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Temporal Plasticity Involved in Recovery from Manual Dexterity Deficit after Motor Cortex Lesion in Macaque Monkeys

Yumi Murata, Noriyuki Higo, Takuya Hayashi, Yukio Nishimura, Yoko Sugiyama, Takao Oishi, Hideo Tsukada, Tadashi Isa and Hirotaka Onoe
Journal of Neuroscience 7 January 2015, 35 (1) 84-95; https://doi.org/10.1523/JNEUROSCI.1737-14.2015
Yumi Murata
1Human Technology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 3058568, Japan,
2Research Fellow of the Japan Society for the Promotion of Science, Chiyoda-ku, Tokyo, 1020083, Japan,
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Noriyuki Higo
1Human Technology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 3058568, Japan,
3Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Kawaguchi, Saitama, 3320012, Japan,
4Precursory Research for Embryonic Science and Technology, Japan Science and Technology Agency, Kawaguchi, Saitama, 3320012, Japan,
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Takuya Hayashi
5Division of Bio-Function Dynamics Imaging, Center for Life Science Technologies, RIKEN, Kobe, Hyogo, 6500047, Japan,
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Yukio Nishimura
4Precursory Research for Embryonic Science and Technology, Japan Science and Technology Agency, Kawaguchi, Saitama, 3320012, Japan,
6Department of Developmental Physiology, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Aichi, 4448585, Japan,
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Yoko Sugiyama
1Human Technology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 3058568, Japan,
7Graduate School of Comprehensive Human Science, University of Tsukuba, Tsukuba, Ibaraki, 3058577, Japan,
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Takao Oishi
1Human Technology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki 3058568, Japan,
3Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Kawaguchi, Saitama, 3320012, Japan,
8Department of Cellular and Molecular Biology, Primate Research Institute, Kyoto University, Inuyama, Aichi, 4848506, Japan, and
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Hideo Tsukada
3Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Kawaguchi, Saitama, 3320012, Japan,
9Central Research Laboratory, Hamamatsu Photonics K.K., Hamamatsu, Shizuoka, 4348601, Japan
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Tadashi Isa
3Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Kawaguchi, Saitama, 3320012, Japan,
6Department of Developmental Physiology, National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Aichi, 4448585, Japan,
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Hirotaka Onoe
3Core Research for Evolutional Science and Technology, Japan Science and Technology Agency, Kawaguchi, Saitama, 3320012, Japan,
5Division of Bio-Function Dynamics Imaging, Center for Life Science Technologies, RIKEN, Kobe, Hyogo, 6500047, Japan,
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Abstract

The question of how intensive motor training restores motor function after brain damage or stroke remains unresolved. Here we show that the ipsilesional ventral premotor cortex (PMv) and perilesional primary motor cortex (M1) of rhesus macaque monkeys are involved in the recovery of manual dexterity after a lesion of M1. A focal lesion of the hand digit area in M1 was made by means of ibotenic acid injection. This lesion initially caused flaccid paralysis in the contralateral hand but was followed by functional recovery of hand movements, including precision grip, during the course of daily postlesion motor training. Brain imaging of regional cerebral blood flow by means of H215O-positron emission tomography revealed enhanced activity of the PMv during the early postrecovery period and increased functional connectivity within M1 during the late postrecovery period. The causal role of these areas in motor recovery was confirmed by means of pharmacological inactivation by muscimol during the different recovery periods. These findings indicate that, in both the remaining primary motor and premotor cortical areas, time-dependent plastic changes in neural activity and connectivity are involved in functional recovery from the motor deficit caused by the M1 lesion. Therefore, it is likely that the PMv, an area distant from the core of the lesion, plays an important role during the early postrecovery period, whereas the perilesional M1 contributes to functional recovery especially during the late postrecovery period.

  • brain activation
  • functional compensation
  • macaque monkey
  • precision grip
  • primate

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The Journal of Neuroscience: 35 (1)
Journal of Neuroscience
Vol. 35, Issue 1
7 Jan 2015
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Temporal Plasticity Involved in Recovery from Manual Dexterity Deficit after Motor Cortex Lesion in Macaque Monkeys
Yumi Murata, Noriyuki Higo, Takuya Hayashi, Yukio Nishimura, Yoko Sugiyama, Takao Oishi, Hideo Tsukada, Tadashi Isa, Hirotaka Onoe
Journal of Neuroscience 7 January 2015, 35 (1) 84-95; DOI: 10.1523/JNEUROSCI.1737-14.2015

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Temporal Plasticity Involved in Recovery from Manual Dexterity Deficit after Motor Cortex Lesion in Macaque Monkeys
Yumi Murata, Noriyuki Higo, Takuya Hayashi, Yukio Nishimura, Yoko Sugiyama, Takao Oishi, Hideo Tsukada, Tadashi Isa, Hirotaka Onoe
Journal of Neuroscience 7 January 2015, 35 (1) 84-95; DOI: 10.1523/JNEUROSCI.1737-14.2015
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Keywords

  • brain activation
  • functional compensation
  • macaque monkey
  • precision grip
  • primate

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