Cammarota M, Paratcha G, Levi de Stein M, Bernabeu R, Izquierdo I, Medina J H
Instituto de Biología Celular y Neurociencias, Facultad de Medicina, UBA, Buenos Aires, Argentina.
Neurochem Res. 1997 Apr;22(4):499-505. doi: 10.1023/a:1027324214060.
Several lines of evidence indicate that protein kinase C (PKC) is involved in long-term potentiation (LTP) and in certain forms of learning. Recently, we found a learning-specific, time-dependent increase in [3H]phorbol dibutyrate binding to membrane-associated PKC in the hippocampus of rats subjected to an inhibitory avoidance task. Here we confirm and extend this observation, describing that a one trial inhibitory avoidance learning was associated with rapid and specific increases in B-50/GAP-43 phosphorylation in vitro and in PKC activity in hippocampal synaptosomal membranes. The increased phosphorylation of B-50/GAP-43, was seen at 30 min (+35% relative to naive or shocked control groups), but not at 10 or 60 min after training. This learning-associated increase in the phosphorylation of B-50/GAP-43 is mainly due to an increase in the activity of PKC. This is based on three different sets of data: 1) PKC activity increased by 24% in hippocampal synaptosomal membranes of rats sacrificed 30 min after training; 2) B-50/GAP-43 immunoblots revealed no changes in the amount of this protein among the different experimental groups; 3) phosphorylation assays, performed in the presence of bovine purified PKC or in the presence of the selective PKC inhibitor CGP 41231, exhibited no differences in B-50/GAP-43 phosphorylation between naive and trained animals. In conclusion, these results support the contention that hippocampal PKC participates in the early neural events of memory formation of an aversively-motivated learning task.
多项证据表明,蛋白激酶C(PKC)参与长时程增强(LTP)及某些形式的学习过程。最近,我们发现,在接受抑制性回避任务的大鼠海马体中,[3H]佛波醇二丁酸酯与膜相关PKC的结合呈现出学习特异性、时间依赖性的增加。在此,我们证实并扩展了这一观察结果,描述了单次试验的抑制性回避学习与体外B-50/GAP-43磷酸化及海马突触体膜中PKC活性的快速、特异性增加相关。B-50/GAP-43磷酸化增加在训练后30分钟时可见(相对于未处理或仅受电击的对照组增加了35%),但在训练后10分钟或60分钟时未出现。这种与学习相关的B-50/GAP-43磷酸化增加主要是由于PKC活性的增加。这基于三组不同的数据:1)训练后30分钟处死的大鼠海马突触体膜中PKC活性增加了24%;2)B-50/GAP-43免疫印迹显示不同实验组中该蛋白的量没有变化;3)在存在牛纯化PKC或选择性PKC抑制剂CGP 41231 的情况下进行的磷酸化测定显示,未处理动物和训练动物之间B-50/GAP-43磷酸化没有差异。总之,这些结果支持了海马体PKC参与厌恶性动机学习任务记忆形成早期神经事件的观点。