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Neural substrates of envisioning the future
Open accessAbstract
The ability to envision specific future episodes is a ubiquitous mental phenomenon that has seldom been discussed in the neuroscience literature. In this study, subjects underwent functional MRI while using event cues (e.g., Birthday) as a guide to vividly envision a personal future event, remember a personal memory, or imagine an event involving a familiar individual. Two basic patterns of data emerged. One set of regions (e.g., within left lateral premotor cortex; left precuneus; right posterior cerebellum) was more active while envisioning the future than while recollecting the past (and more active in both of these conditions than in the task involving imagining another person). These regions appear similar to those emerging from the literature on imagined (simulated) bodily movements. A second set of regions (e.g., bilateral posterior cingulate; bilateral parahippocampal gyrus; left occipital cortex) demonstrated indistinguishable activity during the future and past tasks (but greater activity in both tasks than the imagery control task); similar regions have been shown to be important for remembering previously encountered visual-spatial contexts. Hence, differences between the future and past tasks are attributed to differences in the demands placed on regions that underlie motor imagery of bodily movements, and similarities in activity for these two tasks are attributed to the reactivation of previously experienced visual–spatial contexts. That is, subjects appear to place their future scenarios in well known visual–spatial contexts. Our results offer insight into the fundamental and little-studied capacity of vivid mental projection of oneself in the future.
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“Perhaps it is not altogether surprising therefore that recent fMRI studies have found comprehensive overlap in the activation patterns associated with recalling the past and thinking about plausible self-relevant future events (Addis et al., 2007; Szpunar et al., 2007).”
From Using Imagination to Understand the Neural Basis of Episodic Memory (2007) · cites this paper as Szpunar et al., 2007
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“Previous studies that have compared episodic memory and future thinking were unable to make this distinction because these features were present to a similar degree in both autobiographical memories and personal future scenarios (Atance and O'Neill, 2001; Addis et al., 2007; Szpunar et al., 2007).”
From Using Imagination to Understand the Neural Basis of Episodic Memory (2007) · cites this paper as Szpunar et al., 2007
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“Episodic memories are thought to be involved in a variety of important cognitive processes beyond simply recalling past events.”
From Episodic Memory in AI Agents Poses Risks that Should be Studied and Mitigated (2025) · cites this paper as [77]
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“First, brain imaging studies have shown that similar brain regions are recruited during recall of episodic memories and other tasks [77].”
From Episodic Memory in AI Agents Poses Risks that Should be Studied and Mitigated (2025) · cites this paper as [77]
In the citing paper
“Neuroimaging has revealed that memory and imagination engage the same brain networks, including the default mode network (DMN; Addis, Wong, & Schacter, 2007;Okuda et al., 2003;Szpunar, Watson, & McDermott, 2007; see Figure 1).”
From Mental Time Travel? A Neurocognitive Model of Event Simulation. (2020) · cites this paper as Szpunar, Watson, & McDermott, 2007
In the citing paper
“When imagining non-personal events (i.e., events that do not feature the self), the involvement of self-schemas decreases linearly with psychological closeness to the protagonist (de Vito, Gamboz, & Brandimonte, 2012) as does the engagement of ventromedial prefrontal regions mediating self-schemas (e.g., D' Argembeau et al., 2010;Szpunar et al., 2007).”
From Mental Time Travel? A Neurocognitive Model of Event Simulation. (2020) · cites this paper as Szpunar et al., 2007
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“The overall proportional resolution of non-personal simulations is also likely lower, with a greater proportion of lower-resolution elements such as general semantic knowledge (Szpunar et al., 2007).”
From Mental Time Travel? A Neurocognitive Model of Event Simulation. (2020) · cites this paper as Szpunar et al., 2007
In the citing paper
“With lower reliance on self-schema, as well as reductions in complexity, associative strength, elaborateness and proportional resolution, it is not surprising that imagining non-personal events is associated with lower activity levels in many DMN regions relative to imagining personal events (including parahippocampal cortex, posterior cingulate, and cuneus; e.g., D' Argembeau et al., 2010;Szpunar”
From Mental Time Travel? A Neurocognitive Model of Event Simulation. (2020) · cites this paper as Szpunar et al., 2007
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Citations
Cites
Co-Planar Stereotaxic Atlas of the Human Brain
Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798
Co-planar stereotaxic atlas of the human brain
Laitinen, L. (1989) · Clinical Neurology and Neurosurgery · doi:10.1016/0303-8467(89)90128-5 · Cited by 7,565
The precuneus: a review of its functional anatomy and behavioural correlates
Cavanna, A. E., & Trimble, M. R. (2006) · Brain · doi:10.1093/brain/awl004 · Cited by 5,128
Tulving, E. (1985) · Canadian Psychology / Psychologie canadienne · doi:10.1037/h0080017 · Cited by 4,638
Dynamic magnetic resonance imaging of human brain activity during primary sensory stimulation.
