Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University, Baltimore, Maryland, USA,
Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Dev Neurosci. 2019;41(1-2):17-33. doi: 10.1159/000496602. Epub 2019 May 20.
Therapeutic hypothermia is the standard of clinical care for moderate neonatal hypoxic-ischemic encephalopathy. We investigated the independent and interactive effects of hypoxia-ischemia (HI) and temperature on neuronal survival and injury in basal ganglia and cerebral cortex in neonatal piglets. Male piglets were randomized to receive HI injury or sham procedure followed by 29 h of normothermia, sustained hypothermia induced at 2 h, or hypothermia with rewarming during fentanyl-nitrous oxide anesthesia. Viable and injured neurons and apoptotic profiles were counted in the anterior putamen, posterior putamen, and motor cortex at 29 h after HI injury or sham procedure. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) identified genomic DNA fragmentation to confirm cell death. Though hypothermia after HI preserved viable neurons in the anterior and posterior putamen, hypothermia prevented neuronal injury in only the anterior putamen. Hypothermia initiated 2 h after injury did not protect against apoptotic cell death in either the putamen or motor cortex, and rewarming from hypothermia was associated with increased apoptosis in the motor cortex. In non-HI shams, sustained hypothermia during anesthesia was associated with neuronal injury and corresponding viable neuron loss in the anterior putamen and motor cortex. TUNEL confirmed increased neurodegeneration in the putamen of hypothermic shams. Anesthetized, normothermic shams did not show abnormal neuronal cytopathology in the putamen or motor cortex, thereby demonstrating minimal contribution of the anesthetic regimen to neuronal injury during normothermia. We conclude that the efficacy of hypothermic protection after HI is region specific and that hypothermia during anesthesia in the absence of HI may be associated with neuronal injury in the developing brain. Studies examining the potential interactions between hypothermia and anesthesia, as well as with longer durations of hypothermia, are needed.
治疗性低温是中重度新生儿缺氧缺血性脑病的临床治疗标准。我们研究了缺氧缺血(HI)和温度对新生仔猪基底节和大脑皮层神经元存活和损伤的独立和交互作用。雄性仔猪随机接受 HI 损伤或假手术,然后接受 29 小时的正常体温、2 小时开始的持续低温或芬太尼-氧化亚氮麻醉时的复温低温。HI 损伤或假手术后 29 小时,在前纹状体、后纹状体和运动皮层中计数存活和损伤神经元以及凋亡谱。末端脱氧核苷酸转移酶 dUTP 缺口末端标记(TUNEL)鉴定基因组 DNA 片段化以确认细胞死亡。尽管 HI 后低温保存了前纹状体和后纹状体中的存活神经元,但低温仅能预防前纹状体的神经元损伤。损伤后 2 小时开始的低温不能预防纹状体和运动皮层中的凋亡细胞死亡,而从低温复温与运动皮层中凋亡增加有关。在非 HI 假手术中,麻醉期间的持续低温与前纹状体和运动皮层的神经元损伤和相应的存活神经元丢失有关。TUNEL 证实了低温假手术纹状体中的神经退行性变增加。麻醉、正常体温的假手术未显示纹状体或运动皮层中神经元细胞病理学异常,从而证明在正常体温下麻醉方案对神经元损伤的影响很小。我们得出结论,HI 后低温保护的疗效具有区域特异性,并且在没有 HI 的情况下麻醉期间的低温可能与发育中大脑的神经元损伤有关。需要研究低温与麻醉之间以及与更长时间低温之间的潜在相互作用。