Kellermann Kristine, Gordan M Lucia, Nollert Georg, Blobner Manfred, Kochs Eberhard F, Jungwirth Bettina
Klinik für Anesthesiologie, Technische Universität München, Klinikum rechts der Isar, Ismaningerstrasse 22, 81675 München, Germany.
Perfusion. 2009 Nov;24(6):429-36. doi: 10.1177/0267659109358655.
Inflammatory response is discussed as a contributor to neurologic deficits following cardiac surgery using deep hypothermic circulatory arrest (DHCA). Nuclear Factor Kappa B (NFkappaB) presents a central transcription factor whose expression pattern and subsequent role very much depend on the type and manner of cerebral injury. This study was designed to assess the time course of cerebral NFkappaB expression in relation to neurologic performance over 28 days following 45min of DHCA in rats.
With Institutional Review Board approval, 30 rats were subjected to cardiopulmonary bypass (CPB) with 45min of DHCA (rectal temperature 15-18 degrees Celsius) and randomly assigned to 1, 3, 7, 14 and 28 days of postoperative survival. Untreated animals served as control (n=6). Cerebral NFkappaB expression was analyzed immunohistochemically, cyclooxygenase-2 (COX-2) and inhibitor of kappa B-alpha (IkappaBalpha) using Western Blot and the number of eosinophilic neurons with hematoxylin and eosin (HE) staining. Neurologic outcome was assessed pre- and postoperatively.
Neuronal expression of NFkappaB in the hippocampus peaked at day one, remaining elevated in the motor cortex until day 28. Rats showed neurologic deficits on postoperative day one. Cerebral COX-2 was increased during the first postoperative week and IkappaBalpha peaked on day 14. Histologic damage in the motor cortex and hippocampus persisted until day 28. No systemic inflammation was detectable postoperatively.
Postoperative day one presents with the highest NFkappaB-expression in the ischemia-sensitive hippocampus, accompanied by neurologic dysfunction and histologic damage following 45min of DHCA in rats.
炎症反应被认为是心脏手术中使用深低温循环停搏(DHCA)后导致神经功能缺损的一个因素。核因子κB(NFκB)是一种核心转录因子,其表达模式及后续作用在很大程度上取决于脑损伤的类型和方式。本研究旨在评估大鼠在45分钟DHCA后28天内脑NFκB表达的时间进程及其与神经功能表现的关系。
经机构审查委员会批准,30只大鼠接受了45分钟DHCA(直肠温度15 - 18摄氏度)的体外循环(CPB),并随机分配至术后存活1天、3天、7天、14天和28天组。未处理的动物作为对照(n = 6)。采用免疫组织化学方法分析脑NFκB表达,用蛋白质免疫印迹法分析环氧化酶-2(COX-2)和κBα抑制蛋白(IkBα),并用苏木精-伊红(HE)染色法检测嗜酸性神经元数量。术前和术后评估神经功能结局。
海马体中NFκB的神经元表达在第1天达到峰值,在运动皮层中一直升高至第28天。大鼠在术后第1天出现神经功能缺损。术后第一周脑COX-2增加,IkBα在第14天达到峰值。运动皮层和海马体的组织学损伤持续至第28天。术后未检测到全身炎症反应。
术后第1天,缺血敏感的海马体中NFκB表达最高,大鼠在45分钟DHCA后伴有神经功能障碍和组织学损伤。