Nagasawa H, Araki T, Kogure K
Department of Neurology, Institute of Brain Diseases, Tohoku University School of Medicine, Sendai, Japan.
Brain Res Bull. 1994;35(4):347-52. doi: 10.1016/0361-9230(94)90112-0.
We studied the chronological changes of protein kinase C (PKC) and muscarinic acetylcholine receptor binding activities of the rat brain which were determined by using [3H]phorbol 12,13-dibutyrate (PDBu) and [3H]quinuclidinyl benzilate (QNB) autoradiographic methods, respectively, after 90 min of right middle cerebral artery (MCA) occlusion and after such occlusion, followed by different periods of recirculation. After the ischemic insult followed by 3 h of recirculation, [3H]PDBu binding sites were found to be significantly decreased in the cerebral cortex and lateral segment of the caudate putamen, both supplied by the occluded MCA; thereafter, the binding sites decreased progressively in those ischemic foci. On the contrary, there was no alteration on day 1, but 3 days after ischemic insult, a significant decrease of [3H]QNB binding sites was first detected in those ischemic foci. Moreover, 3 days after ischemic insult, both [3H]PDBu and [3H]QNB binding sites were concurrently reduced in the ipsilateral thalamus and 1 week after the ischemia, in the substantia nigra, in which both areas had not been directly affected by the original ischemic insult. These alterations of PKC in the postischemic brain areas developed concurrently with 45Ca accumulation, which was detected in our previous study. These results suggest that postischemic alterations of second-messenger (PKC) and neurotransmitter receptor systems were involved not only in the ischemic foci due to ischemia-induced energy failure, but also in the exo-focal remote areas prior to the histologic changes where neuronal damage might be caused by transsynaptic delayed degeneration.
我们采用放射自显影法,分别用[3H]佛波醇12,13 - 二丁酸酯(PDBu)和[3H]喹核醇基苯甲酸酯(QNB)研究了大鼠大脑蛋白激酶C(PKC)和毒蕈碱型乙酰胆碱受体结合活性的时间变化,实验在大脑中动脉(MCA)右侧闭塞90分钟后及闭塞后不同时间段再灌注后进行。缺血损伤后再灌注3小时,发现由闭塞的MCA供血的大脑皮质和尾状核壳外侧段的[3H]PDBu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。相反,缺血损伤后第1天无变化,但缺血损伤后3天,首先在这些缺血灶中检测到[3H]QNB结合位点显著减少。此外,缺血损伤后3天,同侧丘脑的[3H]PDBu和[3H]QNB结合位点同时减少,缺血1周后,黑质中的结合位点减少,而这两个区域均未直接受到原始缺血损伤的影响。缺血后脑区PKC的这些变化与我们之前研究中检测到的45Ca积累同时发生。这些结果表明,缺血后第二信使(PKC)和神经递质受体系统的改变不仅与缺血诱导的能量衰竭导致的缺血灶有关,还与组织学变化之前的局灶外远处区域有关,在这些区域神经元损伤可能由跨突触延迟变性引起。