Department of Neurobiology and Anatomy, W.M. Keck Center for the Neurobiology of Learning and Memory, The University of Texas Medical School at Houston, Houston, Texas, USA.
Nat Neurosci. 2011 Dec 25;15(2):294-7. doi: 10.1038/nn.2990.
Learning and memory are influenced by the temporal pattern of training stimuli. However, the mechanisms that determine the effectiveness of a particular training protocol are not well understood. We tested the hypothesis that the efficacy of a protocol is determined in part by interactions among biochemical cascades that underlie learning and memory. Previous findings suggest that the protein kinase A (PKA) and extracellular signal-regulated kinase (ERK) cascades are necessary to induce long-term synaptic facilitation (LTF) in Aplysia, a neuronal correlate of memory. We developed a computational model of the PKA and ERK cascades and used it to identify a training protocol that maximized PKA and ERK interactions. In vitro studies confirmed that the protocol enhanced LTF. Moreover, the protocol enhanced the levels of phosphorylation of the transcription factor CREB1. Behavioral training confirmed that long-term memory also was enhanced by the protocol. These results illustrate the feasibility of using computational models to design training protocols that improve memory.
学习和记忆受到训练刺激的时间模式的影响。然而,决定特定训练方案有效性的机制尚不清楚。我们假设,方案的功效在一定程度上取决于构成学习和记忆基础的生化级联反应之间的相互作用。先前的研究结果表明,蛋白激酶 A(PKA)和细胞外信号调节激酶(ERK)级联反应对于诱导 Aplysia 中的长时突触易化(LTF)是必需的,Aplysia 是记忆的神经元相关物。我们开发了一个 PKA 和 ERK 级联的计算模型,并使用它来确定最大限度地增加 PKA 和 ERK 相互作用的训练方案。体外研究证实,该方案增强了 LTF。此外,该方案增强了转录因子 CREB1 的磷酸化水平。行为训练证实,该方案也增强了长期记忆。这些结果说明了使用计算模型设计可提高记忆的训练方案的可行性。