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Cited by 394Vestibular and auditory disordersMemory and Neural MechanismsSpatial Cognition and Navigation

Vestibular pathways involved in cognition.

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Hitier, Martin, Besnard, Stephane, Smith, Paul F.·2014·Frontiers in Integrative Neuroscience
DOI 10.3389/fnint.2014.00059PMC PMC4107830
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Abstract

Recent discoveries have emphasized the role of the vestibular system in cognitive processes such as memory, spatial navigation and bodily self-consciousness. A precise understanding of the vestibular pathways involved is essential to understand the consequences of vestibular diseases for cognition, as well as develop therapeutic strategies to facilitate recovery. The knowledge of the "vestibular cortical projection areas", defined as the cortical areas activated by vestibular stimulation, has dramatically increased over the last several years from both anatomical and functional points of view. Four major pathways have been hypothesized to transmit vestibular information to the vestibular cortex: (1) the vestibulo-thalamo-cortical pathway, which probably transmits spatial information about the environment via the parietal, entorhinal and perirhinal cortices to the hippocampus and is associated with spatial representation and self-versus object motion distinctions; (2) the pathway from the dorsal tegmental nucleus via the lateral mammillary nucleus, the anterodorsal nucleus of the thalamus to the entorhinal cortex, which transmits information for estimations of head direction; (3) the pathway via the nucleus reticularis pontis oralis, the supramammillary nucleus and the medial septum to the hippocampus, which transmits information supporting hippocampal theta rhythm and memory; and (4) a possible pathway via the cerebellum, and the ventral lateral nucleus of the thalamus (perhaps to the parietal cortex), which transmits information for spatial learning. Finally a new pathway is hypothesized via the basal ganglia, potentially involved in spatial learning and spatial memory. From these pathways, progressively emerges the anatomical network of vestibular cognition.

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  • Exteroceptive sensory information is continuously acquired from the environment to inform the relationship between one's self and surroundings.

    “Exteroceptive sensory information is continuously acquired from the environment to inform the relationship between one’s self and surroundings (Lopez et al., 2008; Hitier et al., 2014).”

    From How Processing of Sensory Information From the Internal and External Worlds Shape the Perception and Engagement With the World in the Aftermath of Trauma: Implications for PTSD (2021) · cites this paper as Hitier et al., 2014

    The section on posterior parietal and medial superior temporal cortices describes visual information locating objects relative to the head, supporting the claim that environmental sensory information helps represent the relationship between self and surroundings. The paper does not establish that such information is acquired continuously. (LLM, conf=0.78)

    Experimental — accuracy not yet measured

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References 229 · Cited by 394

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  1. Aggleton J. P. Vann S. D. Oswald C. J. P. Good M. (2000). Identifying cortical inputs to the rat hippocampus that subserve allocentric spatial processes: a simple problem with a complex answer. Hippocampus 10, 466– 474 10.1002/1098-1063(2000)10:4<466::AID-HIPO13>3.0.CO;2-Y 10985286 · DOI
  2. Akbarian S. Berndl K. Grüsser O. J. Guldin W. Pause M. Schreiter U. (1988). Responses of single neurons in the parietoinsular vestibular cortex of primates. Ann. N Y Acad. Sci. 545, 187– 202 10.1111/j.1749-6632.1988.tb19564.x 3149165 · DOI
  3. Akbarian S. Grüsser O.-J. Guldin W. O. (1992). Thalamic connections of the vestibular cortical fields in the squirrel monkey (Saimiri sciureus). J. Comp. Neurol. 326, 423– 441 10.1002/cne.903260308 1469120 · DOI
  4. Akbarian S. Grüsser O.-J. Guldin W. O. (1993). Corticofugal projections to the vestibular nuclei in squirrel monkeys: further evidence of multiple cortical vestibular fields. J. Comp. Neurol. 332, 89– 104 10.1002/cne.903320107 7685782 · DOI
  5. Akbarian S. Grüsser O. J. Guldin W. O. (1994). Corticofugal connections between the cerebral cortex and brainstem vestibular nuclei in the macaque monkey. J. Comp. Neurol. 339, 421– 437 10.1002/cne.903390309 7510732 · DOI
  6. Amino Y. Kyuhou S. Matsuzaki R. Gemba H. (2001). Cerebello–thalamo–cortical projections to the posterior parietal cortex in the macaque monkey. Neurosci. Lett. 309, 29– 32 10.1016/S0304-3940(01)02018-3 11489539 · DOI
  7. Andersen R. A. (1997). Multimodal integration for the representation of space in the posterior parietal cortex. Philos. Trans. R. Soc. Lond. B Biol. Sci. 352, 1421– 1428 10.1098/rstb.1997.0128 9368930 PMC1692052 · DOI · Paper page
  8. Andersen R. A. Asanuma C. Essick G. Siegel R. M. (1990). Corticocortical connections of anatomically and physiologically defined subdivisions within the inferior parietal lobule. J. Comp. Neurol. 296, 65– 113 10.1002/cne.902960106 2358530 · DOI
  9. Angaut P. Cicirata F. Serapide F. (1985). Topographic organization of the cerebellothalamic projections in the rat. An autoradiographic study. Neuroscience 15, 389– 401 10.1016/0306-4522(85)90221-0 4022330 · DOI
  10. Angelaki D. E. Cullen K. E. (2008). Vestibular system: the many facets of a multimodal sense. Annu. Rev. Neurosci. 31, 125– 150 10.1146/annurev.neuro.31.060407.125555 18338968 · DOI
  11. Angelaki D. E. Yakusheva T. A. Green A. M. Dickman J. D. Blazquez P. M. (2010). Computation of egomotion in the macaque cerebellar vermis. Cerebellum 9, 174– 182 10.1007/s12311-009-0147-z 20012388 PMC3640361 · DOI
