Kato H, Araki T, Hara H, Kogure K
Department of Neurology, Tohoku University School of Medicine, Sendai, Japan.
Brain Res. 1991 Jul 5;553(1):33-8. doi: 10.1016/0006-8993(91)90226-l.
We performed quantitative autoradiography to determine sequential alterations in the binding of muscarinic cholinergic and adenosine A1 receptors and of an L-type calcium channel blocker in the gerbil hippocampus following repeated brief ischemic insults. [3H]Quinuclidinyl benzilate (QNB). [3H]cyclohexyladenosine (CHA) and [3H]PN200-110 were used to label muscarinic and adenosine A1 receptors and L-type calcium channels, respectively. Changes at 1 h, 6 h, 1 day, 4 days and 1 month after three 2-min ischemic insults were compared with changes after single 2- or 6-min ischemia. Two-minute ischemia, which causes no histopathological neuronal damage, produced no persistent alterations in binding sites. We observed a transient and mild increase in binding activities, especially in [3H]CHA binding, at 1 h of recirculation. Following 6-min ischemia and three 2-min ischemic insults. [3H]QNB and [3H]PN200-110 binding decreased by more than 50% in the CA1 subfield by 1 month, but [3H]CHA binding decreased transiently by 20-30% at 4 days when delayed neuronal death of hippocampal CA1 pyramidal cells took place. Reductions in binding, especially in [3H]QNB binding, following three 2-min ischemic insults were greater and appeared earlier than those after 6-min ischemia. Furthermore, alterations extended to the CA3 subfield and the dentate gyrus following repeated insults. Thus, alterations in receptor binding after repeated ischemic insults were greater than those after equivalent single period of ischemia.
我们进行了定量放射自显影,以确定在沙土鼠海马体中,反复短暂缺血性损伤后毒蕈碱胆碱能受体、腺苷A1受体及L型钙通道阻滞剂结合的顺序性变化。[3H]奎宁环基苯甲酸酯(QNB)、[3H]环己基腺苷(CHA)和[3H]PN200-110分别用于标记毒蕈碱受体、腺苷A1受体和L型钙通道。将三次2分钟缺血性损伤后1小时、6小时、1天、4天和1个月时的变化,与单次2分钟或6分钟缺血后的变化进行比较。两分钟的缺血不会造成组织病理学上的神经元损伤,也不会使结合位点产生持续性改变。我们观察到,再灌注1小时时,结合活性出现短暂且轻微的增加,尤其是[3H]CHA结合活性。6分钟缺血及三次2分钟缺血性损伤后,到1个月时,CA1亚区的[3H]QNB和[3H]PN200-110结合减少超过50%,但在海马CA1锥体细胞发生延迟性神经元死亡的4天时,[3H]CHA结合短暂减少20%-30%。三次2分钟缺血性损伤后结合的减少,尤其是[3H]QNB结合的减少,比6分钟缺血后更明显且出现得更早。此外,反复损伤后,变化扩展至CA3亚区和齿状回。因此,反复缺血性损伤后受体结合的变化比同等单次缺血后的变化更大。