The Role of Glutamate Neurotransmission in Mismatch Negativity (MMN), A Measure of Auditory Synaptic Plasticity and Change-detection

被引:24
作者
Harms, Lauren [1 ,2 ,3 ]
Parras, Gloria G. [4 ,5 ]
Michie, Patricia T. [2 ,3 ,6 ]
Malmierca, Manuel S. [4 ,5 ,7 ]
机构
[1] Univ Newcastle, Sch Biomed Sci & Pharm, Callaghan, NSW, Australia
[2] Univ Newcastle, Hunter Med Res Inst, Callaghan, NSW, Australia
[3] Univ Newcastle, Ctr Brain & Mental Hlth Res, Callaghan, NSW, Australia
[4] Inst Neurosci Leon INCYL, Cognit & Auditory Neurosci Lab, Salamanca, Spain
[5] Salamanca Inst Biomed Res IBSAL, Salamanca, NSW, Spain
[6] Univ Newcastle, Sch Psychol, Callaghan, NSW, Australia
[7] Univ Salamanca, Fac Med, Dept Cell Biol & Pathol, Salamanca, Spain
关键词
mismatch negativity; predictive coding; NMDA receptor; GABA; neuromodulation; animal model;
D O I
10.1016/j.neuroscience.2020.01.046
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mismatch negativity (MMN) is an electrophysiological signature that occurs in response to unexpected stimuli. It is often referred to as a measure of memory-based change detection, because the elicitation of a prediction error response relies on the formation of a prediction, which in turn, is dependent upon intact memory of previous auditory stimulation. As such, the MMN is altered in conditions in which memory is affected, such as Alzheimer's disease, schizophrenia and healthy aging. The most prominent pharmacological finding for MMN strengthens the link between MMN and synaptic plasticity, as glutamate N-methyl-D-aspartate receptor (NMDA-R) antagonists reduce the MMN response. However, recent data has begun to demonstrate that the link between NMDA-R function and MMN is not as clear as once thought, with low dose and low affinity NMDA-R antagonists observed to facilitate MMN. (c) 2020 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:106 / 113
页数:8
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