Literature DB >> 7983548

Neural basis for motor learning in the vestibuloocular reflex of primates. II. Changes in the responses of horizontal gaze velocity Purkinje cells in the cerebellar flocculus and ventral paraflocculus.

S G Lisberger1, T A Pavelko, H M Bronte-Stewart, L S Stone.   

Abstract

1. We made extracellular recordings from Purkinje cells in the flocculus and ventral paraflocculus of awake monkeys before and after motor learning in the vestibuloocular reflex (VOR). Three samples were recorded 1) after miniaturizing spectacles had reduced the gain of the VOR (eye speed divided by head speed) to 0.4; 2) when the gain of the VOR was near 1.0; and 3) after magnifying spectacles had increased the gain of the VOR to 1.6. 2. We studied Purkinje cells that showed stronger modulation of simple-spike firing rate during horizontal than during vertical pursuit. These cells corresponded to the previously identified "horizontal gaze velocity Purkinje cells" or HGVP-cells. During pursuit of smooth target motion with the head stationary, HGVP-cells showed strong modulation of firing rate with increases for ipsiversive eye motion (toward the side of recording). When the monkey canceled his VOR by tracking a target that moved exactly with him during sinusoidal head rotation in the horizontal plane, HGVP-cells again showed strong modulation of firing rate with increases for ipsiversive head motion. 3. The responses of HGVP-cells during pursuit with the head stationary and during cancellation of the VOR reveal separate components of firing rate related to eye and head velocity. We used these two behavioral conditions to test for effects of motor learning on the head and eye velocity components of the simple-spike firing of HGVP-cells. Our data confirm the previous observation that motor learning causes the sensitivity to head velocity to be larger when the gain of the VOR is high and smaller when the gain of the VOR is low. Thus we agree with the previous conclusion that changes in the vestibular sensitivity of HGVP-cells, measured during sinusoidal head motion at low frequencies, are in the wrong direction to cause changes in the gain of the VOR. 4. To determine whether the simple-spike output from the HGVP-cells plays a role in the VOR after motor learning, we recorded simple-spike firing during the VOR evoked by transient, rapid changes in head velocity in darkness. When the gain of the VOR was low, firing rate increased during the VOR evoked by ipsiversive head motion and decreased during the VOR evoked by contraversive head motion. When the gain of the VOR was high, the direction selectivity of the responses was reversed.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Keywords:  Non-programmatic

Mesh:

Year:  1994        PMID: 7983548     DOI: 10.1152/jn.1994.72.2.954

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  53 in total

1.  The cerebellum's role in reading: a functional MR imaging study.

Authors:  R K Fulbright; A R Jenner; W E Mencl; K R Pugh; B A Shaywitz; S E Shaywitz; S J Frost; P Skudlarski; R T Constable; C M Lacadie; K E Marchione; J C Gore
Journal:  AJNR Am J Neuroradiol       Date:  1999 Nov-Dec       Impact factor: 3.825

2.  The response of vestibulo-ocular reflex pathways to electrical stimulation after canal plugging.

Authors:  Dianne M Broussard; Juimiin A Hong
Journal:  Exp Brain Res       Date:  2003-01-17       Impact factor: 1.972

3.  Modeling spatial tuning of adaptation of the angular vestibulo-ocular reflex.

Authors:  Yongqing Xiang; Sergei B Yakushin; Theodore Raphan
Journal:  Exp Brain Res       Date:  2012-06-04       Impact factor: 1.972

4.  Cerebellar signatures of vestibulo-ocular reflex motor learning.

Authors:  Pablo M Blazquez; Yutaka Hirata; Shane A Heiney; Andrea M Green; Stephen M Highstein
Journal:  J Neurosci       Date:  2003-10-29       Impact factor: 6.167

5.  Roles of the cerebellum in pursuit-vestibular interactions.

Authors:  Kikuro Fukushima
Journal:  Cerebellum       Date:  2003       Impact factor: 3.847

6.  Synaptic shunting by a baseline of synaptic conductances modulates responses to inhibitory input volleys in cerebellar Purkinje cells.

Authors:  Lisa Kreiner; Dieter Jaeger
Journal:  Cerebellum       Date:  2004       Impact factor: 3.847

7.  Reversal of motor learning in the vestibulo-ocular reflex in the absence of visual input.

Authors:  Marlene R Cohen; Geoffrey W Meissner; Robert J Schafer; Jennifer L Raymond
Journal:  Learn Mem       Date:  2004 Sep-Oct       Impact factor: 2.460

8.  Further evidence for selective difficulty of upward eye pursuit in juvenile monkeys: Effects of optokinetic stimulation, static roll tilt, and active head movements.

Authors:  Satoshi Kasahara; Teppei Akao; Junko Fukushima; Sergei Kurkin; Kikuro Fukushima
Journal:  Exp Brain Res       Date:  2005-11-30       Impact factor: 1.972

Review 9.  Neuroscience and learning: lessons from studying the involvement of a region of cerebellar cortex in eyeblink classical conditioning.

Authors:  Ronald P Villarreal; Joseph E Steinmetz
Journal:  J Exp Anal Behav       Date:  2005-11       Impact factor: 2.468

10.  Cerebellar Purkinje cells control eye movements with a rapid rate code that is invariant to spike irregularity.

Authors:  Hannah L Payne; Ranran L French; Christine C Guo; Td Barbara Nguyen-Vu; Tiina Manninen; Jennifer L Raymond
Journal:  Elife       Date:  2019-05-03       Impact factor: 8.140

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