  12. Antoine M. W. Hübner C. A. Arezzo J. C. Hébert J. M. (2013). A causative link between inner ear defects and long-term striatal dysfunction. Science 341, 1120– 1123 10.1126/science.1240405 24009395 PMC4731229 · DOI
  13. Aravamuthan B. R. Angelaki D. E. (2012). Vestibular responses in the macaque pedunculopontine nucleus and central mesencephalic reticular formation. Neuroscience 223, 183– 199 10.1016/j.neuroscience.2012.07.054 22864184 PMC3484682 · DOI
  14. Arnolds D. Lopes da Silva F. H. Boeijinga P. Kamp A. Aitink W. (1984). Hippocampal EEG and motor activity in the cat: the role of eye movements and body acceleration. Behav. Brain Res. 12, 121– 135 10.1016/0166-4328(84)90035-4 6466432 · DOI
  15. Atallah H. E. Lopez-Paniagua D. Rudy J. W. O’Reilly R. C. (2006). Separate neural substrates for skill learning and performance in the ventral and dorsal striatum. Nat. Neurosci. 10, 126– 131 10.1038/nn1817 17187065 · DOI · Paper page
  16. Aumann T. D. Rawson J. A. Finkelstein D. I. Horne M. K. (1994). Projections from the lateral and interposed cerebellar nuclei to the thalamus of the rat: a light and electron microscopic study using single and double anterograde labelling. J. Comp. Neurol. 349, 165– 181 10.1002/cne.903490202 7860776 · DOI
  17. Baek J. H. Zheng Y. Darlington C. L. Smith P. F. (2010). Evidence that spatial memory deficits following bilateral vestibular deafferentation in rats are probably permanent. Neurobiol. Learn. Mem. 94, 402– 413 10.1016/j.nlm.2010.08.007 20736074 · DOI
  18. Barmack N. H. (2003). Central vestibular system: vestibular nuclei and posterior cerebellum. Brain Res. Bull. 60, 511– 541 10.1016/s0361-9230(03)00055-8 12787870 · DOI
  19. Bassant M. H. Poindessous-Jazat F. (2001). Ventral tegmental nucleus of Gudden: a pontine hippocampal theta generator? Hippocampus 11, 809– 813 10.1002/hipo.1096 11811675 · DOI
  20. Bassett J. P. Taube J. S. (2001). Neural correlates for angular head velocity in the rat dorsal tegmental nucleus. J. Neurosci. 21, 5740– 5751 11466446 PMC6762668
  21. Bassett J. P. Tullman M. L. Taube J. S. (2007). Lesions of the tegmentomammillary circuit in the head direction system disrupt the head direction signal in the anterior thalamus. J. Neurosci. 27, 7564– 7577 10.1523/jneurosci.0268-07.2007 17626218 PMC6672597 · DOI
  22. Bense S. Stephan T. Yousry T. A. Brandt T. Dieterich M. (2001). Multisensory cortical signal increases and decreases during vestibular galvanic stimulation (fMRI). J. Neurophysiol. 85, 886– 899 11160520
  23. Beraneck M. Lambert F. M. (2009). Impaired perception of gravity leads to altered head direction signals: what can we learn from vestibular-deficient mice? J. Neurophysiol. 102, 12– 14 10.1152/jn.00351.2009 19458147 · DOI
  24. Besnard S. Machado M. L. Vignaux G. Boulouard M. Coquerel A. Bouet V. (2012). Influence of vestibular input on spatial and nonspatial memory and on hippocampal NMDA receptors. Hippocampus 22, 814– 826 10.1002/hipo.20942 21538662 · DOI
  25. Biazoli C. E. Jr. Goto M. Campos A. M. P. Canteras N. S. (2006). The supragenual nucleus: a putative relay station for ascending vestibular signs to head direction cells. Brain Res. 1094, 138– 148 10.1016/j.brainres.2006.03.101 16684515 · DOI
  26. Björnsdotter M. Löken L. Olausson H. Vallbo A. Wessberg J. (2009). Somatotopic organization of gentle touch processing in the posterior insular cortex. J. Neurosci. 29, 9314– 9320 10.1523/JNEUROSCI.0400-09.2009 19625521 PMC6665561 · DOI
  27. Blair H. T. Cho J. Sharp P. E. (1998). Role of the lateral mammillary nucleus in the rat head direction circuit: a combined single unit recording and lesion study. Neuron 21, 1387– 1397 10.1016/s0896-6273(00)80657-1 9883731 · DOI
  28. Blair H. T. Sharp P. E. (1996). Visual and vestibular influences on head-direction cells in the anterior thalamus of the rat. Behav. Neurosci. 110, 643– 660 10.1037/0735-7044.110.4.643 8864258 · DOI
  29. Bland B. H. Oddie S. D. (1998). Anatomical, electrophysiological and pharmacological studies of ascending brainstem hippocampal synchronizing pathways. Neurosci. Biobehav. Rev. 22, 259– 273 10.1016/s0149-7634(97)00013-4 9579317 · DOI
  30. Blanks R. H. I. Precht W. Torigoe Y. (1983). Afferent projections to the cerebellar flocculus in the pigmented rat demonstrated by retrograde transport of horseradish peroxidase. Exp. Brain Res. 52, 293– 306 10.1007/bf00236639 6641889 · DOI
  31. Bottini G. Sterzi R. Paulesu E. Vallar G. Cappa S. F. Erminio F. (1994). Identification of the central vestibular projections in man: a positron emission tomography activation study. Exp. Brain Res. 99, 164– 169 10.1007/bf00241421 7925790 · DOI
  32. Brandt T. Dieterich M. (1999). The vestibular cortex: its locations, functions and disorders. Ann. N Y Acad. Sci. 871, 293– 312 10.1111/j.1749-6632.1999.tb09193.x 10372080 · DOI
  33. Brandt T. Schautzer F. Hamilton D. A. Brüning R. Markowitsch H. J. Kalla R. (2005). Vestibular loss causes hippocampal atrophy and impaired spatial memory in humans. Brain 128, 2732– 2741 10.1093/brain/awh617 16141283 · DOI
  34. Bremmer F. (2005). Navigation in space–the role of the macaque ventral intraparietal area. J. Physiol. 566, 29– 35 10.1113/jphysiol.2005.082552 15845586 PMC1464721 · DOI
  35. Brodal A. Brodal P. (1985). Observations on the secondary vestibulocerebellar projections in the macaque monkey. Exp. Brain Res. 58, 62– 74 10.1007/bf00238954 3987852 · DOI
  36. Brown J. E. Taube J. S. (2007). “ Neural representations supporting spatial navigation and memory,” in Representation and Brain, ed Funahashi S. (Japan: Springer), 219– 248
  37. Brun V. H. Leutgeb S. Wu H.-Q. Schwarcz R. Witter M. P. Moser E. I. (2008). Impaired spatial representation in CA1 after lesion of direct input from entorhinal cortex. Neuron 57, 290– 302 10.1016/j.neuron.2007.11.034 18215625 · DOI
  38. Burwell R. D. Amaral D. G. (1998). Cortical afferents of the perirhinal, postrhinal and entorhinal cortices of the rat. J. Comp. Neurol. 398, 179– 205 10.1002/(sici)1096-9861(19980824)398:2<179::aid-cne3>3.0.co;2-y 9700566 · DOI
