Literature DB >> 20707989

Origin and timing of voltage-sensitive dye signals within layers of the turtle cerebellar cortex.

Michael Ariel1, Michael E Brown.   

Abstract

Optical recording techniques were applied to the turtle cerebellum to localize synchronous responses to microstimulation of its cortical layers and reveal the cerebellum's three-dimensional processing. The in vitro yet intact cerebellum was first immersed in voltage-sensitive dye and its responses while intact were compared to those measured in thick cerebellar slices. Each slice is stained throughout its depth, even though the pial half appeared darker during epi-illumination and lighter during trans-illumination. Optical responses were shown to be mediated by the voltage-sensitive dye because the evoked signals had opposite polarity for 540- and 710-nm light, but no response to 850-nm light. Molecular layer stimulation of the intact cerebellum evoked slow transverse beams. Similar beams were observed in the molecular layer of thick transverse slices but not sagittal slices. With low currents, beams in transverse slices were restricted to sublayers within the molecular layer, conducting slowly away from the stimulus site. These excitatory beams were observed nearly all the way across the turtle cerebellum, distances of 4-6mm. Microstimulation of the granule cell layer of both transverse or sagittal slices evoked a local membrane depolarization restricted to a radial wedge, but these radial responses did not activate measurable molecular layer beams in transverse slices. White matter microstimulation in sagittal slices (near the ventricular surface of the turtle cerebellum) activated the granule cell and Purkinje cell layers, but not the molecular layer. These responses were nearly synchronous, were primarily caudal to the stimulation, and were blocked by cobalt ions. Therefore, synaptic responses in all cerebellar layers contribute to optical signals recorded in intact cerebellum in vitro (Brown and Ariel, 2009). Rapid radial signaling connects a sagittally-oriented, fast-conduction system of the deep layers with the transverse-oriented, slow-conducting molecular layer, thereby permitting complex temporal processing between two tangential but orthogonal paths in the cerebellar cortex.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20707989      PMCID: PMC2951884          DOI: 10.1016/j.brainres.2010.08.011

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  56 in total

1.  Optical measurements of synchronized activity in isolated mammalian cerebellum.

Authors:  D Cohen; Y Yarom
Journal:  Neuroscience       Date:  1999       Impact factor: 3.590

2.  Imaging parallel fiber and climbing fiber responses and their short-term interactions in the mouse cerebellar cortex in vivo.

Authors:  R L Dunbar; G Chen; W Gao; K C Reinert; R Feddersen; T J Ebner
Journal:  Neuroscience       Date:  2004       Impact factor: 3.590

3.  Correlations between purkinje cell single-unit activity and simultaneously recorded field potentials in the immediately underlying granule cell layer.

Authors:  Huo Lu; Mitra J Hartmann; James M Bower
Journal:  J Neurophysiol       Date:  2005-05-31       Impact factor: 2.714

4.  Inferior olive oscillation as the temporal basis for motricity and oscillatory reset as the basis for motor error correction.

Authors:  R R Llinás
Journal:  Neuroscience       Date:  2009-04-22       Impact factor: 3.590

5.  Spatial pattern coding of sensory information by climbing fiber-evoked calcium signals in networks of neighboring cerebellar Purkinje cells.

Authors:  Simon R Schultz; Kazuo Kitamura; Arthur Post-Uiterweer; Julija Krupic; Michael Häusser
Journal:  J Neurosci       Date:  2009-06-24       Impact factor: 6.167

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Journal:  J Neurophysiol       Date:  1974-07       Impact factor: 2.714

8.  Quantitative analysis of converging spinal and cuneate mossy fibre afferent projections to the rat cerebellar anterior lobe.

Authors:  J M Alisky; D L Tolbert
Journal:  Neuroscience       Date:  1997-09       Impact factor: 3.590

9.  Tactile projections to granule cells in caudal vermis of the rat's cerebellum.

Authors:  J W Joseph; G M Shambes; J M Gibson; W Welker
Journal:  Brain Behav Evol       Date:  1978       Impact factor: 1.808

10.  Principles of organization of a cerebro-cerebellar circuit. Micromapping the projections from cerebral (SI) to cerebellar (granule cell layer) tactile areas of rats.

Authors:  J M Bower; D H Beermann; J M Gibson; G M Shambes; W Welker
Journal:  Brain Behav Evol       Date:  1981       Impact factor: 1.808

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  1 in total

1.  A novel path for rapid transverse communication of vestibular signals in turtle cerebellum.

Authors:  Michael E Brown; John R Martin; Jack Rosenbluth; Michael Ariel
Journal:  J Neurophysiol       Date:  2010-12-22       Impact factor: 2.714

  1 in total

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