Updated on 2025/11/10

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写真a

 
Mitsuru Sato
 
Organization
Yokohama City University Hospital Neurosurgery Assistant Professor
Title
Assistant Professor
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Degree

  • 博士(医学) ( 2021.2   横浜市立大学 )

Research Areas

  • Life Science / Neurosurgery

Research History

  • Yokohama City University Hospital, Neurosurgery   Assistant Professor

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Research Projects

  • Edonerpic Maleate treatment for chronic compressive cervical spine disease

    Grant number:21K16614  2021.4 - 2024.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Early-Career Scientists

    SATO Mitsuru

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    Grant amount:\4550000 ( Direct Cost: \3500000 、 Indirect Cost:\1050000 )

    As an animal model, we used a 12-week-old Wistar rat cervical spinal cord chronic compression model in which a water-absorbing and swelling material was introduced into the spinal canal. The drug was T817-MA, a neurotrophic factor-like compound. A rotarod was used for rehabilitation. The model was divided into four groups: T817-MA administration and rehabilitation group, T817-MA administration and no rehabilitation group, distilled water administration and rehabilitation group, and distilled water administration and no rehabilitation group. Two types of kinematic analysis were performed: a rotarod walking test and a ladder walking test, and both showed a significant improvement in walking condition in the rehabilitation group treated with T817-MA compared to other groups.

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  • Novel treatment for cervical spinal cord injury: Efficacy of Edonerpic Maleate

    Grant number:18K16593  2018.4 - 2021.3

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Early-Career Scientists

    SATO Mitsuru

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    Grant amount:\4160000 ( Direct Cost: \3200000 、 Indirect Cost:\960000 )

    A comparative study of recovery between the T-817MA-treated group and the non-treated group using a 12-week-old Long-Evans rat frozen coagulation spinal cord injury model showed excellent recovery results in the T-817MA-treated group. Due to the difference in the composition of spinal motor neurons between rats and primates, we started experiments in primates with the aim of early clinical application. A spinal cord half-cut injury model was created in Japanese macaques, and a functional recovery experiment was attempted in the same manner as in rats. It was confirmed that there was a difference in functional recovery between the T-817-administered individuals and the non-administered individuals.

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