Nagasawa H, Araki T, Kogure K
Department of Neurology, Institute of Brain Diseases, Tohoku University School of Medicine, Sendai, Japan.
J Neurol Sci. 1994 Jan;121(1):27-31. doi: 10.1016/0022-510x(94)90152-x.
We studied the postischemic alteration of muscarinic acetylcholine binding sites in the rat brain using in vitro [3H]quinuclidinyl benzilate (QNB) autoradiography. Transient ischemia was induced by the occlusion of the middle cerebral artery (MCA) for 90 min and such occlusion followed by various recirculation periods of up to 4 weeks. After 90 min of ischemia followed by 3 days of recirculation, [3H]QNB binding sites were found to be significantly decreased in the cerebral cortex (P < 0.01) and lateral segment of the caudate putamen (P < 0.05), both supplied by the occluded MCA; thereafter, the binding sites decreased progressively in those ischemic foci. Moreover, 3 days after the ischemia, significant decreases of [3H]QNB binding sites were observed in the ipsilateral thalamus and the amygdala, and also in the substantia nigra 1 week after the ischemia, areas which had not been directly affected by the original ischemic insult. This postischemic phenomenon observed in the thalamus and the substantia nigra developed concurrently with 45Ca accumulation, which was detected there in our previous study. These results indicate that alteration of muscarinic acetylcholine binding sites may be involved not only in the ischemic foci, but also in the exo-focal remote areas, in which delayed neuronal degeneration due to neuronal network disturbances after the ischemia was observed. We suggest that multifocal postischemic alterations of muscarinic acetylcholine binding sites may exacerbate the clinical symptoms of patients during the chronic stage of stroke.
我们采用体外[3H]喹核酯(QNB)放射自显影术,研究了大鼠脑内毒蕈碱型乙酰胆碱结合位点的缺血后改变。通过大脑中动脉(MCA)闭塞90分钟诱导短暂性缺血,随后进行长达4周的不同再灌注期。缺血90分钟后再灌注3天,发现由闭塞的MCA供血的大脑皮质(P<0.01)和尾状核壳核外侧段(P<0.05)的[3H]QNB结合位点显著减少;此后,这些缺血灶中的结合位点逐渐减少。此外,缺血后3天,在同侧丘脑和杏仁核中观察到[3H]QNB结合位点显著减少,在缺血后1周,黑质中也观察到显著减少,这些区域未受到最初缺血损伤的直接影响。在丘脑和黑质中观察到的这种缺血后现象与45Ca积累同时出现,这在我们之前的研究中已在那里检测到。这些结果表明,毒蕈碱型乙酰胆碱结合位点的改变可能不仅涉及缺血灶,还涉及灶外远隔区域,在这些区域观察到缺血后由于神经网络紊乱导致的延迟性神经元变性。我们认为,毒蕈碱型乙酰胆碱结合位点的多灶性缺血后改变可能会加重中风慢性期患者的临床症状。