Abstract
Unblurred vision is mandatory for the orderly processing of visual information during eye and head movements; image slip on the retina of only a few degrees per second diminishes visual acuity (Westheimer and McKee, 1975). Several mechanisms have developed to generate slow eye movements which are aimed at preventing blurring of images on the retina during movements. Head movements induce in all mammals slow eye movements, i.e. compensatory eye movements, into the direction opposite to the head movement via the vestibulo-ocular reflex arc (VOR). Movements of large parts of the visual surround or of single objects induce slow eye movements into the direction of the moving pattern. Continuous rotation of the visual surround induces in foveate and afoveate animals a typical repetitive sequence of eye movements, optokinetic nystagmus (OKN). In foveate animals movement of a single target object can elicit smooth pursuit eye movements.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Alley K (1977) Anatomical basis for the interaction between cerebellar flocculus and brainstem. In: Baker R, Berthoz A (eds) Control of gaze by brainstem neurons. Dev Neurosci 1: 109–117
Allum JHJ, Graf W, Dichgans J, Schmidt CL (1976) Visual-vestibular interaction in the vestibular nuclei of the goldfish. Exp Brain Res 26: 463–485
Angaut P, Brodai A (1967) The projection of the “vestibulo-cerebellum” onto the vestibular nuclei in the cat. Arch Ital Biol 105: 441–479
Barmack NH (1979) Immediate and sustained influences of visual olivocerebellar activity on eye movement. In: Talbott RE, Humphrey DR (eds) Posture and movement. Raven Press, New York, pp 123–168
Collewijn H (1981) The optokinetic system: In: Zuber BL (ed) Models of oculomotor behavior and control. CRC Press, West Plam Beach, Fla, pp 111–137
Batini C, Ito M, Kado RT, Jastreboff PJ, Misashita Y (1979) Interaction between the horizontal vestibulo-ocular reflex and optokinetic response in rabbits. Exp Brain Res 37: 1–15
Blanks RHI, Precht W (1978) Response properties of vestibular afferents in alert cats during opto-kinetic and vestibular stimulation. Neurosci Lett 10: 225–229
Blanks RHI, Precht W (1983) Responses of units in the rat cerebellar flocculus during optokinetic and vestibular stimulation. Exp Brain Res 53: 1–15
Brodai A, Hoivik B (1964) Site and mode of termination of primary vestibulocerebellar fibers in the cat. Arch Ital Biol 101: 1–21
Buettner UW, Büttner U (1979) Vestibular nuclei activity in the alert monkey during suppression of vestibular and optokinetic nystagmus. Exp Brain Res 37: 581–593
Büttner U, Waespe W (1981) Vestibular nerve activity in the alert monkey during vestibular and optokinetic nystagmus. Exp Brain Res 41: 310–315
Büttner U, Waespe W (1984) Purkinje cell activity in the primate flocculus during optokinetic stim-ulation, smooth pursuit eye movements and VOR-suppression. Exp Brain Res 55: 97–104
Büttner U, Boyle R, Schreiter U (1983) Vestibular nuclei activity in the alert monkey during con-stant velocity and sinusoidal optokinetic stimulation. Soc Neurosci Abstr 9: 315
Carpenter MB, Stein BM, Peter P (1972) Primary vestibulo-cerebellar fibers in the monkey: distribution of fibers arising from distinctive cell groups of the vestibular ganglia. Am J Anat 135: 221–250
Cazin L, Precht W, Lannou J (1980) Pathways mediating optokinetic responses of vestibular nucleus neurons in the rat. Pflüger’s Arch 384: 19–29
Cohen B, Uemura T, Takemori S (1973) Effects of labyrinthectomy on optokinetic nystagmus (OKN) and optokinetic after-nystagmus ( OKAN ). Equil Res 3: 88–93
Cohen B, Matsuo V, Raphan T (1977) Quantitative analysis of the velocity characteristics of optokinetic nystagmus and optokinetic after-nystagmus. J Physiol 270: 321–344
