Neuroscience and Behavioral Physiology

, Volume 43, Issue 1, pp 46–55 | Cite as

Activation of Brain Structures Demonstrated by fMRI Data on Viewing Video Clips and Recall of the Actions Shown

  • V. L. Ushakov
  • V. M. Verkhlyutov
  • P. A. Sokolov
  • M. V. Ublinskii
  • V. B. Strelets
  • A. Yu. Agrafonov
  • A. V. Petryaikin
  • T. A. Akhadov
Article
  • 118 Downloads

Functional magnetic resonance imaging scans were obtained in 12 healthy volunteers using a tomograph with a 3-T field magnet. Stimulation was with emotionally calm and emotionally arousing video clips. The experiment consisted of seven series: two series watching the fixation point and two types of video clips, one series with sequential viewing of two types of video clip, two series with viewing video clips followed by recall, and two series with watching the fixation point followed by recall of video clips. Viewing of video clips induced the greatest increases in metabolism, in the visual cortex. Activation was more marked on viewing of emotionally arousing video clips. Apart from the occipital lobe, activity involved the temporal, parietal, and, to a lesser extent, the frontal cortex. Activation of the motor cortex was not seen in all subjects. An “interference” effect was seen on sequential viewing of video clips, whereby increases in metabolism became minimal. Immediate recall of video clips after viewing induced the greatest level of activation of the posterior frontal and motor cortex. Delayed recall produced maximal activation in the anterior parts of the frontal cortex. Metabolism in the visual cortex decreased on recall. The greatest reduction in the visual cortex was seen with immediate recall. Immediate and delayed recall activated structures associated with maintaining consciousness, memory, and the mirror neuron system.

