The effect of NMDA-R antagonist, MK-801, on neuronal mismatch along the rat auditory thalamocortical pathway
Efficient sensory processing requires that the brain maximize its response to unexpected stimuli, while suppressing responsivity to expected events. Mismatch negativity (MMN) is an auditory event‐related potential that occurs when a regular pattern is interrupted by an event that violates
the expected properties of the pattern. According to the predictive coding framework there are two mechanisms underlying the MMN: repetition suppression and prediction error. MMN has been found to be reduced in individuals with schizophrenia, an effect believed to be underpinned by glutamate N‐methyl‐d‐aspartate receptor (NMDA‐R) dysfunction. In the current study, we aimed to test how the NMDA‐R antagonist, MK‐801 in the anaesthetized rat, affected repetition suppression and prediction error processes along the auditory thalamocortical pathway. We found that low‐dose systemic administration of MK‐801 differentially affect thalamocortical responses, namely, increasing thalamic repetition suppression and cortical prediction error. Results demonstrate an enhancement of neuronal mismatch, also confirmed by large scale‐responses. Furthermore, MK‐801 produces faster and stronger dynamics of adaptation along the thalamocortical hierarchy. Clearly more research
is required to understand how NMDA‐R antagonism and dosage affects processes contributing to MMN. Nonetheless, because a low dose of an NMDA‐R antagonist increased neuronal mismatch, the outcome has implications for schizophrenia treatment.
