Behavior of the oculomotor vermis for five different types of saccade

Journal of Neurophysiology

Volumn 104, Issue 6, 2010, Pages 3667-3676

  Kojima, Yoshiko ^a   Soetedjo, Robijanto ^a   Fuchs, Albert F ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ARTICLE; CELL ACTIVITY; CEREBELLUM VERMIS; HAPLORHINI; MALE; NONHUMAN; OCULOMOTOR SYSTEM; PRIORITY JOURNAL; PURKINJE CELL; QUANTITATIVE ANALYSIS; SACCADIC EYE MOVEMENT;

ACTION POTENTIALS; ANIMALS; CEREBELLAR CORTEX; CLASSIFICATION; MACACA MULATTA; MALE; MEMORY; PHOTIC STIMULATION; PURKINJE CELLS; REACTION TIME; SACCADES;

EID: 78650919040     PISSN: 00223077     EISSN: 15221598     Source Type: Journal    
DOI: 10.1152/jn.00558.2010     Document Type: Article

References (43)

1. Alahyane N, Salemme R, Urquizar C, Cotti J, Guillaume A, Vercher JL, Pélisson D. Oculomotor plasticity: Are mechanisms of adaptation for reactive and voluntary saccades separate? Brain Res 1135: 107-121, 2007.
2. Barash S, Melikyan A, Sivakov A, Zhang M, Glickstein M, Thier P. Saccadic dysmetria and adaptation after lesions of the cerebellar cortex. J Neurosci 19: 10931-10939, 1999.
3. Catz N, Dicke PW, Thier P. Cerebellar-dependent motor learning is based on pruning a Purkinje cell population response. Proc Natl Acad Sci USA 105: 7309-7314, 2008.
4. Catz N, Dicke PW, Thier P. Cerebellar complex spike firing is suitable to induce as well as to stabilize motor learning. Curr Biol 15: 2179-2189, 2005.
5. Dias EC, Segraves MA. Muscimol-induced inactivation of monkey frontal eye field: Effects on visually and memory-guided saccades. J Neurophysiol 81: 2191-2214, 1999.
6. Deubel H. Separate adaptive mechanisms for the control of reactive and volitional saccadic eye movements. Vision Res 35: 3529-3540, 1995.
7. Deubel H. Separate mechanisms for the adaptive control of reactive, volitional, and memory-guided saccadic eye movements. In: Attention and Performance XVII Cognitive Regulation of Performance: Interaction of Theory and Application, edited by Gopher D, Koriat A. Cambridge, MA: MIT Press, 1999, p. 697-721.
8. Fisher B, Boch R. Saccadic eye movements after extremely short reaction times. Brain Res 260: 21-26, 1983.
9. Fischer B, Ramsperger E. Human express saccades: Extremely short reaction times of goal directed eye movements. Exp Brain Res 57: 191-195, 1984.
10. Fischer B, Weber H, Biscaldi M, Aiple F, Otto P, Stuhr V. Separate populations of visually guided saccades in humans: Reaction times and amplitudes. Exp Brain Res 92: 528-541, 1993.
11. Fischer B, Weber H. Express saccades and visual attention. Behav Brain Sci 16: 553-567, 1993.
12. Fuchs AF, Reiner D, Pong M. Transfer of gain changes from targeting to other types of saccade in the monkey: Constraints on possible sites of saccadic gain adaptation. J Neurophysiol 76: 2522-2535, 1996.
13. Fuchs A, Robinson F, Straube A. Role of the caudal fastigial nucleus in saccade generation. I. Neuronal discharge patterns. J Neurophysiol 70: 1723-1740, 1993.
14. Fuchs AF, Robinson DA. A method for measuring horizontal and vertical eye movement chronically in the monkey. J Appl Physiol 21: 1068-1070, 1966.
15. Gaymard B, Ploner CJ, Rivaud S, Vermersch AI, Pierrot-Deseilligny C. Cortical control of saccades. Exp Brain Res 123: 159-163, 1998.
16. Hopp JJ, Fuchs AF. The characteristics and neuronal substrate of saccadic eye movement plasticity. Prog Neurobiol 72: 27-53, 2004.
17. Hopp JJ, Fuchs AF. Identifying sites of saccade amplitude plasticity in humans: Transfer of adaptation between different types of saccade. Exp Brain Res 202: 129-45, 2010.
18. Huerta MF, Krubitzer LA, Kaas JH. Frontal eye field as defined by intracortical microstimulation in squirrel monkeys, owl monkeys, and macaque monkeys. I. Subcortical connections. J Comp Neurol 253: 415-39, 1986.
19. Iwamoto Y, Kaku Y. Saccade adaptation as a model of learning in voluntary movements. Exp Brain Res 204: 145-162, 2010.
