Search bioRxiv⌕ Search

bioRxiv · 10.1101/2023.01.29.526087

Modulation of perception by visual, auditory, and audiovisual reward predicting cues

Abstract

Rewards influence information processing in the primary sensory areas specialized to process stimuli from a specific sensory modality. In real life situations, we receive sensory inputs not only from one single modality, but stimuli are often multisensory. It is however not known whether the reward-driven modulation of perception follows the same principles when reward is cued through a single or multiple sensory modalities. We previously showed that task-irrelevant reward cues modulate perception both intra- as well as cross-modally, likely through a putative enhancement in the integration of the stimulus parts into a coherent object. In this study, we explicitly test this possibility by assessing whether reward enhances the integration of unisensory components of a multisensory object in accordance with the supra-additive principle of multisensory integration. Towards this aim, we designed a simple detection task using reward predicting cues that were either unisensory (auditory or visual, both above the detection threshold) or multisensory (audiovisual). We conducted two experiments, behavioral (experiment 1) and simultaneous behavioral and neuroimaging testing (experiment 2). We expected that reward speeds up reaction times in response to all stimulus configurations, and that additionally the reward effects in multisensory cues fulfill the supra-additive principle of multisensory integration. We observed that reward decreased response times in both experiments with the strongest effect found for the multisensory stimuli in experiment 1. However, this behavioral effect did not fulfill the supra-additive principle. Neuroimaging results demonstrated sensory supra-additivity at the classical areas involved in multisensory integration such as the Superior Temporal areas (STS), while reward modulation was found in the midbrain and fronto-parietal areas, reflecting the typical areas that receive dopaminergic projections. However, reward did not enhance the supra-additivity in the STS compared to a no reward condition. Instead, we observed that some of the reward-related areas showed a sub-additive modulation by rewards and areas exhibiting a weaker supra-additive response to audiovisual stimuli, namely the fusiform gyrus, were modulated by rewards of audiovisual stimuli as measured by a conjunction analysis. Overall, our results indicate that reward does not enhance the multisensory integration through a supra-additive rule. These findings inspire a model where reward and sensory integration processes are regulated by two independent mechanisms, where sensory information is integrated at an early stage in a supra-additive manner, while reward modulates perception at a later stage sub-additively. Moreover, an associative area in the Fusiform gyrus exhibits a convergence of both reward and multisensory integration signals, indicating that it may be a hub to integrate different types of signals including rewards to disambiguate the information from different sensory modalities.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Antono, J. E., Pooresmaeili, A.. 2023-01-31. Modulation of perception by visual, auditory, and audiovisual reward predicting cues. https://doi.org/10.1101/2023.01.29.526087

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Rab10 and Arhgef7 interact to promote axon extension by linking vesicle supply and exocytosis

The formation of functional neural circuits begins with the extension of a single axon by immature neurons. Axon elongation requires an expansion of the plasma membrane that depends on the polarization of vesicle trafficking and exocytosis. It is not completely understood how the increased transport of vesicles into the growing axon is linked to their subsequent insertion into the plasma membrane. An analysis of early stages of neuronal differentiation indicates that an asymmetry in neurite length precedes axon specification and the accumulation of PPVs in the nascent axon. We show that increasing the transport of vesicles in unpolarized neurons is sufficient to promote the extension of additional axons. This effect indicates that an increased supply of vesicles stimulates their subsequent insertion into the membrane to allow neurite growth. The link between vesicle transport and exocytosis is mediated by the interaction of Rab10 with Arhgef7. Rab10 stimulates Arhgef7 activity on PPVs as a GEF for Cdc42b to promote axon extension through exocyst-dependent exocytosis, suggesting that their interaction links the increased supply of PPVs to their exocytosis.

neuroscience↗

Subcellular Spatial Profiling Unveils Links Between Neuritic Plaques with Selective Tau Vulnerability in Alzheimer's Disease

Alzheimer's disease (AD) features widespread extracellular amyloid-{beta} plaques but selective intraneuronal tau accumulation in cortical layers II/III and V, while layer IV remains relatively resistant. Here, we combined subcellular spatial transcriptomics with co-registered A{beta} and pTau immunohistochemistry to determine why neurons exposed to comparable plaque-associated pathology differ in somatic pTau accumulation. Plaque-associated neuritic stress occurred similarly across layers, but layer IV neurons showed attenuated pTau accumulation and reduced somatic expression of a shared neurite-soma stress program involving DCTN1, CALM3, NORAD, and PIN1. Trajectory analysis within layers identified tau-vulnerable and resistant neuronal states implicating calcium signaling, retrograde transport, and lysosomal function. Notably, astrocytic APOE-neuronal LRP1 co-expression increased significantly along the pTau-vulnerable trajectory, and APOE {epsilon}4 was associated with stronger coupling of local plaque pathology to pTau-associated molecular programs. These findings reveal neuronal programs and neuron-glia interactions underlying selective tau vulnerability and resistance in AD, highlighting potential tau-targeting therapeutics.

neuroscience↗

Widespread oscillatory suppression in autism persists in the absence of psychotropic medication.

Purpose: Investigate the neural oscillatory activity associated with autism spectrum disorder (ASD) using electroencephalographic (EEG) recordings in children and adolescents. Compare the corresponding oscillatory power between ASD patients taking psychotropic medication with a drug-naive group. Methods: ASD diagnosis was done using DSM-IV and CARS (Childhood Autism Rating Scale). EEG recordings employed 22 scalp electrodes (10/20 system). ASD vs. neurotypical groups were matched for sex and age (5 females; average age: ~10 years old). We analyzed the resting state (eyes open) EEG power spectrum during ~2-minute recordings. The multitaper FFT method was used to estimate spectral power for the delta, theta, alpha, beta and gamma frequency bands. We pooled together data from several electrodes to compute comprehensive power spectra and assess the oscillatory behavior of macro brain regions. Results: We observed widespread (~4Hz - 20Hz) oscillatory suppression comprising the theta, alpha and beta frequency bands. The most widespread and robust ASD-associated power suppression was in the high theta and alpha bands. Delta and gamma bands showed no significant power change for any of the brain regions studied. Results from a subgroup of patients (N = 9) who never used psychotropics confirmed these findings, indicating that they are not an artifact of medication. Conclusion: Suppression in theta, alpha and beta oscillations may offer insights into the neurophysiological underpinnings of autism and could be used as an accessible and comprehensive tool in ASD diagnosis, regardless of the patients being or not on medication.

neuroscience↗