Human perceptual learning is delayed by the NMDA receptor partial agonist D-cycloserine

<p><strong>Background:</strong> The optimisation of learning has long been a focus of scientific research, particularly in relation to improving psychological treatment and recovery of brain function. Previously, partial NMDA agonists have been shown to augment reward learning, pro...

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Main Authors: Dempsey-Jones, H, Steudte-Schmiedgen, S, Browning, M, Makin, T, Woud, ML, Harmer, CJ, Margraf, J, Reinecke, A
Format: Journal article
Language:English
Published: SAGE Publications 2021
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author Dempsey-Jones, H
Steudte-Schmiedgen, S
Browning, M
Makin, T
Woud, ML
Harmer, CJ
Margraf, J
Reinecke, A
author_facet Dempsey-Jones, H
Steudte-Schmiedgen, S
Browning, M
Makin, T
Woud, ML
Harmer, CJ
Margraf, J
Reinecke, A
author_sort Dempsey-Jones, H
collection OXFORD
description <p><strong>Background:</strong> The optimisation of learning has long been a focus of scientific research, particularly in relation to improving psychological treatment and recovery of brain function. Previously, partial NMDA agonists have been shown to augment reward learning, procedural learning and psychological therapy, but many studies also report no impact of these compounds on the same processes.</p> <p><strong>Aims:</strong> Here we investigate whether administration of an NMDA partial agonist (D- cycloserine) modulates a previously unexplored process – tactile perceptual learning. Further, we use a longitudinal design to investigate whether NMDA-related learning effects vary with time, thereby providing a potentially simple explanation for apparent mixed effects in previous research.</p> <p><strong>Methods:</strong> Thirty-four volunteers were randomised to receive one dose of 250mg D-cycloserine or placebo two hours before tactile sensitivity training. Tactile perception was measured using psychophysical methods before and after training, and 24/48 hours later.</p> <p><strong>Results:</strong> The placebo group showed immediate within-day tactile perception gains, but no further improvements between-days. In contrast, tactile perception remained at baseline on day one in the D-cycloserine group (no within-day learning), but showed significant overnight gains on day two. Both groups were equivalent in tactile perception by the final testing – indicating NMDA effects changed the timing, but not overall amount of tactile learning.</p> <p><strong>Conclusions:</strong> In sum, we provide first evidence for modulation of perceptual learning by administration of a partial NMDA agonist. Resolving how the effects of such compounds become apparent over time will assist the optimisation of testing schedules, and may help resolve discrepancies across the learning and cognition domains.</p>
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spelling oxford-uuid:c9372bf2-3ca8-4bf4-b60b-d8726288005b2022-03-27T06:57:34ZHuman perceptual learning is delayed by the NMDA receptor partial agonist D-cycloserineJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:c9372bf2-3ca8-4bf4-b60b-d8726288005bEnglishSymplectic ElementsSAGE Publications2021Dempsey-Jones, HSteudte-Schmiedgen, SBrowning, MMakin, TWoud, MLHarmer, CJMargraf, JReinecke, A<p><strong>Background:</strong> The optimisation of learning has long been a focus of scientific research, particularly in relation to improving psychological treatment and recovery of brain function. Previously, partial NMDA agonists have been shown to augment reward learning, procedural learning and psychological therapy, but many studies also report no impact of these compounds on the same processes.</p> <p><strong>Aims:</strong> Here we investigate whether administration of an NMDA partial agonist (D- cycloserine) modulates a previously unexplored process – tactile perceptual learning. Further, we use a longitudinal design to investigate whether NMDA-related learning effects vary with time, thereby providing a potentially simple explanation for apparent mixed effects in previous research.</p> <p><strong>Methods:</strong> Thirty-four volunteers were randomised to receive one dose of 250mg D-cycloserine or placebo two hours before tactile sensitivity training. Tactile perception was measured using psychophysical methods before and after training, and 24/48 hours later.</p> <p><strong>Results:</strong> The placebo group showed immediate within-day tactile perception gains, but no further improvements between-days. In contrast, tactile perception remained at baseline on day one in the D-cycloserine group (no within-day learning), but showed significant overnight gains on day two. Both groups were equivalent in tactile perception by the final testing – indicating NMDA effects changed the timing, but not overall amount of tactile learning.</p> <p><strong>Conclusions:</strong> In sum, we provide first evidence for modulation of perceptual learning by administration of a partial NMDA agonist. Resolving how the effects of such compounds become apparent over time will assist the optimisation of testing schedules, and may help resolve discrepancies across the learning and cognition domains.</p>
spellingShingle Dempsey-Jones, H
Steudte-Schmiedgen, S
Browning, M
Makin, T
Woud, ML
Harmer, CJ
Margraf, J
Reinecke, A
Human perceptual learning is delayed by the NMDA receptor partial agonist D-cycloserine
title Human perceptual learning is delayed by the NMDA receptor partial agonist D-cycloserine
title_full Human perceptual learning is delayed by the NMDA receptor partial agonist D-cycloserine
title_fullStr Human perceptual learning is delayed by the NMDA receptor partial agonist D-cycloserine
title_full_unstemmed Human perceptual learning is delayed by the NMDA receptor partial agonist D-cycloserine
title_short Human perceptual learning is delayed by the NMDA receptor partial agonist D-cycloserine
title_sort human perceptual learning is delayed by the nmda receptor partial agonist d cycloserine
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