Abstract
1. The production of a goal-directed saccadic gaze shift involves the specification of movement amplitude and direction, and the decision to trigger the movement. Behavioural and neurophysiological data suggest that these two functions involve separate processes which may interact. 2. The medio-posterior cerebellar areas are classically assigned a major contribution to the control of saccade metrics, and previous cerebellar lesion studies have revealed marked dysmetria of visually triggered gaze shifts. In contrast, these studies did not provide evidence for a cerebellar role in saccadic initiation. 3. In the present study, we investigated in the head-unrestrained cat the deficits in both the initiation and the metrics control of saccadic gaze shifts following pharmacological inactivation of the caudal part of the fastigial nucleus (cFN). 4. After cFN inactivation, latencies for contraversive gaze shifts increased to about 137 +/- 28% of normal, and latencies for ipsiversive gaze shifts decreased to about 84 +/- 8% of normal. Similar changes in head movement latency were observed, such that the temporal coupling between eye and head components remained largely unaffected. 5. Contraversive gaze shifts were more hypometric as their latency increased. In contrast, the degree of hypermetria in ipsiversive gaze shifts was unrelated to latency. 6. These results suggest a functional role of the medio-posterior cerebellum in gaze shift initiation and in storing information about the target location and/or the desired gaze shift amplitude.
Full text
PDF














Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Becker W., Jürgens R. An analysis of the saccadic system by means of double step stimuli. Vision Res. 1979;19(9):967–983. doi: 10.1016/0042-6989(79)90222-0. [DOI] [PubMed] [Google Scholar]
- Carpenter R. H., Williams M. L. Neural computation of log likelihood in control of saccadic eye movements. Nature. 1995 Sep 7;377(6544):59–62. doi: 10.1038/377059a0. [DOI] [PubMed] [Google Scholar]
- Cohen B., Goto K., Shanzer S., Weiss A. H. Eye movements induced by electric stimulation of the cerebellum in the alert cat. Exp Neurol. 1965 Oct;13(2):145–162. doi: 10.1016/0014-4886(65)90105-6. [DOI] [PubMed] [Google Scholar]
- Fuchs A. F., Kaneko C. R., Scudder C. A. Brainstem control of saccadic eye movements. Annu Rev Neurosci. 1985;8:307–337. doi: 10.1146/annurev.ne.08.030185.001515. [DOI] [PubMed] [Google Scholar]
- Fuchs A. F., Robinson F. R., Straube A. Role of the caudal fastigial nucleus in saccade generation. I. Neuronal discharge pattern. J Neurophysiol. 1993 Nov;70(5):1723–1740. doi: 10.1152/jn.1993.70.5.1723. [DOI] [PubMed] [Google Scholar]
- Fujikado T., Noda H. Saccadic eye movements evoked by microstimulation of lobule VII of the cerebellar vermis of macaque monkeys. J Physiol. 1987 Dec;394:573–594. doi: 10.1113/jphysiol.1987.sp016885. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Goffart L., Pelisson D. Cerebellar contribution to the spatial encoding of orienting gaze shifts in the head-free cat. J Neurophysiol. 1994 Nov;72(5):2547–2550. doi: 10.1152/jn.1994.72.5.2547. [DOI] [PubMed] [Google Scholar]
- Gruart A., Delgado-García J. M. Signalling properties of identified deep cerebellar nuclear neurons related to eye and head movements in the alert cat. J Physiol. 1994 Jul 1;478(Pt 1):37–54. doi: 10.1113/jphysiol.1994.sp020228. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guitton D. Control of eye-head coordination during orienting gaze shifts. Trends Neurosci. 1992 May;15(5):174–179. doi: 10.1016/0166-2236(92)90169-9. [DOI] [PubMed] [Google Scholar]
- Kalesnykas R. P., Hallett P. E. Fixation conditions, the foveola and saccadic latency. Vision Res. 1996 Oct;36(19):3195–3203. doi: 10.1016/0042-6989(96)00029-6. [DOI] [PubMed] [Google Scholar]
- Langer T. P., Kaneko C. R. Brainstem afferents to the omnipause region in the cat: a horseradish peroxidase study. J Comp Neurol. 1984 Dec 10;230(3):444–458. doi: 10.1002/cne.902300312. [DOI] [PubMed] [Google Scholar]
- Lewis R. F., Zee D. S. Ocular motor disorders associated with cerebellar lesions: pathophysiology and topical localization. Rev Neurol (Paris) 1993;149(11):665–677. [PubMed] [Google Scholar]
- Martin J. H. Autoradiographic estimation of the extent of reversible inactivation produced by microinjection of lidocaine and muscimol in the rat. Neurosci Lett. 1991 Jun 24;127(2):160–164. doi: 10.1016/0304-3940(91)90784-q. [DOI] [PubMed] [Google Scholar]
- May P. J., Hartwich-Young R., Nelson J., Sparks D. L., Porter J. D. Cerebellotectal pathways in the macaque: implications for collicular generation of saccades. Neuroscience. 1990;36(2):305–324. doi: 10.1016/0306-4522(90)90428-7. [DOI] [PubMed] [Google Scholar]