  39. Büttner U. Buettner U. W. (1978). Parietal cortex (2v) neuronal activity in the alert monkey during natural vestibular and optokinetic stimulation. Brain Res. 153, 392– 397 10.1016/0006-8993(78)90421-3 99209 · DOI
  40. Buzsáki G. (2002). Theta oscillations in the Hippocampus. Neuron 33, 325– 340 10.1016/s0896-6273(02)00586-x 11832222 · DOI · Paper page
  41. Calton J. L. Stackman R. W. Goodridge J. P. Archey W. B. Dudchenko P. A. Taube J. S. (2003). Hippocampal place cell instability after lesions of the head direction cell network. J. Neurosci. 23, 9719– 9731 14585999 PMC6740880
  42. Calton J. L. Turner C. S. Cyrenne D. L. M. Lee B. R. Taube J. S. (2008). Landmark control and updating of self-movement cues are largely maintained in head direction cells after lesions of the posterior parietal cortex. Behav. Neurosci. 122, 827– 840 10.1037/0735-7044.122.4.827 18729636 PMC2771080 · DOI
  43. Carpenter M. B. Stein B. M. Peter P. (1972). Primary vestibulocerebellar fibers in the monkey: distribution of fibers arising from distinctive cell groups of the vestibular ganglia. Am. J. Anat. 135, 221– 249 10.1002/aja.1001350209 4627955 · DOI
  44. Chafee M. V. Averbeck B. B. Crowe D. A. (2007). Representing spatial relationships in posterior parietal cortex: single neurons code object-referenced position. Cereb. Cortex 17, 2914– 2932 10.1093/cercor/bhm017 17389630 · DOI
  45. Chen A. DeAngelis G. C. Angelaki D. E. (2013). Functional specializations of the ventral intraparietal area for multisensory heading discrimination. J. Neurosci. 33, 3567– 3581 10.1523/jneurosci.4522-12.2013 23426684 PMC3727431 · DOI
  46. Chen L. L. Lin L. H. Green E. J. Barnes C. A. McNaughton B. L. (1994). Head-direction cells in the rat posterior cortex. I. Anatomical distribution and behavioral modulation. Exp. Brain Res. 101, 8– 23 10.1007/bf00243212 7843305 · DOI · Paper page
  47. Chung K. Wallace J. Kim S.-Y. Kalyanasundaram S. Andalman A. S. Davidson T. J. (2013). Structural and molecular interrogation of intact biological systems. Nature 497, 332– 337 10.1038/nature12107 23575631 PMC4092167 · DOI · Paper page
  48. Clark B. J. Bassett J. P. Wang S. S. Taube J. S. (2010). Impaired head direction cell representation in the anterodorsal thalamus after lesions of the retrosplenial cortex. J. Neurosci. 30, 5289– 5302 10.1523/jneurosci.3380-09.2010 20392951 PMC2861549 · DOI
  49. Clark B. J. Brown J. E. Taube J. S. (2012). Head direction cell activity in the anterodorsal thalamus requires intact supragenual nuclei. J. Neurophysiol. 108, 2767– 2784 10.1152/jn.00295.2012 22875899 PMC3545120 · DOI
  50. Clark B. J. Taube J. S. (2012). Vestibular and attractor network basis of the head direction cell signal in subcortical circuits. Front. Neural Circuits 6: 7 10.3389/fncir.2012.00007 22454618 PMC3308332 · DOI
  51. Cooper B. G. Manka T. F. Mizumori S. J. (2001). Finding your way in the dark: the retrosplenial cortex contributes to spatial memory and navigation without visual cues. Behav. Neurosci. 115, 1012– 1028 10.1037//0735-7044.115.5.1012 11584914 · DOI
  52. Cooper B. G. Mizumori S. J. Y. (2001). Temporary inactivation of the retrosplenial cortex causes a transient reorganization of spatial coding in the hippocampus. J. Neurosci. 21, 3986– 4001 11356886 PMC6762703
  53. Crowe D. A. Averbeck B. B. Chafee M. V. (2008). Neural ensemble decoding reveals a correlate of viewer-to object-centered spatial transformation in monkey parietal cortex. J. Neurosci. 28, 5218– 5228 10.1523/jneurosci.5105-07.2008 18480278 PMC3844802 · DOI
  54. Cuthbert P. C. Gilchrist D. P. Hicks S. L. MacDougall H. G. Curthoys I. S. (2000). Electrophysiological evidence for vestibular activation of the guinea pig hippocampus. Neuroreport 11, 1443– 1447 10.1097/00001756-200005150-00018 10841354 · DOI
  55. Deutschländer A. Bense S. Stephan T. Schwaiger M. Brandt T. Dieterich M. (2002). Sensory system interactions during simultaneous vestibular and visual stimulation in PET. Hum. Brain Mapp. 16, 92– 103 10.1002/hbm.10030 11954059 PMC6871812 · DOI
  56. Dieterich M. Bense S. Lutz S. Drzezga A. Stephan T. Bartenstein P. (2003). Dominance for vestibular cortical function in the non-dominant hemisphere. Cereb. Cortex 13, 994– 1007 10.1093/cercor/13.9.994 12902399 · DOI
  57. Duffy C. J. (1998). MST neurons respond to optic flow and translational movement. J. Neurophysiol. 80, 1816– 1827 9772241
  58. Ekstrom A. D. Kahana M. J. Caplan J. B. Fields T. A. Isham E. A. Newman E. L. (2003). Cellular networks underlying human spatial navigation. Nature 425, 184– 188 10.1038/nature01964 12968182 · DOI · Paper page
  59. Epema A. H. Gerrits N. M. Voogd J. (1990). Secondary vestibulocerebellar projections to the flocculus and uvulo-nodular lobule of the rabbit: a study using HRP and double fluorescent tracer techniques. Exp. Brain Res. 80, 72– 82 10.1007/bf00228849 2358039 · DOI
  60. Falconer C. J. Mast F. W. (2012). Balancing the mind. Exp. Psychol. 59, 332– 339 10.1027/1618-3169/a000161 22750744 · DOI
  61. Fasold O. von Brevern M. Kuhberg M. Ploner C. J. Villringer A. Lempert T. (2002). Human vestibular cortex as identified with caloric stimulation in functional magnetic resonance imaging. Neuroimage 17, 1384– 1393 10.1006/nimg.2002.1241 12414278 · DOI
  62. Ferrè E. R. Vagnoni E. Haggard P. (2013). Galvanic vestibular stimulation influences randomness of number generation. Exp. Brain Res. 224, 233– 241 10.1007/s00221-012-3302-6 23111396 · DOI
  63. Ferretti V. Roullet P. Sargolini F. Rinaldi A. Perri V. Del Fabbro M. (2010). Ventral striatal plasticity and spatial memory. Proc. Natl. Acad. Sci. U S A 107, 7945– 7950 10.1073/pnas.0911757107 20351272 PMC2867912 · DOI
  64. Ferretti V. Sargolini F. Oliverio A. Mele A. Roullet P. (2007). Effects of intra-accumbens NMDA and AMPA receptor antagonists on short-term spatial learning in the Morris water maze task. Behav. Brain Res. 179, 43– 49 10.1016/j.bbr.2007.01.009 17289166 · DOI
  65. Fetsch C. R. Wang S. Gu Y. DeAngelis G. C. Angelaki D. E. (2007). Spatial reference frames of visual, vestibular and multimodal heading signals in the dorsal subdivision of the medial superior temporal area. J. Neurosci. 27, 700– 712 10.1523/JNEUROSCI.3553-06.2007 17234602 PMC1995026 · DOI
