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2017 Fiscal Year Final Research Report

In vivo imagimg for macrophage subtypes associated with neuropathic pain.

Research Project

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Project/Area Number 15K11308
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Surgical dentistry
Research InstitutionHealth Sciences University of Hokkaido (2017)
Niigata University (2015-2016)

Principal Investigator

Terumitsu Makoto  北海道医療大学, 歯学部, 教授 (60401767)

Co-Investigator(Kenkyū-buntansha) 吉川 博之  新潟大学, 医歯学総合病院, 助教 (20547575)
瀬尾 憲司  新潟大学, 医歯学系, 教授 (40242440)
佐藤 由美子  新潟大学, 医歯学総合病院, 特任助教 (70709857)
倉田 行伸  新潟大学, 医歯学系, 助教 (20464018)
Co-Investigator(Renkei-kenkyūsha) KOMAKI Yuji  公益財団法人実験動物中央研究所, 実験動物研究部, 研究員 (10548499)
KURATA Shigenobu  新潟大学, 大学院医歯学総合研究科, 助教 (20464018)
YAMAZAKI Maiko  新潟大学, 医歯学総合病院, 医員 (40625422)
Project Period (FY) 2015-04-01 – 2018-03-31
Keywords三叉神経 / 神経障害性疼痛 / 神経炎症 / マクロファージ / USPIO / MRI
Outline of Final Research Achievements

Abnormal nerve regeneration after traumatic nerve injury is responsible for neuropathic pain. Pathological neuroinflammation is thought to persist in the disordered nerve. We hypothesized that some subtypes of macrophage are involved in this process, which exacerbates inflammation or enhances tissue regeneration. We established a rat model of neuropathic pain in the trigeminal nerve. A phagocytic macrophage ingests ultra-small iron particles administered systemically as a contrast agent. Thereafter, 7.0T MRI was used to observe the activation of the phagocytic macrophage in the chronic phase of nerve injury. The results suggest that a subtype of macrophage caused to enhance excessive tissue growth responsive to the inflammation, and was involved in pathological nerve regeneration.

Free Research Field

歯科麻酔

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Published: 2019-03-29  

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