Calcium and Spike Timing-Dependent Plasticity

被引:19
|
作者
Inglebert, Yanis [1 ,2 ]
Debanne, Dominique [1 ]
机构
[1] Aix Marseille Univ, INSERM, UNIS, UMR1072, Marseille, France
[2] McGill Univ, Dept Pharmacol & Therapeut & Cell Informat Syst, Montreal, PQ, Canada
关键词
synaptic plasticity; synapse; STDP; hippocampus; learning; memory; calcium; LONG-TERM DEPRESSION; PRESYNAPTIC NEURONAL EXCITABILITY; PROPAGATING ACTION-POTENTIALS; SYNAPTIC PLASTICITY; NMDA RECEPTORS; DOPAMINE-RECEPTORS; CA2+ TRANSIENTS; PYRAMIDAL CELLS; RAT; HIPPOCAMPUS;
D O I
10.3389/fncel.2021.727336
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Since its discovery, spike timing-dependent synaptic plasticity (STDP) has been thought to be a primary mechanism underlying the brain's ability to learn and to form new memories. However, despite the enormous interest in both the experimental and theoretical neuroscience communities in activity-dependent plasticity, it is still unclear whether plasticity rules inferred from in vitro experiments apply to in vivo conditions. Among the multiple reasons why plasticity rules in vivo might differ significantly from in vitro studies is that extracellular calcium concentration use in most studies is higher than concentrations estimated in vivo. STDP, like many forms of long-term synaptic plasticity, strongly depends on intracellular calcium influx for its induction. Here, we discuss the importance of considering physiological levels of extracellular calcium concentration to study functional plasticity.</p>
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页数:9
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