  66. Floresco S. B. Todd C. L. Grace A. A. (2001). Glutamatergic afferents from the hippocampus to the nucleus accumbens regulate activity of ventral tegmental area dopamine neurons. J. Neurosci. 21, 4915– 4922 11425919 PMC6762358
  67. Fredrickson J. M. Figge U. Scheid P. Kornhuber H. H. (1966). Vestibular nerve projection to the cerebral cortex of the rhesus monkey. Exp. Brain Res. 2, 318– 327 10.1007/bf00234777 4959658 · DOI
  68. Fyhn M. Hafting T. Treves A. Moser M.-B. Moser E. I. (2007). Hippocampal remapping and grid realignment in entorhinal cortex. Nature 446, 190– 194 10.1038/nature05601 17322902 · DOI · Paper page
  69. Fyhn M. Molden S. Witter M. P. Moser E. I. Moser M.-B. (2004). Spatial representation in the entorhinal cortex. Science 305, 1258– 1264 10.1126/science.1099901 15333832 · DOI · Paper page
  70. Gasbarri A. Verney C. Innocenzi R. Campana E. Pacitti C. (1994). Mesolimbic dopaminergic neurons innervating the hippocampal formation in the rat: a combined retrograde tracing and immunohistochemical study. Brain Res. 668, 71– 79 10.1016/0006-8993(94)90512-6 7704620 · DOI
  71. Gavrilov V. V. Wiener S. I. Berthoz A. (1995). Enhanced hippocampal theta EEG during whole body rotations in awake restrained rats. Neurosci. Lett. 197, 239– 241 10.1016/0304-3940(95)11918-m 8552308 · DOI
  72. Gavrilov V. V. Wiener S. I. Berthoz A. (1996). Whole-body rotations enhance hippocampal theta rhythmic slow activity in awake rats passively transported on a mobile robot. Ann. N Y Acad. Sci. 781, 385– 398 10.1111/j.1749-6632.1996.tb15714.x 8694429 · DOI
  73. Geesaman B. J. Andersen R. A. (1996). The analysis of complex motion patterns by form/cue invariant MSTd neurons. J. Neurosci. 16, 4716– 4732 8764659 PMC6579023
  74. Golob E. J. Taube J. S. (1997). Head direction cells and episodic spatial information in rats without a hippocampus. Proc. Natl. Acad. Sci. U S A 94, 7645– 7650 10.1073/pnas.94.14.7645 9207146 PMC23876 · DOI
  75. Golob E. J. Taube J. S. (1999). Head direction cells in rats with hippocampal or overlying neocortical lesions: evidence for impaired angular path integration. J. Neurosci. 19, 7198– 7211 10436073 PMC6782884
  76. Goodlett C. R. Hamre K. M. West J. R. (1992). Dissociation of spatial navigation and visual guidance performance in Purkinje cell degeneration (pcd) mutant mice. Behav. Brain Res. 47, 129– 141 10.1016/s0166-4328(05)80119-6 1590945 · DOI
  77. Goodridge J. P. Taube J. S. (1997). Interaction between the postsubiculum and anterior thalamus in the generation of head direction cell activity. J. Neurosci. 17, 9315– 9330 9364077 PMC6573595
  78. Graf W. Gerrits N. Yatim-Dhiba N. Ugolini G. (2002). Mapping the oculomotor system: the power of transneuronal labelling with rabies virus. Eur. J. Neurosci. 15, 1557– 1562 10.1046/j.1460-9568.2002.01994.x 12028367 · DOI
  79. Grüsser O.-J. Pause M. Schreiter U. (1982). “ Neuronal responses in the parieto—insular vestibular cortex of alert Java monkeys (Maccaca fascicularis),” in Physiological and Pathological Aspects of Eye Movements, eds Roucoux A. Crommelinck M. (Netherland: Springer), 251– 270
  80. Grüsser O. J. Pause M. Schreiter U. (1990a). Localization and responses of neurones in the parieto-insular vestibular cortex of awake monkeys (Macaca fascicularis). J. Physiol. 430, 537– 557 2086773 PMC1181752
  81. Grüsser O. J. Pause M. Schreiter U. (1990b). Vestibular neurones in the parieto-insular cortex of monkeys (Macaca fascicularis): visual and neck receptor responses. J. Physiol. 430, 559– 583 2086774 PMC1181753
  82. Guldin W. O. Akbarian S. Grüsser O.-J. (1992). Cortico-cortical connections and cytoarchitectonics of the primate vestibular cortex: a study in squirrel monkeys (Saimiri sciureus). J. Comp. Neurol. 326, 375– 401 10.1002/cne.903260306 1281845 · DOI
  83. Guldin W. O. Mirring S. Grüsser O.-J. (1993). Connections from the neocortex to the vestibular brain stem nuclei in the common marmoset. Neuroreport 5, 113– 116 10.1097/00001756-199311180-00004 8110998 · DOI
  84. Hafting T. Fyhn M. Molden S. Moser M.-B. Moser E. I. (2005). Microstructure of a spatial map in the entorhinal cortex. Nature 436, 801– 806 10.1038/nature03721 15965463 · DOI · Paper page
  85. Haroian A. J. Massopust L. C. Young P. A. (1981). Cerebellothalamic projections in the rat: an autoradiographic and degeneration study. J. Comp. Neurol. 197, 217– 236 10.1002/cne.901970205 7276233 · DOI
  86. Hartmann M. Farkas R. Mast F. W. (2012a). Self-motion perception influences number processing: evidence from a parity task. Cogn. Process. 13, 189– 192 10.1007/s10339-012-0484-6 22802038 · DOI
  87. Hartmann M. Grabherr L. Mast F. W. (2012b). Moving along the mental number line: interactions between whole-body motion and numerical cognition. J. Exp. Psychol. Hum. Percept. Perform. 38, 1416– 1427 10.1037/a0026706 22201471 · DOI
  88. Heath R. G. Dempesy C. W. Fontana C. J. Myers W. A. (1978). Cerebellar stimulation: effects on septal region, hippocampus and amygdala of cats and rats. Biol. Psychiatry 13, 501– 529 728506
  89. Heath R. G. Harper J. W. (1974). Ascending projections of the cerebellar fastigial nucleus to the hippocampus, amygdala and other temporal lobe sites: evoked potential and histological studies in monkeys and cats. Exp. Neurol. 45, 268– 287 10.1016/0014-4886(74)90118-6 4422320 · DOI
  90. Hilber P. Jouen F. Delhaye-Bouchaud N. Mariani J. Caston J. (1998). Differential roles of cerebellar cortex and deep cerebellar nuclei in learning and retention of a spatial task: studies in intact and cerebellectomized Lurcher mutant mice. Behav. Genet. 28, 299– 308 10.1023/A:1021675514883 9803022 · DOI
  91. Hoffmann L. C. Berry S. D. (2009). Cerebellar theta oscillations are synchronized during hippocampal theta-contingent trace conditioning. Proc. Natl. Acad. Sci. U S A 106, 21371– 21376 10.1073/pnas.0908403106 19940240 PMC2795537 · DOI