20. Iwamoto Y, Yoshida K. Saccadic dysmetria following inactivation of the primate fastigial oculomotor region. Neurosci Lett 325: 211-215, 2002.
21. Judge SJ, Richmond BJ, Chu FC. Implantation of magnetic search coils for measurement of eye position: An improved method. Vision Res 20: 535-538, 1980.
22. Kojima Y, Soetedjo R, Fuchs AF. Changes in simple spike activity of some Purkinje cells in the oculomotor vermis during saccade adaptation are appropriate to participate in motor learning. J Neurosci 30: 3715-3727, 2010a.
23. Kojima Y, Soetedjo R, Fuchs AF. Monkey oculomotor vermis does not distinguish different types of saccade. Soc Neurosci Abstr 40: 778, 2010b.
24. Künzle H, Akert K. Efferent connections of cortical, area 8 (frontal eye field) in Macaca fascicularis. A reinvestigation using the autoradiographic technique. J Comp Neurol 173: 147-164, 1977.
25. Leichnetz GR, Smith DJ, Spencer RF. Cortical projections to the paramedian tegmental and basilar pons in the monkey. J Comp Neurol 228: 388-408, 1984a.
26. Leichnetz GR, Spencer RF, Smith DJ. Cortical projections to nuclei adjacent to the oculomotor complex in the medial dien-mesencephalic tegmentum in the monkey. J Comp Neurol 228: 359-387, 1984b.
27. Leichnetz GR. The prefrontal cortico-oculomotor trajectories in the monkey. J Neurol Sci 49: 387-396, 1981.
28. Munoz DP, Wurtz RH. Saccade-related activity in monkey superior colliculus. I. Characteristics of burst and buildup cells. J Neurophysiol 73: 2313-2333, 1995.
29. Ohtsuka K, Noda H. Burst discharges of fastigial neurons in macaque monkeys are driven by vision- and memory-guided saccades but not by spontaneous saccades. Neurosci Res 15: 224-228, 1992.
30. Ohtsuka K, Noda H. Discharge properties of Purkinje cells in the oculomotor vermis during visually guided saccades in the macaque monkey. J Neurophysiol 74: 1828-1840, 1995.
31. Ritchie L. Effects of cerebellar lesions on saccadic eye movements. J Neurophysiol 39: 1246-1256, 1976.
32. Robinson DA. A method of measuring eye movement using a scleral search coil in a magnetic field. IEEE Trans Biomed Electron 10: 137-145, 1963.
33. Robinson FR, Straube A, Fuchs AF. Role of the caudal fastigial nucleus in saccade generation. II. Effects of muscimol inactivation. J Neurophysiol 70: 1741-1758, 1993.
34. Robinson FR, Fuchs AF, Noto C. Cerebellar influences on saccadic plasticity. Ann NY Acad Sci 956: 155-164, 2002.
35. Scudder CA, Kaneko CRS, Fuchs AF. The brainstem burst generator for saccadic eye movements. A modern synthesis. Exp Brain Res 142: 439-462, 2002.
36. Soetedjo R, Fuchs AF. Complex spike activity of Purkinje cells in the oculomotor vermis during behavioral adaptation of monkey saccades. J Neurosci 26: 7741-7755, 2006.
37. Soetedjo R, Kaneko CR, Fuchs AF. Evidence against a moving hill in the superior colliculus during saccadic eye movements in the monkey. J Neurophysiol 87: 2778-2789, 2002.
38. Soetedjo R, Kojima Y, Fuchs AF. Complex spike activity in the oculomotor vermis of the cerebellum: A vectorial error signal for saccade motor learning? J Neurophysiol 100: 1949-1966, 2008.
39. Straube A, Deubel H, Spuler A, Buttner U. Differential effect of a bilateral deep cerebellar nuclei lesion on externally and internally triggered saccades in humans. Neuroophthalmology 15: 67-74, 1995.
40. Takagi M, Zee DS, Tamargo RJ. Effects of lesions of the oculomotor vermis on eye movements in primate: Saccades. J Neurophysiol 80: 1911-1931, 1998.
41. Thier P, Dicke PW, Haas R, Barash S. Encoding of movement time by populations of cerebellar Purkinje cells. Nature 405: 72-76, 2000.
42. Tilikete C, Pélisson D. Ocular motor syndromes of the brainstem and cerebellum. Curr Opin Neurol 21: 22-28, 2008.
43. Vilis T, Hore J. Characteristics of saccadic dysmetria in monkeys during reversible lesions of medial cerebellar nuclei. J Neurophysiol 46: 828-838, 1981.