The posterior parietal cortex contributes to visuomotor processing for saccades in blindsight macaques.


Journal

Communications biology
ISSN: 2399-3642
Titre abrégé: Commun Biol
Pays: England
ID NLM: 101719179

Informations de publication

Date de publication:
04 03 2021
Historique:
received: 08 06 2020
accepted: 04 02 2021
entrez: 5 3 2021
pubmed: 6 3 2021
medline: 11 8 2021
Statut: epublish

Résumé

Patients with damage to the primary visual cortex (V1) lose visual awareness, yet retain the ability to perform visuomotor tasks, which is called "blindsight." To understand the neural mechanisms underlying this residual visuomotor function, we studied a non-human primate model of blindsight with a unilateral lesion of V1 using various oculomotor tasks. Functional brain imaging by positron emission tomography showed a significant change after V1 lesion in saccade-related visuomotor activity in the intraparietal sulcus area in the ipsi- and contralesional posterior parietal cortex. Single unit recordings in the lateral bank of the intraparietal sulcus (lbIPS) showed visual responses to targets in the contralateral visual field on both hemispheres. Injection of muscimol into the ipsi- or contralesional lbIPSs significantly impaired saccades to targets in the V1 lesion-affected visual field, differently from previous reports in intact animals. These results indicate that the bilateral lbIPSs contribute to visuomotor function in blindsight.

Identifiants

pubmed: 33664430
doi: 10.1038/s42003-021-01804-z
pii: 10.1038/s42003-021-01804-z
pmc: PMC7933420
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

278

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Auteurs

Rikako Kato (R)

Department of Developmental Physiology, National Institute for Physiological Sciences, Okazaki, Japan.
Department of Neuroscience, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Takuya Hayashi (T)

Laboratory for Brain Connectomics Imaging, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.
Center of Molecular Imaging Science, RIKEN, Kobe, Japan.

Kayo Onoe (K)

Laboratory for Brain Connectomics Imaging, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan.
Center of Molecular Imaging Science, RIKEN, Kobe, Japan.

Masatoshi Yoshida (M)

Department of Developmental Physiology, National Institute for Physiological Sciences, Okazaki, Japan.
School of Life Sciences, the Graduate University of Advanced Studies (SOKENDAI), Hayama, Japan.
Center for Human Nature, Artificial Intelligence, and Neuroscience (CHAIN), Hokkaido University, Sapporo, Japan.

Hideo Tsukada (H)

Central Research Laboratory, Hamamatsu Photonics K.K., Hamamatsu, Japan.

Hirotaka Onoe (H)

Center of Molecular Imaging Science, RIKEN, Kobe, Japan.
Human Brain Research Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Tadashi Isa (T)

Department of Developmental Physiology, National Institute for Physiological Sciences, Okazaki, Japan. isa.tadashi.7u@kyoto-u.ac.jp.
Department of Neuroscience, Graduate School of Medicine, Kyoto University, Kyoto, Japan. isa.tadashi.7u@kyoto-u.ac.jp.
School of Life Sciences, the Graduate University of Advanced Studies (SOKENDAI), Hayama, Japan. isa.tadashi.7u@kyoto-u.ac.jp.
Human Brain Research Center, Graduate School of Medicine, Kyoto University, Kyoto, Japan. isa.tadashi.7u@kyoto-u.ac.jp.
Institute for the Advanced Study of Human Biology (WPI-ASHBi), Kyoto University, Kyoto, Japan. isa.tadashi.7u@kyoto-u.ac.jp.

Takuro Ikeda (T)

Department of Developmental Physiology, National Institute for Physiological Sciences, Okazaki, Japan. taikeda-ns@umin.ac.jp.
Department of Cognitive Neuroscience, Primate Research Institute, Kyoto University, Inuyama, Japan. taikeda-ns@umin.ac.jp.

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Classifications MeSH