  92. Hoover W. B. Vertes R. P. (2007). Anatomical analysis of afferent projections to the medial prefrontal cortex in the rat. Brain Struct. Funct. 212, 149– 179 10.1007/s00429-007-0150-4 17717690 · DOI · Paper page
  93. Horii A. Russell N. A. Smith P. F. Darlington C. L. Bilkey D. K. (2004). Vestibular influences on CA1 neurons in the rat hippocampus: an electrophysiological study in vivo. Exp. Brain Res. 155, 245– 250 10.1007/s00221-003-1725-9 14666395 · DOI
  94. Hubbard E. M. Piazza M. Pinel P. Dehaene S. (2005). Interactions between number and space in parietal cortex. Nat. Rev. Neurosci. 6, 435– 448 10.1038/nrn1684 15928716 · DOI
  95. Hüfner K. Hamilton D. A. Kalla R. Stephan T. Glasauer S. Ma J. (2007). Spatial memory and hippocampal volume in humans with unilateral vestibular deafferentation. Hippocampus 17, 471– 485 10.1002/hipo.20283 17397043 · DOI
  96. Irle E. Sarter M. Guldin W. O. Markowitsch H. J. (1984). Afferents to the ventral tegmental nucleus of Gudden in the mouse, rat and cat. J. Comp. Neurol. 228, 509– 541 10.1002/cne.902280406 6436341 · DOI
  97. Jacobs J. (2014). Hippocampal theta oscillations are slower in humans than in rodents: implications for models of spatial navigation and memory. Philos. Trans. R. Soc. Lond. B Biol. Sci. 369: 20130304 10.1098/rstb.2013.0304 24366145 PMC3866455 · DOI
  98. Jacobs J. Weidemann C. T. Miller J. F. Solway A. Burke J. F. Wei X.-X. (2013). Direct recordings of grid-like neuronal activity in human spatial navigation. Nat. Neurosci. 16, 1188– 1190 10.1038/nn.3466 23912946 PMC3767317 · DOI · Paper page
  99. Klam F. Graf W. (2006). Discrimination between active and passive head movements by macaque ventral and medial intraparietal cortex neurons. J. Physiol. 574, 367– 386 10.1113/jphysiol.2005.103697 16556655 PMC1817758 · DOI
  100. Koenig J. Linder A. N. Leutgeb J. K. Leutgeb S. (2011). The spatial periodicity of grid cells is not sustained during reduced theta oscillations. Science 332, 592– 595 10.1126/science.1201685 21527713 · DOI · Paper page
  101. Korte G. E. Mugnaini E. (1979). The cerebellar projection of the vestibular nerve in the cat. J. Comp. Neurol. 184, 265– 277 10.1002/cne.901840204 762284 · DOI
  102. Kotchabhakdi N. Rinvik E. Walberg F. Yingchareon K. (1980). The vestibulothalamic projections in the cat studied by retrograde axonal transport of horseradish peroxidase. Exp. Brain Res. 40, 405– 418 10.1007/bf00236149 7439283 · DOI
  103. Kotchabhakdi N. Walberg F. (1978). Cerebellar afferent projections from the vestibular nuclei in the cat: an experimental study with the method of retrograde axonal transport of horseradish peroxidase. Exp. Brain Res. 31, 591– 604 10.1007/bf00239814 350598 · DOI
  104. Lai H. Tsumori T. Shiroyama T. Yokota S. Nakano K. Yasui Y. (2000). Morphological evidence for a vestibulo-thalamo-striatal pathway via the parafascicular nucleus in the rat. Brain Res. 872, 208– 214 10.1016/s0006-8993(00)02457-4 10924695 · DOI
  105. Lang W. Büttner-Ennever J. A. Büttner U. (1979). Vestibular projections to the monkey thalamus: an autoradiographic study. Brain Res. 177, 3– 17 10.1016/0006-8993(79)90914-4 115546 · DOI
  106. Leung L.-W. S. Yim C. Y. (1986). Intracellular records of theta rhythm in hippocampal CA1 cells of the rat. Brain Res. 367, 323– 327 10.1016/0006-8993(86)91611-2 3008923 · DOI
  107. Leutgeb S. Leutgeb J. K. Moser M.-B. Moser E. I. (2005). Place cells, spatial maps and the population code for memory. Curr. Opin. Neurobiol. 15, 738– 746 10.1016/j.conb.2005.10.002 16263261 · DOI
  108. Leutgeb S. Ragozzino K. E. Mizumori S. J. Y. (2000). Convergence of head direction and place information in the CA1 region of hippocampus. Neuroscience 100, 11– 19 10.1016/s0306-4522(00)00258-x 10996454 · DOI
  109. Liedgren S. R. Milne A. C. Schwarz D. W. Tomlinson R. D. (1976). Representation of vestibular afferents in somatosensory thalamic nuclei of the squirrel monkey (Saimiri sciureus). J. Neurophysiol. 39, 601– 612 820837
  110. Liu R. Chang L. Wickern G. (1984). The dorsal tegmental nucleus: an axoplasmic transport study. Brain Res. 310, 123– 132 10.1016/0006-8993(84)90015-5 6434154 · DOI
  111. Liu P. Gliddon C. M. Lindsay L. Darlington C. L. Smith P. F. (2004). Nitric oxide synthase and arginase expression changes in the rat perirhinal and entorhinal cortices following unilateral vestibular damage: a link to deficits in object recognition? J. Vestib. Res. 14, 411– 418 15735325
  112. Lopez C. Blanke O. (2011). The thalamocortical vestibular system in animals and humans. Brain Res. Rev. 67, 119– 146 10.1016/j.brainresrev.2010.12.002 21223979 · DOI · Paper page
  113. Lubenov E. V. Siapas A. G. (2009). Hippocampal theta oscillations are travelling waves. Nature 459, 534– 539 10.1038/nature08010 19489117 · DOI
  114. Lugli L. Baroni G. Anelli F. Borghi A. M. Nicoletti R. (2013). Counting is easier while experiencing a congruent motion. PLoS One 8: e64500 10.1371/journal.pone.0064500 23691234 PMC3654906 · DOI
  115. Machado M.-L. Lelong-Boulouard V. Philoxene B. Davis A. Denise P. Besnard S. (2014). Vestibular loss promotes procedural response during a spatial task in rats. Hippocampus 24, 591– 597 10.1002/hipo.22251 24464878 · DOI
  116. Maciewicz R. Phipps B. S. Bry J. Highstein S. M. (1982). The vestibulothalamic pathway: contribution of the ascending tract of Deiters. Brain Res. 252, 1– 11 10.1016/0006-8993(82)90973-8 7172013 · DOI
  117. Maiti A. Snider R. S. (1975). Cerebellar control of basal forebrain seizures: amygdala and hippocampus. Epilepsia 16, 521– 533 10.1111/j.1528-1157.1975.tb06082.x 810347 · DOI
  118. Marlinski V. McCrea R. A. (2008). Activity of ventroposterior thalamus neurons during rotation and translation in the horizontal plane in the alert squirrel monkey. J. Neurophysiol. 99, 2533– 2545 10.1152/jn.00761.2007 18337373 · DOI
  119. Matsunami K. Cohen B. (1975). Afferent modulation of unit activity in globus pallidus and caudate nucleus: changes induced by vestibular nucleus and pyramidal tract stimulation. Brain Res. 91, 140– 146 10.1016/0006-8993(75)90473-4 1131694 · DOI
