Relation of Brain Stimulation Induced Changes in MEP Amplitude and BOLD Signal

被引:3
|
作者
Krivanekova, Lucia [1 ]
Baudrexel, Simon [1 ]
Bliem, Barbara [1 ]
Ziemann, Ulf [1 ]
机构
[1] Goethe Univ Frankfurt, Dept Neurol, D-60528 Frankfurt, Germany
关键词
Primary motor cortex; Primary somatosensory cortex; Transcranial magnetic stimulation; Paired associative stimulation; Cortical plasticity; MEP; FMRI; BOLD signal; TRANSCRANIAL MAGNETIC STIMULATION; HUMAN MOTOR CORTEX; PAIRED ASSOCIATIVE STIMULATION; PRIMARY SOMATOSENSORY CORTEX; THETA-BURST STIMULATION; CORTICAL PLASTICITY; CORTICOSPINAL EXCITABILITY; FMRI SIGNAL; MODULATION; ACTIVATION;
D O I
10.1016/j.brs.2012.06.004
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Non-invasive human brain stimulation can induce long-term plasticity reflected by changes in putative markers of synaptic activation, such as the motor evoked potential (MEP) amplitude elicited by transcranial magnetic stimulation or the task-dependent blood oxygenation level-dependent (BOLD) signal measured by functional magnetic resonance imaging. Objective: To study the relationship between brain stimulation induced changes in MEP amplitude and BOLD signal. Methods: Paired associative stimulation of the hand area of the left primary somatosensory cortex (S1-PAS) was applied in 15 healthy subjects to induce excitability change in the adjacent primary motor cortex (M1) [Krivanekova et al. 2011, Eur J Neurosci 34:1292-1300]. Before and after S1-PAS, MEP amplitude in a right hand muscle, and the BOLD signal during a right hand motor or somatosensory activation task were measured. Results: S1-PAS resulted in substantial individual MEP and BOLD signal changes, but these changes did not correlate in M1 or S1. Conclusions: Findings indicate that MEP amplitude and BOLD signal within the tested M1 reflect physiologically distinct aspects of synaptic excitability change. Therefore, it is suggested that MEP amplitude and BOLD signal are complementary rather than interchangeable markers of synaptic excitability. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:330 / 339
页数:10
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