Kato H, Araki T, Hara H, Kogure K
Department of Neurology, Tohoku University School of Medicine, Sendai, Japan.
Brain Res Bull. 1991 Dec;27(6):759-65. doi: 10.1016/0361-9230(91)90208-2.
Using [3H]inositol 1,4,5-triphosphate (IP3), [3H]phorbol 12,13-dibutyrate (PDBu) and [3H]forskolin, we performed quantitative autoradiography to determine sequential alterations in second-messenger systems in the gerbil hippocampus following repeated brief ischemic insults. Changes following three 2-min ischemic insults were compared with those following single 2- or 6-min ischemia. [3H]IP3 binding was extremely sensitive to ischemic insult, and more than 80% of the binding sites were lost after destruction of CA1 pyramidal cells following 6-min ischemia and three 2-min ischemic insults. Furthermore, a 30% reduction was observed after 2-min ischemia which leads to no neuronal loss. [3H]PDBu binding in the CA1 subfield decreased by 1 day after three 2-min ischemic insults and by 4 days after 6-min ischemia, and 40-50% reductions were observed at 1 month. In contrast, [3H]forskolin binding was relatively preserved. [3H]PDBu and [3H]forskolin binding transiently increased early in the reperfusion period. We also observed a difference in the pattern and severity of alterations between repeated ischemic insults and single ischemia.
我们使用[3H]肌醇1,4,5 - 三磷酸(IP3)、[3H]佛波醇12,13 - 二丁酸酯(PDBu)和[3H]福斯高林,进行了定量放射自显影,以确定沙鼠海马在反复短暂缺血性损伤后第二信使系统的顺序性变化。将三次2分钟缺血性损伤后的变化与单次2分钟或6分钟缺血后的变化进行比较。[3H]IP3结合对缺血性损伤极为敏感,在6分钟缺血和三次2分钟缺血性损伤后CA1锥体细胞破坏后,超过80%的结合位点丧失。此外,在2分钟缺血后观察到30%的减少,此时未导致神经元丢失。在三次2分钟缺血性损伤后1天,CA1亚区的[3H]PDBu结合减少,在6分钟缺血后4天减少,在1个月时观察到40 - 50%的减少。相比之下,[3H]福斯高林结合相对保留。[3H]PDBu和[3H]福斯高林结合在再灌注早期短暂增加。我们还观察到反复缺血性损伤和单次缺血之间在变化模式和严重程度上的差异。