bioRxiv Science⌕ Search

Biology subjects

Mueller-Dahlhaus, F.

Publications and source records attributed to Mueller-Dahlhaus, F..

3 recordsLinked to original sources

Boredom and the representation of information content in the neocortex

Boredom - a pervasive mental state - promotes the pursuit of novel information by assigning negative value to monotonous conditions. Yet, how the brain extracts and represents the information content of ongoing sensory experience remains poorly understood. Here, we combine behavioral assays, neurophysiological recordings and computational modeling across humans and mice to investigate how sensory information shapes boredom-related behavior. In a cross-species choice task, both humans and mice robustly avoid monotonous sources of sensory stimulation. We formalize perceived monotony using empirical entropy as a measure of information content and show that monotony avoidance scales directly with low entropy and in humans correlates with boredom experience. Human electroencephalography and mesoscopic calcium imaging in mice reveal that the recruitment of neocortical activity tracks stimulus entropy. Two-photon calcium imaging in the auditory cortex of mice further uncovers a stimulus-invariant population code for entropy, supported by neurons tuned to information content. A recurrent network model reproduced this code through an interplay of afferent depression and recurrent facilitation. Together, we demonstrate how the information content of sensory experience is represented in cortical population activity, providing a basis for boredom-related avoidance behavior. Thus, our findings link synaptic and neuronal dynamics to boredom, acting as a safeguard mechanism to ensure high information input to the brain.

neuroscience↗

Understanding the neural mechanisms of emotion-cognition interaction via high resolution mapping in space, time, frequency, and information transfer

Interactions between emotional and cognitive processing play a critical role in determining human behavior. The ability to efficiently control these interactions is essential for goal-directed behavior. Previous research on emotion-cognition interaction in humans has primarily focused on its neural topography using techniques with either low temporal resolution (fMRI) or low spatial resolution (ERP), leaving the underlying neuronal mechanisms and their behavioral implications poorly understood. Here, we used EEG recordings from a large cohort of human participants (N=121) and employed source-reconstruction with finite-element head modeling during an emotional Flanker task. Our findings reveal a neural interaction between emotional interference and cognitive control within the pars triangularis of the right inferior frontal gyrus (rIFG). These results align spatially and conceptually with meta-analytic evidence from fMRI studies on interference inhibition processes, supporting the idea that the rIFG is crucial for interference inhibition, regardless of the interfering information type. Notably, the neural interaction between emotion and cognition in the rIFG was transient, peaking during the transition from emotional to cognitive processing, and was most pronounced in the beta-frequency band. Furthermore, conditional Granger-causality analysis of information flow indicated that the pars triangularis of the rIFG communicated with other functional subdivisions of the rIFG and parieto-occipital areas (such as the Precuneus and V2) in a frequency-specific manner. This information flow predicted individual emotional and cognitive interference effects on behavior. Overall, our findings highlight the functional and temporal segregation and integration of emotion, cognition, and their interaction in the rIFG. Furthermore, rIFGs top-down modulation of visuo-attentional areas, ultimately shaping behavioral performance, underscores the importance of stimulus interference inhibition for emotion-cognition interaction. Author summaryUnderstanding the interplay between emotion and cognition is crucial for understanding human behavior. Our study investigates the role of transient oscillatory activity using source-localized EEG in a large cohort. We identify a spatial overlap of the interaction of emotion and cognition processing in the rIFGs pars triangularis, aligning closely with localizations indicated by meta-analytic fMRI evidence. This interaction, primarily in the beta-frequency (around 20Hz) band, is transient, peaking during the shift from emotional to cognitive processing. Granger-causality analysis reveals frequency-specific communication patterns within the rIFG and parieto-occipital areas, predicting individual emotional and cognitive interference effects. Our findings elucidate the functional and temporal dynamics of emotion-cognition interaction within the rIFG, providing insights into the nuanced neural processes shaping human behavior.

neuroscience↗

TMS-EEG signatures of glutamatergic neurotransmission in human cortex

Neuronal activity in the brain is regulated by an excitation-inhibition balance. Glutamate is the main excitatory neurotransmitter. Transcranial magnetic stimulation (TMS) evoked electroencephalographic (EEG) potentials (TEPs) represent a novel way to quantify pharmacological effects on neuronal activity in the human cortex. Here we tested TEPs under the influence of a single oral dose of two anti-glutamatergic drugs, perampanel, an AMPA-receptor antagonist, and dextromethorphan, an NMDA-receptor antagonist, and nimodipine, an L-type voltage-gated calcium channel blocker in 16 healthy adults in a pseudorandomized, double-blinded, placebo-controlled, crossover design. Single-pulse TMS was delivered to the left motor cortex and TEPs were obtained pre-and post-drug intake. Dextromethorphan specifically increased the amplitude of the N45, a negative potential around 45 ms after the TMS pulse, while perampanel reduced the P70 amplitude in the non-stimulated hemisphere. Nimodipine and placebo had no effect on TEPs. These data extend previous pharmaco-TMS-EEG studies by demonstrating that the N45 is regulated by a balance of GABAAergic inhibition and NMDA-receptor-mediated glutamatergic excitation. In contrast, AMPA-receptor-mediated glutamatergic neurotransmission contributes to interhemispherically propagated activity reflected in the P70. These data are important to understand the physiology of TEPs as markers of excitability and propagated activity in the human cortex in health and disease.

neuroscience↗