  120. McCrea R. A. Baker R. (1985). Anatomical connections of the nucleus prepositus of the cat. J. Comp. Neurol. 237, 377– 407 10.1002/cne.902370308 2995460 · DOI
  121. McNaughton B. Barnes C. Gerrard J. Gothard K. Jung M. Knierim J. (1996). Deciphering the hippocampal polyglot: the hippocampus as a path integration system. J. Exp. Biol. 199, 173– 185 8576689
  122. McNaughton B. L. Battaglia F. P. Jensen O. Moser E. I. Moser M.-B. (2006). Path integration and the neural basis of the’cognitive map’. Nat. Rev. Neurosci. 7, 663– 678 10.1038/nrn1932 16858394 · DOI · Paper page
  123. Meng H. May P. J. Dickman J. D. Angelaki D. E. (2007). Vestibular signals in primate thalamus: properties and origins. J. Neurosci. 27, 13590– 13602 10.1523/jneurosci.3931-07.2007 18077671 PMC6673608 · DOI
  124. Middleton F. A. Strick P. L. (2000). Basal ganglia and cerebellar loops: motor and cognitive circuits. Brain Res. Brain Res. Rev. 31, 236– 250 10.1016/s0165-0173(99)00040-5 10719151 · DOI · Paper page
  125. Mizumori S. J. Y. Puryear C. B. Martig A. K. (2009). Basal ganglia contributions to adaptive navigation. Behav. Brain Res. 199, 32– 42 10.1016/j.bbr.2008.11.014 19056429 · DOI
  126. Mizumori S. J. Williams J. D. (1993). Directionally selective mnemonic properties of neurons in the lateral dorsal nucleus of the thalamus of rats. J. Neurosci. 13, 4015– 4028 8366357 PMC6576470
  127. Moffat S. D. Elkins W. Resnick S. M. (2006). Age differences in the neural systems supporting human allocentric spatial navigation. Neurobiol. Aging 27, 965– 972 10.1016/j.neurobiolaging.2005.05.011 15982787 · DOI
  128. Morecraft R. J. Geula C. Mesulam M. (1993). Architecture of connectivity within a cingulo-fronto-parietal neurocognitive network for directed attention. Arch. Neurol. 50, 279– 284 10.1001/archneur.1993.00540030045013 8442707 · DOI
  129. Moser E. I. Kropff E. Moser M. B. (2008). Place cells, grid cells and the brain’s spatial representation system. Annu. Rev. Neurosci. 31, 69– 89 10.1146/annurev.neuro.31.061307.090723 18284371 · DOI · Paper page
  130. Muir G. M. Brown J. E. Carey J. P. Hirvonen T. P. Della Santina C. C. Minor L. B. (2009). Disruption of the head direction cell signal after occlusion of the semicircular canals in the freely moving chinchilla. J. Neurosci. 29, 14521– 14533 10.1523/jneurosci.3450-09.2009 19923286 PMC2821030 · DOI
  131. Mullen R. J. Eicher E. M. Sidman R. L. (1976). Purkinje cell degeneration, a new neurological mutation in the mouse. Proc. Natl. Acad. Sci. U S A 73, 208– 212 10.1073/pnas.73.1.208 1061118 PMC335870 · DOI
  132. Mumby D. G. (2001). Perspectives on object-recognition memory following hippocampal damage: lessons from studies in rats. Behav. Brain Res. 127, 159– 181 10.1016/s0166-4328(01)00367-9 11718890 · DOI
  133. Nagata S. (1986). The vestibulothalamic connections in the rat: a morphological analysis using wheat germ agglutinin-horseradish peroxidase. Brain Res. 376, 57– 70 10.1016/0006-8993(86)90899-1 3013377 · DOI
  134. Neo P. Carter D. Zheng Y. Smith P. Darlington C. McNaughton N. (2012). Septal elicitation of hippocampal theta rhythm did not repair cognitive and emotional deficits resulting from vestibular lesions. Hippocampus 22, 1176– 1187 10.1002/hipo.20963 21748822 · DOI
  135. Newman P. P. Reza H. (1979). Functional relationships between the hippocampus and the cerebellum: an electrophysiological study of the cat. J. Physiol. 287, 405– 426 430426 PMC1281503
  136. Niedermeyer E. (2008). Hippocampic theta rhythm. Clin. EEG Neurosci. 39, 191– 193 10.1177/155005940803900408 19044217 · DOI
  137. Nieuwenhuys R. Voogd J. Van Huijzen C. (2008). The Human Central Nervous System. Berlin: Springer
  138. Niven J. E. Laughlin S. B. (2008). Energy limitation as a selective pressure on the evolution of sensory systems. J. Exp. Biol. 211, 1792– 1804 10.1242/jeb.017574 18490395 · DOI · Paper page
  139. O’Keefe J. (1976). Place units in the hippocampus of the freely moving rat. Exp. Neurol. 51, 78– 109 10.1016/0014-4886(76)90055-8 1261644 · DOI · Paper page
  140. O’Keefe J. (1993). Hippocampus, theta, and spatial memory. Curr. Opin. Neurobiol. 3, 917– 924 10.1016/0959-4388(93)90163-s 8124075 · DOI
  141. Ödkvist L. M. Schwarz D. W. F. Fredrickson J. M. Hassler R. (1974). Projection of the vestibular nerve to the area 3a arm field in the squirrel monkey (Saimiri sciureus). Exp. Brain Res. 21, 97– 105 10.1007/bf00234260 4213802 · DOI
  142. Olshausen B. A. Field D. J. (2004). Sparse coding of sensory inputs. Curr. Opin. Neurobiol. 14, 481– 487 10.1016/j.conb.2004.07.007 15321069 · DOI · Paper page
  143. Partridge J. Rayner J. Awan S. (2010). The cerebellar cognitive affective syndrome. Br. J. Hosp. Med.(Lond.) 71, 712– 713 10.12968/hmed.2010.71.12.712 21135772 · DOI
  144. Pfeiffer B. E. Foster D. J. (2013). Hippocampal place-cell sequences depict future paths to remembered goals. Nature 497, 74– 79 10.1038/nature12112 23594744 PMC3990408 · DOI · Paper page
  145. Pignatelli M. Beyeler A. Leinekugel X. (2012). Neural circuits underlying the generation of theta oscillations. J. Physiol. Paris 106, 81– 92 10.1016/j.jphysparis.2011.09.007 21964249 · DOI
  146. Potegal M. Copack P. de Jong J. M. B. V. Krauthamer G. Gilman S. (1971). Vestibular input to the caudate nucleus. Exp. Neurol. 32, 448– 465 10.1016/0014-4886(71)90011-2 5110227 · DOI
  147. Quiroga R. Q. Kreiman G. Koch C. Fried I. (2008). Sparse but not “grandmother-cell”coding in the medial temporal lobe. Trends Cogn. Sci. 12, 87– 91 10.1016/j.tics.2007.12.003 18262826 · DOI
  148. Reep R. L. Chandler H. C. King V. Corwin J. V. (1994). Rat posterior parietal cortex: topography of corticocortical and thalamic connections. Exp. Brain Res. 100, 67– 84 10.1007/bf00227280 7813654 · DOI
  149. Reichova I. Sherman S. M. (2004). Somatosensory corticothalamic projections: distinguishing drivers from modulators. J. Neurophysiol. 92, 2185– 2197 10.1152/jn.00322.2004 15140908 · DOI
