Timing-dependent modulation of associative plasticity by general network excitability in the human motor cortex

被引:175
|
作者
Nitsche, Michael A. [1 ]
Roth, Amelie [1 ]
Kuo, Min-Fang [1 ]
Fischer, Anja K. [1 ]
Liebetanz, David [1 ]
Lang, Nicolas [1 ]
Tergau, Frithjof [1 ]
Paulus, Walter [1 ]
机构
[1] Univ Gottingen, Dept Clin Neurophysiol, D-37075 Gottingen, Germany
来源
JOURNAL OF NEUROSCIENCE | 2007年 / 27卷 / 14期
关键词
homeostatic plasticity; paired associative stimulation; tDCS; TMS; motor cortex; human; DIRECT-CURRENT STIMULATION; TRANSCRANIAL MAGNETIC STIMULATION; CORTICAL NEUROPLASTICITY; HOMEOSTATIC PLASTICITY; SYNAPTIC PLASTICITY; DC-STIMULATION; CONSOLIDATION; FACILITATION; MECHANISMS; INDUCTION;
D O I
10.1523/JNEUROSCI.5348-06.2007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Associative neuroplasticity, which encompasses the modification of synaptic strength by coactivation of two synaptic inputs, has been linked to learning processes. Because unlimited plasticity destabilizes neuronal networks, homeostatic rules were proposed and experimentally proven that control for the amount and direction of plasticity dependent on background network activity. Accordingly, low background activity would enhance facilitatory plasticity, whereas high background activity would inhibit it. However, the impact of background excitability on associative plasticity has not been studied so far in humans. Facilitatory associative plasticity was induced by paired associative stimulation (PAS) in the human motor cortex, whereas background activity was enhanced or diminished by transcranial direct current stimulation (tDCS). When applied before PAS, excitability-enhancing tDCS also boosted the efficacy of PAS, whereas excitability-diminishing tDCS turned it into inhibition. Thus, previous background activity does not influence associative plasticity homeostatically. When tDCS and PAS were applied simultaneously, now in accordance with homeostatic rules of neuroplasticity, reduced background activity resulted in a prolonged excitability enhancement by PAS, whereas enhanced background activity turned it into inhibition. We conclude that background network activity can influence associative plasticity homeostatically. However, only simultaneous modulation of both parameters is in accordance with homeostatic concepts. These findings might be of importance for the development of plasticity-inducing stimulation protocols supporting information processing in humans.
引用
收藏
页码:3807 / 3812
页数:6
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