Neuromagnetic activation following active and passive finger movements

被引:43
|
作者
Onishi, Hideaki [1 ]
Sugawara, Kazuhiro [1 ]
Yamashiro, Koya [1 ]
Sato, Daisuke [1 ]
Suzuki, Makoto [1 ]
Kirimoto, Hikari [1 ]
Tamaki, Hiroyuki [1 ]
Murakami, Hiroatsu [2 ]
Kameyama, Shigeki [2 ]
机构
[1] Niigata Univ Hlth & Welf, Inst Human Movement & Med Sci, Kita Ku, Niigata 9503198, Japan
[2] Nishi Niigata Chuo Natl Hosp, Dept Neurosurg, Niigata, Japan
来源
BRAIN AND BEHAVIOR | 2013年 / 3卷 / 02期
基金
日本学术振兴会;
关键词
Magnetoencephalography; MEF1; MEG; MRCF; PPC; S2; SEF; SMA; EVOKED MAGNETIC-FIELDS; SUPPLEMENTARY MOTOR AREA; SECONDARY SOMATOSENSORY CORTEX; SPATIOTEMPORAL SOURCE ANALYSIS; LATENCY PERIPHERAL INPUTS; POSTERIOR PARIETAL CORTEX; MEDIAN NERVE-STIMULATION; SPACE SEPARATION METHOD; CORTICAL ACTIVATION; VOLUNTARY MOVEMENT;
D O I
10.1002/brb3.126
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The detailed time courses of cortical activities and source localizations following passive finger movement were studied using whole-head magnetoencephalography (MEG). We recorded motor-related cortical magnetic fields following voluntary movement and somatosensory-evoked magnetic fields following passive movement (PM) in 13 volunteers. The most prominent movement-evoked magnetic field (MEF1) following active movement was obtained approximately 35.3 +/- 8.4 msec after movement onset, and the equivalent current dipole (ECD) was estimated to be in the primary motor cortex (Brodmann area 4). Two peaks of MEG response associated with PM were recorded from 30 to 100 msec after movement onset. The earliest component (PM1) peaked at 36.2 +/- 8.2 msec, and the second component (PM2) peaked at 86.1 +/- 12.1 msec after movement onset. The peak latency and ECD localization of PM1, estimated to be in area 4, were the same as those of the most prominent MEF following active movement. ECDs of PM2 were estimated to be not only in area 4 but also in the supplementary motor area (SMA) and the posterior parietal cortex (PPC) over the hemisphere contralateral to the movement, and in the secondary somatosensory cortex (S2) of both hemispheres. The peak latency of each source activity was obtained at 54-109 msec in SMA, 64-114 msec in PPC, and 84-184 msec in the S2. Our results suggest that the magnetic waveforms at middle latency (50-100 msec) after PM are different from those after active movement and that these waveforms are generated by the activities of several cortical areas, that is, area 4 and SMA, PPC, and S2. In this study, the time courses of the activities in SMA, PPC, and S2 accompanying PM in humans were successfully recorded using MEG with a multiple dipole analysis system.
引用
收藏
页码:178 / 192
页数:15
相关论文
共 50 条
  • [41] The electroencephalographic β synchronization following extension and flexion finger movements in humans
    Stancak, A
    NEUROSCIENCE LETTERS, 2000, 284 (1-2) : 41 - 44
  • [42] Individual trial-to-trial variability of different components of neuromagnetic signals associated with self-paced finger movements
    Vvedensky, V. L.
    NEUROSCIENCE LETTERS, 2014, 569 : 94 - 98
  • [43] Functional overlap of cortical finger representation: A neuromagnetic study
    Biermann, K
    Schmitz, F
    Konezak, J
    Witte, OW
    Freund, HJ
    Schnitzler, A
    EUROPEAN JOURNAL OF NEUROSCIENCE, 1998, 10 : 137 - 137
  • [44] Study on corticospinal excitability during passive symmetry and asymmetry finger movements by TMS
    Graduate School of Maebashi Institute of Technology, 460-1, Kamisadori-machi, Maebashi, Gunma
    371-0816, Japan
    不详
    372-0006, Japan
    不详
    371-0816, Japan
    IEEJ Trans. Electron. Inf. Syst., 12 (1791-1796):
  • [45] MEG-compatible pneumatic stimulator to elicit passive finger and toe movements
    Piitulainen, Harri
    Bourguignon, Mathieu
    Hari, Riitta
    Jousmaki, Veikko
    NEUROIMAGE, 2015, 112 : 310 - 317
  • [46] Development of a Passive Prosthetic Hand That Restores Finger Movements Made by Additive Manufacturing
    da Silveira Romero, Rodrigo Cezar
    Machado, Andre Argueso
    Costa, Kliftom Amorim
    Rodrigues Guilherme Reis, Paulo Henrique
    Brito, Pedro Paiva
    Santos Vimieiro, Claysson Bruno
    APPLIED SCIENCES-BASEL, 2020, 10 (12):
  • [47] Detecting and correcting for head movements in neuromagnetic measurements
    Uutela, K
    Taulu, S
    Hämäläinen, M
    NEUROIMAGE, 2001, 14 (06) : 1424 - 1431
  • [48] Somatosensory evoked magnetic fields following passive finger movement
    Xiang, J
    Hoshiyama, M
    Koyama, S
    Kaneoke, Y
    Suzuki, H
    Watanabe, S
    Naka, D
    Kakigi, R
    BRAIN TOPOGRAPHY TODAY, 1997, 1147 : 92 - 96
  • [49] Deciphering brain activation during wrist movements: comparative fMRI and fNIRS analysis of active, passive, and imagery states
    Jalalvandi, Maziar
    Sharini, Hamid
    Shafaghi, Lida
    Alam, Nader Riyahi
    EXPERIMENTAL BRAIN RESEARCH, 2025, 243 (01)
  • [50] A Reliability Study on Brain Activation During Active and Passive Arm Movements Supported by an MRI-Compatible Robot
    Natalia Estévez
    Ningbo Yu
    Mike Brügger
    Michael Villiger
    Marie-Claude Hepp-Reymond
    Robert Riener
    Spyros Kollias
    Brain Topography, 2014, 27 : 731 - 746