Brain Activity Associated with the Illusion of Motion Evoked by Different Vibration Stimulation Devices: An fNIRS Study

Ryota Imai, Kazuki Hayashida, Hideki Nakano, Shu Morioka, Ryota Imai, Kazuki Hayashida, Hideki Nakano, Shu Morioka

Abstract

[Purpose] A number of different stimulation devices are used in basic and clinical research studies, and their frequencies of use vary. However, whether or not they are equally effective has not been investigated. The purpose of the present study was to investigate neural activity in the brain during the illusion of motion evoked by stimulating the tendons of the wrist extensor muscles using various vibration devices. [Subjects] Twelve right-handed university students with no history of nervous system disorder or orthopedic disease participated in the study. [Methods] The wrist extensor tendon was stimulated using 3 different devices: 1) a vibration stimulation device (SL-0105 LP; Asahi Seisakusho Co., Ltd., Saitama, Japan), frequency 80 Hz; 2) a handy massager (YCM-20; Yamazen Corporation, Osaka, Japan), frequency 70 Hz; and 3) a handy massager (Thrive MD-01; Thrive Co., Ltd., Osaka, Japan), frequency 91.7 Hz. Brain activity was recorded during stimulation by using functional near-infrared spectroscopy. [Results] Increased neural activity was observed in both the premotor cortices and the parietal region in both hemispheres in all 3 cases. The level and localization of neural activity was comparable for all 3 stimulation devices used. [Conclusion] This suggests that subjects experience the illusion of motion while the tendon is being stimulated using any vibration device.

Keywords: Illusion of motion; Tendon vibration; fNIRS.

Figures

Fig. 1.
Fig. 1.
Measurements using functional near-infrared spectroscopy. We employed a 49-channel system, with 30 optodes. Fifteen light sources (red numbers) and 15 detectors (blue numbers) covered the frontoparietal area. Solid white numbers denote measuring channels, which were divided into 8 regions of interest.

References

    1. Naito E: Sensing limb movements in the motor cortex: how humans sense limb movement. Neuroscientist, 2004, 10: 73–82
    1. Goodwin GM, McCloskey DI, Matthews PB: The contribution of muscle afferents to kinaesthesia shown by vibration induced illusions of movement and by the effects of paralysing joint afferents. Brain, 1972, 95: 705–748
    1. Roll JP, Vedel JP: Kinaesthetic role of muscle afferents in man, studied by tendon vibration and microneurography. Exp Brain Res, 1982, 47: 177–190
    1. Naito E, Ehrsson HH: Kinesthetic illusion of wrist movement activates motor-related areas. Neuroreport, 2001, 12: 3805–3809
    1. Naito E, Ehrsson HH, Geyer S, et al. : Illusory arm movements activate cortical motor areas: a positron emission tomography study. J Neurosci, 1999, 19: 6134–6144
    1. Casini L, Romaiguère P, Ducorps A, et al. : Cortical correlates of illusory hand movement perception in humans: a MEG study. Brain Res, 2006, 1121: 200–206
    1. Keinrath C, Wriessnegger S, Müller-Putz GR, et al. : Post-movement beta synchronization after kinesthetic illusion, active and passive movements. Int J Psychophysiol, 2006, 62: 321–327
    1. Naito E, Kochiyama T, Kitada R, et al. : Internally simulated movement sensations during motor imagery activate cortical motor areas and the cerebellum. J Neurosci, 2002, 22: 3683–3691
    1. Gay A, Parratte S, Salazard B, et al. : Proprioceptive feedback enhancement induced by vibratory stimulation in complex regional pain syndrome type I: an open comparative pilot study in 11 patients. Joint Bone Spine, 2007, 74: 461–466
    1. Goble DJ, Coxon JP, Van Impe A, et al. : Brain activity during ankle proprioceptive stimulation predicts balance performance in young and older adults. J Neurosci, 2011, 31: 16344–16352
    1. Roll R, Kavounoudias A, Albert F, et al. : Illusory movements prevent cortical disruption caused by immobilization. Neuroimage, 2012, 62: 510–519
    1. Hagura N, Oouchida Y, Aramaki Y, et al. : Visuokinesthetic perception of hand movement is mediated by cerebro-cerebellar interaction between the left cerebellum and right parietal cortex. Cereb Cortex, 2009, 19: 176–186
    1. Jasdzewski G, Strangman G, Wagner J, et al. : Differences in the hemodynamic response to event-related motor and visual paradigms as measured by near-infrared spectroscopy. Neuroimage, 2003, 20: 479–488
    1. Miyai I, Tanabe HC, Sase I, et al. : Cortical mapping of gait in humans: a near-infrared spectroscopic topography study. Neuroimage, 2001, 14: 1186–1192
    1. Hoshi Y, Kobayashi N, Tamura M: Interpretation of near-infrared spectroscopy signals: a study with a newly developed perfused rat brain model. J Appl Physiol 1985, 2001, 90: 1657–1662
    1. Schroeter ML, Zysset S, Kruggel F, et al. : Age dependency of the hemodynamic response as measured by functional near-infrared spectroscopy. Neuroimage, 2003, 19: 555–564
    1. Strangman G, Franceschini MA, Boas DA: Factors affecting the accuracy of near-infrared spectroscopy concentration calculations for focal changes in oxygenation parameters. Neuroimage, 2003, 18: 865–879
    1. D’Esposito M, Deouell LY, Gazzaley A: Alterations in the BOLD fMRI signal with ageing and disease: a challenge for neuroimaging. Nat Rev Neurosci, 2003, 4: 863–872
    1. Hesselmann V, Zaro Weber O, Wedekind C, et al. : Age related signal decrease in functional magnetic resonance imaging during motor stimulation in humans. Neurosci Lett, 2001, 308: 141–144
    1. Riecker A, Grodd W, Klose U, et al. : Relation between regional functional MRI activation and vascular reactivity to carbon dioxide during normal aging. J Cereb Blood Flow Metab, 2003, 23: 565–573
    1. Winer BJ: Statistical principles in experimental design. New York: Mc Graw-Hill. 1991
    1. Naito E, Roland PE, Ehrsson HH: I feel my hand moving: a new role of the primary motor cortex in somatic perception of limb movement. Neuron, 2002, 36: 979–988
    1. Naito E, Ehrsson HH: Somatic sensation of hand-object interactive movement is associated with activity in the left inferior parietal cortex. J Neurosci, 2006, 26: 3783–3790
    1. Naito E, Scheperjans F, Eickhoff SB, et al. : Human superior parietal lobule is involved in somatic perception of bimanual interaction with an external object. J Neurophysiol, 2008, 99: 695–703
    1. Roll JP, Albert F, Thyrion C, et al. : Inducing any virtual two-dimensional movement in humans by applying muscle tendon vibration. J Neurophysiol, 2009, 101: 816–823
    1. Thyrion C, Roll JP: Perceptual integration of illusory and imagined kinesthetic images. J Neurosci, 2009, 29: 8483–8492
    1. Kito T, Hashimoto T, Yoneda T, et al. : Sensory processing during kinesthetic aftereffect following illusory hand movement elicited by tendon vibration. Brain Res, 2006, 1114: 75–84
    1. Sharma N, Baron JC, Rowe JB: Motor imagery after stroke: relating outcome to motor network connectivity. Ann Neurol, 2009, 66: 604–616

Source: PubMed

3
S'abonner