Abstract

In bistable vision, subjective perception wavers between two interpretations of a constant ambiguous stimulus. This dissociation between conscious perception and sensory stimulation has motivated various empirical studies on the neural correlates of bistable perception, but the neurocomputational mechanism behind endogenous perceptual transitions has remained elusive. Here, we recurred to a generic Bayesian framework of predictive coding and devised a model that casts endogenous perceptual transitions as a consequence of prediction errors emerging from residual evidence for the suppressed percept. Data simulations revealed close similarities between the model’s predictions and key temporal characteristics of perceptual bistability, indicating that the model was able to reproduce bistable perception. Fitting the predictive coding model to behavioural data from an fMRI-experiment on bistable perception, we found a correlation across participants between the model parameter encoding perceptual stabilization and the behaviourally measured frequency of perceptual transitions, corroborating that the model successfully accounted for participants’ perception. Formal model comparison with established models of bistable perception based on mutual inhibition and adaptation, noise or a combination of adaptation and noise was used for the validation of the predictive coding model against the established models. Most importantly, model-based analyses of the fMRI data revealed that prediction error time-courses derived from the predictive coding model correlated with neural signal time-courses in bilateral inferior frontal gyri and anterior insulae. Voxel-wise model selection indicated a superiority of the predictive coding model over conventional analysis approaches in explaining neural activity in these frontal areas, suggesting that frontal cortex encodes prediction errors that mediate endogenous perceptual transitions in bistable perception. Taken together, our current work provides a theoretical framework that allows for the analysis of behavioural and neural data using a predictive coding perspective on bistable perception. In this, our approach posits a crucial role of prediction error signalling for the resolution of perceptual ambiguities.

Highlights

  • During bistable perception, observers experience fluctuations between two mutually exclusive interpretations of a constant ambiguous input

  • Behavioural and fMRI data, we provide evidence that prediction errors stemming from the suppressed stimulus interpretation mediate perceptual transitions and correlate with neural activity in inferior frontal gyrus and insula

  • We investigated which voxels were more active during perceptual transitions as compared to baseline (‘transitions vs. baseline’, Fig 4A): For the ‘PE model’, we found significant activations of motor-related areas in left precentral gyrus ([-36 -16 67], T = 12.23) extending to left postcentral gyrus ([-63 -19 25], T = 8.62) as well as significant clusters in regions previously associated with transition-related activity during bistable perception: right inferior frontal gyrus ([54 17 13], T = 7.96), right inferior parietal lobulus (54 -37 52, T = 9.32) and right middle frontal gyrus ([39 44 31], T = 7.57)

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Summary

Introduction

Observers experience fluctuations between two mutually exclusive interpretations of a constant ambiguous input. Previous neuroimaging work [4, 5, 6, 7, 8, 9, 10] has sought to distill the neural processes underlying bistable perception by recurring to a ‘replay’ condition, in which physical stimulus changes mimic the perceptual alternations induced by ambiguous stimuli This approach revealed a right-lateralized assembly of fronto-parietal areas whose activity is enhanced during endogenously evoked transitions (ambiguity) as compared to exogenously evoked transitions (replay) [4, 5, 7, 9]. Transitions in bistable vision are primarily a result of adaptation and inhibition within visual cortex, while switch-related activations in fronto-parietal areas reflect a mere ‘feedforward’ consequence of neural events at sensory processing levels [6, 10]. We sought to resolve this debate by using model-based fMRI to empirically test a theoretical model that has the potential to integrate these two seemingly contradictory views of perceptual bistability

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