Literature DB >> 35763171

Egomotion-related visual areas respond to goal-directed movements.

Martina Bellagamba1,2, Valentina Sulpizio2,3, Patrizia Fattori4, Gaspare Galati2,3, Claudio Galletti4, Teresa Maltempo1,2, Sabrina Pitzalis5,6.   

Abstract

Integration of proprioceptive signals from the various effectors with visual feedback of self-motion from the retina is necessary for whole-body movement and locomotion. Here, we tested whether the human visual motion areas involved in processing optic flow signals simulating self-motion are also activated by goal-directed movements (as saccades or pointing) performed with different effectors (eye, hand, and foot), suggesting a role in visually guiding movements through the external environment. To achieve this aim, we used a combined approach of task-evoked activity and effective connectivity (PsychoPhysiological Interaction, PPI) by fMRI. We localized a set of six egomotion-responsive visual areas through the flow field stimulus and distinguished them into visual (pIPS/V3A, V6+ , IPSmot/VIP) and visuomotor (pCi, CSv, PIC) areas according to recent literature. We tested their response to a visuomotor task implying spatially directed delayed eye, hand, and foot movements. We observed a posterior-to-anterior gradient of preference for eye-to-foot movements, with posterior (visual) regions showing a preference for saccades, and anterior (visuomotor) regions showing a preference for foot pointing. No region showed a clear preference for hand pointing. Effective connectivity analysis showed that visual areas were more connected to each other with respect to the visuomotor areas, particularly during saccades. We suggest that visual and visuomotor egomotion regions can play different roles within a network that integrates sensory-motor signals with the aim of guiding movements in the external environment.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Functional magnetic resonance; Optic flow; Pointing; Superior parietal lobule; Visuomotor control

Mesh:

Year:  2022        PMID: 35763171     DOI: 10.1007/s00429-022-02523-9

Source DB:  PubMed          Journal:  Brain Struct Funct        ISSN: 1863-2653            Impact factor:   3.748


  67 in total

1.  An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest.

Authors:  Rahul S Desikan; Florent Ségonne; Bruce Fischl; Brian T Quinn; Bradford C Dickerson; Deborah Blacker; Randy L Buckner; Anders M Dale; R Paul Maguire; Bradley T Hyman; Marilyn S Albert; Ronald J Killiany
Journal:  Neuroimage       Date:  2006-03-10       Impact factor: 6.556

Review 2.  Intention, action planning, and decision making in parietal-frontal circuits.

Authors:  Richard A Andersen; He Cui
Journal:  Neuron       Date:  2009-09-10       Impact factor: 17.173

3.  Cortical surface-based analysis. I. Segmentation and surface reconstruction.

Authors:  A M Dale; B Fischl; M I Sereno
Journal:  Neuroimage       Date:  1999-02       Impact factor: 6.556

4.  Neural mechanisms for discounting head-roll-induced retinal motion.

Authors:  Jac Billington; Andrew T Smith
Journal:  J Neurosci       Date:  2015-03-25       Impact factor: 6.167

Review 5.  Opportunities and limitations of intrinsic functional connectivity MRI.

Authors:  Randy L Buckner; Fenna M Krienen; B T Thomas Yeo
Journal:  Nat Neurosci       Date:  2013-06-25       Impact factor: 24.884

Review 6.  Understanding the parietal lobe syndrome from a neurophysiological and evolutionary perspective.

Authors:  Roberto Caminiti; Matthew V Chafee; Alexandra Battaglia-Mayer; Bruno B Averbeck; David A Crowe; Apostolos P Georgopoulos
Journal:  Eur J Neurosci       Date:  2010-06-09       Impact factor: 3.386

7.  Sensitivity of human visual and vestibular cortical regions to egomotion-compatible visual stimulation.

Authors:  Velia Cardin; Andrew T Smith
Journal:  Cereb Cortex       Date:  2009-12-24       Impact factor: 5.357

8.  Processing of Egomotion-Consistent Optic Flow in the Rhesus Macaque Cortex.

Authors:  Benoit R Cottereau; Andrew T Smith; Samy Rima; Denis Fize; Yseult Héjja-Brichard; Luc Renaud; Camille Lejards; Nathalie Vayssière; Yves Trotter; Jean-Baptiste Durand
Journal:  Cereb Cortex       Date:  2017-01-01       Impact factor: 5.357

Review 9.  Vestibular System and Self-Motion.

Authors:  Zhixian Cheng; Yong Gu
Journal:  Front Cell Neurosci       Date:  2018-11-22       Impact factor: 5.505

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