The role of the striatum in goal activation of cascaded actions
Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-go...
Ausführliche Beschreibung
Autor*in: |
Ness, Vanessa [verfasserIn] |
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E-Artikel |
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Englisch |
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2013transfer abstract |
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10 |
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Übergeordnetes Werk: |
Enthalten in: Articles That May Change Your Practice: Pelvic Binders Revisited - MacDonald, Russell D. ELSEVIER, 2023, an international journal in behavioural and cognitive neuroscience, Amsterdam [u.a.] |
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Übergeordnetes Werk: |
volume:51 ; year:2013 ; number:13 ; pages:2562-2571 ; extent:10 |
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DOI / URN: |
10.1016/j.neuropsychologia.2013.09.032 |
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Katalog-ID: |
ELV022325182 |
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245 | 1 | 4 | |a The role of the striatum in goal activation of cascaded actions |
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520 | |a Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. | ||
520 | |a Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. | ||
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650 | 7 | |a Stop-change |2 Elsevier | |
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700 | 1 | |a Beste, Christian |4 oth | |
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10.1016/j.neuropsychologia.2013.09.032 doi GBVA2013022000020.pica (DE-627)ELV022325182 (ELSEVIER)S0028-3932(13)00334-5 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 44.71 bkl Ness, Vanessa verfasserin aut The role of the striatum in goal activation of cascaded actions 2013transfer abstract 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. Action selection Elsevier Striatum Elsevier Caudate Elsevier Stop-change Elsevier Action chunking Elsevier Beste, Christian oth Enthalten in Elsevier Science MacDonald, Russell D. ELSEVIER Articles That May Change Your Practice: Pelvic Binders Revisited 2023 an international journal in behavioural and cognitive neuroscience Amsterdam [u.a.] (DE-627)ELV009449108 volume:51 year:2013 number:13 pages:2562-2571 extent:10 https://doi.org/10.1016/j.neuropsychologia.2013.09.032 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.71 Verkehrsmedizin VZ AR 51 2013 13 2562-2571 10 045F 610 |
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10.1016/j.neuropsychologia.2013.09.032 doi GBVA2013022000020.pica (DE-627)ELV022325182 (ELSEVIER)S0028-3932(13)00334-5 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 44.71 bkl Ness, Vanessa verfasserin aut The role of the striatum in goal activation of cascaded actions 2013transfer abstract 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. Action selection Elsevier Striatum Elsevier Caudate Elsevier Stop-change Elsevier Action chunking Elsevier Beste, Christian oth Enthalten in Elsevier Science MacDonald, Russell D. ELSEVIER Articles That May Change Your Practice: Pelvic Binders Revisited 2023 an international journal in behavioural and cognitive neuroscience Amsterdam [u.a.] (DE-627)ELV009449108 volume:51 year:2013 number:13 pages:2562-2571 extent:10 https://doi.org/10.1016/j.neuropsychologia.2013.09.032 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.71 Verkehrsmedizin VZ AR 51 2013 13 2562-2571 10 045F 610 |
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10.1016/j.neuropsychologia.2013.09.032 doi GBVA2013022000020.pica (DE-627)ELV022325182 (ELSEVIER)S0028-3932(13)00334-5 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 44.71 bkl Ness, Vanessa verfasserin aut The role of the striatum in goal activation of cascaded actions 2013transfer abstract 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. Action selection Elsevier Striatum Elsevier Caudate Elsevier Stop-change Elsevier Action chunking Elsevier Beste, Christian oth Enthalten in Elsevier Science MacDonald, Russell D. ELSEVIER Articles That May Change Your Practice: Pelvic Binders Revisited 2023 an international journal in behavioural and cognitive neuroscience Amsterdam [u.a.] (DE-627)ELV009449108 volume:51 year:2013 number:13 pages:2562-2571 extent:10 https://doi.org/10.1016/j.neuropsychologia.2013.09.032 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.71 Verkehrsmedizin VZ AR 51 2013 13 2562-2571 10 045F 610 |
allfieldsGer |
10.1016/j.neuropsychologia.2013.09.032 doi GBVA2013022000020.pica (DE-627)ELV022325182 (ELSEVIER)S0028-3932(13)00334-5 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 44.71 bkl Ness, Vanessa verfasserin aut The role of the striatum in goal activation of cascaded actions 2013transfer abstract 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. Action selection Elsevier Striatum Elsevier Caudate Elsevier Stop-change Elsevier Action chunking Elsevier Beste, Christian oth Enthalten in Elsevier Science MacDonald, Russell D. ELSEVIER Articles That May Change Your Practice: Pelvic Binders Revisited 2023 an international journal in behavioural and cognitive neuroscience Amsterdam [u.a.] (DE-627)ELV009449108 volume:51 year:2013 number:13 pages:2562-2571 extent:10 https://doi.org/10.1016/j.neuropsychologia.2013.09.032 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.71 Verkehrsmedizin VZ AR 51 2013 13 2562-2571 10 045F 610 |
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10.1016/j.neuropsychologia.2013.09.032 doi GBVA2013022000020.pica (DE-627)ELV022325182 (ELSEVIER)S0028-3932(13)00334-5 DE-627 ger DE-627 rakwb eng 610 610 DE-600 610 VZ 44.71 bkl Ness, Vanessa verfasserin aut The role of the striatum in goal activation of cascaded actions 2013transfer abstract 10 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. Action selection Elsevier Striatum Elsevier Caudate Elsevier Stop-change Elsevier Action chunking Elsevier Beste, Christian oth Enthalten in Elsevier Science MacDonald, Russell D. ELSEVIER Articles That May Change Your Practice: Pelvic Binders Revisited 2023 an international journal in behavioural and cognitive neuroscience Amsterdam [u.a.] (DE-627)ELV009449108 volume:51 year:2013 number:13 pages:2562-2571 extent:10 https://doi.org/10.1016/j.neuropsychologia.2013.09.032 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 44.71 Verkehrsmedizin VZ AR 51 2013 13 2562-2571 10 045F 610 |
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The role of the striatum in goal activation of cascaded actions |
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Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. |
abstractGer |
Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. |
abstract_unstemmed |
Successful multitasking requires subjects to flexibly activate task goals important to accomplish the task at hand. However, the neural mechanisms underlying goal activation in multitasking are unknown. Based on neurobiological models of action selection, we expected that the extent to which task-goals are processed with some overlap that strongly depends on striatal structures. Therefore, we applied a stop-change paradigm to examine multitasking using fMRI and manipulated the delay between the stop stimulus and the subsequently following change signal towards a new GO response (stop-change delay; SCD). The manipulation of the SCD was introduced to achieve varying amounts of overlap of the two task-goals (stop goal, change goal). This manipulation allowed the calculation of a stop-change delay-reaction time function (SCD-RT function), with the slope of this function, reflecting on the degree of overlap between the stop and the change goal. Data analysis revealed that change trials, independent of their SCD, showed an activation pattern encompassing frontal and parietal cortical regions. Contrasting the two main SCD (long vs. short SCD) conditions with each other showed a stronger BOLD (blood oxygenation level dependent) signal activation of the caudate and the right inferior frontal gyrus in trials with a long SCD compared to trials with a short SCD. Follow-up analyses showed that activation differences of the caudate between the two SCDs drive the effect. Integrating the fMRI data with the slope of the SCD-RT function indicated that the degree of overlap of stop and change processes is determined by the degree of striatal activation on a serial-to-parallel continuum. In conclusion, the findings acknowledge the role of the basal ganglia as an important structure determining action selection processes via a network of neocortical and striatal structures, in terms of an extended multiple demand system. |
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