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Dias Maile, A. A.

Publications and source records attributed to Dias Maile, A. A..

3 recordsLinked to original sources

Cholinergic and noradrenergic modulation of perceptual decision making and learning

Decision making often requires the integration of noisy bottom-up sensory evidence with top-down prior expectations learned from past experiences. Acetylcholine and noradrenaline have been proposed to shape these computations, yet it remains unclear whether they directly influence the weighting of sensory evidence and prior expectations during decision making or instead shape the learning process that gives rise to these expectations. To disentangle this, healthy participants (n = 62) completed a perceptual decision-making task under the influence of either the muscarinic acetylcholine receptor antagonist biperiden, the {beta}-adrenoceptor antagonist propranolol, or placebo, in a within-subject crossover design. The task required the integration of sensory evidence with learned expectations. The reliability of these two sources of information varied independently. We show that both drugs led to a faster updating of current beliefs in response to new evidence. Under propranolol, these effects were specific to reward outcomes, whereas under biperiden, faster updating in response to both reward and non-reward outcomes resulted in less stable beliefs. Notably, neither drug affected the degree to which choices were governed by the strength of the sensory evidence. Together, these findings suggest that acetylcholine and noradrenaline guide perceptual decision making by modulating the updating of top-down prior expectations in response to new bottom-up evidence during learning.

neuroscience↗

Role of GABA and NMDA receptors in shaping cortical timescales and large-scale network dynamics

Cortical brain regions integrate information across different timescales, ranging from fast sensory processing to longer integration windows, allowing cognitive functions like working memory. At the large-scale, brain regions organize into transient network states that rapidly switch over time and similarly contribute to cognition. Both cortical timescales and large-scale network dynamics are proposed to be determined by the balance between recurrent synaptic excitation and GABAergic inhibition. Here, we pharmacologically manipulated synaptic transmission at GABAA and NMDA receptors in 60 healthy male participants and acquired resting-state magnetoencephalography. Neuronal timescales followed a hierarchical gradient with shorter timescales in early sensory regions. Increasing GABAergic activity prolonged neuronal timescales across cortical regions. This effect was most prominent in the frontal default mode and in the dorsal attention network. Notably, dynamic network analyses revealed that the occurrence probability of the frontal default mode network increased, whereas the occurrence of the dorsal attention network was reduced. NMDA receptor modulation resulted in no significant changes. Together, these findings provide causal evidence that GABAergic inhibition is a key regulator of cortical temporal organization, linking microscale synaptic mechanisms to neuronal timescales and network dynamics that support diverse cognitive function.

neuroscience↗

Bidirectional modulation of reward-guided decision making by dopamine

RationaleThe neuromodulator dopamine is known to play a key role in reward-guided decision making, where choice options are often characterized by multiple attributes. Different decision strategies can be used to merge these choice attributes with personal preferences (e.g., risk preferences) and integrate them into a single subjective value. While the influence of dopamine on risk preferences has been investigated, it is unknown whether dopamine is also involved in arbitrating between decision strategies. ObjectiveIn the present study, we investigate the effects of pharmacological dopamine manipulations on arbitrating between different decision strategies in a healthy sample. Methods31 healthy male participants performed a reward-guided decision-making task under the influence of the dopamine D2/D3-receptor antagonist amisulpride (400 mg), the dopamine precursor L-DOPA (100 mg L-DOPA + 25 mg cardidopa), or placebo in a double-blind within-subject design. The effect of dopamine on reward-guided decisions and decision strategies was analyzed using hierarchical implementations of regressions and Bayesian models. ResultsNotably, we observed that the dopaminergic interventions shifted the (overall) weighting of option attributes without changing how option attributes are integrated into a subjective value (decision strategy). These effects were bidirectional: Amisulpride reduced whereas L-DOPA increased the degree to which choices were influenced by both reward magnitude and reward probability. These effects occurred in the absence of changes in statistically optimal behavior. ConclusionTogether, our data provide evidence for a role of dopamine in controlling the influence of value parameters on choice irrespective of decision strategies.

neuroscience↗