Reymann Klaus G, Frey Julietta U
Department for Neurophysiology, Leibniz Institute for Neurobiology, Brenneckestrasse 6, D-39118 Magdeburg, Germany.
Neuropharmacology. 2007 Jan;52(1):24-40. doi: 10.1016/j.neuropharm.2006.07.026. Epub 2006 Aug 21.
Our review focuses on the mechanisms which enable the late maintenance of hippocampal long-term potentiation (LTP; >3h), a phenomenon which is thought to underlie prolonged memory. About 20 years ago we showed for the first time that the maintenance of LTP - like memory storage--depends on intact protein synthesis and thus, consists of at least two temporal phases. Here we concentrate on mechanisms required for the induction of the transient early-LTP and of the protein synthesis-dependent late-LTP. Our group has shown that the induction of late-LTP requires the associative activation of heterosynaptic inputs, i.e. the synergistic activation of glutamatergic and modulatory, reinforcing inputs within specific, effective time windows. The induction of late-LTP is characterized by novel, late-associative properties such as 'synaptic tagging' and 'late-associative reinforcement'. Both phenomena require the associative setting of synaptic tags as well as the availability of plasticity-related proteins (PRPs) and they are restricted to functional dendritic compartments, in general. 'Synaptic tagging' guarantees input specificity and thus the specific processing of afferent signals for the establishment of late-LTP. 'Late-associative reinforcement' describes a process where early-LTP by the co-activation of modulatory inputs can be transformed into late-LTP in activated synapses where a tag is set. Recent evidence from behavioral experiments, which studied processes of emotional and cognitive reinforcement of LTP, point to the physiological relevance of the above mechanisms during cellular and system's memory formation.
我们的综述聚焦于能够使海马体长期增强效应(LTP;>3小时)得以晚期维持的机制,这一现象被认为是长期记忆的基础。大约20年前,我们首次表明,LTP(类似记忆存储)的维持依赖于完整的蛋白质合成,因此至少由两个时间阶段组成。在这里,我们专注于瞬时早期LTP和蛋白质合成依赖性晚期LTP诱导所需的机制。我们小组已经表明,晚期LTP的诱导需要异突触输入的联合激活,即在特定的有效时间窗口内谷氨酸能和调节性、增强性输入的协同激活。晚期LTP的诱导具有“突触标记”和“晚期联合增强”等新的晚期联合特性。这两种现象都需要突触标记的联合设置以及可塑性相关蛋白(PRP)的可用性,并且通常仅限于功能性树突区室。“突触标记”保证了输入特异性,从而保证了传入信号用于建立晚期LTP的特异性处理。“晚期联合增强”描述了一个过程,即通过调节性输入的共同激活,早期LTP可以在设置了标记的激活突触中转化为晚期LTP。最近来自行为实验的证据,这些实验研究了LTP的情感和认知增强过程,指出了上述机制在细胞和系统记忆形成过程中的生理相关性。