Cargando…
The rat suprachiasmatic nucleus: the master clock ticks at 30 Hz
KEY POINTS: Light‐responsive neurones in the rat suprachiasmatic nucleus discharge with a harmonic distribution of interspike intervals, whereas unresponsive neurones seldom do. This harmonic patterning has a fundamental frequency of close to 30 Hz, and is the same in light‐on cells as in light‐off...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929337/ https://www.ncbi.nlm.nih.gov/pubmed/27061101 http://dx.doi.org/10.1113/JP272331 |
_version_ | 1782440589410697216 |
---|---|
author | Tsuji, Takahiro Tsuji, Chiharu Ludwig, Mike Leng, Gareth |
author_facet | Tsuji, Takahiro Tsuji, Chiharu Ludwig, Mike Leng, Gareth |
author_sort | Tsuji, Takahiro |
collection | PubMed |
description | KEY POINTS: Light‐responsive neurones in the rat suprachiasmatic nucleus discharge with a harmonic distribution of interspike intervals, whereas unresponsive neurones seldom do. This harmonic patterning has a fundamental frequency of close to 30 Hz, and is the same in light‐on cells as in light‐off cells, and is unaffected by exposure to light. Light‐on cells are more active than light‐off cells in both subjective day and subjective night, and both light‐on cells and light‐off cells respond more strongly to changes in light intensity during the subjective night than during the subjective day. Paired recordings indicate that the discharge of adjacent light‐responsive cells is very tightly synchronized. The gap junction inhibitor carbenoxolone increases the spontaneous activity of suprachiasmatic nucleus neurones but does not block the harmonic discharge patterning. ABSTRACT: The suprachiasmatic nucleus (SCN) of the hypothalamus has an essential role in orchestrating circadian rhythms of behaviour and physiology. In the present study, we recorded from single SCN neurons in urethane‐anaesthetized rats, categorized them by the statistical features of their electrical activity and by their responses to light, and examined how activity in the light phase differs from activity in the dark phase. We classified cells as light‐on cells or light‐off cells according to how their firing rate changed in acute response to light, or as non‐responsive cells. In both sets of light‐responsive neurons, responses to light were stronger at subjective night than in subjective day. Neuronal firing patterns were analysed by constructing hazard functions from interspike interval data. For most light‐responsive cells, the hazard functions showed a multimodal distribution, with a harmonic sequence of modes, indicating that spike activity was driven by an oscillatory input with a fundamental frequency of close to 30 Hz; this harmonic pattern was rarely seen in non‐responsive SCN cells. The frequency of the rhythm was the same in light‐on cells as in light‐off cells, was the same in subjective day as at subjective night, and was unaffected by exposure to light. Paired recordings indicated that the discharge of adjacent light‐responsive neurons was very tightly synchronized, consistent with electrical coupling. |
format | Online Article Text |
id | pubmed-4929337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49293372016-10-04 The rat suprachiasmatic nucleus: the master clock ticks at 30 Hz Tsuji, Takahiro Tsuji, Chiharu Ludwig, Mike Leng, Gareth J Physiol Neuroscience ‐ cellular/molecular KEY POINTS: Light‐responsive neurones in the rat suprachiasmatic nucleus discharge with a harmonic distribution of interspike intervals, whereas unresponsive neurones seldom do. This harmonic patterning has a fundamental frequency of close to 30 Hz, and is the same in light‐on cells as in light‐off cells, and is unaffected by exposure to light. Light‐on cells are more active than light‐off cells in both subjective day and subjective night, and both light‐on cells and light‐off cells respond more strongly to changes in light intensity during the subjective night than during the subjective day. Paired recordings indicate that the discharge of adjacent light‐responsive cells is very tightly synchronized. The gap junction inhibitor carbenoxolone increases the spontaneous activity of suprachiasmatic nucleus neurones but does not block the harmonic discharge patterning. ABSTRACT: The suprachiasmatic nucleus (SCN) of the hypothalamus has an essential role in orchestrating circadian rhythms of behaviour and physiology. In the present study, we recorded from single SCN neurons in urethane‐anaesthetized rats, categorized them by the statistical features of their electrical activity and by their responses to light, and examined how activity in the light phase differs from activity in the dark phase. We classified cells as light‐on cells or light‐off cells according to how their firing rate changed in acute response to light, or as non‐responsive cells. In both sets of light‐responsive neurons, responses to light were stronger at subjective night than in subjective day. Neuronal firing patterns were analysed by constructing hazard functions from interspike interval data. For most light‐responsive cells, the hazard functions showed a multimodal distribution, with a harmonic sequence of modes, indicating that spike activity was driven by an oscillatory input with a fundamental frequency of close to 30 Hz; this harmonic pattern was rarely seen in non‐responsive SCN cells. The frequency of the rhythm was the same in light‐on cells as in light‐off cells, was the same in subjective day as at subjective night, and was unaffected by exposure to light. Paired recordings indicated that the discharge of adjacent light‐responsive neurons was very tightly synchronized, consistent with electrical coupling. John Wiley and Sons Inc. 2016-05-29 2016-07-01 /pmc/articles/PMC4929337/ /pubmed/27061101 http://dx.doi.org/10.1113/JP272331 Text en © 2016 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Neuroscience ‐ cellular/molecular Tsuji, Takahiro Tsuji, Chiharu Ludwig, Mike Leng, Gareth The rat suprachiasmatic nucleus: the master clock ticks at 30 Hz |
title | The rat suprachiasmatic nucleus: the master clock ticks at 30 Hz |
title_full | The rat suprachiasmatic nucleus: the master clock ticks at 30 Hz |
title_fullStr | The rat suprachiasmatic nucleus: the master clock ticks at 30 Hz |
title_full_unstemmed | The rat suprachiasmatic nucleus: the master clock ticks at 30 Hz |
title_short | The rat suprachiasmatic nucleus: the master clock ticks at 30 Hz |
title_sort | rat suprachiasmatic nucleus: the master clock ticks at 30 hz |
topic | Neuroscience ‐ cellular/molecular |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929337/ https://www.ncbi.nlm.nih.gov/pubmed/27061101 http://dx.doi.org/10.1113/JP272331 |
work_keys_str_mv | AT tsujitakahiro theratsuprachiasmaticnucleusthemasterclockticksat30hz AT tsujichiharu theratsuprachiasmaticnucleusthemasterclockticksat30hz AT ludwigmike theratsuprachiasmaticnucleusthemasterclockticksat30hz AT lenggareth theratsuprachiasmaticnucleusthemasterclockticksat30hz AT tsujitakahiro ratsuprachiasmaticnucleusthemasterclockticksat30hz AT tsujichiharu ratsuprachiasmaticnucleusthemasterclockticksat30hz AT ludwigmike ratsuprachiasmaticnucleusthemasterclockticksat30hz AT lenggareth ratsuprachiasmaticnucleusthemasterclockticksat30hz |