Cohen B, Suzuki J, Raphan T, Matsuo V, deJong V (1982) Selective labyrinthine lesions and nystagmus induced by rotation about off-vertical axis. In: Lennerstrand G, Keller E, Zee DS (eds) Functional basis of ocular motility disorders. Pergamon Press, Oxford New York, pp 337–346
Collewijn H (1976) Impairment of optokinetic (after)nystagmus by labyrinthectomy in the rabbit. Exp Neurol 52: 146–156
Collewijn H (1981) The optokinetic system: In: Zuber BL (ed) Models of oculomotor behavior and control. CRC Press, West Plam Beach, Fla, pp 111–137
Dow RS (1938) Efferent connections of the flocculo-nodular lobe in macacca mulatta. J Comp Neurol 68: 297–305
Dubois MFW, Collewijn H (1979) The optokinetic reactions of the rabbit: relation to the visual streak. Vision Res 19: 9–17
Duensing F, Schaefer KP (1958) Die Aktivität einzelner Neurone im Bereich der Vestibulariskerne bei Horizontalbeschleunigung unter besonderer Berücksichtigung des vestibulären Nystagmus. Arch Psychiat Nervenkr 198: 225–252
Fuchs AF (1967) Saccadic and smooth pursuit eye movements in the monkey. J Physiol 191: 609–631
Fukuda J, Highstein SM, Ito M (1972) Cerebellar inhibitory control of the vestibulo-ocular reflex investigated in rabbit 3rd nucleus. Exp Brain Res 14: 511–526
Ghelarducci B, Ito M, Yagi N (1975) Impulse discharges from flocculus Purkinje cells of alert rabbits during visual stimulation combined with horizontal head rotation. Brain Res 87: 66–72
Goldberg JM, Fernandez C (1981) Physiological mechanisms of the nystagmus produced by rota-tions about an earth-horizontal axis. Ann NY Acad Sci 374: 40–43
Gonshor A, Melvill Jones G (1976) Extreme vestibulo-ocular adaptation induced by prolonged optical reversal of vision. J Physiol 256: 381–414
Gutman J, Zelig S, Bergmann F (1964) Optokinetic nystagmus in the labyrinthectomized rabbit. Confin Neurol 24: 158–162
Haines DE (1977) Cerebellar corticonuclear and corticovestibular fibers of the flocculonodular lobe in a prosimian primate (Galago senegalensis). J Comp Neurol 174: 607–630
Henn V, Young L, Finley C (1974) Vestibular nucleus units in alert monkeys are also influenced by moving visual fields. Brain Res 71: 144–149
Henn V, Cohen B, Young LR (1980) Visual-vestibular interaction in motion perception and the generation of nystagmus. Neurosci Res Progr Bull 18: 459–651
Holmes G (1917) The symptoms of acute cerebellar injuries due to gunshot injuries. Brain 40: 461–535
Ito M (1972) Neural design of the cerebellar motor control system. Brain Res 40: 81–84
Ito M (1976) Cerebellar learning control of vestibulo-ocular mechanisms. In: Desirayu T (ed) Mech-anisms in transmission of signals for conscious behavior. Elsevier, Amsterdam New York, pp 1–22
Ito M (1982) Cerebellar control of the vestibuloocular reflex, around the flocculus hypothesis. Annu Rev Neurosci 5: 275–296
Ito M, Jastreboff PJ, Miyashita Y (1982) Specific effects of unilateral lesions in the flocculus upon eye movements in albino rabbits. Exp Brain Res 45: 233–242
Keller EL (1976) Behavior of horizontal semicircular canal afferents in alert monkey during vestibular and optokinetic stimulation. Exp Brain Res 24: 459–471
Keller EL, Daniels PD (1975) Oculomotor related interaction of vestibular and visual stimulation in vestibular nuclei cells in alert monkeys. Exp Neurol 46: 187–198
Keller EL, Kamath BY (1975) Characteristics of head rotation and eye movement-related neurons in alert monkey vestibular nucleus. Brain Res 100: 182–187
Keller EL, Precht W (1979) Visual-vestibular responses in vestibular nuclear neurons in intact and cerebellectomized, alert cat. Neuroscience 4: 1599–1613
King WM, Lisberger SG, Fuchs AF (1976) Responses of fibers in medial longitudinal fasciculus ( MLF) of alert monkeys during horizontal and vertical conjugate eye movements evoked by vestibular or visual stimuli. J Neurophysiol 39: 1135–1149
