Literature DB >> 8433134

Output organization of intermediate cerebellum of the monkey.

P L van Kan1, J C Houk, A R Gibson.   

Abstract

1. The goal of this study was to investigate the motor organization of monkey nucleus interpositus (NI) and neighboring regions of the lateral nucleus (NL) by correlating discharge of single neurons with active movements. Neurons were surveyed during free-form movements as well as during operation of six devices that required movement about specific forelimb joints. The paradigm allowed us to test the hypothesis that discharge of individual cells relates to movements about individual joints. 2. One hundred sixty-two isolated nuclear neurons from two monkeys were studied. Eighty-three percent showed large increases in discharge (an average of 3 times resting rate for forelimb neurons) during movement of one body part, either forelimb, hindlimb, mouth/face, or eyes. 3. Anterior interpositus contains neurons related to hindlimb movement in anterior regions and neurons related to forelimb movement in posterior regions. A mouth/face-related area exists in the dorsal-posterior regions and is continuous with a mouth/face area in the dorsal regions of NL. Posterior interpositus (NIP) showed no clear separation between forelimb and hindlimb neurons: forelimb neurons were encountered throughout the nucleus, and hindlimb neurons were encountered in the medial-anterior two thirds. A distinct eye movement area exists in lateral, posterior, and ventral regions of NIP. This area borders regions of NL that also contain eye movement-related neurons. 4. Forelimb interpositus neurons discharged strongly during reach and grasp; discharge rates were recorded for 41 neurons during a stereotyped reach and the average depth of modulation was 149 imp/s. Nineteen neurons that modulated during device tracking were also tested during reaching, and the depth of modulation was much greater during reaching. 5. Fifty-nine forelimb neurons were tested with device tracking. Twenty-seven (46%) produced no audible modulation, regardless of the joint being exercised. The remaining 32 neurons modulated during movement on at least one device (mean depth of modulation = 84 imp/s). Comparison of discharge during use of different devices revealed no strong evidence for device-specific discharge. 6. Discharge modulations during device tracking were phasic, preceded movement, and, for a small number of cells, showed consistent parametric relations to duration, amplitude, and velocity of movement. 7. Despite a clear somatotopy within NI and NL, there is no finer mapping based on active movements about individual joints within forelimb regions. Discharge modulation depends on movements involving the whole limb. Progress in understanding the function of intermediate cerebellum depends on determining the variables required to elicit consistent and high modulation of neural discharge.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1993        PMID: 8433134     DOI: 10.1152/jn.1993.69.1.57

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


  55 in total

1.  Effects of accuracy constraints on reach-to-grasp movements in cerebellar patients.

Authors:  M K Rand; Y Shimansky; G E Stelmach; V Bracha; J R Bloedel
Journal:  Exp Brain Res       Date:  2000-11       Impact factor: 1.972

2.  Cerebellar Purkinje cell simple spike discharge encodes movement velocity in primates during visuomotor arm tracking.

Authors:  J D Coltz; M T Johnson; T J Ebner
Journal:  J Neurosci       Date:  1999-03-01       Impact factor: 6.167

3.  Evidence for a motor somatotopy in the cerebellar dentate nucleus--an FMRI study in humans.

Authors:  Michael Küper; Markus Thürling; Roxana Stefanescu; Stefan Maderwald; Johannes Roths; Hans G Elles; Mark E Ladd; Jörn Diedrichsen; Dagmar Timmann
Journal:  Hum Brain Mapp       Date:  2011-09-21       Impact factor: 5.038

4.  Timing and causality in the generation of learned eyelid responses.

Authors:  Raudel Sánchez-Campusano; Agnès Gruart; José M Delgado-García
Journal:  Front Integr Neurosci       Date:  2011-08-30

5.  Unravelling cerebellar pathways with high temporal precision targeting motor and extensive sensory and parietal networks.

Authors:  Fahad Sultan; Mark Augath; Salah Hamodeh; Yusuke Murayama; Axel Oeltermann; Alexander Rauch; Peter Thier
Journal:  Nat Commun       Date:  2012-06-26       Impact factor: 14.919

6.  Dynamic changes in the cerebellar-interpositus/red-nucleus-motoneuron pathway during motor learning.

Authors:  Raudel Sánchez-Campusano; Agnès Gruart; José M Delgado-García
Journal:  Cerebellum       Date:  2011-12       Impact factor: 3.847

7.  Information processing in the hemisphere of the cerebellar cortex for control of wrist movement.

Authors:  Saeka Tomatsu; Takahiro Ishikawa; Yoshiaki Tsunoda; Jongho Lee; Donna S Hoffman; Shinji Kakei
Journal:  J Neurophysiol       Date:  2015-10-14       Impact factor: 2.714

Review 8.  Corollary Discharge Signals in the Cerebellum.

Authors:  Abigail L Person
Journal:  Biol Psychiatry Cogn Neurosci Neuroimaging       Date:  2019-05-02

9.  The cerebellar interpositus nucleus and the dynamic control of learned motor responses.

Authors:  Raudel Sánchez-Campusano; Agnès Gruart; José M Delgado-García
Journal:  J Neurosci       Date:  2007-06-20       Impact factor: 6.167

10.  Role of cerebellar interpositus nucleus in the genesis and control of reflex and conditioned eyelid responses.

Authors:  Lydia Jiménez-Díaz; Juan de Dios Navarro-López; Agnès Gruart; José M Delgado-García
Journal:  J Neurosci       Date:  2004-10-13       Impact factor: 6.167

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