Literature DB >> 22101492

The organization of cortical activity in the anterior lobe of the cat cerebellum during hindlimb stepping.

M S Valle1, J Eian, G Bosco, R E Poppele.   

Abstract

We recorded from over 280 single cortical neurons throughout the medial anterior lobe of the cat cerebellum during passive movements of the hindlimbs resembling stepping on a moving treadmill. We used three stepping patterns, unilateral stepping of either the ipsilateral or contralateral leg and bipedal stepping in an alternating gait pattern. We found that over 60% of the neurons, mostly Purkinje cells, responded to stepping of one or both legs, and over 40% to more than one type of stepping pattern. Responsive cells were distributed throughout the five anterior lobules, and the highest concentration was found in traditional hindlimb areas in lobules 2 and 3. A comparison of response waveforms showed that they are similar for neighboring cells in many parts of the cerebellar cortex, and they tend to form local blob-like groupings. Response patterns, i.e., relationship among responses to each stepping type, tended to be similar within a local group. The groupings extend further in the parasagittal dimension (up to about a third of a lobule) than in the transverse dimension (about 1 mm), and they may form functional modules. A principal component analysis also showed that the responses were composed of a four basis waveforms (principal components) that explained about 80% of the response waveform variance that were nearly identical to those derived from dorsal spinocerebellar tract (DSCT) responses to similar stepping movements. We reconstructed the locations of the recorded neurons on a 2D map of the cerebellar cortex showing the spatial distribution of responsive cells according to their response characteristics. We propose, on the basis of these results, that the sensory input to the cerebellum from the hindlimbs is distributed to multiple zones that may each contribute to a different component of cerebellar function.

Mesh:

Year:  2011        PMID: 22101492     DOI: 10.1007/s00221-011-2938-y

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  52 in total

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Authors:  M S Valle; G Bosco; R Poppele
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Journal:  AMA Arch Neurol Psychiatry       Date:  1955-12

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Authors:  J S Lou; J R Bloedel
Journal:  J Neurophysiol       Date:  1992-08       Impact factor: 2.714

4.  Kinematic and non-kinematic signals transmitted to the cat cerebellum during passive treadmill stepping.

Authors:  G Bosco; J Eian; R E Poppele
Journal:  Exp Brain Res       Date:  2005-10-28       Impact factor: 1.972

5.  Cutaneous receptive fields and topography of mossy fibres and climbing fibres projecting to cat cerebellar C3 zone.

Authors:  M Garwicz; H Jorntell; C F Ekerot
Journal:  J Physiol       Date:  1998-10-01       Impact factor: 5.182

6.  Representation of multiple kinematic parameters of the cat hindlimb in spinocerebellar activity.

Authors:  G Bosco; R E Poppele
Journal:  J Neurophysiol       Date:  1997-09       Impact factor: 2.714

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Authors:  D M Armstrong; S A Edgley
Journal:  J Physiol       Date:  1988-06       Impact factor: 5.182

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Authors:  P L van Kan; A R Gibson; J C Houk
Journal:  J Neurophysiol       Date:  1993-01       Impact factor: 2.714

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Authors:  R Leicht; R F Schmidt
Journal:  Exp Brain Res       Date:  1977-04-21       Impact factor: 1.972

10.  Different responses of rat cerebellar Purkinje cells and Golgi cells evoked by widespread convergent sensory inputs.

Authors:  Tahl Holtzman; Thimali Rajapaksa; Abteen Mostofi; Steve A Edgley
Journal:  J Physiol       Date:  2006-05-18       Impact factor: 5.182

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  6 in total

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Journal:  Exp Brain Res       Date:  2017-08-23       Impact factor: 1.972

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Journal:  PLoS One       Date:  2014-10-28       Impact factor: 3.240

5.  Persistent motor dysfunction despite homeostatic rescue of cerebellar morphogenesis in the Car8 waddles mutant mouse.

Authors:  Lauren N Miterko; Joshua J White; Tao Lin; Amanda M Brown; Kevin J O'Donovan; Roy V Sillitoe
Journal:  Neural Dev       Date:  2019-03-12       Impact factor: 3.842

6.  Purkinje cell misfiring generates high-amplitude action tremors that are corrected by cerebellar deep brain stimulation.

Authors:  Amanda M Brown; Joshua J White; Meike E van der Heijden; Joy Zhou; Tao Lin; Roy V Sillitoe
Journal:  Elife       Date:  2020-03-17       Impact factor: 8.140

  6 in total

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