Long-Term Enhancement of NMDA Receptor Function in Inhibitory Neurons Preferentially Modulates Potassium Channels and Cell Adhesion Molecules
Affiliation
Department of Physiology, University of ArizonaIssue Date
2022Keywords
cell adhesion moleculeselectrophysiological recording
NMDAR-positive allosteric modulator
potassium channels
RNA-seq
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Frontiers Media S.A.Citation
Xia, D., Zhang, X., Deng, D., Ma, X., Masri, S., Wang, J., Bao, S., Hu, S., & Zhou, Q. (2022). Long-Term Enhancement of NMDA Receptor Function in Inhibitory Neurons Preferentially Modulates Potassium Channels and Cell Adhesion Molecules. Frontiers in Pharmacology.Journal
Frontiers in PharmacologyRights
Copyright © 2022 Xia, Zhang, Deng, Ma, Masri, Wang, Bao, Hu and Zhou. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Effectively enhancing the activity of inhibitory neurons has great therapeutic potentials since their reduced function/activity has significant contributions to pathology in various brain diseases. We showed previously that NMDAR positive allosteric modulator GNE-8324 and M-8324 selectively increase NMDAR activity on the inhibitory neurons and elevates their activity in vitro and in vivo. Here we examined the impact of long-term administering M-8324 on the functions and transcriptional profiling of parvalbumin-containing neurons in two representative brain regions, primary auditory cortex (Au1) and prelimbic prefrontal cortex (PrL-PFC). We found small changes in key electrophysiological parameters and RNA levels of neurotransmitter receptors, Na+ and Ca2+ channels. In contrast, large differences in cell adhesion molecules and K+ channels were found between Au1 and PrL-PFC in drug-naïve mice, and differences in cell adhesion molecules became much smaller after M-8324 treatment. There was also minor impact of M-8324 on cell cycle and apoptosis, suggesting a fine safety profile. Copyright © 2022 Xia, Zhang, Deng, Ma, Masri, Wang, Bao, Hu and Zhou.Note
Open access journalISSN
1663-9812Version
Final published versionae974a485f413a2113503eed53cd6c53
10.3389/fphar.2021.796179
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Except where otherwise noted, this item's license is described as Copyright © 2022 Xia, Zhang, Deng, Ma, Masri, Wang, Bao, Hu and Zhou. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).

