Bistability of prefrontal states gates access to consciousness
Abhilash Dwarakanath, Vishal Kapoor, Joachim Werner, Shervin Safavi, Leonid A. Fedorov, Nikos K. Logothetis, Theofanis I. Panagiotaropoulos
bioRxiv Preprint Server January 29, 2020 preprint DOI: 10.1101/2020.01.29.924928 via bioRxiv
Summary
AI-generated from the abstractAccess of sensory information to consciousness depends on neural activity crossing a threshold in the prefrontal cortex (PFC), yet how brain state fluctuations interact with conscious content is unclear. Using multielectrode recordings during a no-report binocular rivalry task in animals, two distinct prefrontal states were identified: low-frequency (1-9 Hz) bursts that precede spontaneous switches in conscious perception (perceptual update), and beta-band (20-40 Hz) bursts correlated with stable perception. Beta bursts synchronize neural ensembles coding the perceived stimulus. Similar fluctuations occur during rest, suggesting they are endogenous. The findings indicate that global cortical states, not selective spiking, drive internal switches in conscious perception.
Study at a glance
| Characteristics | Experimental study |
|---|---|
| Citations | 15 |
| Key finding | Two distinct prefrontal cortical states—low-frequency bursts preceding perceptual updates and beta-band bursts correlated with stable perception—mediate spontaneous switches in conscious perception during binocular rivalry. |
Abstract
Access of sensory information to consciousness is thought to be mediated through ignition of neural activity in the prefrontal cortex (PFC). Ignition occurs once activity elicited by sensory input crosses a threshold, which has been shown to depend on brain state fluctuations. However, the neural correlates of fluctuations and their interaction with the neural representations of conscious contents within the PFC remain largely unknown. To understand the role of prefrontal state fluctuations in conscious access, we combined multielectrode intracortical recordings with a no-report binocular rivalry (BR) paradigm that induces spontaneously-driven changes in conscious perception. During BR, antagonistic coupling of two prefrontal states, characterised by dominance of low frequency (1-9Hz) or beta (20-40Hz) local field potentials (LFP), reflect competition between two states of visual consciousness; perceptual update and stability, respectively. Low frequency perisynaptic bursts precede spontaneous transitions in conscious perception, signalling upcoming perceptual update of conscious content. We therefore show that it is a global cortical state that seems to drive internal switches, rather than the spiking activity of selective neuronal ensembles, which subsequently, only report the active percept. Beta band bursts were found to be correlated with periods of stable conscious perception, and selectively synchronised the neural ensemble coding for the consciously perceived stimulus. Similar ongoing fluctuations in the LFPs, with dynamics resembling the distribution of perceptual dominance periods during BR, dominated the prefrontal cortex during resting-state, thus pointing to their default, endogenous nature. Our results suggest that the two modes of conscious perception: perceptual update, and stability, can be associated with distinct prefrontal cortical states.