Recruitment of the middle temporal area by tactile motion in congenital blindness
Abstract
We used positron emission tomography to investigate whether tactile motion discrimination activates the dorsal visual stream in congenitally blind (CB) participants compared with sighted controls. The tactile stimuli consisted of either static dots, dots moving coherently in one of two possible directions, or in random directions. Although CB and sighted controls performed equally well on the motion discrimination task, only CB showed increased activation in the right middle temporal area. In addition, CB also activated other visual areas including the cuneus and extrastriate area V3. These results indicate that the dorsal visual pathway is activated by tactile motion stimuli in CB, therefore providing additional support for the cross-modal plasticity hypothesis.
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Object vision and spatial vision: Two cortical pathways
Mishkin, M., Ungerleider, L. G., & Macko, K. A. (1983) · Trends in Neurosciences · doi:10.1016/0166-2236(83)90190-x · Cited by 2,947 · see citing works
Neuroscience: Exploring the brain
Wood, I. K. (1996) · Journal of Child and Family Studies · doi:10.1007/bf02234670 · Cited by 1,529 · see citing works
Early ‘visual’ cortex activation correlates with superior verbal memory performance in the blind
Amedi, A., Raz, N., Pianka, P., Malach, R., & Zohary, E. (2003) · Nature Neuroscience · doi:10.1038/nn1072 · Cited by 591 · see citing works
Goebel, R., Khorram‐Sefat, D., Muckli, L., Hacker, H., & Singer, W. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00181.x · Cited by 570 · see citing works
Multisensory convergence in calcarine visual areas in macaque monkey
Rockland, K. S., & Ojima, H. (2003) · International Journal of Psychophysiology · doi:10.1016/s0167-8760(03)00121-1 · Cited by 564 · see citing works
A Positron Emission Tomographic Study of Auditory Localization in the Congenitally Blind
Weeks, R., Horwitz, B., Aziz‐Sultan, M. A., Tian, B., Wessinger, C. M., Cohen, L. G., Hallett, M., & Rauschecker, J. P. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-07-02664.2000 · Cited by 486 · see citing works
Beyond sensory images: Object-based representation in the human ventral pathway
Pietrini, P., Furey, M. L., Ricciardi, E., Gobbini, M. I., Wu, C. W. ‐., Cohen, L. G., Guazzelli, M., & Haxby, J. V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400707101 · Cited by 484 · see citing works
A Comparison of Visual and Auditory Motion Processing in Human Cerebral Cortex
Lewis, J. W. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.9.873 · Cited by 381 · see citing works
Adaptive Changes in Early and Late Blind: A fMRI Study of Braille Reading
Burton, H., Snyder, A. Z., Conturo, T. E., Akbudak, E., Ollinger, J. M., & Raichle, M. E. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00285.2001 · Cited by 369 · see citing works
The Neurology of Consciousness
VALKENBURG, C. T. V. (2009) · Elsevier eBooks · doi:10.1016/b978-0-12-374168-4.x0001-9 · Cited by 366 · see citing works
Ptito, M. (2005) · Brain · doi:10.1093/brain/awh380 · Cited by 310 · see citing works
Self-citationTactile motion activates the human middle temporal/V5 (MT/V5) complex
Hagen, M. C., Franzén, O. G., McGlone, F. P., Essick, G. K., Dancer, C., & Pardo, J. V. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02139.x · Cited by 253 · see citing works
Adaptive Changes in Early and Late Blind: A fMRI Study of Verb Generation to Heard Nouns
Burton, H., Snyder, A. Z., Diamond, J. B., & Raichle, M. E. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00129.2002 · Cited by 233 · see citing works
Diffusion Tensor Imaging Reveals White Matter Reorganization in Early Blind Humans
Shimony, J. S., Burton, H., Epstein, A. A., McLaren, D. G., Sun, S.-W., & Snyder, A. Z. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj102 · Cited by 233 · see citing works
Auditory motion perception activates visual motion areas in early blind subjects
Poirier, C., Collignon, O., Scheiber, C., Renier, L., Vanlierde, A., Tranduy, D., Veraart, C., & De Volder, A. G. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2005.11.036 · Cited by 227 · see citing works
Neural Synergy Between Kinetic Vision and Touch
Blake, R., Sobel, K. V., & James, T. W. (2004) · Psychological Science · doi:10.1111/j.0956-7976.2004.00691.x · Cited by 225 · see citing works
Alterations of the visual pathways in congenital blindness
Ptito, M., Schneider, F., Paulson, O. B., & Kupers, R. C. (2008) · Experimental Brain Research · doi:10.1007/s00221-008-1273-4 · Cited by 219 · see citing works
Self-citationFunctional connectivity between somatosensory and visual cortex in early blind humans
