Ding Xu-Dong, Zheng Ning-Ning, Cao Yan-Yan, Zhao Guang-Yi, Zhao Ping
a Department of Anesthesiology, Shengjing Hospital , China Medical University , Shenyang , China.
b Department of Pathophysiology, College of Basic Medical Science , China Medical University , Shenyang , China.
Int J Neurosci. 2016;126(3):249-56. doi: 10.3109/00207454.2015.1005291. Epub 2015 Jul 14.
BACKGROUND/AIMS: To investigate the protection effect of dexmedetomidine preconditioning on global cerebral ischemic injury following asphyxial cardiac arrest (CA) in rats.
Seventy-two rats were randomly assigned into three groups, sham group (no asphyxia), control group (asphyxia only), and dexmedetomidine preconditioned group (asphyxia + dexmedetomidine). Dexmedetomidine was administered 5 minutes before an 8 min of asphyxia. Rats were resuscitated by a standardized method. Blood O(2) and CO(2) partial pressures were, pH, base excess (BE), and blood glucose concentration measured before asphyxial CA and 1 h after resuscitation. Neurological deficit score (NDS) was measured at 12, 24, 48, and 72 h after CA. Histopathologic changes in the hippocampal region were observed by H&E staining and histopathologic damage score. Ultrastructural morphology was observed by transmission electron microscopy. HIF-1 and VEGF expression were measured by immunostaining of serial sections obtained from brain tissue.
Asphyxial CA -induced global cerebral ischemic decreased PaO(2), pH, BE and increased PaCO(2), blood glucose. Dexmedetomidine preconditioning improved neurologic outcome, which was associated with reduction in histopathologic injury measured by H&E staining, the histopathologic damage score and electron microscopy. Dexmedetomidine preconditioning also elevated HIF-1α and VEGF expression after global cerebral ischemia following asphyxial CA.
Dexmedetomidine preconditioning protected against cerebral ischemic injury and was associated with upregulation of HIF-1α and VEGF expression.
背景/目的:探讨右美托咪定预处理对大鼠窒息性心脏骤停(CA)后全脑缺血损伤的保护作用。
将72只大鼠随机分为三组,假手术组(无窒息)、对照组(仅窒息)和右美托咪定预处理组(窒息+右美托咪定)。在窒息8分钟前5分钟给予右美托咪定。采用标准化方法对大鼠进行复苏。在窒息性心脏骤停前及复苏后1小时测量血氧分压、二氧化碳分压、pH值、碱剩余(BE)和血糖浓度。在心脏骤停后12、24、48和72小时测量神经功能缺损评分(NDS)。通过苏木精-伊红(H&E)染色观察海马区的组织病理学变化并进行组织病理学损伤评分。通过透射电子显微镜观察超微结构形态。通过对脑组织连续切片进行免疫染色来测量缺氧诱导因子-1(HIF-1)和血管内皮生长因子(VEGF)的表达。
窒息性心脏骤停诱导的全脑缺血降低了动脉血氧分压、pH值、碱剩余,并升高了动脉血二氧化碳分压、血糖。右美托咪定预处理改善了神经功能结局,这与通过H&E染色、组织病理学损伤评分和电子显微镜测量的组织病理学损伤减轻有关。右美托咪定预处理还提高了窒息性心脏骤停后全脑缺血时HIF-1α和VEGF的表达。
右美托咪定预处理可预防脑缺血损伤,并与HIF-1α和VEGF表达上调有关。