A year in research · 28 selected publications · five research threads
In 2016, we decomposed action control into sensory selection, feature binding, response choice, inhibition and evaluation—and showed that each can change independently.
This component-based view made apparently paradoxical findings intelligible: children could switch more flexibly than adults, alcohol could help or harm depending on workload, and a clinical group could behave normally while showing altered neural processing.
01 · EVENT CODING
Voluntary event coding separated stimulus categorization, feature unbinding and response selection into distinct EEG processes; reward selectively changed the earliest of these.[1] Perceptual conflicts could already impair later stopping, with the recruited network depending on sensory-integration complexity.[2] Concurrent information shifted inhibition in both directions through theta-network architecture.[3]
Conscious and subliminal conflict began as distinct processes but interacted from early perception through response selection.[4] Backward inhibition, by contrast, depended mainly on current attentional selection rather than later N2 or P3 processes, and reward reduced that attentional inhibition specifically.[5,6]
In plain terms: A controlled action is assembled from separable operations, so an experimental effect must be assigned to the stage that actually changed.
02 · NEUROCHEMISTRY
D1- and D2-receptor variants differentially influenced inhibition subprocesses, and tyrosine benefited working memory and stopping most in people with a genotype associated with lower striatal dopamine.[7,8] Transcutaneous vagus nerve stimulation suggested that norepinephrine was more important than simultaneous GABAergic modulation for its inhibitory effects.[9]
Deep brain stimulation of globus pallidus compensated controlled-inhibition deficits in pantothenate kinase-associated neurodegeneration while leaving automatic behaviour relatively distinct.[10] Wilson's disease similarly showed compromised neural evaluation of successful stopping even without greater behavioural impulsivity.[11]
In plain terms: Neurochemical and basal-ganglia effects are process- and person-specific, not uniform changes in performance.
03 · DEVELOPMENT AND ADAPTATION
Late-childhood participants unexpectedly outperformed young adults in memory-based task switching, illustrating that development need not be a monotonic improvement.[12] Older adults used less efficient task-goal strategies during action cascading because response-selection processes in temporoparietal cortex changed.[13] Deaf adults showed better action cascading through reorganized downstream sensorimotor processes rather than early sensory differences alone.[14]
Fatigue, simulated scanner noise and response mode each changed selected parts of the processing cascade.[15,16] Single-subject prediction indicated that early allocation of resources during responding was especially important for individual stopping success.[17]
In plain terms: Age and sensory experience reshape particular routes through the system; they do not simply add or subtract a general capacity.
04 · CLINICAL SPECIFICITY
Tourette syndrome involved weaker binding of perceptual features and reduced recruitment of higher-order sensorimotor-gating regions.[18,19] The moment-to-moment relation between premonitory urges and tics was variable, and voluntary suppression partly decoupled the two.[20]
In adolescent autism, multisensory content altered attention and conflict monitoring during inhibition.[21] In ADHD, attentional filtering differed broadly, but medial-prefrontal response selection was the process that predicted impulsive errors; theta/beta neurofeedback modulated this relevant mechanism.[22,23]
In plain terms: Clinical explanation improves when binding, gating and response choice are measured separately and related to behaviour.
05 · CONTEXT AND STRATEGY
High-dose alcohol and binge drinking had highly specific effects that reversed with mental workload rather than producing a universal inhibition deficit.[24,25] Combined interference sources interacted through theta activity and partly distinct frontal and parietal regions.[26]
A causal TMS/EEG test questioned a broad role for frontopolar cortex in multi-component behaviour.[27] Excessive control could itself be non-adaptive by suppressing useful implicit learning through right prefrontal mechanisms.[28] These studies encouraged narrower causal claims tied to actual task demands.
In plain terms: The functional value of control depends on workload, information structure and whether automatic regularities should be used.
The 2016 programme established a detailed component logic for action control. That logic connected molecules, networks and behaviour while clarifying why development, clinical variation and intoxication can produce selective—and sometimes counterintuitive—effects.
Curated from PubMed records returned for Beste C[au] in 2016. Citation numbers in the story link to entries below. DOI links open the publisher landing page; PubMed links open the indexed record.
Petruo VA, Stock AK, Münchau A, Beste C. NeuroImage. 2016;135:324-32.
DOI: 10.1016/j.neuroimage.2016.05.007 · PubMed
Chmielewski WX, Beste C. Scientific reports. 2016;6:26289.
DOI: 10.1038/srep26289 · PubMed
Chmielewski WX, Mückschel M, Dippel G, Beste C. Brain structure & function. 2016;221(8):3949-3961.