Keywords

functional magnetic resonance imaging mirror neurons memory consciousness 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    G. N. Boldyreva, L. A. Zhavoronkova, E. V. Sharova, S. B. Buklina, A. S. Migalev, D. V. Pyashina, I. N. Pronin, and V. N. Kornienko, “fMRI-EEG studies of brain responses in healthy humans under functional loading,” Fiziol. Cheloveka, 35, No. 3, 20–30 (2009).PubMedGoogle Scholar
  2. 2.
    V. M. Verkhlyutov, V. L. Ushakov, and V. B. Strelets, “Decreases in the latency of the N170 component of evoked potentials on repeated presentation of images of faces,” Zh. Vyssh. Nerv. Deyat., 59, No. 3, 272–282 (2009).Google Scholar
  3. 3.
    I. G. Silkis, “Involvement of the trisynaptic hippocampal pathway in the formation of neural ‘object-place’ representations,” Zh. Vyssh. Nerv. Deyat., 59, No. 6, 643–659 (2009).Google Scholar
  4. 4.
    J. Bonaiuto and M. A. Arbib, “Extending the mirror neuron system model, II: what did I just do? A new role for mirror neurons,” Biol. Cybernet., 102, No. 4, 341–359 (2010).CrossRefGoogle Scholar
  5. 5.
    G. Buccino, F. Binkofski, and L. Riggio, “The mirror neuron system and action recognition,” Brain Lang., 89, No. 2, 370–376 (2004).PubMedCrossRefGoogle Scholar
  6. 6.
    G. Di Pellegrino, L. Fadiga, L. Fogassi, V. Gallese, and V. Rizzolatti, “Understanding motor events: a neurophysiological study,” Exp. Brain Res., 91, No. 1, 176–180 (1992).PubMedCrossRefGoogle Scholar
  7. 7.
    F. Edin, T. Klingberg, P. Johansson, F. McNab, J. Tegnér, and A. Compte, “Mechanism for top-down control of working memory capacity,” Proc. Natl. Acad. Sci. USA, 106, No. 16, 6802–6807 (2009).PubMedCrossRefGoogle Scholar
  8. 8.
    K. J. Friston, J. Ashburner, S. J. Kiebel, T. E. Nichols, and W. D. Penny, Statistical Parametric Mapping: The Analysis of Functional Brain Images, Academic Press, London (2007).Google Scholar
  9. 9.
    M. Fyhn, S. Molden, M. P. Witter, E. I. Moser, and M. B. Moser, “Spatial representation in the entorhinal cortex,” Science, 305, 1258–1264 (2004).PubMedCrossRefGoogle Scholar
  10. 10.
    V. Gallese, L. Fadiga, L. Fogassi, and G. Rizzolatti, “Action recognition in the premotor cortex,” Brain, 119, No. 2, 593–609 (1996).PubMedCrossRefGoogle Scholar
  11. 11.
    T. Hafting, M. Fyhn, S. Molden, M. B. Moser, and E. I. Moser, “Microstructure of a spatial map in the entorhinal cortex,” Nature, 436, 801–806 (2005).PubMedCrossRefGoogle Scholar
  12. 12.
    J. H. Han, S. A. Kushner, A. P. Yiu, H. L. Hsiang, T. Buch, A. Waisman, B. Bontempi, R. L. Neve, P. W. Frankland, and S. A. Josselyn, “Selective erasure of a fear memory,” Science, 323, No. 5920, 1492–1496 (2009).PubMedCrossRefGoogle Scholar
  13. 13.
    M. Iacoboni, R. P. Woods, M. Brass, H. Bekkering, J. C. Mazziotta, and G. Rizzolatti, “Cortical mechanisms of human imitation,” Science, 286, No. 5449, 2526–2528 (1999).PubMedCrossRefGoogle Scholar
  14. 14.
    J. L. Lancaster, M. G. Woldorff, L. M. Parsons, M. Liotti, C. S. Freitas, L. Rainey, P. V. Kochunov, D. Nickerson, S. A. Mikiten, and P. T. Fox, “Automated Talairach Atlas labels for functional brain mapping,” Hum. Brain Mapping, No. 10, 120–131 (2000).CrossRefGoogle Scholar
  15. 15.
    S. Laureys, S. Antoine, M. Boly, S. Elincx, M. E. Faymonville, J. Berré, B. Sadzot, M. Ferring, X. De Tiége, P. van Bogaert, I. Hansen, P. Damas, N. Mavroudakis, B. Lambermont, G. Del Fiore, J. Aerts, C. Degueldre, C. Phillips, G. Franck, J. L. Vincent, M. Lamy, A. Luxen, G. Moonen, S. Goldman, and P. Maquet, “Brain function in the vegetative state,” Acta Neurol. Belg., 102, No. 4, 177–185 (2002).PubMedGoogle Scholar
  16. 16.
    M. M. Monti, A. Vanhaudenhuyse, M. R. Coleman, M. Boly, J. D. Pickard, I. Tshibanda, A. M. Owen, and S. Laureys, “Wilful modulation of brain activity in disorders of consciousness,” N. Eng. J. Med., 362, No. 7, 648–649 (2010).CrossRefGoogle Scholar
  17. 17.
    A. M. Owen, M. R. Coleman, M. Boly, M. H. Davis, S. Laureys, and J. D. Pickard, “Detecting awareness in the vegetative state,” Science, 313, No. 5792, 1402 (2006).PubMedCrossRefGoogle Scholar
  18. 18.
    L. Palmer and G. A. Lynch, “A Kantian view of space,” Science, 328, No. 5985, 1487–1488 (2010).PubMedCrossRefGoogle Scholar
  19. 19.
    G. Rizzolatti, L. Fadiga, V. Gallese, and L. Fogassi, “Premotor cortex and the recognition of motor actions,” Brain Res. Cogn. Brain Res., 3, No. 2, 131–141 (1996).PubMedCrossRefGoogle Scholar
  20. 20.
    W. B. Scoville and B. Milner, “Loss of recent memory after bilateral hippocampal lesions,” J. Neurol. Neurosurg. Psychiatry, 20, 11–21 (1957).PubMedCrossRefGoogle Scholar
  21. 21.
    L. R. Squire, “Memory and the hippocampus: a synthesis from findings with rats, monkeys, and humans,” Psychol. Rev., 99, 195–231 (1992).PubMedCrossRefGoogle Scholar
  22. 22.
    J. Talairach and P. Tournoux, Co-Planar Stereotaxic Atlas of the Human Brain, Thieme Med. Publ. Inc., New York (1988).Google Scholar
  23. 23.
    J. J. Todd, D. Fougnie, and R. Marois, “Visual short-term memory load suppresses temporo-parietal junction activity and induces inattentional blindness,” Science, 16, No. 12, 965–972 (2005).Google Scholar
  24. 24.
    V. M. Verkhlyutov, G. V. Gapienko,V. L. Ushakov, et al., “MRI morphometry of the cerebral ventricles in patients with attention deficit hyperactivity disorder,” Neurosci. Behav. Physiol., 40, No. 3, 295–305 (2010).PubMedCrossRefGoogle Scholar
  25. 25.
    R. P. Vertes,W. B. Hoover, K. Szigeti-Buck, and C. Leranth, “Nucleus reuniens of the midline thalamus: link between the medial prefrontal cortex and the hippocampus,” Brain Res. Bull., 71, No. 6, 601–609 (2007).PubMedCrossRefGoogle Scholar
  26. 26.
    J. Wang, Y. Awi, Y. Weng, K. Ng, Y. Z. Huang, L. Ying, J. Liu, and C. J. Wang, “Functional MRI in the assessment of cortical activation during gait-related imaginary tasks,” Neural. Transm., 116, No. 9, 1087–1092 (2009).CrossRefGoogle Scholar
  27. 27.
    T. J. Wills, F. Cacucci, N. Burgess, and J. O’Keefe, “Development of the hippocampal cognitive map in preweanling rats,” Science, 328, No. 5985, 1573–1576 (2010).PubMedCrossRefGoogle Scholar
  28. 28.
    M. M. Zeineh, S. A. Engel, P. M. Thompson, and S. Y. Bookheimer, “Dynamics of the hippocampus during encoding and retrieval of face-name pairs,” Science, 299, 577–580 (2003).PubMedCrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media New York 2012

Authors and Affiliations

  • V. L. Ushakov
    • 1
  • V. M. Verkhlyutov
    • 1
  • P. A. Sokolov
    • 1
  • M. V. Ublinskii
    • 1
  • V. B. Strelets
    • 2
  • A. Yu. Agrafonov
    • 3
  • A. V. Petryaikin
    • 3
  • T. A. Akhadov
    • 3
  1. 1.National Nuclear Research University – Moscow Engineering-Physics Institute (NIYaU MIFI)MoscowRussia
  2. 2.Institute of Higher Nervous Activity and NeurophysiologyRussian Academy of SciencesMoscowRussia
  3. 3.Research Institute of Emergency Pediatric Surgery and TraumatologyMoscowRussia

Personalised recommendations