Back

Influence of attention mechanisms on cerebellar and basal ganglia activity during vocal emotion decoding

Ceravolo, L.; Thomasson, M.; Constantin, I. M.; Stiennon, E.; Chassot, E.; Pierce, J.; Cionca, A.; Grandjean, D.; Sveikata, L.; Assal, F.; Peron, J.

2026-02-04 neuroscience
10.1101/2024.11.20.624507 bioRxiv
Show abstract

Emotional prosody processing involves a widespread network of brain regions, but the specific roles of the cerebellum and basal ganglia in explicit and implicit tasks are not well known or understood. This study investigated how the cerebellum and basal ganglia contribute to explicit (emotion categorization) and implicit (gender categorization) processing of emotional prosody, namely when attention is directly versus implicitly oriented towards the emotion of the voice stimuli, respectively. Twenty-eight healthy French-speaking participants (average age: 65 years old) underwent high-resolution functional MRI while performing explicit and implicit vocal emotion processing tasks. Neuroimaging results revealed--and replicated--that both tasks recruited a widespread network, including the superior temporal cortex, inferior frontal cortex, primary motor and somatosensory cortices, basal ganglia, and cerebellum. The explicit task elicited stronger activations in the basal ganglia (caudate nucleus, putamen) and cerebellar regions (Crus I/II, lobules VI, VIIb, and X), consistent with higher cognitive control demands. In contrast, the implicit task was associated with activations in cerebellar lobules IV-V, VI, VIII, and IX, along with the thalamus. Regression-based functional connectivity analyses further demonstrated stronger connectivity between the right cerebellar lobule IX and the putamen, as well as the cerebellar vermis (XII), particularly during implicit processing. These findings highlight the distinct contributions of the cerebellum and basal ganglia to emotional prosody processing, with explicit tasks engaging associative and cognitive control networks, while implicit tasks rely more on sensorimotor and automatic neural processing mechanisms.

Matching journals

The top 3 journals account for 50% of the predicted probability mass.

1
Human Brain Mapping
295 papers in training set
Top 0.1%
22.7%
2
NeuroImage
813 papers in training set
Top 0.4%
22.7%
3
Cerebral Cortex
357 papers in training set
Top 0.1%
10.2%
50% of probability mass above
4
Imaging Neuroscience
242 papers in training set
Top 0.5%
6.4%
5
The Journal of Neuroscience
928 papers in training set
Top 2%
4.9%
6
Communications Biology
886 papers in training set
Top 3%
3.1%
7
Scientific Reports
3102 papers in training set
Top 44%
2.8%
8
NeuroImage: Clinical
132 papers in training set
Top 2%
2.1%
9
Journal of Cognitive Neuroscience
119 papers in training set
Top 0.9%
1.7%
10
Brain Research
35 papers in training set
Top 0.8%
1.7%
11
Neuropsychologia
77 papers in training set
Top 0.7%
1.5%
12
Neuroscience & Biobehavioral Reviews
43 papers in training set
Top 0.4%
1.5%
13
Brain Structure and Function
83 papers in training set
Top 0.3%
1.3%
14
eneuro
389 papers in training set
Top 7%
1.2%
15
Frontiers in Human Neuroscience
67 papers in training set
Top 2%
1.2%
16
iScience
1063 papers in training set
Top 29%
0.8%
17
Cerebral Cortex Communications
36 papers in training set
Top 0.2%
0.8%
18
Frontiers in Neuroscience
223 papers in training set
Top 7%
0.8%
19
Brain and Language
11 papers in training set
Top 0.1%
0.8%
20
eLife
5422 papers in training set
Top 59%
0.7%
21
Nature Communications
4913 papers in training set
Top 64%
0.7%
22
Neurobiology of Language
28 papers in training set
Top 0.2%
0.6%
23
PLOS ONE
4510 papers in training set
Top 71%
0.6%
24
Advanced Science
249 papers in training set
Top 23%
0.5%
25
Social Cognitive and Affective Neuroscience
29 papers in training set
Top 0.3%
0.5%
26
Proceedings of the National Academy of Sciences
2130 papers in training set
Top 49%
0.5%