Homola Ales, Zoremba Norbert, Slais Karel, Kuhlen Ralf, Syková Eva
Department of Neuroscience and Centre for Cell Therapy and Tissue Repair, 2nd Medical Faculty, Prague, Czech Republic.
Neurosci Lett. 2006 Aug 14;404(1-2):137-42. doi: 10.1016/j.neulet.2006.05.028. Epub 2006 Jun 6.
It has been shown that global anoxia leads to dramatic changes in the diffusion properties of the extracellular space (ECS). In this study, we investigated how changes in ECS volume and geometry in the rat somatosensory cortex during and after transient hypoxia/ischemia correlate with extracellular concentrations of energy-related metabolites and glutamate. Adult male Wistar rats (n = 12) were anesthetized and subjected to hypoxia/ischemia for 30 min (ventilation with 10% oxygen and unilateral carotid artery occlusion). The ECS diffusion parameters, volume fraction and tortuosity, were determined from concentration-time profiles of tetramethylammonium applied by iontophoresis. Concentrations of lactate, glucose, pyruvate and glutamate in the extracellular fluid (ECF) were monitored by microdialysis (n = 9). During hypoxia/ischemia, the ECS volume fraction decreased from initial values of 0.19 +/- 0.03 (mean +/- S.E.M.) to 0.07 +/- 0.01 and tortuosity increased from 1.57 +/- 0.01 to 1.88 +/- 0.03. During reperfusion the volume fraction returned to control values within 20 min and then increased to 0.23 +/- 0.01, while tortuosity only returned to original values (1.53 +/- 0.06). The concentrations of lactate and glutamate, and the lactate/pyruvate ratio, substantially increased during hypoxia/ischemia, followed by continuous recovery during reperfusion. The glucose concentration decreased rapidly during hypoxia/ischemia with a subsequent return to control values within 20 min of reperfusion. We conclude that transient hypoxia/ischemia causes similar changes in ECS diffusion parameters as does global anoxia and that the time course of the reduction in ECS volume fraction correlates with the increase of extracellular concentration of glutamate. The decrease in the ECS volume fraction can therefore contribute to an increased accumulation of toxic metabolites, which may aggravate functional deficits and lead to damage of the central nervous system (CNS).
研究表明,全脑缺氧会导致细胞外间隙(ECS)扩散特性发生显著变化。在本研究中,我们调查了大鼠体感皮层在短暂缺氧/缺血期间及之后ECS体积和几何形状的变化如何与能量相关代谢物和谷氨酸的细胞外浓度相关。成年雄性Wistar大鼠(n = 12)麻醉后进行30分钟的缺氧/缺血处理(用10%氧气通气并单侧颈动脉闭塞)。通过离子电泳施加的四甲基铵的浓度-时间曲线确定ECS扩散参数、体积分数和曲折度。通过微透析监测细胞外液(ECF)中乳酸、葡萄糖、丙酮酸和谷氨酸的浓度(n = 9)。在缺氧/缺血期间,ECS体积分数从初始值0.19±0.03(平均值±标准误)降至0.07±0.01,曲折度从1.57±0.01增加到1.88±0.03。在再灌注期间,体积分数在20分钟内恢复到对照值,然后增加到0.23±0.01,而曲折度仅恢复到原始值(1.53±0.06)。乳酸和谷氨酸的浓度以及乳酸/丙酮酸比值在缺氧/缺血期间大幅增加,随后在再灌注期间持续恢复。葡萄糖浓度在缺氧/缺血期间迅速下降,随后在再灌注20分钟内恢复到对照值。我们得出结论,短暂缺氧/缺血引起的ECS扩散参数变化与全脑缺氧相似,并且ECS体积分数降低的时间进程与细胞外谷氨酸浓度的增加相关。因此,ECS体积分数的降低可能导致有毒代谢物积累增加,这可能加重功能缺陷并导致中枢神经系统(CNS)损伤。