 摘要: 目的:研究在正常和高血压条件下血管紧张素Ⅱ(AngⅡ)对心肌细胞中基质金属酶蛋白-2(MMP-2)和组织金属酶蛋白抑制物-1(TIMP-1)表达的影响,观察其对氧化应激的影响。方法: AngⅡ预处理体外培养的原代心肌细胞,利用试剂盒检测细胞中丙二醛水平、谷胱甘肽过氧化物酶(GPx)和超氧化物歧化酶(SOD)活力的变化;同时利用实时定量PCR (qRT-PCR)和蛋白免疫印迹(Western blot)方法检测细胞中MMP-2和TIMP-1基因信使核糖核苷酸(mRNA)和蛋白的表达变化。建立大鼠高血压模型,检测模型大鼠及缬沙坦治疗大鼠心肌组织中丙二醛、GPx和SOD酶活力的变化,并运用qRT-PCR和Western blot方法分析心肌组织中MMP-2和TIMP-1基因mRNA和蛋白的表达变化。 结果: AngⅡ预处理能显著提高心肌细胞中氧化应激水平,同时AngⅡ预处理上调心肌细胞中MMP-2和TIMP-1基因表达。在高血压大鼠中,心肌组织的氧化应激水平明显高于假手术组,而经AngⅡ受体阻断剂缬沙坦处理后氧化应激水平则下降。并且,缬沙坦治疗也能降低高血压大鼠心肌组织中MMP-2和TIMP-1基因表达。 结论: AngⅡ可同时上调氧化应激并调控MMP-2基因和TIMP-1基因在心肌细胞中的表达,但其具体机制还不完全清楚,仍需进一步探讨。

       

      Abstract: AIM:To investigate the effect of angiotensin II (AngII) on the expressions of matrix metalloproteinase-2 (MMP-2) and tissue inhibitors of metalloproteinase-1 (TIMP-1). METHODS: Cultured cardiomycytes were pretreated with AngII. The level of malonaldehyde (MDA) and enzyme activity of glutathione peroxidase (GPx) and superoxide dismutase (SOD) were detected by commercial kits. The mRNA and protein expressions of MMP-2 and TIMP-1 in cardiomyocytes were analyzed by qRT-PCR and Western blot. The rat hypertension model was established and the levels of MDA in the heart tissue of model rats and valsartan-treated rats were detected along with the enzyme activity of GPx and SOD. Expressions of MMP-2 and TIMP-1 were also analyzed by qRT-PCR and Western blot. RESULTS: Pretreatment with AngII significantly increased the oxidative stress in myocardial cells and also induced the upregulation of the expressions of MMP-2 and TIMP-1. In hypertensive rats, the oxidative stress in myocardial tissue was significantly higher than that in sham group, but the stress decreased after valsartan treatment. Valsartan also reduced the expressions of MMP-2 and TIMP-1 gene in myocardial tissue of hypertensive rats. CONCLUSION: Oxidative stress increase via AngII is involved in the regulation of MMP-2 and TIMP-1 expression. The mechanism deserves further research.

       

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