Chen Mengjiao, Ren Wei, Wang Xingang
School of Physics and Information Technology, Shaanxi Normal University Xi'an, China.
Key Laboratory of Modern Teaching Technology, Ministry of Education, Shaanxi Normal University Xi'an, China.
Front Comput Neurosci. 2016 Oct 19;10:104. doi: 10.3389/fncom.2016.00104. eCollection 2016.
Long-term potentiation (LTP) of synaptic strength is strongly implicated in learning and memory. On the other hand, depotentiation, the reversal of synaptic strength from potentiated LTP state to the pre-LTP level, is required in extinction of the obsolete memory. A generic tristable system, which couples the phosphatase and kinase switches, exclusively explains how moderate and high elevation of intracellular calcium concentration triggers long-term depression (LTD) and LTP, respectively. The present study, introducing calcium influx and calcium release from internal store into the tristable system, further show that significant elevation of cytoplasmic calcium concentration switches activation of both kinase and phosphatase to their basal states, thereby depotentiate the synaptic strength. A phase-plane analysis of the combined model was employed to explain the previously reported depotentiation in experiments and predict a threshold-like effect with calcium concentration. The results not only reveal a mechanism of NMDAR- and mGluR-dependent depotentiation, but also predict further experiments about the role of internal calcium store in induction of depotentiation and extinction of established memories.
突触强度的长期增强(LTP)与学习和记忆密切相关。另一方面,去增强作用,即突触强度从增强的LTP状态逆转到LTP前水平,是消除过时记忆所必需的。一种将磷酸酶和激酶开关耦合在一起的通用三稳态系统,专门解释了细胞内钙浓度的适度升高和高度升高分别如何触发长期抑制(LTD)和LTP。本研究将钙内流和内质网钙释放引入三稳态系统,进一步表明细胞质钙浓度的显著升高会将激酶和磷酸酶的激活切换到其基础状态,从而使突触强度去增强。采用组合模型的相平面分析来解释先前实验中报道的去增强作用,并预测钙浓度的阈值样效应。这些结果不仅揭示了NMDAR和mGluR依赖性去增强作用的机制,还预测了关于内质网钙库在去增强作用诱导和已建立记忆消除中的作用的进一步实验。