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Observation of Static Pictures of Dynamic Actions Enhances the Activity of Movement-Related Brain Areas
Open accessAbstract
BACKGROUND: Physiological studies of perfectly still observers have shown interesting correlations between increasing effortfulness of observed actions and increases in heart and respiration rates. Not much is known about the cortical response induced by observing effortful actions. The aim of this study was to investigate the time course and neural correlates of perception of implied motion, by presenting 260 pictures of human actions differing in degrees of dynamism and muscular exertion. ERPs were recorded from 128 sites in young male and female adults engaged in a secondary perceptual task. PRINCIPAL FINDINGS: Our results indicate that even when the stimulus shows no explicit motion, observation of static photographs of human actions with implied motion produces a clear increase in cortical activation, manifest in a long-lasting positivity (LP) between 350-600 ms that is much greater to dynamic than less dynamic actions, especially in men. A swLORETA linear inverse solution computed on the dynamic-minus-static difference wave in the time window 380-430 ms showed that a series of regions was activated, including the right V5/MT, left EBA, left STS (BA38), left premotor (BA6) and motor (BA4) areas, cingulate and IF cortex. CONCLUSIONS AND SIGNIFICANCE: Overall, the data suggest that corresponding mirror neurons respond more strongly to implied dynamic than to less dynamic actions. The sex difference might be partially cultural and reflect a preference of young adult males for highly dynamic actions depicting intense muscular activity, or a sporty context.
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“complex visual stimuli, including actions, reach PMC and motor areas in around 300ms”
From Mirror neurons: from origin to function (2014) · cites this paper as Proverbio, Riva, & Zani, 2009
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“It has been demonstrated (by using both TMS and event related potentials) that static images with implied motion perception activate both motor and visual areas (Urgesi et al., 2006; Proverbio et al., 2009).”
From Corticomotor Excitability during Observation and Imagination of a Work of Art (2011) · cites this paper as Proverbio et al., 2009
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Cites
Rizzolatti, G., & Craighero, L. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144230 · Cited by 7,433
Cattaneo, L., & Rizzolatti, G. (2009) · Archives of Neurology · doi:10.1001/archneurol.2009.41 · Cited by 3,137
Cortical mechanisms of human imitation
Iacoboni, M., Woods, R. P., Brass, M., Bekkering, H., Mazziotta, J. C., & Rizzolatti, G. (1999) · Science · doi:10.1126/science.286.5449.2526 · Cited by 2,683
Neural simulation of action: a unifying mechanism for motor cognition.
Jeannerod, M. (2001) · NeuroImage · doi:10.1006/nimg.2001.0832 · Cited by 2,563
Action observation activates premotor and parietal areas in a somatotopic manner: an fMRI study
Buccino, G., Binkofski, F., Fink, G. R., Fadiga, L., Fogassi, L., Gallese, V., Seitz, R. J., Zilles, K., Rizzolatti, G., & Freund, H. ‐. (2001) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2001.01385.x · Cited by 2,488
A cortical area selective for visual processing of the human body
Downing, P. E., Jiang, Y., Shuman, M., & Kanwisher, N. (2001) · Science · doi:10.1126/science.1063414 · Cited by 2,043
Imitation, empathy, and mirror neurons
Iacoboni, M. (2009) · Annual Review of Psychology · doi:10.1146/annurev.psych.60.110707.163604 · Cited by 1,606
Arbib, M. A. (2005) · Behavioral and Brain Sciences · doi:10.1017/s0140525x05000038 · Cited by 1,164
Mapping motor representations with positron emission tomography
Decety, J., Perani, D., Jeannerod, M., Bettinardi, V., Tadary, B., Woods, R., Mazziotta, J. C., & Fazio, F. (1994) · Nature · doi:10.1038/371600a0 · Cited by 976
Brain Areas Involved in Perception of Biological Motion
Grossman, E. D., Donnelly, M. P. W., Price, R. R., Pickens, D. R., Morgan, V. L., Neighbor, G., & Blake, R. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/089892900562417 · Cited by 917
Research works printed but not linked: 1
- J Decety, 1994, Mapping motor representations with PET., Nature, 600, 10.1038/371600a0 · DOI · Paper page
