Testing the dopamine overdose hypothesis in action control: A study in people with Parkinson's disease

被引:0
作者
Ruitenberg, Marit F. L. [1 ,2 ,3 ]
Abrahamse, Elger L. [4 ,5 ]
Santens, Patrick [6 ]
Notebaert, Wim [3 ]
机构
[1] Leiden Univ, Dept Hlth Med & Neuropsychol, Leiden, Netherlands
[2] Leiden Inst Brain & Cognit, Leiden, Netherlands
[3] Univ Ghent, Dept Expt Psychol, Ghent, Belgium
[4] Tilburg Univ, Dept Commun & Cognit, Tilburg, Netherlands
[5] Atlantico Medio Univ, Dept Educ Sci, Las Palmas Gran Canaria, Spain
[6] Ghent Univ Hosp, Dept Neurol, Ghent, Belgium
关键词
action control; dopamine; movement; Parkinson's disease; MONTREAL COGNITIVE ASSESSMENT; EVENT CODING TEC; RELEASE FORMULATION; CONFLICT ADAPTATION; DUAL-RELEASE; MEDICATION; PERCEPTION; LEVODOPA; MOCA; PHARMACOKINETICS;
D O I
10.1111/jnp.12296
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
Prior work on patients with Parkinson's disease (PD) has shown that the administration of dopaminergic medication in the early to intermediate stages of PD benefits (motor) functions associated with the dopamine-depleted dorsal striatal circuitry but may 'overdose' and interfere with (cognitive) functions associated with the relatively intact ventral striatal circuitry. The present study aimed to elucidate this so-called dopamine overdose hypothesis for the action control domain. Using a within-subject design in a sample of 13 people with PD, we evaluated the effect of dopaminergic medication on two cognitive processes underlying goal-directed behaviour, namely action selection and initiation through event binding and conflict adaptation. We also investigated whether individual differences in the magnitude of medication effects were associated across these processes. Results showed no indications that dopaminergic medication affects action selection and initiation or conflict adaptation in PD patients. Additionally, we observed no correlations between both cognitive processes nor between individual differences in medication effects. Our findings do not support the notion that dopaminergic medication modulates action control processes, suggesting that the dopamine overdose hypothesis may only apply to a specific set of cognitive processes and should potentially be refined.
引用
收藏
页码:264 / 278
页数:15
相关论文
共 53 条
[1]   A CLASSIFICATION OF HAND PREFERENCE BY ASSOCIATION ANALYSIS [J].
ANNETT, M .
BRITISH JOURNAL OF PSYCHOLOGY, 1970, 61 (03) :303-&
[2]   Additive Effects of Item-Specific and Congruency Sequence Effects in the Vocal Stroop Task [J].
Aschenbrenner, Andrew J. ;
Balota, David A. .
FRONTIERS IN PSYCHOLOGY, 2019, 10
[3]  
Beck A. T., 1996, Manual for the Beck Depression Inventory-II
[4]   Conflict monitoring and anterior cingulate cortex: an update [J].
Botvinick, Matthew M. ;
Cohen, Jonathan D. ;
Carter, Cameron S. .
TRENDS IN COGNITIVE SCIENCES, 2004, 8 (12) :539-546
[5]   Conflict monitoring and cognitive control [J].
Botvinick, MM ;
Braver, TS ;
Barch, DM ;
Carter, CS ;
Cohen, JD .
PSYCHOLOGICAL REVIEW, 2001, 108 (03) :624-652
[6]   Measuring Adaptive Control in Conflict Tasks [J].
Braem, Senne ;
Bugg, Julie M. ;
Schmidt, James R. ;
Crump, Matthew J. C. ;
Weissman, Daniel H. ;
Notebaert, Wim ;
Egner, Tobias .
TRENDS IN COGNITIVE SCIENCES, 2019, 23 (09) :769-783
[7]   Evidence for the Sparing of Reactive Cognitive Control With Age [J].
Bugg, Julie M. .
PSYCHOLOGY AND AGING, 2014, 29 (01) :115-127
[8]   In support of a distinction between voluntary and stimulus-driven control: a review of the literature on proportion congruent effects [J].
Bugg, Julie M. ;
Crump, Matthew J. C. .
FRONTIERS IN PSYCHOLOGY, 2012, 3
[9]   Power failure: why small sample size undermines the reliability of neuroscience [J].
Button, Katherine S. ;
Ioannidis, John P. A. ;
Mokrysz, Claire ;
Nosek, Brian A. ;
Flint, Jonathan ;
Robinson, Emma S. J. ;
Munafo, Marcus R. .
NATURE REVIEWS NEUROSCIENCE, 2013, 14 (05) :365-376
[10]   A re-examination of Montreal Cognitive Assessment (MoCA) cutoff scores [J].
Carson, Nicole ;
Leach, Larry ;
Murphy, Kelly J. .
INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY, 2018, 33 (02) :379-388