Wittenberg, G. F., Werhahn, K. J., Wassermann, E. M., Herscovitch, P., & Cohen, L. G. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03630.x · Cited by 151 · see citing works
Visual Motion Area MT+/V5 Responds to Auditory Motion in Human Sight-Recovery Subjects
Sàenz, M., Lewis, L. B., Huth, A. G., Fine, I., & Christof Koch, A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0803-08.2008 · Cited by 134 · see citing works
Brain energy metabolism in early blind subjects: neural activity in the visual cortex
Volder, A. D., Bol, A., Blin, J., Robert, A. R., Arno, P., Grandin, C. B. G., Michel, C. J., & Veraart, C. (1997) · Brain Research · doi:10.1016/s0006-8993(96)01352-2 · Cited by 121 · see citing works
Neural Correlates of Coherent Audiovisual Motion Perception
Baumann, O., & Greenlee, M. W. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhl055 · Cited by 117 · see citing works
CROSS-MODAL PLASTICITY IN EARLY BLINDNESS
Ptito, M., & Kupers, R. C. (2005) · Journal of Integrative Neuroscience · doi:10.1142/s0219635205000951 · Cited by 81 · see citing works
Self-citationSeparate neural pathways for contour and biological-motion cues in motion-defined animal shapes
Ptito, M., Faubert, J., Gjedde, A., & Kupers, R. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00082-x · Cited by 54 · see citing works
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Maidenbaum, S., Abboud, S., & Amedi, A. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.11.007 · Cited by 230 · see citing works
Functional connectivity of visual cortex in the blind follows retinotopic organization principles
Striem-Amit, E., Ovadia-Caro, S., Caramazza, A., Margulies, D. S., Villringer, A., & Amedi, A. (2015) · Brain · doi:10.1093/brain/awv083 · Cited by 194 · see citing works
Ricciardi, E., Bonino, D., Pellegrini, S., & Pietrini, P. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.10.006 · Cited by 154 · see citing works
Cortical plasticity and preserved function in early blindness
Renier, L., De Volder, A. G., & Rauschecker, J. P. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.01.025 · Cited by 144 · see citing works
‘Visual’ Acuity of the Congenitally Blind Using Visual-to-Auditory Sensory Substitution
Striem-Amit, E., Guendelman, M., & Amedi, A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033136 · Cited by 117 · see citing works
Designing sensory-substitution devices: Principles, pitfalls and potential1
Kristjánsson, Á., Moldoveanu, A., Jóhannesson, Ó. I., Balan, O., Spagnol, S., Valgeirsdóttir, V. V., & Unnthorsson, R. (2016) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-160647 · Cited by 116 · see citing works
“Additionally, tactile motion discrimination activates dorsal visual stream areas in the congenitally blind (Ptito et al., 2009).”
BackgroundAuditory, tactile, and audiotactile information processing following visual deprivation
Occelli, V., Spence, C., & Zampini, M. (2013) · Psychological Bulletin · doi:10.1037/a0028416 · Cited by 43 · see citing works
The role of visual deprivation and experience on the performance of sensory substitution devices
Stronks, H. C., Nau, A. C., Ibbotson, M. R., & Barnes, N. (2015) · Brain Research · doi:10.1016/j.brainres.2015.06.033 · Cited by 31 · see citing works
Sulpizio, V., Strappini, F., Fattori, P., Galati, G., Galletti, C., Pecchinenda, A., & Pitzalis, S. (2022) · Brain Structure and Function · doi:10.1007/s00429-022-02549-z · Cited by 12 · see citing works
- Authors
- Ptito, M., Matteau, I., Gjedde, A., & Kupers, R.
- Affiliations
- Université de Montréal (CA)
- University of Copenhagen (DK)
- Corresponding author
- Kupers, Ron
- Venue
- Neuroreport
- Published
- 2009-04-22
- Volume
- 20
- Issue
- 6
- Pages
- 543-547
- ISSN
- 0959-4965 (ISSN-L)
- OpenAlex
- W1967976608
- Cited by
- 65
- References
- 23
- Citations by year
- 2025: 2 · 2024: 2 · 2023: 3 · 2022: 5 · 2021: 3 · 2020: 3 · 2019: 4 · 2018: 4 · 2017: 3 · 2016: 5 · 2015: 8 · 2014: 4 · 2013: 7 · 2012: 5
- FWCI
- 1.94
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Neuroreport (publishedVersion)
- PubMed (publishedVersion)
- Research at the University of Copenhagen (University of Copenhagen) (submittedVersion)
- Funders
- Sundhed og Sygdom, Det Frie Forskningsråd
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Tactile and Sensory Interactions
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Multisensory perception and integration
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Keywords
- congenital blindness, middle temporal area, dorsal stream, cross-modal plasticity, visual cortex activation, cuneus, visual motion perception
- MeSH terms
- Adult, Blindness, Humans, Middle Aged, Motion Perception, Physical Stimulation, Temporal Lobe, Visual Pathways, Positron-Emission Tomography, Touch Perception, Young Adult
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