Tissue Na, K, and Ca changes in regional cerebral ischemia: their measurement and interpretation.

W Young, V DeCrescito, E S Flamm, M Hadani, H Rappaport, P Cornu
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引用次数: 28

Abstract

A simple and reliable method of quantifying tissue damage is described. This method, based on atomic absorption spectroscopic determinations of Na, K, and Ca concentrations in small brain samples, was applied to the rat middle cerebral artery occlusion model (MCAo). At the infarct site by 24 hours, Na concentration more than doubled, Ca concentration increased by greater than 70%, and K concentration fell nearly 80%; these changes are consistent with a greater than 80% disruption of cells. A remarkable acceleration of ionic shifts occurred between 4 and 6 hours after MCAo. At 4 hours, only 20-30% of the ionic shifts found at 24 hours had occurred; by 6 hours, 80-100% of the ionic shifts found at 24 hours had taken place. Since the measurements reflect ionic movement into and out of the tissue, they are likely to represent irreversible tissue damage. Although blood brain barrier breakdown may have contributed to an increased rate of ionic shifts, large ionic gradients must have been present between the extracellular space and the vascular compartment at 4-6 hours to drive the ionic shifts. Our results suggest an upper time limit of 4 hours for treatments of acute ischemic tissue damage in the rat MCAo model. The methods and analytical approach described may be useful for determining the time window for therapeutic intervention in acute CNS injuries, as well as for evaluating treatment effects.

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局部脑缺血时组织Na、K和Ca的变化:测量和解释。
描述了一种简单可靠的定量组织损伤的方法。该方法基于原子吸收光谱法测定小脑样品中Na、K和Ca的浓度,并应用于大鼠大脑中动脉闭塞模型(MCAo)。24h梗死部位Na浓度增加一倍以上,Ca浓度增加70%以上,K浓度下降近80%;这些变化与超过80%的细胞破坏相一致。在MCAo后4 ~ 6小时,离子位移发生显著加速。在4小时时,仅发生了24小时时发现的20-30%的离子位移;到6小时时,24小时内发现的80-100%的离子转移已经发生。由于测量反映了离子进出组织的运动,它们很可能代表了不可逆的组织损伤。尽管血脑屏障的破坏可能导致离子移动速率的增加,但在细胞外空间和血管间室之间必须在4-6小时内存在较大的离子梯度来驱动离子移动。提示MCAo模型大鼠急性缺血性组织损伤的治疗时间上限为4小时。所描述的方法和分析方法可能有助于确定急性中枢神经系统损伤治疗干预的时间窗口,以及评估治疗效果。
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