  150. Retailleau A. Etienne S. Guthrie M. Boraud T. (2012). Where is my reward and how do I get it? Interaction between the hippocampus and the basal ganglia during spatial learning. J. Physiol. Paris 106, 72– 80 10.1016/j.jphysparis.2011.10.002 22033208 · DOI
  151. Risey J. Briner W. (1990–1991). Dyscalculia in patients with vertigo. J. Vestib. Res. 1, 31– 37 1670135
  152. Robinson C. J. Burton H. (1980). Organization of somatosensory receptive fields in cortical areas 7b, retroinsula, postauditory and granular insula of M. fascicularis. J. Comp. Neurol. 192, 69– 92 10.1002/cne.901920105 7410614 · DOI
  153. Rochefort C. Lefort J. M. Rondi-Reig L. (2013). The cerebellum: a new key structure in the navigation system. Front. Neural Circuits 7: 35 10.3389/fncir.2013.00035 23493515 PMC3595517 · DOI
  154. Rockland K. S. Van Hoesen G. W. (1999). Some temporal and parietal cortical connections converge in CA1 of the primate hippocampus. Cereb. Cortex 9, 232– 237 10.1093/cercor/9.3.232 10355903 · DOI
  155. Rondi-Reig L. Burguière E. (2005). Is the cerebellum ready for navigation? Prog. Brain Res. 148, 199– 212 10.1016/s0079-6123(04)48017-0 15661192 · DOI
  156. Rondi-Reig L. Le Marec N. Caston J. Mariani J. (2002). The role of climbing and parallel fibers inputs to cerebellar cortex in navigation. Behav. Brain Res. 132, 11– 18 10.1016/s0166-4328(01)00381-3 11853853 · DOI
  157. Russell N. A. Horii A. Smith P. F. Darlington C. L. Bilkey D. K. (2003). Long-term effects of permanent vestibular lesions on hippocampal spatial firing. J. Neurosci. 23, 6490– 6498 12878690 PMC6740646
  158. Russell N. A. Horii A. Smith P. F. Darlington C. L. Bilkey D. K. (2006). Lesions of the vestibular system disrupt hippocampal theta rhythm in the rat. J. Neurophysiol. 96, 4– 14 10.1152/jn.00953.2005 16772515 · DOI
  159. Sargolini F. Fyhn M. Hafting T. McNaughton B. L. Witter M. P. Moser M.-B. (2006). Conjunctive representation of position, direction and velocity in entorhinal cortex. Science 312, 758– 762 10.1126/science.1125572 16675704 · DOI · Paper page
  160. Schmahmann J. D. (1996). From movement to thought: anatomic substrates of the cerebellar contribution to cognitive processing. Hum. Brain Mapp. 4, 174– 198 10.1002/(sici)1097-0193(1996)4:3<174::aid-hbm3>3.0.co;2-0 20408197 · DOI
  161. Schmahmann J. D. (2001). The cerebellar cognitive affective syndrome: clinical correlations of the dysmetria of thought hypothesis. Int. Rev. Psychiatry 13, 313– 322 10.1080/09540260127522 · DOI
  162. Schmahmann J. D. (2004). Disorders of the cerebellum: ataxia, dysmetria of thought and the cerebellar cognitive affective syndrome. J. Neuropsychiatry Clin. Neurosci. 16, 367– 378 10.1176/appi.neuropsych.16.3.367 15377747 · DOI
  163. Schmahmann J. D. Sherman J. C. (1998). The cerebellar cognitive affective syndrome. Brain 121, 561– 579 10.1093/brain/121.4.561 9577385 · DOI · Paper page
  164. Schneider R. J. Friedman D. P. Mishkin M. (1993). A modality-specific somatosensory area within the insula of the rhesus monkey. Brain Res. 621, 116– 120 10.1016/0006-8993(93)90305-7 8221062 · DOI
  165. Seemungal B. Yousif N. Bronstein A. M. Naushahi J. Nandi D. (2010). Human pedunculopontine nucleus displays vestibular reactivity. J. Neurol. Neurosurg. Psychiatry 81: e43 10.1136/jnnp.2010.226340.106 · DOI
  166. Semba K. Fibiger H. C. (1992). Afferent connections of the laterodorsal and the pedunculopontine tegmental nuclei in the rat: a retro-and antero-grade transport and immunohistochemical study. J. Comp. Neurol. 323, 387– 410 10.1002/cne.903230307 1281170 · DOI
  167. Sharp P. E. (1999). Complimentary roles for hippocampal versus subicular/entorhinal place cells in coding place, context and events. Hippocampus 9, 432– 443 10.1002/(sici)1098-1063(1999)9:4<432::aid-hipo9>3.3.co;2-g 10495024 · DOI
  168. Sharp P. E. Koester K. (2008). Lesions of the mammillary body region severely disrupt the cortical head direction, but not place cell signal. Hippocampus 18, 766– 784 10.1002/hipo.20436 18446828 · DOI
  169. Sharp P. E. Tinkelman A. Cho J. (2001). Angular velocity and head direction signals recorded from the dorsal tegmental nucleus of gudden in the rat: implications for path integration in the head direction cell circuit. Behav. Neurosci. 115, 571– 588 10.1037//0735-7044.115.3.571 11439447 · DOI
  170. Sherman S. M. (2007). The thalamus is more than just a relay. Curr. Opin. Neurobiol. 17, 417– 422 10.1016/j.conb.2007.07.003 17707635 PMC2753250 · DOI
  171. Sherman S. M. Guillery R. W. (2011). Distinct functions for direct and transthalamic corticocortical connections. J. Neurophysiol. 106, 1068– 1077 10.1152/jn.00429.2011 21676936 · DOI · Paper page
  172. Shibata H. Honda Y. (2012). Thalamocortical projections of the anterodorsal thalamic nucleus in the rabbit. J. Comp. Neurol. 520, 2647– 2656 10.1002/cne.23057 22314639 · DOI
  173. Shin J. (2010). Passive rotation-induced theta rhythm and orientation homeostasis response. Synapse 64, 409– 415 10.1002/syn.20742 20034015 · DOI
  174. Shinder M. E. Taube J. S. (2010). Differentiating ascending vestibular pathways to the cortex involved in spatial cognition. J. Vestib. Res. 20, 3– 23 10.3233/VES-2010-0344 20555163 · DOI
  175. Shinder M. E. Taube J. S. (2011). Active and passive movement are encoded equally by head direction cells in the anterodorsal thalamus. J. Neurophysiol. 106, 788– 800 10.1152/jn.01098.2010 21613594 PMC3154800 · DOI
  176. Shiromani P. J. Armstrong D. M. Berkowitz A. Jeste D. V. Gillin J. C. (1988). Distribution of choline acetyltransferase immunoreactive somata in the feline brainstem: implications for REM sleep generation. Sleep 11, 1– 16 2896380
  177. Shiroyama T. Kayahara T. Yasui Y. Nomura J. Nakano K. (1999). Projections of the vestibular nuclei to the thalamus in the rat: a Phaseolus vulgaris leucoagglutinin study. J. Comp. Neurol. 407, 318– 332 10.1002/(sici)1096-9861(19990510)407:3<318::aid-cne2>3.3.co;2-8 10320214 · DOI
  178. Smith P. F. (1997). Vestibular-hippocampal interactions. Hippocampus 7, 465– 471 10.1002/(sici)1098-1063(1997)7:5<465::aid-hipo3>3.0.co;2-g 9347344 · DOI
