Neuropathic pain inhibitor, RAP-103, is a potent inhibitor of microglial CCL1/CCR8-Reference-Cited by-同舟云学术

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Neuropathic pain inhibitor, RAP-103, is a potent inhibitor of microglial CCL1/CCR8

Published:2018-10 Issue: Volume:119 Page:184-189
ISSN:0197-0186
Container-title:Neurochemistry International
language:en
Short-container-title:Neurochemistry International

Author:

Noda Mami,Tomonaga Daichi,Kitazono Kota,Yoshioka Yusaku,Liu Jiadai,Rousseau Jean-Philippe,Kinkead Richard^ORCID,Ruff Michael R.,Pert Candace B.

Funder

Research Support Center, Graduate School of Medical Sciences, Kyushu University

Natural Sciences and Engineering Research Council (NSERC) of Canada

NSERC

Respiratory Health Network of the Fonds de Recherche en Santé du Québec

Publisher

Elsevier BV

Subject

Cell Biology,Cellular and Molecular Neuroscience

Reference50 articles.

1. Impaired neuropathic pain responses in mice lacking the chemokine receptor CCR2;Abbadie;Proc Natl Acad Sci U S A,2003

2. Inhibition of inflammatory and neuropathic pain by targeting a mu opioid receptor/chemokine Receptor5 heteromer (MOR-CCR5);Akgun;J. Med. Chem.,2015

3. CCL-1 in the spinal cord contributes to neuropathic pain induced by nerve injury;Akimoto;Cell Death Dis.,2013

4. M- and T-tropic HIVs promote apoptosis in rat neurons;Bachis;J. Neuroimmune Pharmacol.,2009

5. Functional inhibition of chemokine receptor CCR2 by dicer-substrate-siRNA prevents pain development;Begin-Lavallee;Mol. Pain,2016

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