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Dolcos, F., Katsumi, Y., Moore, M., Berggren, N., de Gelder, B., Derakshan, N., Hamm, A. O., Koster, E. H. W., Ladouceur, C. D., Okon‐Singer, H., et al. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.08.017 · Cited by 247
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Urgesi, C., Savonitto, M. M., Fabbro, F., & Aglioti, S. M. (2011) · Psychological Research · doi:10.1007/s00426-011-0383-y · Cited by 129
Dio, C. D., Ardizzi, M., Massaro, D., Cesare, G. D., Gilli, G., Marchetti, A., & Gallese, V. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00705 · Cited by 122
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Borgomaneri, S., Gazzola, V., & Avenanti, A. (2012) · Brain stimulation · doi:10.1016/j.brs.2012.03.011 · Cited by 102
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Amoruso, L., Sedeño, L., Huepe, D., Tomio, A., Kamienkowski, J. E., Hurtado, E., Cardona, J. F., González, M. Á. Á., Rieznik, A. A., Sigman, M., et al. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.05.005 · Cited by 94
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Candidi, M., Leone‐Fernandez, B., Barber, H. A., Carreiras, M., & Aglioti, S. M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07305.x · Cited by 43
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Del Casale, A., Ferracuti, S., Rapinesi, C., De Rossi, P., Angeletti, G., Sani, G., Kotzalidis, G. D., & Girardi, P. (2015) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2016.01.001 · Cited by 39
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Osaka, N., Matsuyoshi, D., Ikeda, T., & Osaka, M. (2010) · NeuroReport · doi:10.1097/wnr.0b013e328335b371 · Cited by 60
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Wamain, Y., Tallet, J., Zanone, P.-G., & Longcamp, M. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.07.020 · Cited by 25
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Jia, L., Xu, Y., Sweeney, J. A., Wang, C., Sung, B., & Wang, J. (2019) · Frontiers in Psychology · doi:10.3389/fpsyg.2019.02117 · Cited by 3
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Nather, F. C., Anelli, V., Ennes, G., & Bueno, J. L. O. (2015) · Paidéia (Ribeirão Preto) · doi:10.1590/1982-43272561201513 · Cited by 3
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Zheng, W. (2024) · Behavioral Sciences · doi:10.3390/bs14111092 · Cited by 2
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Heinrich, M. (2022) · Springer eBooks · doi:10.1007/978-3-658-22321-2_11 · Cited by 2
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Yashiro, R., Sawayama, M., Yamashita, A., & Amano, K. (2026) · Imaging Neuroscience · doi:10.1162/imag.a.1309 · Cited by 1
Coffman, B. A. (2014) · UNM’s Digital Repository (University of New Mexico) · Cited by 1
Gozzano, N. (2016) · Recherches en danse · doi:10.4000/danse.1374 · Cited by 1
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Metadata
- Authors
- Proverbio, A. M., Riva, F., & Zani, A.
- Affiliations
- University of Milano-Bicocca (IT)
- Institute of Molecular Bioimaging and Physiology (IT)
- Corresponding author
- Proverbio, Alice Mado
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2009-05-06
- Volume
- 4
- Issue
- 5
- Pages
- e5389
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC2671843
- OpenAlex
- W2146356260
- Cited by
- 108
- References
- 32
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 3 · 2023: 7 · 2022: 4 · 2021: 9 · 2020: 6 · 2019: 6 · 2018: 4 · 2017: 3 · 2016: 5 · 2015: 9 · 2014: 12 · 2013: 6 · 2012: 10
- FWCI
- 11.75
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS ONE (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- BOA (University of Milano-Bicocca) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Figshare (submittedVersion, cc-by)
- Funders
- Università degli Studi di Milano-Bicocca
- Topics
- Social Sciences › Psychology › Social Psychology › Action Observation and Synchronization
- Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
- Life Sciences › Neuroscience › Cognitive Neuroscience › Aesthetic Perception and Analysis
- Keywords
- implied motion, mirror neurons, event-related potentials, sex differences, MT/V5, premotor cortex, STS, cingulate cortex, muscular exertion
- MeSH terms
- Adult, Brain Mapping, Cerebral Cortex, Electroencephalography, Evoked Potentials, Visual, Female, Humans, Male, Motion Perception, Movement, Evoked Potentials, Motor, Observation, Young Adult
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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