DOI: 10.1007/s00429-015-1137-1 · PubMed
Stock AK, Friedrich J, Beste C. Cortex; a journal devoted to the study of the nervous system and behavior. 2016;85:75-89.
DOI: 10.1016/j.cortex.2016.09.027 · PubMed
Zhang R, Stock AK, Fischer R, Beste C. Brain structure & function. 2016;221(9):4575-4587.
DOI: 10.1007/s00429-016-1186-0 · PubMed
Zhang R, Stock AK, Beste C. NeuroImage. 2016;142:163-171.
DOI: 10.1016/j.neuroimage.2016.05.080 · PubMed
Beste C, Stock AK, Epplen JT, Arning L. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology. 2016;26(6):1029-36.
DOI: 10.1016/j.euroneuro.2016.03.002 · PubMed
Colzato LS, Steenbergen L, Sellaro R, Stock AK, Arning L, Beste C. Cortex; a journal devoted to the study of the nervous system and behavior. 2016;82:217-224.
DOI: 10.1016/j.cortex.2016.06.010 · PubMed
Beste C, Steenbergen L, Sellaro R, Grigoriadou S, et al.. Brain stimulation. 2016;9(6):811-818.
DOI: 10.1016/j.brs.2016.07.004 · PubMed
Mückschel M, Smitka M, Hermann A, von der Hagen M, Beste C. Brain structure & function. 2016;221(4):2251-7.
DOI: 10.1007/s00429-015-1041-8 · PubMed
Stock AK, Reuner U, Gohil K, Beste C. Archives of toxicology. 2016;90(7):1623-30.
DOI: 10.1007/s00204-015-1609-3 · PubMed
Wolff N, Roessner V, Beste C. Scientific reports. 2016;6:28954.
DOI: 10.1038/srep28954 · PubMed
Stock AK, Gohil K, Beste C. Brain structure & function. 2016;221(5):2767-75.
DOI: 10.1007/s00429-015-1071-2 · PubMed
Gohil K, Hahne A, Beste C. Scientific reports. 2016;6:28259.
DOI: 10.1038/srep28259 · PubMed
Kobald SO, Getzmann S, Beste C, Wascher E. Scientific reports. 2016;6:28371.
DOI: 10.1038/srep28371 · PubMed
Dippel G, Chmielewski W, Mückschel M, Beste C. Brain structure & function. 2016;221(8):4091-4101.
DOI: 10.1007/s00429-015-1148-y · PubMed
Stock AK, Popescu F, Neuhaus AH, Beste C. Journal of neurophysiology. 2016;115(3):1252-62.
DOI: 10.1152/jn.00969.2015 · PubMed
Beste C, Tübing J, Seeliger H, Bäumer T, Brandt V, Stock AK, Münchau A. Cortex; a journal devoted to the study of the nervous system and behavior. 2016;83:160-6.
DOI: 10.1016/j.cortex.2016.07.015 · PubMed
Buse J, Beste C, Herrmann E, Roessner V. The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry. 2016;17(3):187-97.
DOI: 10.3109/15622975.2015.1112033 · PubMed
Brandt VC, Beck C, Sajin V, Baaske MK, et al.. Cortex; a journal devoted to the study of the nervous system and behavior. 2016;77:24-37.
DOI: 10.1016/j.cortex.2016.01.008 · PubMed
Chmielewski WX, Wolff N, Mückschel M, Roessner V, Beste C. Psychological medicine. 2016;46(13):2705-16.
DOI: 10.1017/S0033291716001008 · PubMed
Bluschke A, Roessner V, Beste C. Psychological medicine. 2016;46(6):1277-87.
DOI: 10.1017/S0033291715002822 · PubMed
Bluschke A, Broschwitz F, Kohl S, Roessner V, Beste C. Scientific reports. 2016;6:31178.
DOI: 10.1038/srep31178 · PubMed
Stock AK, Schulz T, Lenhardt M, Blaszkewicz M, Beste C. Addiction biology. 2016;21(1):136-45.
DOI: 10.1111/adb.12170 · PubMed
Stock AK, Riegler L, Chmielewski WX, Beste C. Archives of toxicology. 2016;90(6):1429-36.
DOI: 10.1007/s00204-015-1565-y · PubMed
Mückschel M, Stock AK, Dippel G, Chmielewski W, Beste C. NeuroImage. 2016;125:342-349.
DOI: 10.1016/j.neuroimage.2015.09.075 · PubMed
Gohil K, Dippel G, Beste C. Scientific reports. 2016;6:22317.
DOI: 10.1038/srep22317 · PubMed
Stock AK, Steenbergen L, Colzato L, Beste C. Human brain mapping. 2016;37(12):4511-4522.
DOI: 10.1002/hbm.23325 · PubMed