- Munoz D. P., Guitton D., Pélisson D. Control of orienting gaze shifts by the tectoreticulospinal system in the head-free cat. III. Spatiotemporal characteristics of phasic motor discharges. J Neurophysiol. 1991 Nov;66(5):1642–1666. doi: 10.1152/jn.1991.66.5.1642. [DOI] [PubMed] [Google Scholar]
- Munoz D. P., Wurtz R. H. Fixation cells in monkey superior colliculus. I. Characteristics of cell discharge. J Neurophysiol. 1993 Aug;70(2):559–575. doi: 10.1152/jn.1993.70.2.559. [DOI] [PubMed] [Google Scholar]
- Munoz D. P., Wurtz R. H. Fixation cells in monkey superior colliculus. II. Reversible activation and deactivation. J Neurophysiol. 1993 Aug;70(2):576–589. doi: 10.1152/jn.1993.70.2.576. [DOI] [PubMed] [Google Scholar]
- Noda H., Murakami S., Yamada J., Tamada J., Tamaki Y., Aso T. Saccadic eye movements evoked by microstimulation of the fastigial nucleus of macaque monkeys. J Neurophysiol. 1988 Sep;60(3):1036–1052. doi: 10.1152/jn.1988.60.3.1036. [DOI] [PubMed] [Google Scholar]
- Ohtsuka K., Noda H. Discharge properties of Purkinje cells in the oculomotor vermis during visually guided saccades in the macaque monkey. J Neurophysiol. 1995 Nov;74(5):1828–1840. doi: 10.1152/jn.1995.74.5.1828. [DOI] [PubMed] [Google Scholar]
- Ohtsuka K., Noda H. Saccadic burst neurons in the oculomotor region of the fastigial nucleus of macaque monkeys. J Neurophysiol. 1991 Jun;65(6):1422–1434. doi: 10.1152/jn.1991.65.6.1422. [DOI] [PubMed] [Google Scholar]
- Ohtsuka K., Noda H. The effect of microstimulation of the oculomotor vermis on discharges of fastigial neurons and visually-directed saccades in macaques. Neurosci Res. 1991 May;10(4):290–295. doi: 10.1016/0168-0102(91)90086-e. [DOI] [PubMed] [Google Scholar]
- Ohtsuka K., Sato H., Noda H. Saccadic burst neurons in the fastigial nucleus are not involved in compensating for orbital nonlinearities. J Neurophysiol. 1994 May;71(5):1976–1980. doi: 10.1152/jn.1994.71.5.1976. [DOI] [PubMed] [Google Scholar]
- Ottes F. P., Van Gisbergen J. A., Eggermont J. J. Latency dependence of colour-based target vs nontarget discrimination by the saccadic system. Vision Res. 1985;25(6):849–862. doi: 10.1016/0042-6989(85)90193-2. [DOI] [PubMed] [Google Scholar]
- Pernier J., Jeannerod M., Gerin P. Elaboration et décision des saccades: adaptation à la trace du stimulus. Vision Res. 1969 Sep;9(9):1149–1165. doi: 10.1016/0042-6989(69)90053-4. [DOI] [PubMed] [Google Scholar]
- ROBINSON D. A. A METHOD OF MEASURING EYE MOVEMENT USING A SCLERAL SEARCH COIL IN A MAGNETIC FIELD. IEEE Trans Biomed Eng. 1963 Oct;10:137–145. doi: 10.1109/tbmel.1963.4322822. [DOI] [PubMed] [Google Scholar]
- Robinson F. R., Straube A., Fuchs A. F. Role of the caudal fastigial nucleus in saccade generation. II. Effects of muscimol inactivation. J Neurophysiol. 1993 Nov;70(5):1741–1758. doi: 10.1152/jn.1993.70.5.1741. [DOI] [PubMed] [Google Scholar]
- Roldán M., Reinoso-Suárez F. Cerebellar projections to the superior colliculus in the cat. J Neurosci. 1981 Aug;1(8):827–834. doi: 10.1523/JNEUROSCI.01-08-00827.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shimizu N., Naito M., Yoshida M. Eye-head co-ordination in patients with Parkinsonism and cerebellar ataxia. J Neurol Neurosurg Psychiatry. 1981 Jun;44(6):509–515. doi: 10.1136/jnnp.44.6.509. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Steriade M. Two channels in the cerebellothalamocortical system. J Comp Neurol. 1995 Mar 27;354(1):57–70. doi: 10.1002/cne.903540106. [DOI] [PubMed] [Google Scholar]
- Sugimoto T., Mizuno N., Uchida K. Distribution of cerebellar fiber terminals in the midbrain visuomotor areas: an autoradiographic study in the cat. Brain Res. 1982 Apr 29;238(2):353–370. doi: 10.1016/0006-8993(82)90110-x. [DOI] [PubMed] [Google Scholar]
- Urquizar C., Pélisson D. A non-contact system for 2-dimensional trajectory recording. J Neurosci Methods. 1992 Jun;43(1):77–82. doi: 10.1016/0165-0270(92)90069-p. [DOI] [PubMed] [Google Scholar]
- Vilis T., Hore J. Characteristics of saccadic dysmetria in monkeys during reversible lesions of medial cerebellar nuclei. J Neurophysiol. 1981 Oct;46(4):828–838. doi: 10.1152/jn.1981.46.4.828. [DOI] [PubMed] [Google Scholar]
- Wyman D., Steinman R. M. Letter: Latency characteristics of small saccades. Vision Res. 1973 Nov;13(11):2173–2175. doi: 10.1016/0042-6989(73)90195-8. [DOI] [PubMed] [Google Scholar]
- Zambarbieri D., Beltrami G., Versino M. Saccade latency toward auditory targets depends on the relative position of the sound source with respect to the eyes. Vision Res. 1995 Dec;35(23-24):3305–3312. doi: 10.1016/0042-6989(95)00065-m. [DOI] [PubMed] [Google Scholar]

