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J Neurophysiol 99: 220-230, 2008. First published October 31, 2007; doi:10.1152/jn.00554.2007
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Premotor Inhibitory Neurons Carry Signals Related to Saccade Adaptation in the Monkey

Yoshiko Kojima1, Yoshiki Iwamoto1, Farrel R. Robinson2, Christopher T. Noto2 and Kaoru Yoshida1

1Department of Neurophysiology, Doctoral Program in Kansei Behavioral and Brain Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan; and 2Department of Biological Structure and National Primate Research Center, University of Washington, Seattle, Washington

Submitted 18 May 2007; accepted in final form 29 October 2007

Cerebellar output changes during motor learning. How these changes cause alterations of motoneuron activity and movement remains an unresolved question for voluntary movements. To answer this question, we examined premotor neurons for saccadic eye movement. Previous studies indicate that cells in the fastigial oculomotor region (FOR) within the cerebellar nuclei on one side exhibit a gradual increase in their saccade-related discharge as the amplitude of ipsiversive saccades adaptively decreases. This change in FOR activity could cause the adaptive change in saccade amplitude because neurons in the FOR project directly to the brain stem region containing premotor burst neurons (BNs). To test this possibility, we recorded the activity of saccade-related burst neurons in the area that houses premotor inhibitory burst neurons (IBNs) and examined their discharge during amplitude-reducing adaptation elicited by intrasaccadic target steps. We specifically analyzed their activity for off-direction (contraversive) saccades, in which the IBN activity would increase to reduce saccade size. Before adaptation, 29 of 42 BNs examined discharged, at least occasionally, for contraversive saccades. As the amplitude of contraversive saccades decreased adaptively, half of BNs with off-direction spike activity showed an increase in the number of spikes (14/29) or an earlier occurrence of spikes (7/14). BNs that were silent during off-direction saccades before adaptation remained silent after adaptation. These results indicate that the changes in the off-direction activity of BNs are closely related to adaptive changes in saccade size and are appropriate to cause these changes.


Address for reprint requests and other correspondence: Y. Iwamoto, Department of Neurophysiology, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8574, Japan (E-mail: iwamoto{at}md.tsukuba.ac.jp)




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