沙鼠后脑短暂缺血后,血脑屏障的缺血性开放可能使脑干听觉诱发电位恶化。

R Hata, M Matsumoto, K Yamamoto, T Ohtsuki, S Ogawa, N Handa, T Kubo, T Matsunaga, T Nishimura, T Kamada
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引用次数: 0

摘要

为了阐明血管源性脑水肿对脑干的影响,我们研究了后脑短暂缺血后脑干听觉诱发电位(BAEP)波形变化与血脑屏障(BBB)紊乱的关系。双侧椎动脉闭塞引起沙鼠后脑缺血。将动物分为三组,分别接受0、5、30分钟的双侧椎体闭塞(BVO-0′、-5′、-30′组);每组N = 4)。再循环2小时后,将埃文斯蓝(EB)溶液注入大鼠隐静脉。循环30min后取脑,记录所有EB宏观染色区域。后脑缺血时BAEP在3 min内消失,BVO-5′组BAEP在再灌注后10 min内重新出现并恢复正常,而BVO-30′组BAEP未恢复正常,最终在再灌注后30 min内消失。BVO-5’组未见EB染色。另一方面,在BVO-30'组,2只动物中脑被盖内侧,3只动物脑桥外侧前庭核周围可见EB染色。这些结果表明脑缺血诱导的BAEP变化的可逆性与脑干血脑屏障紊乱密切相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An ischemic opening of the blood-brain barrier may deteriorate brain stem auditory evoked potentials following transient hindbrain ischemia in gerbils.

To clarify the effect of vasogenic brain edema on the brainstem, the relationships between waveform changes in brainstem auditory evoked potentials (BAEP) and blood-brain barrier (BBB) disturbance following transient hindbrain ischemia were investigated. Hindbrain ischemia was induced in gerbils by bilateral occlusion of the vertebral arteries. The animals were divided into three groups subjected to 0, 5, and 30 min of bilateral vertebral occlusion (BVO-0',-5', and -30' groups; n = 4 in each group). Two hours after recirculation, Evans blue (EB) solution was injected into the saphenous vein. The brains were removed after 30 min of circulation, and all areas stained macroscopically by EB were noted and recorded. During hindbrain ischemia, BAEP disappeared within 3 min. In the BVO-5' group, BAEP reappeared and returned to normal within 10 min after reperfusion, whereas in the BVO-30' group, BAEP never returned to normal and finally disappeared within 30 min after reperfusion. In the BVO-5' group, no EB staining was visible. On the other hand, in the BVO-30' group, EB staining was seen in the medial part of the tegmentum in the midbrain in two animals, and around the vestibular nucleus in the lateral parts of the pons in three. These results demonstrate the close relationship between the reversibility of ischemia-induced changes in BAEP and BBB disturbance in the brainstem.

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