Kwong, K. K., Belliveau, J. W., Chesler, D. A., Goldberg, I. E., Weisskoff, R. M., Poncelet, B. P., Kennedy, D. N., Hoppel, B. E., Cohen, M. S., & Turner, R. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5675 · Cited by 4,212
From Neuropsychology to Mental Structure
Shallice, T. (1988) · doi:10.1017/cbo9780511526817 · Cited by 4,072
Ogawa, S., Tank, D. W., Menon, R., Ellermann, J. M., Kim, S. G., Merkle, H., & Ugurbil, K. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.13.5951 · Cited by 3,681
Imaging Cognition II: An Empirical Review of 275 PET and fMRI Studies
Cabeza, R., & Nyberg, L. (2000) · Journal of Cognitive Neuroscience · doi:10.1162/08989290051137585 · Cited by 3,598
Gusnard, D. A., Akbudak, E., Shulman, G. L., & Raichle, M. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.071043098 · Cited by 2,997
Cohen, J., MacWhinney, B., Flatt, M., & Provost, J. (1993) · Behavior Research Methods, Instruments, & Computers · doi:10.3758/bf03204507 · Cited by 2,802
Buckner, R. L., & Carroll, D. C. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.11.004 · Cited by 2,691
Gazzaniga, M. S., & Bizzi, E. (2000) · Cited by 2,547
Linear Systems Analysis of Functional Magnetic Resonance Imaging in Human V1
Boynton, G., Engel, S., Glover, G., & Heeger, D. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-13-04207.1996 · Cited by 2,522
The Prefrontal Cortex: Anatomy, Physiology, and Neuropsychology of the Frontal Lobe
Fuster, J. M. (1980) · Cited by 2,367
Can cognitive processes be inferred from neuroimaging data?
POLDRACK, R. (2006) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2005.12.004 · Cited by 2,249
Analysis of fMRI Time-Series Revisited—Again
Worsley, K. J., & Friston, K. J. (1995) · NeuroImage · doi:10.1006/nimg.1995.1023 · Cited by 2,198
Stuss, D. T., & Benson, D. F. (1986) · Raven Press eBooks · Cited by 2,102
Processing strategies for time‐course data sets in functional mri of the human brain
Bandettini, P. A., Jesmanowicz, A., Wong, E. C., & Hyde, J. S. (1993) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910300204 · Cited by 1,762
Toward a theory of episodic memory: The frontal lobes and autonoetic consciousness.
Wheeler, M. A., Stuss, D. T., & Tulving, E. (1997) · Psychological Bulletin · doi:10.1037/0033-2909.121.3.331 · Cited by 1,751
Principles of Frontal Lobe Function
Stuss, D. T. (2002) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195134971.001.0001 · Cited by 1,731
Finding the self? An event-related fMRI study
Kelley, W. M., Macrae, C. N., Wyland, C. L., Caglar, S., Inati, S., & Heatherton, T. F. (2002) · Journal of Cognitive Neuroscience · doi:10.1162/08989290260138672 · Cited by 1,606
Cortical midline structures and the self
Northoff, G., & Bermpohl, F. (2004) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2004.01.004 · Cited by 1,446
Atance, C. M., & O'Neill, D. K. (2001) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(00)01804-0 · Cited by 1,300
The functional neuroanatomy of autobiographical memory: a meta-analysis
Svoboda, E., McKinnon, M. C., & Levine, B. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.05.023 · Cited by 1,274
The prefrontal cortex: Anatomy, physiology, and neuropsychology of the frontal lobe
Holmes, G. L. (1989) · Journal of Epilepsy · doi:10.1016/0896-6974(89)90035-2 · Cited by 1,211
Picard, N., & Strick, P. L. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(01)00266-5 · Cited by 1,184
Effect of subjective perspective taking during simulation of action: a PET investigation of agency
Ruby, P., & Decety, J. (2001) · Nature Neuroscience · doi:10.1038/87510 · Cited by 1,182
Mental time travel and the evolution of the human mind.
