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Your Imaging Group Has Coined the Term ‘Dream Imaging.’ Please Summarize the Concept in Relation to Dream Theory

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Dream Consciousness

Part of the book series: Vienna Circle Institute Library ((VCIL,volume 3))

Abstract

The rise of modern imaging techniques has endowed neuroscience with a new quality to enquire into cognition and consciousness. In the 1990s, positron emission tomography (PET) was utilised for the first time to address sleep-specific questions and led to intriguing insights into the neural correlates of sleep. While the brain experiences widespread deactivations during slow wave sleep, REM sleep is again associated with increased cerebral blood flow in the thalamus, visual areas and limbic regions as well as attenuated metabolism in the dorsolateral prefrontal cortex (DLPFC), parietal cortex and the precuneus (Maquet et al. 1996, 1997; Braun et al. 1998). Such a pattern of activation has been related to the phenomenology of REM sleep dreaming. Activation of visual association areas is in line with vivid dream imagery, amygdala activation with dream emotionality, and DLPFC deactivation with the lack of insight, reflexivity and volition commonly experienced in dreams (Hobson and Pace-Schott 2002; Nir and Tononi 2009; Desseilles et al. 2011).

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References

  • Alkire, M. T., & Miller, J. (2005). General anesthesia and the neural correlates of consciousness. Progress in Brain Research, 150, 229–244.

    Article  PubMed  Google Scholar 

  • Andrade, K. C., Spoormaker, V. I., Dresler, M., Wehrle, R., Holsboer, F., Sämann, P. G., & Czisch, M. (2011). Sleep spindles and hippocampal functional connectivity in human NREM sleep. Journal of Neuroscience, 31, 10331–10339.

    Article  CAS  PubMed  Google Scholar 

  • Boly, M., Phillips, C., Tshibanda, L., Vanhaudenhuyse, A., Schabus, M., Dang-Vu, T. T., Moonen, G., Hustinx, R., Maquet, P., & Laureys, S. (2008). Intrinsic brain activity in altered states of consciousness: How conscious is the default mode of brain function? Annals of the New York Academy of Sciences, 1129, 119–129.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Born, A. P., Rostrup, E., Miranda, M. J., Larsson, H. B., & Lou, H. C. (2002). Visual cortex reactivity in sedated children examined with perfusion MRI (FAIR). Magnetic Resonance Imaging, 20, 199–205.

    Article  CAS  PubMed  Google Scholar 

  • Braun, A. R., Balkin, T. J., Wesensten, N. J., Gwadry, F., Carson, R. E., Varga, M., Baldwin, P., Belenky, G., & Herscovitch, P. (1998). Dissociated pattern of activity in visual cortices and their projections during human rapid eye movement sleep. Science, 279, 91–95.

    Article  CAS  PubMed  Google Scholar 

  • Buckner, R. L., Andrews-Hanna, J. R., & Schacter, D. L. (2008). The brain’s default network. Annals of the New York Academy of Sciences, 1124, 1–38.

    Article  PubMed  Google Scholar 

  • Caporro, M., Haneef, Z., Yeh, H. J., Lenartowicz, A., Buttinelli, C., Parvizi, J., & Stern, J. M. (2012). Functional MRI of sleep spindles and K-complexes. Clinical Neurophysiology, 123, 303–309.

    Article  PubMed Central  PubMed  Google Scholar 

  • Czisch, M., & Wehrle, R. (2010). Sleep. In C. Mulert & L. Lemieux (Eds.), EEG–fMRI. Berlin: Springer.

    Google Scholar 

  • Czisch, M., Wetter, T. C., Kaufmann, C., Pollmächer, T., Holsboer, F., & Auer, D. P. (2002). Altered processing of acoustic stimuli during sleep: Reduced auditory activation and visual deactivation detected by a combined fMRI/EEG study. NeuroImage, 16, 251–258.

    Article  PubMed  Google Scholar 

  • Czisch, M., Wehrle, R., Kaufmann, C., Wetter, T. C., Pollmächer, T., & Auer, D. P. (2004). Functional MRI during sleep: BOLD signal decreases and their electrophysiological correlates. The European Journal of Neuroscience, 20, 566–574.

    Article  PubMed  Google Scholar 

  • Czisch, M., Wehrle, R., Stiegler, A., Peters, H., Andrade, K., Holsboer, F., & Sämann, P. G. (2009). Acoustic oddball during NREM sleep: A combined EEG/fMRI study. PloS One, 4, e6749.

    Article  PubMed Central  PubMed  Google Scholar 

  • Dang-Vu, T. T., Schabus, M., Desseilles, M., Albouy, G., Boly, M., Darsaud, A., Gais, S., Rauchs, G., Sterpenich, V., Vandewalle, G., Carrier, J., Moonen, G., Balteau, E., Degueldre, C., Luxen, A., Phillips, C., & Maquet, P. (2008). Spontaneous neural activity during human slow wave sleep. Proceedings of the National Academy of Sciences, 105, 15160–15165.

