Barreiro Christopher J, Williams Jason A, Fitton Torin P, Lange Mary S, Blue Mary E, Kratz Lisa, Barker Peter B, Degaonkar Mahaveer, Gott Vincent L, Troncoso Juan C, Johnston Michael V, Baumgartner William A
Division of Cardiac Surgery, Kennedy-Krieger Research Institute, Baltimore, Maryland, USA.
Ann Thorac Surg. 2006 May;81(5):1593-8. doi: 10.1016/j.athoracsur.2006.01.011.
Studies have confirmed the neuroprotective effect of diazoxide in canines undergoing hypothermic circulatory arrest (HCA). A decreased N-acetyl-asparate:choline (NAA:Cho) ratio is believed to reflect the severity of neurologic injury. We demonstrated that noninvasive measurement of NAA:Cho with magnetic resonance spectroscopy facilitates assessment of neuronal injury after HCA and allows for evaluation of neuroprotective strategies.
Canines underwent 2 hours of HCA at 18 degrees C and were observed for 24 hours. Animals were divided into three groups (n = 15 in each group): normal (unoperated), HCA (HCA only), and HCA+diazoxide (pharmacologic treatment before HCA). The NAA:Cho ratios were obtained 24 hours after HCA by spectroscopy. Brains were immediately harvested for fresh tissue NAA quantification by mass spectrometry. Separate cohorts of HCA (n = 16) and HCA+diazoxide (n = 23) animals were kept alive for 72 hours for daily neurologic assessment.
Cortical NAA:Cho ratios were significantly decreased in HCA versus normal animals (1.01 +/- 0.29 versus 1.31 +/- 0.23; p = 0.004), consistent with severe neurologic injury. Diazoxide pretreatment limited neurologic injury versus HCA alone, reflected in a preserved NAA:Cho ratio (1.21 +/- 0.27 versus 1.01 +/- 0.29; p = 0.05). Data were substantiated with fresh tissue NAA extraction. A significant decrease in cortical NAA was observed in HCA versus normal (7.07 +/- 1.9 versus 8.54 +/- 2.1 micromol/g; p = 0.05), with maintenance of normal NAA levels after diazoxide pretreatment (9.49 +/- 1.1 versus 7.07 +/- 1.9 micromol/g; p = 0.0002). Clinical neurologic scores were significantly improved in the HCA+diazoxide group versus HCA at all time points.
Neurologic injury remains a significant complication of cardiac surgery and is most severe after HCA. Magnetic resonance spectroscopy assessment of NAA:Cho ratios offers an early, noninvasive means of potentially evaluating neurologic injury and the effect of neuroprotective agents.
研究已证实二氮嗪对接受低温循环停搏(HCA)的犬具有神经保护作用。N-乙酰天门冬氨酸与胆碱(NAA:Cho)比值降低被认为反映了神经损伤的严重程度。我们证明,用磁共振波谱对NAA:Cho进行无创测量有助于评估HCA后的神经元损伤,并可用于评估神经保护策略。
犬在18℃下接受2小时的HCA,并观察24小时。动物分为三组(每组n = 15):正常组(未手术)、HCA组(仅接受HCA)和HCA + 二氮嗪组(HCA前进行药物治疗)。HCA后24小时通过波谱获得NAA:Cho比值。立即采集大脑用于通过质谱法定量新鲜组织中的NAA。将单独的HCA组(n = 16)和HCA + 二氮嗪组(n = 23)动物存活72小时以进行每日神经学评估。
与正常动物相比,HCA组的皮质NAA:Cho比值显著降低(1.01±0.29对1.31±0.23;p = 0.004),这与严重的神经损伤一致。与单独的HCA相比,二氮嗪预处理可限制神经损伤,这反映在NAA:Cho比值得以保留(1.21±0.27对1.01±0.29;p = 0.05)。新鲜组织NAA提取证实了该数据。与正常组相比,HCA组的皮质NAA显著降低(7.07±1.9对8.54±2.1微摩尔/克;p = 0.05),而二氮嗪预处理后可维持正常的NAA水平(9.49±1.1对7.07±1.9微摩尔/克;p = 0.0002)。在所有时间点,HCA + 二氮嗪组的临床神经学评分均显著优于HCA组。
神经损伤仍然是心脏手术的一个重要并发症,在HCA后最为严重。磁共振波谱对NAA:Cho比值的评估提供了一种早期、无创的方法,有可能用于评估神经损伤和神经保护剂的效果。