Literature DB >> 7472342

Human cortical regions activated by wide-field visual motion: an H2(15)O PET study.

K Cheng1, H Fujita, I Kanno, S Miura, K Tanaka.   

Abstract

1. Several areas in the monkey dorsal visual pathway, including the dorsal part of the medial superior temporal area, have been found to contain cells responding to movements of a wide visual field and are suggested to be involved in analyzing self-induced motion information. In the present study, positron emission tomography was used to localize human cortical regions responding to wide-field visual motion. Changes in regional cerebral blood flow (rCBF) were measured when subjects maintained fixation and viewed low-contrast (0.15 log units brighter than the background) dots subtending 80 x 80 degrees and moving either coherently or incoherently. Brain foci were localized after activity in a fixation-only paradigm was subtracted from that in the two moving dot paradigms. 2. Both the coherent and incoherent movements significantly activated the primary/secondary visual cortex and surrounding visual areas in the cuneus and superior occipital gyrus. Subtraction of images between the coherent and incoherent movements showed that the activity caused by the two types of movement was comparable in these early visual cortical regions. 3. In the lateral occipitotemporoparietal cortex, the coherent movement specifically activated two separate areas; a posterior focus was located at the border of the right occipitotemporal gyri, and a dorsoanterior focus was located bilaterally in the temporoparietal cortex. The incoherent movement did not activate these regions. 4. A fine anatomic localization using individual magnetic resonance images was performed for the bilateral activation in the temporoparietal cortex, which was found to be located mainly in the depth of the inferior parietal lobule and a small portion of the superior and middle temporal gyri. 5. Both the coherent and incoherent movements activated a part of the superior parietal lobule located within the intraparietal sulcus (Brodmann area 7). The bilateral foci activated by the coherent movement were located more anteriorly than the focus activated by the incoherent movement. Subtraction images between the coherent and incoherent movements, however, did not reveal any significant rCBF increases in the superior parietal lobule. 6. Several other cortical regions known to be involved in visuospatial and visuomotor functions were also activated by the coherent movement, including the frontal eye field (Brodmann area 8) and premotor cortex (Brodmann area 6) in the frontal lobe. 7. The posteriorly located activation at the border of occipito-temporal gyri corresponds to the homologue of the middle temporal area reported in previous activation studies using small to medium-sized motion stimuli. The bilateral activation in the inferior parietal lobule appeared to rely on wide-field motion stimulation.

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Year:  1995        PMID: 7472342     DOI: 10.1152/jn.1995.74.1.413

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  24 in total

1.  Sensory system interactions during simultaneous vestibular and visual stimulation in PET.

Authors:  Angela Deutschländer; Sandra Bense; Thomas Stephan; Markus Schwaiger; Thomas Brandt; Marianne Dieterich
Journal:  Hum Brain Mapp       Date:  2002-06       Impact factor: 5.038

2.  Human visual motion areas determined individually by magnetoencephalography and 3D magnetic resonance imaging.

Authors:  M Bundo; Y Kaneoke; S Inao; J Yoshida; A Nakamura; R Kakigi
Journal:  Hum Brain Mapp       Date:  2000-09       Impact factor: 5.038

3.  The processing of first- and second-order motion in human visual cortex assessed by functional magnetic resonance imaging (fMRI).

Authors:  A T Smith; M W Greenlee; K D Singh; F M Kraemer; J Hennig
Journal:  J Neurosci       Date:  1998-05-15       Impact factor: 6.167

4.  Auditory induced vestibular (otolithic) processing revealed by an independent component analysis: an fMRI parametric analysis.

Authors:  Sun-Young Oh; Rainer Boegle; Matthias Ertl; Peter Zu Eulenburg; Thomas Stephan; Marianne Dieterich
Journal:  J Neurol       Date:  2017-03-07       Impact factor: 4.849

5.  Brain activity during time to contact estimation: an EEG study.

Authors:  Asieh Daneshi; Hamed Azarnoush; Farzad Towhidkhah; Delphine Bernardin; Jocelyn Faubert
Journal:  Cogn Neurodyn       Date:  2019-11-27       Impact factor: 5.082

6.  Functional neuroanatomy of biological motion perception in humans.

Authors:  L M Vaina; J Solomon; S Chowdhury; P Sinha; J W Belliveau
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-11       Impact factor: 11.205

7.  Vection induced by low-level motion extracted from complex animation films.

Authors:  Wataru Suzuki; Takeharu Seno; Wakayo Yamashita; Noritaka Ichinohe; Hiroshige Takeichi; Stephen Palmisano
Journal:  Exp Brain Res       Date:  2019-11-11       Impact factor: 1.972

8.  Impact of early deafness and early exposure to sign language on the cerebral organization for motion processing.

Authors:  D Bavelier; C Brozinsky; A Tomann; T Mitchell; H Neville; G Liu
Journal:  J Neurosci       Date:  2001-11-15       Impact factor: 6.167

9.  Visual detection of motion speed in humans: spatiotemporal analysis by fMRI and MEG.

Authors:  Osamu Kawakami; Yoshiki Kaneoke; Koichi Maruyama; Ryusuke Kakigi; Tomohisa Okada; Norihiro Sadato; Yoshiharu Yonekura
Journal:  Hum Brain Mapp       Date:  2002-06       Impact factor: 5.038

10.  Human v6: the medial motion area.

Authors:  S Pitzalis; M I Sereno; G Committeri; P Fattori; G Galati; F Patria; C Galletti
Journal:  Cereb Cortex       Date:  2009-06-05       Impact factor: 5.357

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