    Article  Google Scholar 

  • Desseilles, M., Dang-Vu, T. T., Sterpenich, V., & Schwartz, S. (2011). Cognitive and emotional processes during dreaming: A neuroimaging view. Consciousness and Cognition, 20(4), 998–1008.

    Article  PubMed  Google Scholar 

  • Dresler, M., Wehrle, R., Spoormaker, V. I., Koch, S., Holsboer, F., Steiger, A., Obrig, H., Sämann, P. G., & Czisch, M. (2009). Neural correlates of consciousness – Insights from sleep imaging. Neuroforum, 15(S1), T24–3C.

    Google Scholar 

  • Dresler, M., Koch, S. P., Wehrle, R., Spoormaker, V. I., Holsboer, F., Steiger, A., Sämann, P. G., Obrig, H., & Czisch, M. (2011). Dreamed movement elicits activation in the sensorimotor cortex. Current Biology, 21, 1–5.

    Article  Google Scholar 

  • Dresler, M., Wehrle, R., Spoormaker, V. I., Koch, S. P., Holsboer, F., Steiger, A., Obrig, H., Sämann, P. G., & Czisch, M. (2012). Neural correlates of dream lucidity obtained from contrasting lucid versus non-lucid REM sleep: A combined EEG/fMRI case study. Sleep, 35, 1017–1020.

    PubMed Central  PubMed  Google Scholar 

  • Edelman, G. M. (2003). Naturalizing consciousness: A theoretical framework. Proceedings of the National Academy of Sciences, 100, 5520–5524.

    Article  CAS  Google Scholar 

  • Ermis, U., Krakow, K., & Voss, U. (2010). Arousal thresholds during human tonic and phasic REM sleep. Journal of Sleep Research, 19, 400–406.

    Article  PubMed  Google Scholar 

  • Fox, M. D., & Raichle, M. E. (2007). Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging. Nature Reviews Neuroscience, 8, 700–711.

    Article  CAS  PubMed  Google Scholar 

  • Hobson, J. A. (2009). The neurobiology of consciousness: Lucid dreaming wakes up. International Journal of Dream Research, 2, 41–44.

    Google Scholar 

  • Hobson, J. A., & McCarley, R. W. (1977). The brain as a dream state generator: an activation-synthesis hypothesis of the dream process. American Journal of Psychiatry, 134, 1335–1348.

    CAS  PubMed  Google Scholar 

  • Hobson, J. A., & Pace-Schott, E. (2002). The cognitive neuroscience of sleep: Neuronal systems, consciousness and learning. Nature Reviews Neuroscience, 3, 679–693.

    Article  CAS  PubMed  Google Scholar 

  • Hong, C. C., Harris, J. C., Pearlson, G. D., Kim, J., Calhoun, V. D., Fallon, J. H., Golay, X., Gillen, J. S., Simmonds, D. J., van Zijl, P. C. M., Zee, D. S., & Pekar, J. J. (2009). fMRI evidence for multisensory recruitment associated with rapid eye movements during sleep. Human Brain Mapping, 30, 1705–1722.

    Article  PubMed Central  PubMed  Google Scholar 

  • Jahnke, K., von Wegner, F., Morzelewski, A., Borisov, S., Maischein, M., Steinmetz, H., & Laufs, H. (2012). To wake or not to wake? The two-sided nature of the human K-complex. NeuroImage, 59, 1631–1638.

    Article  PubMed  Google Scholar 

  • Kaufmann, C., Wehrle, R., Wetter, T. C., Holsboer, F., Auer, D. P., Pollmächer, T., & Czisch, M. (2006). Brain activation and hypothalamic functional connectivity during human NREM sleep: An EEG/fMRI study. Brain, 129, 655–667.

    Article  CAS  PubMed  Google Scholar 

  • LaBerge, S. (1980). Lucid dreaming as a learnable skill: A case study. Perceptual and Motor Skills, 51, 1039–1042.

    Article  Google Scholar 

  • LaBerge, S., Nagel, L., Dement, W. C., & Zarcone, V. (1981). Lucid dreaming verified by volitional communication during REM sleep. Perceptual and Motor Skills, 52, 727–732.

    Article  CAS  Google Scholar 

  • Larson-Prior, L. J., Power, J. D., Vincent, J. L., Nolan, T. S., Coalson, R. S., Zempel, J., Snyder, A. Z., Schlaggar, B. L., Raichle, M. E., & Petersen, S. E. (2011). Modulation of the brain’s functional network architecture in the transition from wake to sleep. Progress in Brain Research, 193, 277–294.

    Article  PubMed  Google Scholar 

  • Maquet, P., Péters, J., Aerts, J., Delfiore, G., Degueldre, C., Luxen, A., & Franck, G. (1996). Functional neuroanatomy of human rapid-eye-movement sleep and dreaming. Nature, 383, 163–166.

    Article  CAS  PubMed  Google Scholar 

  • Maquet, P., Degueldre, C., Delfiore, G., Aerts, J., Péters, J., Luxen, A., & Franck, G. (1997). Functional neuroanatomy of human slow wave sleep. Journal of Neuroscience, 17, 2807–2812.

