Literature DB >> 8989413

Burst responses in thalamic relay cells of the awake behaving cat.

W Guido1, T Weyand.   

Abstract

1. Relay cells of the dorsal lateral geniculate nucleus (LGN) respond in one of two modes: tonic or burst. The purpose of this study was to determine whether, and under what conditions, burst responses occur in LGN cells of an awake, behaving animal. 2. We recorded the extracellular responses of cells located in the A layers of LGN in two cats trained to perform a simple fixation task. In our paradigm, head position was fixed and gaze monitored with the use of the scleral search coil technique. They were trained to fixate on a small target light while we probed the receptive field of an isolated LGN cell with drifting gratings. 3. Many LGN cells (37/48; 77%) recorded in the awake cat showed some form of burst firing. However, the degree of burstiness a given cell displayed was relatively low. The probability of recording a burst response during any second within the fixation task was 0.09. This reflects the fact that during wakefulness, LGN cells are generally in a state of relative depolarization and the low-threshold Ca2+ conductance underlying burst firing is inactivated. 4. The majority of bursts occurred (262/377; 71%) during visual stimulation. These comprised the initial response to the grating and were confined to the early phase of fixation. As the cat continued to hold fixation and as subsequent cycles of the grating passed through the cell's receptive field, the response shifted from a burst to a tonic firing pattern. Some bursts (67/377, 18%) were related to eye movements. All of these were postsaccadic, and most occurred > 150 ms from the onset of the eye movement. Finally, some bursts were neither visually driven nor related to eye movements. However, these spontaneous bursts were infrequent (41/377; 11%) and never rhythmic. 5. Burst firing in LGN cells has a dual purpose. During quiescent states such as slow-wave sleep, they support the decoupling of retinal signals from LGN. During the waking state, bursts can facilitate signal transmission during target acquisition and early phases of fixation.

Entities:  

Mesh:

Year:  1995        PMID: 8989413     DOI: 10.1152/jn.1995.74.4.1782

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  78 in total

1.  Action potential backpropagation and somato-dendritic distribution of ion channels in thalamocortical neurons.

Authors:  S R Williams; G J Stuart
Journal:  J Neurosci       Date:  2000-02-15       Impact factor: 6.167

2.  Thalamic reticular nucleus activation reflects attentional gating during classical conditioning.

Authors:  K McAlonan; V J Brown; E M Bowman
Journal:  J Neurosci       Date:  2000-12-01       Impact factor: 6.167

3.  Thalamic bursting in rats during different awake behavioral states.

Authors:  E E Fanselow; K Sameshima; L A Baccala; M A Nicolelis
Journal:  Proc Natl Acad Sci U S A       Date:  2001-12-18       Impact factor: 11.205

4.  Stimulus-based state control in the thalamocortical system.

Authors:  L M Miller; C E Schreiner
Journal:  J Neurosci       Date:  2000-09-15       Impact factor: 6.167

Review 5.  Dynamic shifting in thalamocortical processing during different behavioural states.

Authors:  Miguel A L Nicolelis; Erika E Fanselow
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-12-29       Impact factor: 6.237

Review 6.  Novel neuronal and astrocytic mechanisms in thalamocortical loop dynamics.

Authors:  Vincenzo Crunelli; Kate L Blethyn; David W Cope; Stuart W Hughes; H Rheinallt Parri; Jonathan P Turner; Tibor I Tòth; Stephen R Williams
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-12-29       Impact factor: 6.237

7.  The initiation of bursts in thalamic neurons and the cortical control of thalamic sensitivity.

Authors:  Alain Destexhe; Terrence J Sejnowski
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-12-29       Impact factor: 6.237

Review 8.  Corticothalamic interactions in the transfer of visual information.

Authors:  Adam M Sillito; Helen E Jones
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-12-29       Impact factor: 6.237

Review 9.  Spike timing and visual processing in the retinogeniculocortical pathway.

Authors:  W Martin Usrey
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-12-29       Impact factor: 6.237

10.  EEG oscillations at 600 Hz are macroscopic markers for cortical spike bursts.

Authors:  Stuart N Baker; Gabriel Curio; Roger N Lemon
Journal:  J Physiol       Date:  2003-06-13       Impact factor: 5.182

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