Literature DB >> 26013316

Changes in cortical N-methyl-D-aspartate receptors and post-synaptic density protein 95 in schizophrenia, mood disorders and suicide.

Brian Dean1, Andrew S Gibbons2, Simone Boer3, Akihito Uezato4, James Meador-Woodruff5, Elizabeth Scarr2, Robert E McCullumsmith6.   

Abstract

OBJECTIVES: In humans, depending on dose, blocking the N-methyl-D-aspartate receptor (NMDAR) with ketamine can cause psychomimetic or antidepressant effects. The overall outcome for drugs such as ketamine depends on dose and the number of its available binding sites in the central nervous system, and to understand something of the latter variable we measure NMDAR in the frontal pole, dorsolateral prefrontal, anterior cingulate and parietal cortices from people with schizophrenia, bipolar disorder, major depressive disorders and age/sex matched controls.
METHOD: We measured levels of NMDARs (using [(3)H]MK-801 binding) and NMDAR sub-unit mRNAs (GRINs: using in situ hybridisation) as well as post-synaptic density protein 95 (anterior cingulate cortex only; not major depressive disorders: an NMDAR post-synaptic associated protein) in bipolar disorder, schizophrenia and controls.
RESULTS: Compared to controls, levels of NMDAR were lower in the outer laminae of the dorsolateral prefrontal cortex (-17%, p = 0.01) in people with schizophrenia. In bipolar disorder, levels of NMDAR binding (laminae IV-VI; -19%, p < 0.01) and GRIN2C mRNA (laminae I-VI; -27%, p < 0.05) were lower in the anterior cingulate cortex and NMDAR binding was lower in the outer lamina IV of the dorsolateral prefrontal cortex (-19%, p < 0.01). In major depressive disorders, levels of GRIN2D mRNA were higher in frontal pole (+22%, p < 0.05). In suicide completers, levels of GRIN2B mRNA were higher in parietal cortex (+20%, p < 0.01) but lower (-35%, p = 0.02) in dorsolateral prefrontal cortex while post-synaptic density protein 95 was higher (+26%, p < 0.05) in anterior cingulate cortex.
CONCLUSION: These data suggest that differences in cortical NMDAR expression and post-synaptic density protein 95 are present in psychiatric disorders and suicide completion and may contribute to different responses to ketamine. © The Royal Australian and New Zealand College of Psychiatrists 2015.

Entities:  

Keywords:  NMDA; Schizophrenia; bipolar disorders; cortex; major depressive disorders

Mesh:

Substances:

Year:  2015        PMID: 26013316     DOI: 10.1177/0004867415586601

Source DB:  PubMed          Journal:  Aust N Z J Psychiatry        ISSN: 0004-8674            Impact factor:   5.744


  18 in total

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3.  Postsynaptic Density-95 Isoform Abnormalities in Schizophrenia.

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4.  Differential genetic associations and expression of PAPST1/SLC35B2 in bipolar disorder and schizophrenia.

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Journal:  J Neural Transm (Vienna)       Date:  2022-05-02       Impact factor: 3.850

5.  Alterations in brain synaptic proteins and mRNAs in mood disorders: a systematic review and meta-analysis of postmortem brain studies.

Authors:  Edison Leung; Ethan W Lau; Andi Liang; Constanza de Dios; Robert Suchting; Linda Östlundh; Joseph C Masdeu; Masahiro Fujita; Marsal Sanches; Jair C Soares; Sudhakar Selvaraj
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7.  Suicidality is a common and serious feature of anti-N-methyl-D-aspartate receptor encephalitis.

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Review 10.  Therapeutic Potential of Selectively Targeting the α2C-Adrenoceptor in Cognition, Depression, and Schizophrenia-New Developments and Future Perspective.

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Journal:  Front Psychiatry       Date:  2017-08-14       Impact factor: 4.157

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