Juzekaeva Elvira, Gainutdinov Azat, Mukhtarov Marat, Khazipov Roustem
Laboratory of Neurobiology, Institute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia.
Aix Marseille Univ, INSERM, INMED, Marseille, France.
Front Cell Neurosci. 2018 Dec 18;12:502. doi: 10.3389/fncel.2018.00502. eCollection 2018.
Cerebral edema is a major, life threatening complication of ischemic brain damage. Previous studies using brain slices have revealed that cellular swelling and a concomitant increase in tissue transparency starts within minutes of the onset of metabolic insult in association with collective anoxic spreading depolarization (aSD). However, the dynamics of tissue swelling in brain slices under ischemia-like conditions remain elusive. Here, we explored the dynamics of brain tissue swelling induced by oxygen-glucose deprivation (OGD) in submerged rat barrel cortex slices. Video monitoring of the vertical and horizontal position of fluorescent dye-filled neurons and contrast slice surface imaging revealed elevation of the slice surface and a horizontal displacement of the cortical tissue during OGD. The OGD-induced tissue movement was also associated with an expansion of the slice borders. Tissue swelling started several minutes after aSD and continued during reperfusion with normal solution. Thirty minutes after aSD, slice borders had expanded by ~130 μm and the slice surface had moved up to attain a height of ~70 μm above control levels, which corresponded to a volume increase of ~30%. Hyperosmotic sucrose solution partially reduced the OGD-induced slice swelling. Thus, OGD-induced cortical slice tissue swelling in brain slices recapitulates many features of ischemic cerebral edema , its onset is tightly linked to aSD and it develops at a relatively slow pace after aSD. We propose that this model of cerebral edema could be useful for the exploration of the pathophysiological mechanisms underlying ischemic cerebral edema and in the search for an efficient treatment to this devastating condition.
脑水肿是缺血性脑损伤的一种主要的、危及生命的并发症。以往使用脑片的研究表明,在代谢损伤开始后的几分钟内,伴随着集体性缺氧性扩散性去极化(aSD),细胞肿胀和组织透明度随之增加。然而,在类似缺血条件下脑片中组织肿胀的动态变化仍不清楚。在此,我们探讨了在浸没的大鼠桶状皮层脑片中,氧糖剥夺(OGD)诱导的脑组织肿胀的动态变化。对充满荧光染料的神经元的垂直和水平位置进行视频监测以及对切片表面进行对比成像,结果显示在OGD期间切片表面升高,皮层组织发生水平位移。OGD诱导的组织移动还与切片边界的扩展有关。组织肿胀在aSD后几分钟开始,并在正常溶液再灌注期间持续。aSD后30分钟,切片边界扩大了约130μm,切片表面向上移动,达到比对照水平高约70μm的高度,这相当于体积增加了约30%。高渗蔗糖溶液部分减轻了OGD诱导的切片肿胀。因此,OGD诱导的脑片皮层切片组织肿胀概括了缺血性脑水肿的许多特征,其发生与aSD紧密相关,并且在aSD后以相对缓慢的速度发展。我们认为这种脑水肿模型可能有助于探索缺血性脑水肿的病理生理机制,并有助于寻找针对这种毁灭性疾病的有效治疗方法。