Suddendorf, T., & Corballis, M. C. (1997) · PubMed · Cited by 1,035
Selective averaging of rapidly presented individual trials using fMRI
Dale, A. M., & Buckner, R. L. (1997) · Human Brain Mapping · doi:10.1002/(sici)1097-0193(1997)5:5 · Cited by 1,034
Schacter, D. L., & Buckner, R. L. (1998) · Neuron · doi:10.1016/s0896-6273(00)80448-1 · Cited by 837
Individual Self, Relational Self, Collective Self
(2015) · doi:10.4324/9781315783024 · Cited by 810
Cerebral Representation of One’s Own Past: Neural Networks Involved in Autobiographical Memory
Fink, G. R., Markowitsch, H. J., Reinkemeier, M., Bruckbauer, T., Kessler, J., & Heiss, W.-D. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-13-04275.1996 · Cited by 803
The power of simulation: Imagining one's own and other's behavior
Decety, J., & Grèzes, J. (2006) · Brain Research · doi:10.1016/j.brainres.2005.12.115 · Cited by 790
When zero is not zero: the problem of ambiguous baseline conditions in fMRI
Stark, C. E. L., & Squire, L. R. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.221462998 · Cited by 724
Frequency of episodic memories as a function of their age
Crovitz, H. F., & Schiffman, H. (1974) · Bulletin of the Psychonomic Society · doi:10.3758/bf03334277 · Cited by 674
Neural systems engaged by planning: A PET study of the Tower of London task
Baker, S. C., Rogers, R. D., Owen, A. M., Frith, C. D., Dolan, R. J., Frackowiak, R. S. J., & Robbins, T. W. (1996) · Neuropsychologia · doi:10.1016/0028-3932(95)00133-6 · Cited by 635
Thinking of the future and past: the roles of the frontal pole and the medial temporal lobes
Okuda, J., Fujii, T., Ohtake, H., Tsukiura, T., Tanji, K., Suzuki, K., Kawashima, R., Fukuda, H., Itoh, M., & Yamadori, A. (2003) · NeuroImage · doi:10.1016/s1053-8119(03)00179-4 · Cited by 607
Remembering the past: two facets of episodic memory explored with positron emission tomography
(1995) · American Journal of Psychiatry · doi:10.1176/ajp.152.11.1576 · Cited by 593
Brain regions involved in prospective memory as determined by positron emission tomography
Burgess, P. W., Quayle, A., & Frith, C. D. (2001) · Neuropsychologia · doi:10.1016/s0028-3932(00)00149-4 · Cited by 575
Conscious thought as simulation of behaviour and perception
Hesslow, G. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(02)01913-7 · Cited by 572
Klein, S. B., Loftus, J., & Kihlstrom, J. F. (2002) · Social Cognition · doi:10.1521/soco.20.5.353.21125 · Cited by 553
The specificity of autobiographical memory and imageability of the future
Williams, J. M. G., Ellis, N. C., Tyers, C., Healy, H., Rose, G., & Macleod, A. K. (1996) · Memory & Cognition · doi:10.3758/bf03197278 · Cited by 526
"Memory of the future": an essay on the temporal organization of conscious awareness.
Ingvar, D. H. (1985) · PubMed · Cited by 519
Mental navigation along memorized routes activates the hippocampus, precuneus, and insula
Ghaëm, O., Mellet, E., Crivello, F., Tzourio‐Mazoyer, N., Mazoyer, B. M., Berthoz, A., & Denis, M. (1997) · Neuroreport · doi:10.1097/00001756-199702100-00032 · Cited by 481
Episodic memory and the self in a case of isolated retrograde amnesia
Levine, B. (1998) · Brain · doi:10.1093/brain/121.10.1951 · Cited by 472
Cabeza, R. E. L., Prince, S. E., Daselaar, S. M., Greenberg, D. L., Budde, M. D., Dolcos, F., LaBar, K. S., & Rubin, D. C. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929042568578 · Cited by 395
Recollective qualities modulate hippocampal activation during autobiographical memory retrieval
Addis, D. R., Moscovitch, M., Crawley, A. P., & McAndrews, M. P. (2004) · Hippocampus · doi:10.1002/hipo.10215 · Cited by 383
What can Functional Neuroimaging Tell the Experimental Psychologist?
