方 舟, 李 泱, 卢才义. 睡眠剥夺对大鼠心肌损伤效应的研究[J]. 心脏杂志, 2011, 23(5): 598-600.
    引用本文: 方 舟, 李 泱, 卢才义. 睡眠剥夺对大鼠心肌损伤效应的研究[J]. 心脏杂志, 2011, 23(5): 598-600.
    Effects of sleep deprivation on rat myocardial damage[J]. Chinese Heart Journal, 2011, 23(5): 598-600.
    Citation: Effects of sleep deprivation on rat myocardial damage[J]. Chinese Heart Journal, 2011, 23(5): 598-600.

    睡眠剥夺对大鼠心肌损伤效应的研究

    Effects of sleep deprivation on rat myocardial damage

    • 摘要: 目的:评估睡眠剥夺(SD)后大鼠心肌组织损伤程度并探讨其机制。方法: 将60只实验大鼠随机分为6组,每组10只。采用改良的多平台SD法(MMPM)建立SD模型,观察SD对心肌组织中缺血修饰白蛋白(IMA)、高敏C反应蛋白(hs-CRP)、还原型谷胱甘肽(GSH)、丙二醛(MDA)、超氧化物酶(SOD)含量的影响。结果: 与笼养组(CC组)和大平台组(TC组)相比,SD后大鼠心肌组织中IMA、hs-CRP、GSH及MDA的含量明显升高(P<0.05),且随着SD时间的延长有明显上升的趋势;而SOD的活性随着SD时间的延长有降低的趋势。结论: SD可引起大鼠心肌发生明显的氧化应激和炎症反应,且随着氧化应激和炎症反应的加重,心肌发生进行性缺血缺氧损害。

       

      Abstract: AIM:To evaluate the severity of myocardial damage after sleep deprivation and to explore its mechanism. METHODS: Sixty rats were randomized into six groups (ten in each group) and sleep deprivation rat models were established by “multi-platform method” (MMPM). Effects of sleep deprivation on the contents of ischemia modified albumin (IMA), high-sensitivity C-reactive protein (hs-CRP), glutathione (GSH), superoxide dismutase (SOD) and malondialdehyde (MDA) in rat myocardium were evaluated. RESULTS: Compared with those in the normal cage control (CC) and tank control (TC) group, the contents of IMA, hs-CRP, GSH and MDA increased (P<0.05). With the elongation of sleep deprivation time, the contents of these markers increased, but the activity of SOD showed a decreasing tendency. CONCLUSION: Sleep deprivation contributes to rat myocardial oxidative stress and inflammation. With the aggravating oxidative stress and inflammation, the damaging effects of ischemia and hypoxia on myocardium become more serious.

       

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