Cargando…
Stimulus contrast modulates burst activity in the lateral geniculate nucleus
Burst activity is a ubiquitous feature of thalamic neurons and is well documented for visual neurons in the lateral geniculate nucleus (LGN). Although bursts are often associated with states of drowsiness, they are also known to convey visual information to cortex and are particularly effective in e...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313900/ https://www.ncbi.nlm.nih.gov/pubmed/37397805 http://dx.doi.org/10.1016/j.crneur.2023.100096 |
_version_ | 1785067205273059328 |
---|---|
author | Sanchez, Alyssa N. Alitto, Henry J. Rathbun, Daniel L. Fisher, Tucker G. Usrey, W. Martin |
author_facet | Sanchez, Alyssa N. Alitto, Henry J. Rathbun, Daniel L. Fisher, Tucker G. Usrey, W. Martin |
author_sort | Sanchez, Alyssa N. |
collection | PubMed |
description | Burst activity is a ubiquitous feature of thalamic neurons and is well documented for visual neurons in the lateral geniculate nucleus (LGN). Although bursts are often associated with states of drowsiness, they are also known to convey visual information to cortex and are particularly effective in evoking cortical responses. The occurrence of thalamic bursts depends on (1) the inactivation gate of T-type Ca(2+) channels (T-channels), which become de-inactivated following periods of increased membrane hyperpolarization, and (2) the opening of the T-channel activation gate, which has voltage-threshold and rate-of-change (δv/δt) requirements. Given the time/voltage relationship for the generation of Ca(2+) potentials that underlie burst events, it is reasonable to predict that geniculate bursts are influenced by the luminance contrast of drifting grating stimuli, with the null phase of higher contrast stimuli evoking greater hyperpolarization followed by a larger dv/dt than the null phase of lower contrast stimuli. To determine the relationship between stimulus contrast and burst activity, we recorded the spiking activity of cat LGN neurons while presenting drifting sine-wave gratings that varied in luminance contrast. Results show that burst rate, reliability, and timing precision are significantly greater with higher contrast stimuli compared with lower contrast stimuli. Additional analysis from simultaneous recordings of synaptically connected retinal ganglion cells and LGN neurons further reveals the time/voltage dynamics underlying burst activity. Together, these results support the hypothesis that stimulus contrast and the biophysical properties underlying the state of T-type Ca(2+) channels interact to influence burst activity, presumably to facilitate thalamocortical communication and stimulus detection. |
format | Online Article Text |
id | pubmed-10313900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-103139002023-07-02 Stimulus contrast modulates burst activity in the lateral geniculate nucleus Sanchez, Alyssa N. Alitto, Henry J. Rathbun, Daniel L. Fisher, Tucker G. Usrey, W. Martin Curr Res Neurobiol Articles from the special issue: Integrating thalamocortical functions from sensation to cognition, edited by Mathieu Wolff and Anna Mitchell Burst activity is a ubiquitous feature of thalamic neurons and is well documented for visual neurons in the lateral geniculate nucleus (LGN). Although bursts are often associated with states of drowsiness, they are also known to convey visual information to cortex and are particularly effective in evoking cortical responses. The occurrence of thalamic bursts depends on (1) the inactivation gate of T-type Ca(2+) channels (T-channels), which become de-inactivated following periods of increased membrane hyperpolarization, and (2) the opening of the T-channel activation gate, which has voltage-threshold and rate-of-change (δv/δt) requirements. Given the time/voltage relationship for the generation of Ca(2+) potentials that underlie burst events, it is reasonable to predict that geniculate bursts are influenced by the luminance contrast of drifting grating stimuli, with the null phase of higher contrast stimuli evoking greater hyperpolarization followed by a larger dv/dt than the null phase of lower contrast stimuli. To determine the relationship between stimulus contrast and burst activity, we recorded the spiking activity of cat LGN neurons while presenting drifting sine-wave gratings that varied in luminance contrast. Results show that burst rate, reliability, and timing precision are significantly greater with higher contrast stimuli compared with lower contrast stimuli. Additional analysis from simultaneous recordings of synaptically connected retinal ganglion cells and LGN neurons further reveals the time/voltage dynamics underlying burst activity. Together, these results support the hypothesis that stimulus contrast and the biophysical properties underlying the state of T-type Ca(2+) channels interact to influence burst activity, presumably to facilitate thalamocortical communication and stimulus detection. Elsevier 2023-06-10 /pmc/articles/PMC10313900/ /pubmed/37397805 http://dx.doi.org/10.1016/j.crneur.2023.100096 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Articles from the special issue: Integrating thalamocortical functions from sensation to cognition, edited by Mathieu Wolff and Anna Mitchell Sanchez, Alyssa N. Alitto, Henry J. Rathbun, Daniel L. Fisher, Tucker G. Usrey, W. Martin Stimulus contrast modulates burst activity in the lateral geniculate nucleus |
title | Stimulus contrast modulates burst activity in the lateral geniculate nucleus |
title_full | Stimulus contrast modulates burst activity in the lateral geniculate nucleus |
title_fullStr | Stimulus contrast modulates burst activity in the lateral geniculate nucleus |
title_full_unstemmed | Stimulus contrast modulates burst activity in the lateral geniculate nucleus |
title_short | Stimulus contrast modulates burst activity in the lateral geniculate nucleus |
title_sort | stimulus contrast modulates burst activity in the lateral geniculate nucleus |
topic | Articles from the special issue: Integrating thalamocortical functions from sensation to cognition, edited by Mathieu Wolff and Anna Mitchell |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313900/ https://www.ncbi.nlm.nih.gov/pubmed/37397805 http://dx.doi.org/10.1016/j.crneur.2023.100096 |
work_keys_str_mv | AT sanchezalyssan stimuluscontrastmodulatesburstactivityinthelateralgeniculatenucleus AT alittohenryj stimuluscontrastmodulatesburstactivityinthelateralgeniculatenucleus AT rathbundaniell stimuluscontrastmodulatesburstactivityinthelateralgeniculatenucleus AT fishertuckerg stimuluscontrastmodulatesburstactivityinthelateralgeniculatenucleus AT usreywmartin stimuluscontrastmodulatesburstactivityinthelateralgeniculatenucleus |