J Physiol Wellcome Trust-funded researchers
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Physiol Volume 574, Number 2, 491-507, July 15, 2006 DOI: 10.1113/jphysiol.2006.108282
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
574/2/491    most recent
jphysiol.2006.108282v2
jphysiol.2006.108282v1
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Holtzman, T.
Right arrow Articles by Edgley, S. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Holtzman, T.
Right arrow Articles by Edgley, S. A.
Related Collections
Right arrow Neuroscience

NEUROSCIENCE

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

Tahl Holtzman1, Thimali Rajapaksa1, Abteen Mostofi1 and Steve A. Edgley1

1 Department of Anatomy, University of Cambridge, Downing Street, Cambridge CB2 3DY, UK

While the synaptic properties of Golgi cell-mediated inhibition of granule cells are well studied, less is known of the afferent inputs to Golgi cells so their role in information processing remains unclear. We investigated the responses of cerebellar cortical Golgi cells and Purkinje cells in Crus I and II of the posterior lobe cerebellar hemisphere to activation of peripheral afferents in vivo, using anaesthetized rats. Recordings were made from 70 Golgi cells and 76 Purkinje cells. Purkinje cells were identified by the presence of climbing fibre responses. Golgi cells were identified by both spontaneous firing pattern and response properties, and identification was confirmed using juxtacellular labelling of single neurones (n = 16). Purkinje cells in Crus II showed continuous firing at relatively high rates (25–60 Hz) and stimulation of peripheral afferents rarely evoked substantial responses. The most common response was a modest, long-latency, long-lasting increase in simple spike output. By comparison, the most common response evoked in Golgi cells by the same stimuli was a long-latency, long-lasting depression of firing, found in ~70% of the Golgi cells tested. The onsets of Golgi cell depressions had shorter latencies than the Purkinje cell excitations. Brief, short-latency excitations and reductions in firing were also evoked in some Golgi cells, and rarely in Purkinje cells, but in most cases long-lasting depressions were the only significant change in spike firing. Golgi cell responses could be evoked using air puff or tactile stimuli and under four different anaesthetic regimens. Long-lasting responses in both neurone types could be evoked from wide receptive fields, in many cases including distal afferents from all four limbs, as well as from trigeminal afferents. These Golgi cell responses are not consistent with the conventional feedback inhibition or ‘gain control’ models of Golgi cell function. They suggest instead that cerebellar cortical activity can be powerfully modulated by the general level of peripheral afferent activation from much of the body. On this basis, Golgi cells may act as a context-specific gate on transmission through the mossy fibre–granule cell pathway.

(Received 6 March 2006; accepted after revision 12 May 2006; first published online 16 May 2006)
Corresponding author S. A. Edgley: Department of Anatomy, Downing Street, University of Cambridge, Cambridge CB2 3DY, UK. Email: sae1000{at}cam.ac.uk




This article has been cited by other articles:


Home page
J. Physiol.Home page
H. Jorntell
Input-output plasticity of peripheral responses in cerebellar Golgi cells in vivo
J. Physiol., October 15, 2008; 586(20): 4789 - 4789.
[Full Text] [PDF]


Home page
J. Physiol.Home page
W. Xu and S. A. Edgley
Climbing fibre-dependent changes in Golgi cell responses to peripheral stimulation
J. Physiol., October 15, 2008; 586(20): 4951 - 4959.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
R. T. Kanichay and R. A. Silver
Synaptic and Cellular Properties of the Feedforward Inhibitory Circuit within the Input Layer of the Cerebellar Cortex
J. Neurosci., September 3, 2008; 28(36): 8955 - 8967.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
N. H. Barmack and V. Yakhnitsa
Functions of Interneurons in Mouse Cerebellum
J. Neurosci., January 30, 2008; 28(5): 1140 - 1152.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
W. Mittmann and M. Hausser
Linking Synaptic Plasticity and Spike Output at Excitatory and Inhibitory Synapses onto Cerebellar Purkinje Cells
J. Neurosci., May 23, 2007; 27(21): 5559 - 5570.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
T. Holtzman, A. Mostofi, C. L. Phuah, and S. A. Edgley
Cerebellar Golgi cells in the rat receive multimodal convergent peripheral inputs via the lateral funiculus of the spinal cord
J. Physiol., November 15, 2006; 577(1): 69 - 80.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
H. Jorntell and C.-F. Ekerot
Properties of somatosensory synaptic integration in cerebellar granule cells in vivo.
J. Neurosci., November 8, 2006; 26(45): 11786 - 11797.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2006 The Physiological Society.