    CAS  PubMed  Google Scholar 

  • Miyauchi, S., Misaki, M., Kan, S., Fukunaga, T., & Koike, T. (2009). Human brain activity time-locked to rapid eye movements during REM sleep. Experimental Brain Research, 192, 657–667.

    Article  PubMed  Google Scholar 

  • Molinari, S., & Foulkes, D. (1969). Tonic and phasic events during sleep: Psychological correlates and implications. Perceptual and Motor Skills, 29, 343–368.

    Article  CAS  PubMed  Google Scholar 

  • Nir, Y., & Tononi, G. (2009). Dreaming and the brain: From phenomenology to neurophysiology. Trends in Cognitive Science, 14, 88–100.

    Article  Google Scholar 

  • Rechtschaffen, A., & Kales, A. (1968). A manual of standardized terminology, techniques and scoring system for sleep stages of human subjects. Washington, DC: NIH.

    Google Scholar 

  • Sämann, P. G., Wehrle, R., Hoehn, D., Spoormaker, V. I., Peters, H., Tully, C., Holsboer, F., & Czisch, M. (2011). Development of the brain’s default mode network from wakefulness to slow wave sleep. Cerebral Cortex, 21(9), 2082–2093.

    Article  PubMed  Google Scholar 

  • Schabus, M., Dang-Vu, T. T., Albouy, G., Balteau, E., Boly, M., Carrier, J., Darsaud, A., Degueldre, C., Desseilles, M., Gais, S., Phillips, C., Rauchs, G., Schnakers, C., Sterpenich, V., Vandewalle, G., Luxen, A., & Maquet, P. (2007). Hemodynamic cerebral correlates of sleep spindles during human non-rapid eye movement sleep. Proceedings of the National Academy of Sciences, 104, 13164–13169.

    Article  CAS  Google Scholar 

  • Schabus, M., Dang-Vu, T. T., Heib, D. P., Boly, M., Desseilles, M., Vandewalle, G., Schmidt, C., Albouy, G., Darsaud, A., Gais, S., Degueldre, C., Balteau, E., Phillips, C., Luxen, A., & Maquet, P. (2012). The fate of incoming stimuli during NREM sleep is determined by spindles and the phase of the slow oscillation. Frontiers in Neurology, 3, 40.

    Article  PubMed Central  PubMed  Google Scholar 

  • Spoormaker, V. I., Czisch, M., & Dresler, M. (2010a). Lucid and non-lucid dreaming: Thinking in networks. International Journal of Dream Research, 3, 49–51.

    Google Scholar 

  • Spoormaker, V. I., Schröter, M. S., Gleiser, P. M., Andrade, K. C., Dresler, M., Wehrle, R., Sämann, P. G., & Czisch, M. (2010b). Development of a large-scale functional brain network during human non-rapid eye movement sleep. Journal of Neuroscience, 30, 11379–11387.

    Article  CAS  PubMed  Google Scholar 

  • Tononi, G. (2004). An information integration theory of consciousness. BMC Neuroscience, 5, 42.

    Article  PubMed Central  PubMed  Google Scholar 

  • Vincent, J. L., Patel, G. H., Fox, M. D., Snyder, A. Z., Baker, J. T., Van Essen, D. C., Zempel, J. M., Snyder, L. H., Corbetta, M., & Raichle, M. E. (2007). Intrinsic functional architecture in the anaesthetized monkey brain. Nature, 447, 83–86.

    Article  CAS  PubMed  Google Scholar 

  • Vincent, J. L., Kahn, I., Snyder, A. Z., Raichle, M. E., & Buckner, R. L. (2008). Evidence for a frontoparietal control system revealed by intrinsic functional connectivity. Journal of Neurophysiology, 100, 3328–3342.

    Article  PubMed Central  PubMed  Google Scholar 

  • Voss, U., Holzmann, R., Tuin, I., & Hobson, J. A. (2009). Lucid dreaming: A state of consciousness with features of both waking and non-lucid dreaming. Sleep, 32, 1191–1200.

    PubMed Central  PubMed  Google Scholar 

  • Wehrle, R., Czisch, M., Kaufmann, C., Wetter, T. C., Holsboer, F., Auer, D. P., & Pollmächer, T. (2005). Rapid eye movement related brain activation in human REM sleep using fMRI. Neuroreport, 16, 853–857.

    Article  PubMed  Google Scholar 

  • Wehrle, R., Kaufmann, C., Wetter, T. C., Holsboer, F., Auer, D., Pollmächer, T., & Czisch, M. (2007). Functional microstates within human REM sleep. European Journal of Neuroscience, 25, 863–871.

    Article  PubMed  Google Scholar 

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Correspondence to Martin Dresler .

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Dresler, M., Spoormaker, V., Wehrle, R., Czisch, M. (2014). Your Imaging Group Has Coined the Term ‘Dream Imaging.’ Please Summarize the Concept in Relation to Dream Theory. In: Tranquillo, N. (eds) Dream Consciousness. Vienna Circle Institute Library, vol 3. Springer, Cham. https://doi.org/10.1007/978-3-319-07296-8_13

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