Logo image
Dizocilpine (MK-801) induces distinct changes of N-methyl-D-aspartic acid receptor subunits in parvalbumin-containing interneurons in young adult rat prefrontal cortex
Journal article   Open access   Peer reviewed

Dizocilpine (MK-801) induces distinct changes of N-methyl-D-aspartic acid receptor subunits in parvalbumin-containing interneurons in young adult rat prefrontal cortex

Dong Xi, Wentong Zhang, Huai-Xing Wang, George G Stradtman and Wen-Jun Gao
The international journal of neuropsychopharmacology, v 12(10), pp 1395-1408
Nov 2009
PMID: 19435549
url
https://doi.org/10.1017/S146114570900042XView
Published, Version of Record (VoR) Open

Abstract

Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors Age Factors Interneurons - drug effects Parvalbumins - metabolism Rats Protein Subunits - biosynthesis Down-Regulation - drug effects Rats, Sprague-Dawley Down-Regulation - genetics Receptors, N-Methyl-D-Aspartate - genetics RNA, Messenger - biosynthesis Animals Interneurons - chemistry Interneurons - metabolism Parvalbumins - analysis Prefrontal Cortex - drug effects RNA, Messenger - antagonists & inhibitors Prefrontal Cortex - metabolism Receptors, N-Methyl-D-Aspartate - biosynthesis Female Prefrontal Cortex - chemistry Protein Subunits - antagonists & inhibitors Dizocilpine Maleate - pharmacology Protein Subunits - genetics
N-methyl-D-aspartic acid receptor (NMDAR) hypofunction has long been implicated in schizophrenia and NMDARs on gamma-aminobutyric acid (GABA)ergic interneurons are proposed to play an essential role in the pathogenesis. However, controversial results have been reported regarding the regulation of NMDAR expression, and direct evidence of how NMDAR antagonists act on specific subpopulations of prefrontal interneurons is missing. We investigated the effects of the NMDAR antagonist dizocilpine (MK-801) on the expression of NMDAR subtypes in the identified interneurons in young adult rat prefrontal cortex (PFC) by using laser microdissection and real-time polymerase chain reaction, combined with Western blotting and immunofluorescent staining. We found that MK-801 induced distinct changes of NMDAR subunits in the parvalbumin-immunoreactive (PV-ir) interneurons vs. pyramidal neurons in the PFC circuitry. The messenger RNA (mRNA) expression of all NMDAR subtypes, including NR1 and NR2A to 2D, exhibited inverted-U dose-dependent changes in response to MK-801 treatment in the PFC. In contrast, subunit mRNAs of NMDARs in PV-ir interneurons were significantly down-regulated at low doses, unaltered at medium doses, and significantly decreased again at high doses, suggesting a biphasic dose response to MK-801. The differential effects of MK-801 in mRNA expression of NMDAR subunits were consistent with the protein expression of NR2A and NR2B subunits revealed with Western blotting and double immunofluorescent staining. These results suggest that PV-containing interneurons in the PFC exhibit a distinct responsiveness to NMDAR antagonism and that NMDA antagonist can differentially and dose-dependently regulate the functions of pyramidal neurons and GABAergic interneurons in the prefrontal cortical circuitry.

Metrics

11 Record Views
70 citations in Scopus

Details

UN Sustainable Development Goals (SDGs)

This publication has contributed to the advancement of the following goals:

#3 Good Health and Well-Being

InCites Highlights

Data related to this publication, from InCites Benchmarking & Analytics tool:

Collaboration types
Domestic collaboration
International collaboration
Web of Science research areas
Clinical Neurology
Neurosciences
Pharmacology & Pharmacy
Psychiatry
Logo image