Literature DB >> 30553898

NMDA receptors of blood lymphocytes anticipate cognitive performance variations in healthy volunteers.

Mitra-Sadat Sadat-Shirazi1, Ghorbangol Ashabi2, Mohammadreza Bahrami Hessari3, Solmaz Khalifeh4, Nazanin Monfared Neirizi5, Maral Matloub5, Mohammad Safarzadeh5, Nasim Vousooghi1, Mohammad-Reza Zarrindast6.   

Abstract

Working memory (WM) system, temporarily stores information and uses this information for complex cognitive tasks. WM connects memory, emotional feelings and perception. Evidence compelling that N-methyl d-aspartate receptor (NMDAR) expression relatively affect WM performance in animal models. It has been suggested some peripheral blood lymphocyte's (PBL) receptors are similar with neuronal receptors in the brain, so we measured PBL's receptors changes as a marker of the neuronal receptor. In this study, we examined one hundred adult men with Wisconsin Card Sorting Test (WCST) as a tool for primary screening for executive function (EF) which include WM. Then, we selected fifty individuals with high and low WCST scores. With digit span and symmetry span tasks, we screened 20 samples for high WM group and 19 samples for low WM group. After separating PBL, we measured mRNA expression level changes in NMDAR subunits with Reverse transcription-polymerase chain reaction method. We demonstrated that GluN2D increased and GluN3A decreased in individuals with high WM compared with the low WM (P < .01 and P < .001, respectively). The expression levels of GluN2A, GluN2B, and GluN3B were not altered between two groups (P > .05). Modifying the PBL receptors could be future approaches to defend memory loss and concentrate the senses over WM-related processes in physiological and pathological statuses. We hypothesized that increasing in GluN2 subunits and decreasing in GluN3 subunits led to improving current via NMDAR and subsequently affect WM.
Copyright © 2018. Published by Elsevier Inc.

Entities:  

Keywords:  NMDA receptor; Peripheral marker; Psychological tests; Working memory

Mesh:

Substances:

Year:  2018        PMID: 30553898     DOI: 10.1016/j.physbeh.2018.12.015

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  2 in total

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Authors:  María J Conde-Dusman; Partha N Dey; Óscar Elía-Zudaire; Isabel Perez-Otaño; Luis G Rabaneda; Carmen García-Lira; Teddy Grand; Victor Briz; Eric R Velasco; Raül Andero; Sergio Niñerola; Angel Barco; Pierre Paoletti; John F Wesseling; Fabrizio Gardoni; Steven J Tavalin
Journal:  Elife       Date:  2021-11-17       Impact factor: 8.140

2.  Transcriptome-wide association study of post-trauma symptom trajectories identified GRIN3B as a potential biomarker for PTSD development.

Authors:  Adriana Lori; Katharina Schultebraucks; Isaac Galatzer-Levy; Nikolaos P Daskalakis; Seyma Katrinli; Alicia K Smith; Amanda J Myers; Ryan Richholt; Matthew Huentelman; Guia Guffanti; Stefan Wuchty; Felicia Gould; Philip D Harvey; Charles B Nemeroff; Tanja Jovanovic; Ekaterina S Gerasimov; Jessica L Maples-Keller; Jennifer S Stevens; Vasiliki Michopoulos; Barbara O Rothbaum; Aliza P Wingo; Kerry J Ressler
Journal:  Neuropsychopharmacology       Date:  2021-06-29       Impact factor: 8.294

  2 in total

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