NeuroImageNeurosciencePeer-reviewed journal article
Indexing sensory plasticity: Evidence for distinct Predictive Coding and Hebbian Learning mechanisms in the cerebral cortex
Meg J. SpriggsiD, Rachael L. SumneriD, Rebecca L. McMillaniD, Rosalyn MoraniD, Ian J. KirkiD, Suresh D MuthukumaraswamyiD
Abstract
HighlightsO_LIERP and DCM study of two sensory plasticity paradigms: roving MMN and visual LTP\nC_LIO_LIFirst demonstration of multiple learning mechanisms under different task demands\nC_LIO_LIEvidence for both Predictive Coding and Hebbian learning mechanisms\nC_LIO_LIThe BDNF Val66Met polymorphism modulates ERPs for both paradigms\nC_LIO_LIHowever, the polymorphism only modulates MMN network connectivity\nC_LI\n\nThe Roving Mismatch Negativity (MMN), and Visual LTP paradigms are widely used as independent measures of sensory plasticity. However, the paradigms are built upon fundamentally different (and seemingly opposing) models of perceptual learning; namely, Predictive Coding (MMN) and Hebbian plasticity (LTP). The aims of the current study were to 1) compare the generative mechanisms of the MMN and visual LTP, therefore assessing whether Predictive Coding and Hebbian mechanisms co-occur in the brain, and 2) assess whether the paradigms identify similar group differences in plasticity. Forty participants were split into two groups based on the BDNF Val66Met polymorphism and were presented with both paradigms. Consistent with Predictive Coding and Hebbian predictions, Dynamic Causal Modelling revealed that the generation of the MMN modulates forward and backward connections in the underlying network, while visual LTP only modulates forward connections. Genetic differences were identified in the ERPs for both paradigms, but were only apparent in backward connections of the MMN network. These results suggest that both Predictive Coding and Hebbian mechanisms are utilized by the brain under different task demands. Additionally, both tasks provide unique insight into plasticity mechanisms, which has important implications for future studies of aberrant plasticity in clinical populations.
- organism: human
- assay: electronic health records
- research focus: cell type annotation
- approach: statistical model
- Citations
- 38
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