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Distinct Cerebellar Regions for Body Motion Discrimination

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Date 2019 Dec 11
PMID 31820788
Citations 13
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Abstract

Visual processing of human movements is critical for adaptive social behavior. Cerebellar activations have been observed during biological motion discrimination in prior neuroimaging studies, and cerebellar lesions may be detrimental for this task. However, whether the cerebellum plays a causal role in biological motion discrimination has never been tested. Here, we addressed this issue in three different experiments by interfering with the posterior cerebellar lobe using transcranial magnetic stimulation (TMS) during a biological discrimination task. In Experiments 1 and 2, we found that TMS delivered at onset of the visual stimuli over the vermis (vermal lobule VI), but not over the left cerebellar hemisphere (left lobule VI/Crus I), interfered with participants' ability to distinguish biological from scrambled motion compared to stimulation of a control site (vertex). Interestingly, when stimulation was delivered at a later time point (300 ms after stimulus onset), participants performed worse when TMS was delivered over the left cerebellar hemisphere compared to the vermis and the vertex (Experiment 3). Our data show that the posterior cerebellum is causally involved in biological motion discrimination and suggest that different sectors of the posterior cerebellar lobe may contribute to the task at different time points.

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References
1.
Janssen A, Oostendorp T, Stegeman D . The effect of local anatomy on the electric field induced by TMS: evaluation at 14 different target sites. Med Biol Eng Comput. 2014; 52(10):873-83. DOI: 10.1007/s11517-014-1190-6. View

2.
Allison , Puce , McCarthy . Social perception from visual cues: role of the STS region. Trends Cogn Sci. 2000; 4(7):267-278. DOI: 10.1016/s1364-6613(00)01501-1. View

3.
Lapenta O, Xavier A, Correa S, Boggio P . Human biological and nonbiological point-light movements: Creation and validation of the dataset. Behav Res Methods. 2016; 49(6):2083-2092. DOI: 10.3758/s13428-016-0843-9. View

4.
Puce A, Perrett D . Electrophysiology and brain imaging of biological motion. Philos Trans R Soc Lond B Biol Sci. 2003; 358(1431):435-45. PMC: 1693130. DOI: 10.1098/rstb.2002.1221. View

5.
Bijsterbosch J, Barker A, Lee K, Woodruff P . Where does transcranial magnetic stimulation (TMS) stimulate? Modelling of induced field maps for some common cortical and cerebellar targets. Med Biol Eng Comput. 2012; 50(7):671-81. DOI: 10.1007/s11517-012-0922-8. View