  179. Smith P. F. (2012). Dyscalculia and vestibular function. Med. Hypotheses 79, 493– 496 10.1016/j.mehy.2012.06.032 22819131 · DOI
  180. Smith P. F. Darlington C. L. Zheng Y. (2010). Move it or lose it—is stimulation of the vestibular system necessary for normal spatial memory? Hippocampus 20, 36– 43 10.1002/hipo.20588 19405142 · DOI
  181. Smith P. F. Horii A. Russell N. Bilkey D. K. Zheng Y. Liu P. (2005). The effects of vestibular lesions on hippocampal function in rats. Prog. Neurobiol. 75, 391– 405 10.1016/j.pneurobio.2005.04.004 15936135 · DOI
  182. Snyder L. H. Grieve K. L. Brotchie P. Andersen R. A. (1998). Separate body-and world-referenced representations of visual space in parietal cortex. Nature 394, 887– 891 10.1038/29777 9732870 · DOI
  183. Solstad T. Boccara C. N. Kropff E. Moser M.-B. Moser E. I. (2008). Representation of geometric borders in the entorhinal cortex. Science 322, 1865– 1868 10.1126/science.1166466 19095945 · DOI · Paper page
  184. Spiegel E. A. Szekely E. G. Gildenberg P. L. (1965). Vestibular responses in midbrain, thalamus, and basal ganglia. Arch. Neurol. 12, 258– 269 10.1001/archneur.1965.00460270034005 14247384 · DOI
  185. Stackman R. W. Clark A. S. Taube J. S. (2002). Hippocampal spatial representations require vestibular input. Hippocampus 12, 291– 303 10.1002/hipo.1112 12099481 PMC1823522 · DOI
  186. Stackman R. W. Taube J. S. (1997). Firing properties of head direction cells in the rat anterior thalamic nucleus: dependence on vestibular input. J. Neurosci. 17, 4349– 4358 9151751 PMC1489676
  187. Stackman R. W. Taube J. S. (1998). Firing properties of rat lateral mammillary single units: head direction, head pitch and angular head velocity. J. Neurosci. 18, 9020– 9037 9787007 PMC1550347
  188. Stephan T. Deutschländer A. Nolte A. Schneider E. Wiesmann M. Brandt T. (2005). Functional MRI of galvanic vestibular stimulation with alternating currents at different frequencies. Neuroimage 26, 721– 732 10.1016/j.neuroimage.2005.02.049 15955481 · DOI
  189. Suzuki M. Kitano H. Ito R. Kitanishi T. Yazawa Y. Ogawa T. (2001). Cortical and subcortical vestibular response to caloric stimulation detected by functional magnetic resonance imaging. Brain Res. Cogn. Brain Res. 12, 441– 449 10.1016/s0926-6410(01)00080-5 11689304 · DOI
  190. Tai S. K. Ma J. Ossenkopp K.-P. Leung L. S. (2012). Activation of immobility-related hippocampal theta by cholinergic septohippocampal neurons during vestibular stimulation. Hippocampus 22, 914– 925 10.1002/hipo.20955 21542057 · DOI
  191. Taube J. S. (2007). The head direction signal: origins and sensory-motor integration. Annu. Rev. Neurosci. 30, 181– 207 10.1146/annurev.neuro.29.051605.112854 17341158 · DOI
  192. Taube J. S. Muller R. U. Ranck J. B. (1990). Head-direction cells recorded from the postsubiculum in freely moving rats. I. Description and quantitative analysis. J. Neurosci. 10, 420– 435 2303851 PMC6570151
  193. Thunnissen I. E. Epema A. H. Gerrits N. M. (1989). Secondary vestibulocerebellar mossy fiber projection to the caudal vermis in the rabbit. J. Comp. Neurol. 290, 262– 277 10.1002/cne.902900207 2480371 · DOI
  194. van der Meer M. A. Johnson A. Schmitzer-Torbert N. C. Redish A. D. (2010). Triple dissociation of information processing in dorsal striatum, ventral striatum and hippocampus on a learned spatial decision task. Neuron 67, 25– 32 10.1016/j.neuron.2010.06.023 20624589 PMC4020415 · DOI
  195. Vann S. D. (2009). Gudden’s ventral tegmental nucleus is vital for memory: re-evaluating diencephalic inputs for amnesia. Brain 132, 2372– 2384 10.1093/brain/awp175 19602577 · DOI
  196. Vertes R. P. Kocsis B. (1997). Brainstem-diencephalo-septohippocampal systems controlling the theta rhythm of the hippocampus. Neuroscience 81, 893– 926 9330355
  197. Vitte E. Derosier C. Caritu Y. Berthoz A. Hasboun D. Soulie D. (1996). Activation of the hippocampal formation by vestibular stimulation: a functional magnetic resonance imaging study. Exp. Brain Res. 112, 523– 526 10.1007/bf00227958 9007554 · DOI
  198. Walberg F. Dietrichs E. (1988). The interconnection between the vestibular nuclei and the nodulus: a study of reciprocity. Brain Res. 449, 47– 53 10.1016/0006-8993(88)91022-0 2456133 · DOI
  199. Waydo S. Kraskov A. Quiroga R. Q. Fried I. Koch C. (2006). Sparse representation in the human medial temporal lobe. J. Neurosci. 26, 10232– 10234 10.1523/jneurosci.2101-06.2006 17021178 PMC6674629 · DOI
  200. Whishaw I. Q. Maaswinkel H. Gonzalez C. L. Kolb B. (2001). Deficits in allothetic and idiothetic spatial behavior in rats with posterior cingulate cortex lesions. Behav. Brain Res. 118, 67– 76 10.1016/s0166-4328(00)00312-0 11163635 · DOI

200 of 215 shown

Authors
Hitier, M., Besnard, S., & Smith, P. F.
Affiliations
  • Inserm (FR)
  • University of Otago (NZ)
Corresponding author
Hitier, Martin
ORCID
Venue
Frontiers in Integrative Neuroscience
Publisher
Frontiers Media SA
Published
2014-07-23
Volume
8
Pages
59-59
ISSN
1662-5145 (ISSN-L)
DOI
10.3389/fnint.2014.00059
PMC
PMC4107830
OpenAlex
W2075593715
Cited by
394
References
229
Citations by year
2026: 31 · 2025: 40 · 2024: 42 · 2023: 51 · 2022: 35 · 2021: 41 · 2020: 39 · 2019: 28 · 2018: 22 · 2017: 29 · 2016: 18 · 2015: 16 · 2014: 2
FWCI
1.75
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Frontiers in Integrative Neuroscience (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Topics
  • Life Sciences › Neuroscience › Neurology › Vestibular and auditory disorders
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
  • Physical Sciences › Engineering › Automotive Engineering › Spatial Cognition and Navigation
Keywords
vestibular system, vestibular pathways, vestibular cortex, spatial navigation, spatial memory, entorhinal cortex, hippocampus, medial septum, supramammillary nucleus, cerebellum, basal ganglia, vestibular disorders, self-motion perception

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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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