Cox-Limpens Kimberly E M, Strackx Eveline, Van den Hove Daniel L A, Van Ekkendonk Joris R A, Jong Marin de, Zimmermann Luc J I, Steinbusch Harry W M, Vles Johan S H, Gavilanes Antonio W D
School for Mental Health and Neuroscience (MHeNS), Faculty of Health, Medicine and Life Sciences, Maastricht University, Universiteitssingel 40, 6229 ER Maastricht, The Netherlands.
CNS Neurol Disord Drug Targets. 2015;14(1):33-40. doi: 10.2174/1871527314666150116112032.
Hypoxic-ischemic preconditioning is an endogenous mechanism in which exposure to a sublethal episode of hypoxia-ischemia protects against a subsequent more severe episode. Although several postnatal models of hypoxic-ischemic preconditioning have been established, hardly any perinatal models exist. Therefore, the objective of this study is to validate a new rodent model. We investigate whether mild fetal asphyxia (FA) as a preconditioning stimulus, protects against severe perinatal asphyxia (PA) when looking at neonatal brain histology. FA was induced at embryonic day 17 (E17) by temporarily clamping the uterine circulation. A caesarean section was performed at E21/22 and PA was induced by submersing the uterine horns, still containing the fetuses, in a water bath. Brains were examined for histological changes at either postnatal day 7 or 14. We used terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) staining to detect apoptotic cell death and a glial fibrillary acidic protein (GFAP) staining to detect reactive astrocytes. Interestingly, the preconditioned group showed significantly less perinatal mortality than non-preconditioned groups. Furthermore, preconditioned animals had significantly less TUNEL-positive cells and less GFAP-positive cells in striatum, prefrontal cortex and hippocampus compared to the non-preconditioned animals that underwent PA. Consequently, mild FA might cause neuroprotection by inducing anti-apoptotic mechanisms and attenuating astrogliosis. Considering the morphological findings in the neonatal brain from this study, together with previously reported long-term behavioral outcomes in this model, we can conclude that this is a suitable experimental model to investigate mechanisms of endogenous neuroprotection in the fetal brain. Identifying these endogenous neuroprotective mechanisms will provide novel potential targets for future pharmacological intervention in asphyctic newborns.
缺氧缺血预处理是一种内源性机制,即暴露于亚致死性缺氧缺血事件可保护机体免受随后更严重事件的影响。尽管已经建立了几种产后缺氧缺血预处理模型,但几乎不存在围产期模型。因此,本研究的目的是验证一种新的啮齿动物模型。我们研究了作为预处理刺激的轻度胎儿窒息(FA),在观察新生鼠脑组学学时,是否能预防严重的围产期窒息(PA)。在胚胎第17天(E17)通过暂时夹闭子宫循环诱导FA。在E21/22进行剖宫产,将仍含有胎儿的子宫角浸入水浴中诱导PA。在出生后第7天或第14天检查大脑的组织学变化。我们使用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)染色来检测凋亡细胞死亡,并使用胶质纤维酸性蛋白(GFAP)染色来检测反应性星形胶质细胞。有趣的是,预处理组的围产期死亡率明显低于未预处理组。此外,与经历PA的未预处理动物相比,预处理动物在纹状体、前额叶皮质和海马体中的TUNEL阳性细胞和GFAP阳性细胞明显更少。因此,轻度FA可能通过诱导抗凋亡机制和减轻星形胶质细胞增生来发挥神经保护作用。考虑到本研究中新生鼠脑的形态学发现,以及该模型中先前报道的长期行为结果,我们可以得出结论,这是一个研究胎儿脑内源性神经保护机制的合适实验模型。确定这些内源性神经保护机制将为未来对窒息新生儿进行药物干预提供新的潜在靶点。