Kuge Y, Hasegawa Y, Yokota C, Minematsu K, Hashimoto N, Miyake Y, Yamaguchi T
Institute for Biofunctional Research Co., Inc., Osaka, Japan.
J Neurol Sci. 2000 Jun 15;176(2):114-23. doi: 10.1016/s0022-510x(00)00327-0.
To clarify the effects of spreading depression (SD) on cerebral circulation and metabolism, we elicited a single or repetitive episode of SD and evaluated CBF and CMRglc three-dimensionally in normal cats (n=4, in each group) using a high-resolution positron emission tomography (PET) scanner. SD was evoked by applying KCl to the left occipital cortex. We then monitored DC potential changes with tungsten electrodes inserted into the left temporal cortex. CBF was measured twice before and three times (immediately, 30-60 min, and 60-120 min) following KCl application using [15O]H(2)O, and CMRglc was determined using 2-[18F]fluoro-2-deoxy-D-glucose immediately following the last CBF measurement. The following results were obtained: (1) a single episode of SD produced a temporary CBF increase, followed by a long-lasting hypoperfusion in the cortex, with no significant changes to CBF observed in the subcortex; (2) no significant CMRglc changes were observed in either cortical or subcortical regions following a single episode of SD; (3) a flow-metabolism uncoupling was observed in the cortical regions concurrently with persistent hypoperfusion; (4) repetitive SD produced significant CBF changes in the cortex; and (5) the cortical CMRglc increased as a result of repeated episodes of SD, with no significant changes observed in the subcortex. Thus, we succeeded in determining three-dimensionally the effects of single and repetitive SD on CBF and CMRglc in cats using a high-resolution PET scanner. The present study provides the first direct evidence of CBF-CMRglc uncoupling occurring concurrently with persistent hypoperfusion following SD.
为阐明扩散性抑制(SD)对脑循环和代谢的影响,我们在正常猫(每组n = 4)中引发单次或重复性SD发作,并使用高分辨率正电子发射断层扫描(PET)扫描仪三维评估脑血流量(CBF)和脑葡萄糖代谢率(CMRglc)。通过将氯化钾应用于左侧枕叶皮质诱发SD。然后,我们用插入左侧颞叶皮质的钨电极监测直流电位变化。在应用氯化钾之前使用[15O]H₂O测量两次CBF,并在应用氯化钾后测量三次(立即、30 - 60分钟和60 - 120分钟),并在最后一次CBF测量后立即使用2 - [18F]氟 - 2 - 脱氧 - D - 葡萄糖测定CMRglc。获得以下结果:(1)单次SD发作导致短暂的CBF增加,随后皮质出现长期灌注不足,而皮质下未观察到CBF有显著变化;(2)单次SD发作后,皮质或皮质下区域均未观察到CMRglc有显著变化;(3)在皮质区域观察到血流 - 代谢解偶联,同时伴有持续性灌注不足;(4)重复性SD导致皮质出现显著的CBF变化;(5)重复性SD发作导致皮质CMRglc增加,皮质下未观察到显著变化。因此,我们成功地使用高分辨率PET扫描仪三维确定了单次和重复性SD对猫CBF和CMRglc的影响。本研究提供了首个直接证据,证明SD后持续性灌注不足同时发生CBF - CMRglc解偶联。