Henson, R. (2005) · The Quarterly Journal of Experimental Psychology Section A · doi:10.1080/02724980443000502 · Cited by 327
Ingvar, D. H. (2009) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.1979.tb02947.x · Cited by 322
Jean Decety, A., & Ingvar, D. H. (1990) · Acta Psychologica · doi:10.1016/0001-6918(90)90056-l · Cited by 305
Recalling yesterday and predicting tomorrow
Grant, J. B., & Suddendorf, T. (2005) · Cognitive Development · doi:10.1016/j.cogdev.2005.05.002 · Cited by 292
Awareness of Deficit after Brain Injury
North, N. T. (1992) · International Journal of Rehabilitation Research · doi:10.1097/00004356-199206000-00013 · Cited by 270
Rosenbaum, R. S., Ziegler, M., Winocur, G., Grady, C. L., & Moscovitch, M. (2004) · Hippocampus · doi:10.1002/hipo.10218 · Cited by 258
Mellet, E., Bricogne, S., Tzourio‐Mazoyer, N., Ghaëm, O., Petit, L., Zago, L., Etard, O., Berthoz, A., Mazoyer, B. M., & Denis, M. (2000) · NeuroImage · doi:10.1006/nimg.2000.0648 · Cited by 221
Chronesthesia: Conscious Awareness of Subjective Time
Tulving, E. (2002) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195134971.003.0020 · Cited by 191
Report of case of bilateral frontal lobe defect.
Ackerly, S., & Benton, A. L. (1948) · PubMed · Cited by 166
Difference Image vs Ratio Image Error Function Forms in PET—PET Realignment
Snyder, A. Z. (1996) · Elsevier eBooks · doi:10.1016/b978-012389760-2/50028-1 · Cited by 130
The prefrontal cortex: Anatomy physiology and neurophysiology of the frontal lobe
Passingham, R. E. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90204-9 · Cited by 104
Research works printed but not linked: 6
- T Suddendorf, MC Corballis Genet Social Gen Psychol Monogr 123, 133–167 (1997).
- DH Ingvar Hum Neurobiol 4, 127–136 (1985).
- DR Addis, AT Wong, DL Schacter Neuropsychologia, in press. (2006).
- DL Schacter, DR Addis Philos Trans R Soc London B, in press.
- RL Buckner, DC Carroll Trends Cogn Sci, in press. (2006).
- SS Ackerley, AL Benton Res Publ Assoc Res Nerv Ment Dis 27, 479–504 (1947).
Cited by
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Buckner, R. L., Andrews‐Hanna, J. R., & Schacter, D. L. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1440.011 · Cited by 9,761
Buckner, R. L., & Carroll, D. C. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2006.11.004 · Cited by 2,691
Remembering the past to imagine the future: the prospective brain
Schacter, D. L., Addis, D. R., & Buckner, R. L. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2213 · Cited by 2,394
Spreng, R. N., Mar, R. A., & Kim, A. S. N. (2009) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2008.21029 · Cited by 2,143
The cognitive neuroscience of constructive memory: remembering the past and imagining the future
Schacter, D. L., & Addis, D. R. (2007) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2007.2087 · Cited by 1,836
Metadata
- Authors
- Szpunar, K. K., Watson, J. M., & McDermott, K. B.
- Affiliations
- Washington University in St. Louis (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2007-01-09
- Volume
- 104
- Issue
- 2
- Pages
- 642-647
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC1761910
- OpenAlex
- W2098699616
- Cited by
- 784
- References
- 60
- Citations by year
- 2026: 18 · 2025: 32 · 2024: 28 · 2023: 33 · 2022: 29 · 2021: 27 · 2020: 29 · 2019: 26 · 2018: 29 · 2017: 44 · 2016: 33 · 2015: 48 · 2014: 56 · 2013: 66 · 2012: 58
- FWCI
- 29.47
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Functions and Memory
- Keywords
- mental time travel, future events, personal memories, event simulation, motor imagery, premotor cortex, precuneus, posterior cerebellum, posterior cingulate cortex, parahippocampal gyrus
- MeSH terms
- Adolescent, Adult, Brain, Female, Forecasting, Humans, Magnetic Resonance Imaging, Male, Memory, Thinking
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