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Effective connectivity underlying reward‐based executive control
by
Hippmann, Bernadette
, Münte, Thomas F.
, Göttlich, Martin
, Weiblen, Ronja
, Tzvi, Elinor
, Jessen, Sarah
in
Adult
/ Cerebral Cortex - diagnostic imaging
/ Cerebral Cortex - physiology
/ Cognitive ability
/ cognitive control
/ Connectome - methods
/ Cortex (cingulate)
/ Decision making
/ Decision Making - physiology
/ Dopamine receptors
/ dynamic causal modeling
/ Executive function
/ Executive Function - physiology
/ fMRI
/ Functional magnetic resonance imaging
/ Humans
/ Magnetic Resonance Imaging
/ Models, Theoretical
/ Monetary incentives
/ Motivation
/ Motivation - physiology
/ Neuroimaging
/ Punishment
/ Reinforcement
/ Reward
/ Switching
/ Ventral tegmentum
/ Young Adult
2021
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Effective connectivity underlying reward‐based executive control
by
Hippmann, Bernadette
, Münte, Thomas F.
, Göttlich, Martin
, Weiblen, Ronja
, Tzvi, Elinor
, Jessen, Sarah
in
Adult
/ Cerebral Cortex - diagnostic imaging
/ Cerebral Cortex - physiology
/ Cognitive ability
/ cognitive control
/ Connectome - methods
/ Cortex (cingulate)
/ Decision making
/ Decision Making - physiology
/ Dopamine receptors
/ dynamic causal modeling
/ Executive function
/ Executive Function - physiology
/ fMRI
/ Functional magnetic resonance imaging
/ Humans
/ Magnetic Resonance Imaging
/ Models, Theoretical
/ Monetary incentives
/ Motivation
/ Motivation - physiology
/ Neuroimaging
/ Punishment
/ Reinforcement
/ Reward
/ Switching
/ Ventral tegmentum
/ Young Adult
2021
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Effective connectivity underlying reward‐based executive control
by
Hippmann, Bernadette
, Münte, Thomas F.
, Göttlich, Martin
, Weiblen, Ronja
, Tzvi, Elinor
, Jessen, Sarah
in
Adult
/ Cerebral Cortex - diagnostic imaging
/ Cerebral Cortex - physiology
/ Cognitive ability
/ cognitive control
/ Connectome - methods
/ Cortex (cingulate)
/ Decision making
/ Decision Making - physiology
/ Dopamine receptors
/ dynamic causal modeling
/ Executive function
/ Executive Function - physiology
/ fMRI
/ Functional magnetic resonance imaging
/ Humans
/ Magnetic Resonance Imaging
/ Models, Theoretical
/ Monetary incentives
/ Motivation
/ Motivation - physiology
/ Neuroimaging
/ Punishment
/ Reinforcement
/ Reward
/ Switching
/ Ventral tegmentum
/ Young Adult
2021
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Effective connectivity underlying reward‐based executive control
Journal Article
Effective connectivity underlying reward‐based executive control
2021
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Overview
Motivational influences on cognitive control play an important role in shaping human behavior. Cognitive facilitation through motivators such as prospective reward or punishment is thought to depend on regions from the dopaminergic mesocortical network, primarily the ventral tegmental area (VTA), inferior frontal junction (IFJ), and anterior cingulate cortex (ACC). However, how interactions between these regions relate to motivated control remains elusive. In the present functional magnetic resonance imaging study, we used dynamic causal modeling (DCM) to investigate effective connectivity between left IFJ, ACC, and VTA in a task‐switching paradigm comprising three distinct motivational conditions (prospective monetary reward or punishment and a control condition). We found that while prospective punishment significantly facilitated switching between tasks on a behavioral level, interactions between IFJ, ACC, and VTA were characterized by modulations through prospective reward but not punishment. Our DCM results show that IFJ and VTA modulate ACC activity in parallel rather than by interaction to serve task demands in reward‐based cognitive control. Our findings further demonstrate that prospective reward and punishment differentially affect neural control mechanisms to initiate decision‐making. Dynamic causal modeling (DCM) in functional magnetic resonance imaging data was applied to investigate effective connectivity between left IFJ, ACC, and VTA in a task‐switching paradigm comprising three distinct motivational conditions (prospective monetary reward or punishment and a control condition). Prospective punishment significantly facilitated switching between tasks on a behavioral level, while interactions between IFJ, ACC, and VTA were characterized by modulations through prospective reward. Our DCM results show that IFJ and VTA modulate ACC activity in parallel rather than by interaction to serve task demands in reward‐based cognitive control.
Publisher
John Wiley & Sons, Inc
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