Literature DB >> 8014919

The cerebellar dorsal granular ridge in an elasmobranch has proprioceptive and electroreceptive representations and projects homotopically to the medullary electrosensory nucleus.

R A Conley1, D Bodznick.   

Abstract

1. Response properties of neurons in the dorsal granular ridge (DGR) of the little skate, Raja erinacea, were studied in decerebrate, curarized fish. Sensory responses included proprioceptive (426 of 952; 45%) and electroreceptive units (526 of 952; 55%). Electroreceptive units responded to weak electric fields with a higher threshold than lower-order units and had large ipsilateral receptive fields, whose exact boundaries were often unclear but contained smaller, identifiable best areas. Proprioceptive units responded to displacement of the ipsilateral fin and were either position- or movement-sensitive. 2. Both proprioceptive and electroreceptive units showed a progression of receptive fields from anterior to posterior body in the rostral to caudal direction along the length of DGR. Sensory maps in DGR projected homotopically to the electrosensory somatotopy in the dorsal nucleus. Peak evoked potentials and units responding to local DGR stimulation occurred only in areas of the dorsal nucleus with receptive fields located within the composite receptive field at the DGR stimulation site. 3. Single shocks to DGR produced a short spike train followed by a prolonged suppression period in the medullary dorsal nucleus. These results have implications for the role of the parallel fiber system in medullary electrosensory processing.

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Year:  1994        PMID: 8014919     DOI: 10.1007/bf00192720

Source DB:  PubMed          Journal:  J Comp Physiol A            Impact factor:   1.836


  19 in total

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Journal:  J Physiol       Date:  1964-10       Impact factor: 5.182

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Authors:  J G New
Journal:  J Comp Physiol A       Date:  1990-07       Impact factor: 1.836

4.  Medullary electrosensory processing in the little skate. II. Suppression of self-generated electrosensory interference during respiration.

Authors:  J G New; D Bodznick
Journal:  J Comp Physiol A       Date:  1990-07       Impact factor: 1.836

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Authors:  S I Terashima; R C Goris
Journal:  Brain Res       Date:  1975-01-17       Impact factor: 3.252

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Authors:  J Bastian; J Courtright
Journal:  J Comp Physiol A       Date:  1991-04       Impact factor: 1.836

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Journal:  J Comp Physiol A       Date:  1986-01       Impact factor: 1.836

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Journal:  J Neurophysiol       Date:  1971-07       Impact factor: 2.714

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Journal:  J Neurosci       Date:  1986-02       Impact factor: 6.167

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Authors:  D Bodznick; A W Schmidt
Journal:  J Comp Neurol       Date:  1984-06-01       Impact factor: 3.215

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  4 in total

1.  Two modes of information processing in the electrosensory system of the paddlefish (Polyodon spathula).

Authors:  Leonie Pothmann; Lon A Wilkens; Michael H Hofmann
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2011-09-30       Impact factor: 1.836

2.  Neural simulations of adaptive reafference suppression in the elasmobranch electrosensory system.

Authors:  M E Nelson; M G Paulin
Journal:  J Comp Physiol A       Date:  1995-12       Impact factor: 1.836

3.  Pyramidal-cell plasticity in weakly electric fish: a mechanism for attenuating responses to reafferent electrosensory inputs.

Authors:  J Bastian
Journal:  J Comp Physiol A       Date:  1995-01       Impact factor: 1.836

4.  Anti-hebbian spike-timing-dependent plasticity and adaptive sensory processing.

Authors:  Patrick D Roberts; Todd K Leen
Journal:  Front Comput Neurosci       Date:  2010-12-31       Impact factor: 2.380

  4 in total

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