Koerner F, Schiller PH (1972) The optokinetic response under open and closed loop conditions in the monkey. Exp Brain Res 14: 318–330
Kommerell G, Klein U (1971) Über die visuelle Regelung der Okulomotorik: die optomotorische Wirkung exzentrischer Nachbilder. Vision Res 11: 905–920
Korte GE, Mugnaini E (1979) The cerebellar projection of the vestibular nerve in the cat. J Comp Neurol 184: 265–278
Holmes G (1917) The symptoms of acute cerebellar injuries due to gunshot injuries. Brain 40: 461–535
Lisberger SG, Fuchs AF (1978a) Role of primate flocculus during rapid behavioral modification of vestibulo-ocular reflex. I. Purkinje cell activity during visually guided horizontal smooth-pursuit eye movements and passive head rotation. J Neurophysiol 41: 733–763
Lisberger SG, Fuchs AF (1978b) Role of primate flocculus duringrapid behavioral modification of vestibulo-ocular reflex. II. Mossy fiber firing patterns during horizontal head rotation and eye movement. J Neurophysiol 41: 764–777
Lisberger SG, Miles FA, Optican LM, Eighmy B (1981) Optokinetic response in monkey: underlying mechanisms and their sensitivity to long-term adaptive changes in vestibuloocular reflex. J Neurophysiol 45: 869–890
Lorente de Nc R (1933) Vestibulo-ocular reflex arc. Arch Neurol Psychiat 30: 245–291
Maekawa K, Takeda T (1976) Electrophysiological identification of the climbing and mossy fiber pathways from the rabbit’s retina to the contralateral cerebellar flocculus. Brain Res 109: 169–174
Miles FA, Lisberger SG (1981) Plasticity in the vestibulo-ocular reflex: a new hypothesis. Annu Rev Neurosci 4: 273–299
Miles FA, Fuller JH, Braitman DJ, Dow BM (1980) Long term adaptive changes in primate vestibulo-ocular reflexes. III. Electrophysiological observations in flocculus of adapted monkeys. J Neurophysiol 43: 1437–1476
Mitsacos A, Reisine H, Highstein SM (1983) The superior vestibular nucleus: An intracellular HRP study in the cat. II. Non-vestibular-oculor neurons. J comp Neurol: 215, 92–107
King WM, Lisberger SG, Fuchs AF (1976) Responses of fibers in medial longitudinal fasciculus ( MLF) of alert monkeys during horizontal and vertical conjugate eye movements evoked by vestibular or visual stimuli. J Neurophysiol 39: 1135–1149
Miyashita Y, Nagao S (1981) Signal contents of Purkinje cell responses in rabbit flocculus to optokinetic stimuli. J Jpn Physiol Soc 43: 317
Mowrer OH (1937) The influence of vision during bodily rotation upon the duration of post-rotational vestibular nystagmus. Acta Otolaryngol 25: 351–364
Nagao S (1983) Effects of vestibulocerebellar lesions upon dynamic characteristics and adaptation of vestibulo-ocular and optokinetic responses in pigmented rabbits. Exp Brain Res 53: 36–46
Neverov VP, Gterc J, Bures J (1980) Electrophysiological correlates of the reversed postoptokinetic nystagmus in the rabbit: Activity of vestibular and floccular neurons. Brain Res 189: 355–367
Waespe W, Henn V (1977a) Neuronal activity in the vestibular nuclei of the alert monkey during vestibular and optokinetic stimulation. Exp Brain Res 27: 523–538
Noda H, Suzuki DA (1978) The role of the flocculus of the monkey in saccadic eye movements. J Physiol 294: 317–334
Noda H, Warabi T (1982) Eye position signals in the flocculus of the monkey during smooth-pursuit eye movements. J Physiol 324: 187–202
Noda H, Asoh R, Shibagaki M (1977) Floccular unit activity associated with eye movements and fixation. In: Baker R, Berthoz A (eds) Control of gaze by brain stem neurons. Elsevier, Amsterdam, pp 371–380
Raphan T, Cohen B (1981) The role of integration in oculomotor control. In: Zuber B (ed) Models of oculomotor behavior and control, CRC Press, West Palm Beach, Fla, pp 91–109
