Theta band oscillation and synchrony in the hippocampal formation and associated structures: the case for its role in sensorimotor integration
Abstract
The current review advances the argument that it is naïve to ascribe a unitary function to the hippocampal formation (HPC). Rather, it is more productive to consider the hippocampal formation as consisting of a number of subsystems, each subsystem defined by its own particular neural circuitry. Among examples of neural circuitry appearing in current hippocampal literature are theta, beta and gamma oscillations, sharp waves, place cells and head orientation cells. Data are reviewed supporting the case that theta band oscillation and synchrony is involved in mechanisms underlying sensorimotor integration. Specifically, the neural circuitry underlying the production of oscillation and synchrony (theta) in limbic cortex and associated structures function in the capacity of providing voluntary motor systems with continually updated feedback on their performance relative to changing environmental (sensory) conditions. A crucial aspect of this performance is the intensity with which the motor programs are initiated and maintained. The ascending brainstem HPC synchronizing pathways make the primary contribution in this regard. These pathways originate in the rostral pontine region, ascend and synapse with caudal diencephalic nuclei, which in turn send projections to the medial septal region. The medial septum functions as the node in the ascending pathways, sending both cholinergic and GABA-ergic projections to the HPC. An updated version of the sensorimotor integration model including anatomical details is presented and discussed.
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Increased connectivity within the theta (3.5-7.5 Hz) and alpha (8-12.5 Hz) frequency bands has been linked to mechanisms underlying sensorimotor integration.
“Increased connectivity within the theta (3.5–7.5 Hz) and alpha (8–12.5 Hz) frequency bands has been linked to mechanisms underlying sensorimotor integration (Bland and Oddie, 2001).”
From Handwriting but not typewriting leads to widespread brain connectivity: a high-density EEG study with implications for the classroom (2024) · cites this paper as Bland and Oddie, 2001
Cites
From motivation to action: Functional interface between the limbic system and the motor system
MOGENSON, G., JONES, D., & YIM, C. (1980) · Progress in Neurobiology · doi:10.1016/0301-0082(80)90018-0 · Cited by 2,331 · see citing works
GABA-containing neurons in the septum control inhibitory interneurons in the hippocampus
Freund, T. F., & Antal, M. (1988) · Nature · doi:10.1038/336170a0 · Cited by 1,283 · see citing works
Kramis, R., Vanderwolf, C. H., & Bland, B. H. (1975) · Experimental Neurology · doi:10.1016/0014-4886(75)90195-8 · Cited by 791 · see citing works
Self-citation(1997) · Neuroscience · doi:10.1016/s0306-4522(97)00239-x · Cited by 707 · see citing works
PHA-L analysis of projections from the supramammillary nucleus in the rat
Vertes, R. P. (1992) · Journal of Comparative Neurology · doi:10.1002/cne.903260408 · Cited by 299 · see citing works
Acsády, L., Halasy, K., & Freund, T. F. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90532-k · Cited by 99 · see citing works
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The role of acetylcholine in learning and memory
Hasselmo, M. E. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.09.002 · Cited by 1,693 · see citing works
Top-down influences on visual processing
Gilbert, C. D., & Li, W. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3476 · Cited by 1,224 · see citing works
Farmer, J., Zhao, X., van Praag, H., Wodtke, K., Gage, F. H., & Christie, B. R. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2003.09.029 · Cited by 836 · see citing works
Frontal-midline theta from the perspective of hippocampal “theta”
Mitchell, D. J., McNaughton, N., Flanagan, D., & Kirk, I. J. (2008) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2008.09.005 · Cited by 549 · see citing works
Hippocampal network patterns of activity in the mouse
Buzsáki, G., Buhl, D. L., Harris, K. D., Csicsvari, J., Czéh, B., & Morozov, A. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00669-3 · Cited by 486 · see citing works
Hasselmo, M. E. (2005) · Hippocampus · doi:10.1002/hipo.20116 · Cited by 502 · see citing works
Korotkova, T., Fuchs, E. C., Ponomarenko, A., von Engelhardt, J., & Monyer, H. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.017 · Cited by 480 · see citing works
