Literature DB >> 15145087

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

R L Dunbar1, G Chen, W Gao, K C Reinert, R Feddersen, T J Ebner.   

Abstract

A major question in the study of cerebellar cortical function is how parallel fiber and climbing fiber inputs interact to shape information processing. Emphasis has been placed on the long-term effects due to conjunctive stimulation of climbing fibers and parallel fibers. Much less emphasis has been placed on short-term interactions and their spatial nature. To address this question the responses to parallel fiber and climbing fiber inputs and their short-term interaction were characterized using optical imaging with Neutral Red in the anesthetized mouse in vivo. Electrical stimulation of the cerebellar surface evoked an increase in fluorescence consisting of a transverse optical beam. The linear relationship between the optical responses and stimulus parameters, high spatial resolution and close coupling to the electrophysiological recordings show the utility of this imaging methodology. The majority of the optical response was due to activation of postsynaptic alpha-amino-3-hydroxyl-5-methyl-4-isoxazole propionate (AMPA) and metabotropic glutamate receptors with a minor contribution from the presynaptic parallel fibers. Stimulation of the inferior olive evoked parasagittal bands that were abolished by blocking AMPA glutamate receptors. Conjunctive stimulation of the cerebellar surface and inferior olive resulted in inhibition of the climbing fiber evoked optical responses. This lateral inhibition of the parasagittal bands extended out from both sides of an activated parallel fiber beam and was mediated by GABA(A) but not GABA(B) receptors. One hypothesized role for lateral inhibition of this type is to spatially focus the interactions between parallel fiber and climbing fiber input on Purkinje cells. In summary optical imaging with Neutral Red permitted visualization of cerebellar cortical responses to parallel fiber and climbing fiber activation. The GABA(A) dependent lateral inhibition of the climbing fiber evoked parasagittal bands by parallel fiber stimulation shows that cerebellar interneurons play a short-term role in shaping the responses of Purkinje cells to climbing fiber input.

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Year:  2004        PMID: 15145087     DOI: 10.1016/j.neuroscience.2004.02.020

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  13 in total

1.  Parasagittally aligned, mGluR1-dependent patches are evoked at long latencies by parallel fiber stimulation in the mouse cerebellar cortex in vivo.

Authors:  Xinming Wang; Gang Chen; Wangcai Gao; Timothy J Ebner
Journal:  J Neurophysiol       Date:  2011-02-02       Impact factor: 2.714

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Authors:  D A Llano; B B Theyel; A K Mallik; S M Sherman; N P Issa
Journal:  J Neurophysiol       Date:  2009-03-25       Impact factor: 2.714

3.  Optogenetic mapping of cerebellar inhibitory circuitry reveals spatially biased coordination of interneurons via electrical synapses.

Authors:  Jinsook Kim; Soojung Lee; Sachiko Tsuda; Xuying Zhang; Brent Asrican; Bernd Gloss; Guoping Feng; George J Augustine
Journal:  Cell Rep       Date:  2014-05-22       Impact factor: 9.423

4.  Role of the metabotropic glutamate receptor subtype 1 in the harmaline-induced tremor in rats.

Authors:  Wacław Kolasiewicz; Katarzyna Kuter; Jadwiga Wardas; Krystyna Ossowska
Journal:  J Neural Transm (Vienna)       Date:  2009-06-24       Impact factor: 3.575

5.  Stimulus-dependent changes in optical responses of the dorsal cochlear nucleus using voltage-sensitive dye.

Authors:  F G Licari; M Shkoukani; J A Kaltenbach
Journal:  J Neurophysiol       Date:  2011-05-04       Impact factor: 2.714

6.  Cerebellar AMPA/KA receptor antagonism by CNQX inhibits vestibuloocular reflex adaptation.

Authors:  Troy L Carter; James G McElligott
Journal:  Exp Brain Res       Date:  2005-08-05       Impact factor: 1.972

7.  Activity-induced tissue oxygenation changes in rat cerebellar cortex: interplay of postsynaptic activation and blood flow.

Authors:  Nikolas Offenhauser; Kirsten Thomsen; Kirsten Caesar; Martin Lauritzen
Journal:  J Physiol       Date:  2005-03-17       Impact factor: 5.182

8.  Low-frequency oscillations in the cerebellar cortex of the tottering mouse.

Authors:  Gang Chen; Laurentiu S Popa; Xinming Wang; Wangcai Gao; Justin Barnes; Claudia M Hendrix; Ellen J Hess; Timothy J Ebner
Journal:  J Neurophysiol       Date:  2008-11-05       Impact factor: 2.714

9.  Reliable coding emerges from coactivation of climbing fibers in microbands of cerebellar Purkinje neurons.

Authors:  Ilker Ozden; Megan R Sullivan; H Megan Lee; Samuel S-H Wang
Journal:  J Neurosci       Date:  2009-08-26       Impact factor: 6.167

10.  Long-term potentiation of the responses to parallel fiber stimulation in mouse cerebellar cortex in vivo.

Authors:  X Wang; G Chen; W Gao; T Ebner
Journal:  Neuroscience       Date:  2009-02-04       Impact factor: 3.590

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