Bernabeu R, Bevilaqua L, Ardenghi P, Bromberg E, Schmitz P, Bianchin M, Izquierdo I, Medina J H
Instituto de Biologia Celular, Facultad de Medicina, Universidad de Buenos Aires, Buenos Aires, Argentina.
Proc Natl Acad Sci U S A. 1997 Jun 24;94(13):7041-6. doi: 10.1073/pnas.94.13.7041.
cAMP/cAMP-dependent protein kinase (PKA) signaling pathway has been recently proposed to participate in both the late phase of long term potentiation in the hippocampus and in the late, protein synthesis-dependent phase of memory formation. Here we report that a late memory consolidation phase of an inhibitory avoidance learning is regulated by an hippocampal cAMP signaling pathway that is activated, at least in part, by D1/D5 receptors. Bilateral infusion of SKF 38393 (7.5 microg/side), a D1/D5 receptor agonist, into the CA1 region of the dorsal hippocampus, enhanced retention of a step-down inhibitory avoidance when given 3 or 6 h, but not immediately (0 h) or 9 h, after training. In contrast, full retrograde amnesia was obtained when SCH 23390 (0.5 microg/side), a D1/D5 receptor antagonist, was infused into the hippocampus 3 or 6 h after training. Intrahippocampal infusion of 8Br-cAMP (1.25 microg/side), or forskolin (0.5 microg/side), an activator of adenylyl cyclase, enhanced memory when given 3 or 6 h after training. KT5720 (0.5 microg/side), a specific inhibitor of PKA, hindered memory consolidation when given immediately or 3 or 6 h posttraining. Rats submitted to the avoidance task showed learning-specific increases in hippocampal 3H-SCH 23390 binding and in the endogenous levels of cAMP 3 and 6 h after training. In addition, PKA activity and P-CREB (phosphorylated form of cAMP responsive element binding protein) immunoreactivity increased in the hippocampus immediately and 3 and 6 h after training. Together, these findings suggest that the late phase of memory consolidation of an inhibitory avoidance is modulated cAMP/PKA signaling pathways in the hippocampus.
环磷酸腺苷/环磷酸腺苷依赖性蛋白激酶(PKA)信号通路最近被认为参与了海马体中长期增强效应的后期阶段以及记忆形成后期依赖蛋白质合成的阶段。在此我们报告,抑制性回避学习的后期记忆巩固阶段受海马体环磷酸腺苷信号通路调控,该通路至少部分由D1/D5受体激活。双侧向背侧海马体CA1区注射D1/D5受体激动剂SKF 38393(7.5微克/侧),在训练后3小时或6小时给予时,增强了一步下抑制性回避的记忆保持,但在训练后立即(0小时)或9小时给予则无此效果。相反,在训练后3小时或6小时向海马体注射D1/D5受体拮抗剂SCH 23390(0.5微克/侧),可导致完全逆行性遗忘。在训练后3小时或6小时向海马体内注射8-溴环磷酸腺苷(1.25微克/侧)或腺苷酸环化酶激活剂福斯高林(0.5微克/侧),可增强记忆。PKA特异性抑制剂KT5720(0.5微克/侧)在训练后立即、3小时或6小时给予时,会阻碍记忆巩固。接受回避任务的大鼠在训练后3小时和6小时,海马体中3H-SCH 23390结合以及环磷酸腺苷内源性水平呈现出学习特异性增加。此外,训练后立即、3小时和6小时,海马体中的PKA活性以及环磷酸腺苷反应元件结合蛋白的磷酸化形式(P-CREB)免疫反应性均增加。这些研究结果共同表明,抑制性回避记忆巩固的后期阶段受海马体中环磷酸腺苷/PKA信号通路的调节。