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2017 Fiscal Year Final Research Report

The role of colony-stimulating factors on microglial proliferation and neuropathic pain in rats

Research Project

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Project/Area Number 16K19220
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Pain science
Research InstitutionHyogo Medical University

Principal Investigator

Okubo Masamichi  兵庫医科大学, 医学部, 助教 (70581495)

Project Period (FY) 2016-04-01 – 2018-03-31
Keywords神経障害性疼痛 / 末梢神経 / 損傷 / マイクログリア / 増殖 / コロニー刺激因子 / 脊髄
Outline of Final Research Achievements

We examined the expression of mRNAs for macrophage-CSF (M-CSF), granulocyte macrophage-CSF (GM-CSF), granulocyte-CSF (G-CSF) and IL-34 in the dorsal root ganglion (DRG) and spinal cord after peripheral nerve injury in rats. RT-PCR and ISHH revealed that M-CSF and IL-34, but not GM- or G-CSF, mRNAs were constitutively expressed in the DRG, and M-CSF robustly increased in injured-DRG neurons. M-CSF receptor mRNA was expressed in naive rats and increased in spinal microglia following peripehral nerve injury. Intrathecal injection of M-CSF receptor inhibitor partially but significantly reversed the proliferation of spinal microglia and mechanical allodynia induced by peripheral nerve injury. Furthermore, intrathecal injection of recombinant M-CSF induced microglial proliferation and mechanical allodynia.

Free Research Field

神経解剖学

URL: 

Published: 2019-03-29  

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