Sleep-Dependent θ Oscillations in the Human Hippocampus and Neocortex
Cantero, J. L., Atienza, M., Stickgold, R., Kahana, M. J., Madsen, J. R., & Kocsis, B. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-34-10897.2003 · Cited by 312 · see citing works
Synch before you speak: Auditory hallucinations in schizophrenia
Ford, J. M., Roach, B. J., Faustman, W. O., & Mathalon, D. H. (2007) · American Journal of Psychiatry · doi:10.1176/ajp.2007.164.3.458 · Cited by 245 · see citing works
Juszczak, G. R., & Swiergiel, A. H. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2008.12.014 · Cited by 211 · see citing works
McNaughton, N., Kocsis, B., & Hajós, M. (2007) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e3282ee82e3 · Cited by 187 · see citing works
Back to front: cerebellar connections and interactions with the prefrontal cortex
Watson, T. C., Becker, N., Apps, R., & Jones, M. W. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00004 · Cited by 176 · see citing works
Out-of-synch and out-of-sorts: dysfunction of motor-sensory communication in schizophrenia
Ford, J. M., Roach, B. J., Faustman, W. O., & Mathalon, D. H. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2007.09.013 · Cited by 136 · see citing works
Ventral hippocampal OLM cells control type 2 theta oscillations and response to predator odor
Mikulovic, S., Restrepo, C. E., Siwani, S., Bauer, P., Pupe, S., Tort, A. B. L., Kullander, K., & Leão, R. N. (2018) · Nature Communications · doi:10.1038/s41467-018-05907-w · Cited by 114 · see citing works
Ose Askvik, E., van der Weel, F. R. (., & van der Meer, A. L. H. (2020) · Frontiers in Psychology · doi:10.3389/fpsyg.2020.01810 · Cited by 86 · see citing works
Van der Weel, F. R. (., & Van der Meer, A. L. H. (2024) · Frontiers in Psychology · doi:10.3389/fpsyg.2023.1219945 · Cited by 85 · see citing works
Distinct contributions of human hippocampal theta to spatial cognition and anxiety
Cornwell, B. R., Arkin, N., Overstreet, C., Carver, F. W., & Grillon, C. (2012) · Hippocampus · doi:10.1002/hipo.22019 · Cited by 73 · see citing works
van der Meer, A. L. H., & van der Weel, F. R. (. (2017) · Frontiers in Psychology · doi:10.3389/fpsyg.2017.00706 · Cited by 62 · see citing works
Remembering forward: Neural correlates of memory and prediction in human motor adaptation
Scheidt, R. A., Zimbelman, J. L., Salowitz, N. M. G., Suminski, A. J., Mosier, K. M., Houk, J., & Simo, L. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.07.072 · Cited by 42 · see citing works
Forro, T., Valenti, O., Lasztoczi, B., & Klausberger, T. (2015) · Cerebral Cortex · doi:10.1093/cercor/bht316 · Cited by 38 · see citing works
Sensory mismatch induces autonomic responses associated with hippocampal theta waves in rats
Aitake, M., Hori, E., Matsumoto, J., Umeno, K., Fukuda, M., Ono, T., & Nishijo, H. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.02.011 · Cited by 17 · see citing works
Rat hippocampal theta rhythm during sensory mismatch
Zou, D., Aitake, M., Hori, E., Umeno, K., Fukuda, M., Ono, T., & Nishijo, H. (2009) · Hippocampus · doi:10.1002/hipo.20524 · Cited by 17 · see citing works
Modulation of normal and altered hippocampal excitability states by septal networks
Colom, L. V., & Garrido‐Sanabria, E. (2007) · Journal of Neuroscience Research · doi:10.1002/jnr.21276 · Cited by 17 · see citing works
Dunn, S. L. S., Town, S. M., Bizley, J. K., & Bendor, D. (2022) · Nature Communications · doi:10.1038/s41467-022-33507-2 · Cited by 17 · see citing works
- Authors
- Bland, B. H., & Oddie, S. D.
- Affiliations
- University of Calgary (CA)
- Corresponding author
- Bland, Brian H.
- Venue
- Behavioural Brain Research
- Publisher
- Elsevier BV
- Published
- 2001-12
- Volume
- 127
- Issue
- 1-2
- Pages
- 119-136
- ISSN
- 0166-4328 (ISSN-L)
- OpenAlex
- W2023802575
- Cited by
- 520
- References
- 6
- Citations by year
- 2026: 8 · 2025: 24 · 2024: 18 · 2023: 17 · 2022: 18 · 2021: 19 · 2020: 18 · 2019: 16 · 2018: 20 · 2017: 28 · 2016: 20 · 2015: 26 · 2014: 34 · 2013: 28 · 2012: 26
- FWCI
- 0.91
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Behavioural Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- theta oscillations, neuronal synchronization, hippocampal formation, sensorimotor integration, limbic cortex, medial septum, cholinergic projections, GABAergic projections, motor feedback
- MeSH terms
- Brain Stem, Electrophysiology, Hippocampus, Humans, Limbic System, Models, Neurological, Neural Pathways, Pons, Psychomotor Performance, Septal Nuclei, Theta Rhythm, Posterior Thalamic Nuclei
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