Literature DB >> 10683572

Role of climbing fibers in determining the spatial patterns of activation in the cerebellar cortex to peripheral stimulation: an optical imaging study.

C L Hanson1, G Chen, T J Ebner.   

Abstract

The spatial patterns of activation in the rat cerebellar cortex evoked by ipsilateral face stimulation were mapped using optical imaging based on the pH sensitive dye, Neutral Red. The aims of the study were to characterize the optical responses evoked by peripheral stimulation and test the hypothesis that the resultant parasagittal banding is due to climbing fiber activation. In the anesthetized rat Crus I and II of the cerebellar cortex were stained with Neutral Red. Epi-fluorescent changes produced by a train of stimuli (5-10s and 4-20 Hz) to the ipsilateral face were monitored in time using a fast, high resolution charge-coupled device camera. The patterns of activation were quantified using a two-dimensional fast Fourier transform analysis that removed signals with high spatial frequencies and minimized the contribution of horizontal structural elements (i.e. blood vessels). The dominant spatial pattern of activation evoked by face stimulation was that of parasagittal bands. The bands were highly frequency-dependent and were elicited most strongly by stimulus frequencies in the range of 6-8 Hz. There was a large fall-off in the response for frequencies above and below. The optical signal evoked by face stimulation built up over a period of 10s and then gradually decayed. Within a folium the individual parasagittal bands exhibited some frequency and temporal specificity. Stimulation of the contralateral inferior olive also resulted in the activation of parasagittal bands with characteristics similar to the bands evoked by face stimulation, including a preferred stimulus frequency which peaked at 10 Hz. Injection of lidocaine into the contralateral inferior olive blocked the parasagittal bands evoked by ipsilateral face stimulation, while control injections of saline had no effect. The results confirm that a parasagittal banding pattern is a dominant feature of the functional architecture of the cerebellar cortex. The parasagittal banding pattern observed with Neutral Red is due primarily to the activation of climbing fiber afferents. The frequency tuning of the responses, with the preference for peripheral stimuli of 6-8 Hz, is in agreement with previous findings that the inferior olive is inherently rhythmic. These observations support the hypothesis that inferior olivary neurons are dynamically coupled into groups that activate parasagittal bands of Purkinje cells in the cerebellar cortex. The frequency tuning also supports the hypothesis that the climbing fiber system is involved with timing. Activation of this afferent system may require stimuli with appropriate frequency content and stimuli synchronized to the rhythmicity of the inferior olive.

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Year:  2000        PMID: 10683572     DOI: 10.1016/s0306-4522(99)00470-4

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


  9 in total

1.  Electrotonically mediated oscillatory patterns in neuronal ensembles: an in vitro voltage-dependent dye-imaging study in the inferior olive.

Authors:  Elena Leznik; Vladimir Makarenko; Rodolfo Llinás
Journal:  J Neurosci       Date:  2002-04-01       Impact factor: 6.167

2.  The entire trajectories of single olivocerebellar axons in the cerebellar cortex and their contribution to Cerebellar compartmentalization.

Authors:  I Sugihara; H S Wu; Y Shinoda
Journal:  J Neurosci       Date:  2001-10-01       Impact factor: 6.167

3.  Molecular, topographic, and functional organization of the cerebellar cortex: a study with combined aldolase C and olivocerebellar labeling.

Authors:  Izumi Sugihara; Yoshikazu Shinoda
Journal:  J Neurosci       Date:  2004-10-06       Impact factor: 6.167

4.  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

5.  Topography and response timing of intact cerebellum stained with absorbance voltage-sensitive dye.

Authors:  Michael E Brown; Michael Ariel
Journal:  J Neurophysiol       Date:  2008-11-12       Impact factor: 2.714

6.  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

7.  Role of calcium, glutamate neurotransmission, and nitric oxide in spreading acidification and depression in the cerebellar cortex.

Authors:  G Chen; R L Dunbar; W Gao; T J Ebner
Journal:  J Neurosci       Date:  2001-12-15       Impact factor: 6.167

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

Authors:  Michael Ariel; Michael E Brown
Journal:  Brain Res       Date:  2010-08-11       Impact factor: 3.252

Review 9.  Cerebellar Modules and Their Role as Operational Cerebellar Processing Units: A Consensus paper [corrected].

Authors:  Richard Apps; Richard Hawkes; Sho Aoki; Fredrik Bengtsson; Amanda M Brown; Gang Chen; Timothy J Ebner; Philippe Isope; Henrik Jörntell; Elizabeth P Lackey; Charlotte Lawrenson; Bridget Lumb; Martijn Schonewille; Roy V Sillitoe; Ludovic Spaeth; Izumi Sugihara; Antoine Valera; Jan Voogd; Douglas R Wylie; Tom J H Ruigrok
Journal:  Cerebellum       Date:  2018-10       Impact factor: 3.847

  9 in total

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