Contribution of Monovalent (Na+ and K+) and Divalent (Ca2+) Ions to the Mechanisms of Synaptic Plasticity

被引:0
|
作者
Smolyaninova, L., V [1 ]
Shiyan, A. A. [1 ]
Maksimov, G., V [1 ]
Orlov, S. N. [1 ]
机构
[1] Moscow Lomonosov State Univ, Fac Biol, Moscow 119992, Russia
基金
俄罗斯基础研究基金会;
关键词
sodium; potassium; calcium; synaptic plasticity; long-term potentiation and depression; gene expression; LONG-TERM POTENTIATION; INOSITOL TRISPHOSPHATE RECEPTORS; ACTIVATED POTASSIUM CHANNELS; C-FOS EXPRESSION; PROTEIN-KINASE-C; NMDA RECEPTOR; PLASMA-MEMBRANE; CALCIUM-CHANNEL; CEREBELLAR PURKINJE; RYANODINE RECEPTOR;
D O I
10.1134/S1990747820050062
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The review presents the mechanisms of participation of ions (Na+, K+, and Ca2+) in the processes of synaptic plasticity in the postsynaptic neuron during long-term potentiation and long-term depression. It is assumed that the main participants are AMPA and NMDA receptors, voltage-dependent Na+, K+, Ca2+ channels, Ca2+ and Na+-activated K+ channels, ATP-sensitive K+ channels, and Ca2+ channels of the endoplasmic reticulum. The review provides their molecular characteristics and discusses their role in long-term potentiation and long-term depression. The significance of changes in the intracellular ratio [Na+](i)/[K+](i) and Ca2+-dependent mechanism are considered for the first time from the signal formation to the level of gene expression. We believe that additional research is needed to identify a subset of neuronal genes whose differential expression contributes to synaptic plasticity, which is implemented with the participation of [Na+](i)/[K+](i)-sensitive Ca2+-independent "excitation-transcription coupling" mechanism.
引用
收藏
页码:1 / 20
页数:20
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