Raphan T, Matsuo V, Cohen B (1979) Velocity storage in the vestibulo-ocular reflex arc ( VOR ). Exp Brain Res 35: 229–248
Rashbass C (1961) The relationship between saccadic and smooth tracking eye movements. J Physiol 159: 326
Robinson DA (1965) The mechanics of human smooth pursuit eye movement. J Physiol 180: 569–591
Robinson DA (1976) Adaptive gain control of vestibuloocular reflex by the cerebellum. J Neurophysiol 39: 954–969
Robinson DA (1981) Control of eye movements. In: Brooks VB (ed) Handbook of physiology, sect 1: the nervous system, vol II. Am Physiol Soc (Bethesda), pp 1275–1320
Sato Y, Kawasaki T, Ikarashi K (1983) Zonal organization of the floccular Purkinje cells projecting to the vestibular nucleus in cats. Brain Res 232: 1–15
Takemori S, Cohen B (1974) Loss of suppression of vestibular nystagmus after flocculus lesion. Brain Res 72: 213–224
Waespe W, Cohen B (1983) Effects of flocculectomy on unit activity in the vestibular nuclei during visual-vestibular interactions. Exp Brain Res 51: 23–35
Waespe W, Henn V (1977a) Neuronal activity in the vestibular nuclei of the alert monkey during vestibular and optokinetic stimulation. Exp Brain Res 27: 523–538
Waespe W, Henn V (1977b) Vestibular nuclei activity during optokinetic after-nystagmus ( OKAN) in the alert monkey. Exp Brain Res 30: 323–330
Waespe W, Henn V (1978) Conflicting visual-vestibular stimulation and vestibular nucleus activity in alert monkeys. Exp Brain Res 33: 203–211
Waespe W, Henn V (1979a) The velocity response of vestibular nucleus neurons during vestibular, visual, and combined angular acceleration. Exp Brain Res 37: 337–347
Noda H, Warabi T (1982) Eye position signals in the flocculus of the monkey during smooth-pursuit eye movements. J Physiol 324: 187–202
Waespe W, Henn V (1981) Visual-vestibular interaction in the flocculus of the alert monkey. II. Purkinje cell activity. Exp Brain Res 43: 439–360
Waespe W, Henn V, Isovilta V (1980) Nystagmus slow-phase velocity during vestibular, optokinetic, and combined stimulation in the monkey. Arch Psychiat Nervenkr 228: 275–286
Waespe W, Buettner U, Henn V (1981) Visual-vestibular interaction in the flocculus of the alert monkey. I. Input activity. Exp Brain Res 43: 337–348
Waespe W, Cohen B, Raphan T (1983) Role of the flocculus and paraflocculus in optokinetic nystagmus and visual-vestibular interactions: effects of lesions. Exp Brain Res 50: 9–33
Waespe W, Rudinger D, Wolfensberger M (1985) Floccular Purkinje cell activity after bilateral neurectomy during optokinetic nystagmus (OKN) and smooth pursuit eye movements in primates (in preparation)
Westheimer G, McKee SP (1975) Visual acuity in the presence of retinal image motion. J Opt Soc Am 65: 847–850
Yingcharoen K, Rinvik E (1983) Ultrastructural degeneration of a projection from the flocculus to the nucleus prepositus hypoglossi in the cat. Exp Brain Res 51: 192–198
Zee DS, Yee RD, Robinson DA (1976) Optokinetic responses in labyrinthine-defective human beings. Brain Res 113: 423–428
Zee DS, Yamazaki A, Butler PH, Gucer G (1981) Effects of ablation of flocculus and paraflocculus on eye movements in primate. J Neurophysiol 46: 878–899
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1984 Springer-Verlag Berlin Heidelberg
About this paper
Cite this paper
Waespe, W., Henn, V. (1984). The Primate Flocculus in Visual-vestibular Interactions: Conceptual, Neurophysiological, and Anatomical Problems. In: Bloedel, J.R., Dichgans, J., Precht, W. (eds) Cerebellar Functions. Proceedings in Life Sciences. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-69980-1_8
Download citation
DOI: https://doi.org/10.1007/978-3-642-69980-1_8
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-69982-5
Online ISBN: 978-3-642-69980-1
eBook Packages: Springer Book Archive