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Dynamic Encoding of Natural Luminance Sequences by LGN Bursts

In the lateral geniculate nucleus (LGN) of the thalamus, visual stimulation produces two distinct types of responses known as tonic and burst. Due to the dynamics of the T-type Ca (2+) channels involved in burst generation, the type of response evoked by a particular stimulus depends on the resting...

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Autores principales: Lesica, Nicholas A, Weng, Chong, Jin, Jianzhong, Yeh, Chun-I, Alonso, Jose-Manuel, Stanley, Garrett B
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1475766/
https://www.ncbi.nlm.nih.gov/pubmed/16756389
http://dx.doi.org/10.1371/journal.pbio.0040209
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author Lesica, Nicholas A
Weng, Chong
Jin, Jianzhong
Yeh, Chun-I
Alonso, Jose-Manuel
Stanley, Garrett B
author_facet Lesica, Nicholas A
Weng, Chong
Jin, Jianzhong
Yeh, Chun-I
Alonso, Jose-Manuel
Stanley, Garrett B
author_sort Lesica, Nicholas A
collection PubMed
description In the lateral geniculate nucleus (LGN) of the thalamus, visual stimulation produces two distinct types of responses known as tonic and burst. Due to the dynamics of the T-type Ca (2+) channels involved in burst generation, the type of response evoked by a particular stimulus depends on the resting membrane potential, which is controlled by a network of modulatory connections from other brain areas. In this study, we use simulated responses to natural scene movies to describe how modulatory and stimulus-driven changes in LGN membrane potential interact to determine the luminance sequences that trigger burst responses. We find that at low resting potentials, when the T channels are de-inactivated and bursts are relatively frequent, an excitatory stimulus transient alone is sufficient to evoke a burst. However, to evoke a burst at high resting potentials, when the T channels are inactivated and bursts are relatively rare, prolonged inhibitory stimulation followed by an excitatory transient is required. We also observe evidence of these effects in vivo, where analysis of experimental recordings demonstrates that the luminance sequences that trigger bursts can vary dramatically with the overall burst percentage of the response. To characterize the functional consequences of the effects of resting potential on burst generation, we simulate LGN responses to different luminance sequences at a range of resting potentials with and without a mechanism for generating bursts. Using analysis based on signal detection theory, we show that bursts enhance detection of specific luminance sequences, ranging from the onset of excitatory sequences at low resting potentials to the offset of inhibitory sequences at high resting potentials. These results suggest a dynamic role for burst responses during visual processing that may change according to behavioral state.
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spelling pubmed-14757662006-07-21 Dynamic Encoding of Natural Luminance Sequences by LGN Bursts Lesica, Nicholas A Weng, Chong Jin, Jianzhong Yeh, Chun-I Alonso, Jose-Manuel Stanley, Garrett B PLoS Biol Research Article In the lateral geniculate nucleus (LGN) of the thalamus, visual stimulation produces two distinct types of responses known as tonic and burst. Due to the dynamics of the T-type Ca (2+) channels involved in burst generation, the type of response evoked by a particular stimulus depends on the resting membrane potential, which is controlled by a network of modulatory connections from other brain areas. In this study, we use simulated responses to natural scene movies to describe how modulatory and stimulus-driven changes in LGN membrane potential interact to determine the luminance sequences that trigger burst responses. We find that at low resting potentials, when the T channels are de-inactivated and bursts are relatively frequent, an excitatory stimulus transient alone is sufficient to evoke a burst. However, to evoke a burst at high resting potentials, when the T channels are inactivated and bursts are relatively rare, prolonged inhibitory stimulation followed by an excitatory transient is required. We also observe evidence of these effects in vivo, where analysis of experimental recordings demonstrates that the luminance sequences that trigger bursts can vary dramatically with the overall burst percentage of the response. To characterize the functional consequences of the effects of resting potential on burst generation, we simulate LGN responses to different luminance sequences at a range of resting potentials with and without a mechanism for generating bursts. Using analysis based on signal detection theory, we show that bursts enhance detection of specific luminance sequences, ranging from the onset of excitatory sequences at low resting potentials to the offset of inhibitory sequences at high resting potentials. These results suggest a dynamic role for burst responses during visual processing that may change according to behavioral state. Public Library of Science 2006-07 2006-06-13 /pmc/articles/PMC1475766/ /pubmed/16756389 http://dx.doi.org/10.1371/journal.pbio.0040209 Text en Copyright: © 2006 Lesica et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Lesica, Nicholas A
Weng, Chong
Jin, Jianzhong
Yeh, Chun-I
Alonso, Jose-Manuel
Stanley, Garrett B
Dynamic Encoding of Natural Luminance Sequences by LGN Bursts
title Dynamic Encoding of Natural Luminance Sequences by LGN Bursts
title_full Dynamic Encoding of Natural Luminance Sequences by LGN Bursts
title_fullStr Dynamic Encoding of Natural Luminance Sequences by LGN Bursts
title_full_unstemmed Dynamic Encoding of Natural Luminance Sequences by LGN Bursts
title_short Dynamic Encoding of Natural Luminance Sequences by LGN Bursts
title_sort dynamic encoding of natural luminance sequences by lgn bursts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1475766/
https://www.ncbi.nlm.nih.gov/pubmed/16756389
http://dx.doi.org/10.1371/journal.pbio.0040209
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