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间歇性低氧对心脏的影响。

Effects of intermittent hypoxia on the heart.

作者信息

Park Ah-Mee, Nagase Hiroko, Kumar Shilpashree Vinod, Suzuki Yuichiro J

机构信息

Department of Pharmacology, Georgetown University Medical Center, Washington, DC 20057, USA.

出版信息

Antioxid Redox Signal. 2007 Jun;9(6):723-9. doi: 10.1089/ars.2007.1460.

Abstract

Obstructive sleep apnea (OSA) is associated with cardiovascular diseases such as hypertension through mechanisms involving intermittent hypoxia (IH). However, it is not yet clear whether IH directly affects the heart. In a mouse model of OSA, we found that IH causes time-dependent alterations of the susceptibility of the heart to oxidative stress. Acute IH can exert preconditioning-like cardioprotection, in part, through the transcriptional activation of genes such as bcl-x(L) and gata4. We cloned the mouse gata4 promoter and identified an IH-responsive region. The exposure of mice to prolonged IH results in the increased susceptibility of the heart to ischemia-reperfusion injury by increasing the oxidative stress status. This might resemble conditions of OSA patients. In our mouse model, further exposure to prolonged IH allowed reversal of the enhancement of myocardial damage. Understanding the complex effects of IH on the heart should help ultimately to develop therapeutic strategies against OSA-induced complications.

摘要

阻塞性睡眠呼吸暂停(OSA)通过涉及间歇性缺氧(IH)的机制与心血管疾病如高血压相关。然而,IH是否直接影响心脏尚不清楚。在一个OSA小鼠模型中,我们发现IH会导致心脏对氧化应激的易感性随时间发生改变。急性IH可部分通过激活bcl-x(L)和gata4等基因的转录来发挥类似预处理的心脏保护作用。我们克隆了小鼠gata4启动子并鉴定出一个IH反应区域。小鼠长时间暴露于IH会通过增加氧化应激状态而导致心脏对缺血-再灌注损伤的易感性增加。这可能类似于OSA患者的情况。在我们的小鼠模型中,进一步长时间暴露于IH可使心肌损伤的增强得到逆转。了解IH对心脏的复杂影响最终应有助于制定针对OSA所致并发症的治疗策略。

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