The NMDAR modulator NYX-2925 alleviates neuropathic pain via a Src-dependent mechanism in the mPFC

Previous studies have shown that oral administration of the NMDAR modulator NYX-2925 alleviates pain in several animal models of neuropathic pain and this appears to be through mPFC, but not spinal, mediated mechanisms. While much is known about the impact of neuropathic pain on NMDAR-mediated signa...

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Main Authors: Gladys Morrison, Marina N. Asiedu, Jessica M. Priebe, Jacqueline Dunning, Nayereh Ghoreishi-Haack, Roger A. Kroes, M. Scott Bowers, Amanda L. Barth, Cassia N. Cearley, Joseph R. Moskal
Format: Article
Language:English
Published: Elsevier 2020-01-01
Series:Neurobiology of Pain
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2452073X19300145
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spelling doaj-135d2d36d9074a59aaae40a10aba95ab2020-11-25T03:12:25ZengElsevierNeurobiology of Pain2452-073X2020-01-017The NMDAR modulator NYX-2925 alleviates neuropathic pain via a Src-dependent mechanism in the mPFCGladys Morrison0Marina N. Asiedu1Jessica M. Priebe2Jacqueline Dunning3Nayereh Ghoreishi-Haack4Roger A. Kroes5M. Scott Bowers6Amanda L. Barth7Cassia N. Cearley8Joseph R. Moskal9Aptinyx Inc., Evanston, IL, United States; Corresponding author at: 1801 Maple Ave Suite 4301, Evanston, IL 60201, United States.Aptinyx Inc., Evanston, IL, United StatesAptinyx Inc., Evanston, IL, United StatesAptinyx Inc., Evanston, IL, United StatesAptinyx Inc., Evanston, IL, United StatesAptinyx Inc., Evanston, IL, United States; Falk Ctr. for Mol. Therapeutics, McCormick School of Engineering, Northwestern University, Evanston, IL, United StatesAptinyx Inc., Evanston, IL, United States; Falk Ctr. for Mol. Therapeutics, McCormick School of Engineering, Northwestern University, Evanston, IL, United StatesAptinyx Inc., Evanston, IL, United StatesAptinyx Inc., Evanston, IL, United StatesAptinyx Inc., Evanston, IL, United States; Falk Ctr. for Mol. Therapeutics, McCormick School of Engineering, Northwestern University, Evanston, IL, United StatesPrevious studies have shown that oral administration of the NMDAR modulator NYX-2925 alleviates pain in several animal models of neuropathic pain and this appears to be through mPFC, but not spinal, mediated mechanisms. While much is known about the impact of neuropathic pain on NMDAR-mediated signaling in the spinal cord, limited studies have focused on the brain. In the current study, we assess signaling changes associated with NMDAR-mediated plasticity in the mPFC and the impact of NYX-2925 administration on the normalization of these signaling changes. We found a decrease in activated Src levels in the mPFC of animals with chronic constriction injury (CCI) of the sciatic nerve. While Src mediated activation of NMDARs was also decreased in CCI animals, the main NMDAR phosphorylation site of CAMKII was not affected. This is in opposition to what has been found in the spinal cord, where both Src and CAMKII activation are increased. Oral administration of NYX-2925 restored levels of activated Src and Src phosphorylation sites on GluN2A and GluN2B in the mPFC, with no effect on activated CAMKII levels. The analgesic effect of NYX-2925 appears dependent on this restoration of Src activation in the mPFC, as co-administering Src activation inhibitors prevented the NYX-2925 analgesic effect. Overall, these data suggest that NMDAR-mediated signaling plays a key role in neuropathic pain, albeit in different directions in the spinal cord vs. the mPFC. Furthermore, the analgesic effect of NYX-2925 appears to involve a restoration of NMDAR-mediated signaling in the mPFC.http://www.sciencedirect.com/science/article/pii/S2452073X19300145Neuropathic painMedial prefrontal cortexNMDAR'sSrc kinaseChronic Constriction injury (CCI)
collection DOAJ
language English
format Article
sources DOAJ
author Gladys Morrison
Marina N. Asiedu
Jessica M. Priebe
Jacqueline Dunning
Nayereh Ghoreishi-Haack
Roger A. Kroes
M. Scott Bowers
Amanda L. Barth
Cassia N. Cearley
Joseph R. Moskal
spellingShingle Gladys Morrison
Marina N. Asiedu
Jessica M. Priebe
Jacqueline Dunning
Nayereh Ghoreishi-Haack
Roger A. Kroes
M. Scott Bowers
Amanda L. Barth
Cassia N. Cearley
Joseph R. Moskal
The NMDAR modulator NYX-2925 alleviates neuropathic pain via a Src-dependent mechanism in the mPFC
Neurobiology of Pain
Neuropathic pain
Medial prefrontal cortex
NMDAR's
Src kinase
Chronic Constriction injury (CCI)
author_facet Gladys Morrison
Marina N. Asiedu
Jessica M. Priebe
Jacqueline Dunning
Nayereh Ghoreishi-Haack
Roger A. Kroes
M. Scott Bowers
Amanda L. Barth
Cassia N. Cearley
Joseph R. Moskal
author_sort Gladys Morrison
title The NMDAR modulator NYX-2925 alleviates neuropathic pain via a Src-dependent mechanism in the mPFC
title_short The NMDAR modulator NYX-2925 alleviates neuropathic pain via a Src-dependent mechanism in the mPFC
title_full The NMDAR modulator NYX-2925 alleviates neuropathic pain via a Src-dependent mechanism in the mPFC
title_fullStr The NMDAR modulator NYX-2925 alleviates neuropathic pain via a Src-dependent mechanism in the mPFC
title_full_unstemmed The NMDAR modulator NYX-2925 alleviates neuropathic pain via a Src-dependent mechanism in the mPFC
title_sort nmdar modulator nyx-2925 alleviates neuropathic pain via a src-dependent mechanism in the mpfc
publisher Elsevier
series Neurobiology of Pain
issn 2452-073X
publishDate 2020-01-01
description Previous studies have shown that oral administration of the NMDAR modulator NYX-2925 alleviates pain in several animal models of neuropathic pain and this appears to be through mPFC, but not spinal, mediated mechanisms. While much is known about the impact of neuropathic pain on NMDAR-mediated signaling in the spinal cord, limited studies have focused on the brain. In the current study, we assess signaling changes associated with NMDAR-mediated plasticity in the mPFC and the impact of NYX-2925 administration on the normalization of these signaling changes. We found a decrease in activated Src levels in the mPFC of animals with chronic constriction injury (CCI) of the sciatic nerve. While Src mediated activation of NMDARs was also decreased in CCI animals, the main NMDAR phosphorylation site of CAMKII was not affected. This is in opposition to what has been found in the spinal cord, where both Src and CAMKII activation are increased. Oral administration of NYX-2925 restored levels of activated Src and Src phosphorylation sites on GluN2A and GluN2B in the mPFC, with no effect on activated CAMKII levels. The analgesic effect of NYX-2925 appears dependent on this restoration of Src activation in the mPFC, as co-administering Src activation inhibitors prevented the NYX-2925 analgesic effect. Overall, these data suggest that NMDAR-mediated signaling plays a key role in neuropathic pain, albeit in different directions in the spinal cord vs. the mPFC. Furthermore, the analgesic effect of NYX-2925 appears to involve a restoration of NMDAR-mediated signaling in the mPFC.
topic Neuropathic pain
Medial prefrontal cortex
NMDAR's
Src kinase
Chronic Constriction injury (CCI)
url http://www.sciencedirect.com/science/article/pii/S2452073X19300145
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