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Postprandial sleep mechanics in Drosophila
Food consumption is thought to induce sleepiness. However, little is known about how postprandial sleep is regulated. Here, we simultaneously measured sleep and food intake of individual flies and found a transient rise in sleep following meals. Depending on the amount consumed, the effect ranged fr...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119887/ https://www.ncbi.nlm.nih.gov/pubmed/27873574 http://dx.doi.org/10.7554/eLife.19334 |
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author | Murphy, Keith R Deshpande, Sonali A Yurgel, Maria E Quinn, James P Weissbach, Jennifer L Keene, Alex C Dawson-Scully, Ken Huber, Robert Tomchik, Seth M Ja, William W |
author_facet | Murphy, Keith R Deshpande, Sonali A Yurgel, Maria E Quinn, James P Weissbach, Jennifer L Keene, Alex C Dawson-Scully, Ken Huber, Robert Tomchik, Seth M Ja, William W |
author_sort | Murphy, Keith R |
collection | PubMed |
description | Food consumption is thought to induce sleepiness. However, little is known about how postprandial sleep is regulated. Here, we simultaneously measured sleep and food intake of individual flies and found a transient rise in sleep following meals. Depending on the amount consumed, the effect ranged from slightly arousing to strongly sleep inducing. Postprandial sleep was positively correlated with ingested volume, protein, and salt—but not sucrose—revealing meal property-specific regulation. Silencing of leucokinin receptor (Lkr) neurons specifically reduced sleep induced by protein consumption. Thermogenetic stimulation of leucokinin (Lk) neurons decreased whereas Lk downregulation by RNAi increased postprandial sleep, suggestive of an inhibitory connection in the Lk-Lkr circuit. We further identified a subset of non-leucokininergic cells proximal to Lkr neurons that rhythmically increased postprandial sleep when silenced, suggesting that these cells are cyclically gated inhibitory inputs to Lkr neurons. Together, these findings reveal the dynamic nature of postprandial sleep. DOI: http://dx.doi.org/10.7554/eLife.19334.001 |
format | Online Article Text |
id | pubmed-5119887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51198872016-11-28 Postprandial sleep mechanics in Drosophila Murphy, Keith R Deshpande, Sonali A Yurgel, Maria E Quinn, James P Weissbach, Jennifer L Keene, Alex C Dawson-Scully, Ken Huber, Robert Tomchik, Seth M Ja, William W eLife Neuroscience Food consumption is thought to induce sleepiness. However, little is known about how postprandial sleep is regulated. Here, we simultaneously measured sleep and food intake of individual flies and found a transient rise in sleep following meals. Depending on the amount consumed, the effect ranged from slightly arousing to strongly sleep inducing. Postprandial sleep was positively correlated with ingested volume, protein, and salt—but not sucrose—revealing meal property-specific regulation. Silencing of leucokinin receptor (Lkr) neurons specifically reduced sleep induced by protein consumption. Thermogenetic stimulation of leucokinin (Lk) neurons decreased whereas Lk downregulation by RNAi increased postprandial sleep, suggestive of an inhibitory connection in the Lk-Lkr circuit. We further identified a subset of non-leucokininergic cells proximal to Lkr neurons that rhythmically increased postprandial sleep when silenced, suggesting that these cells are cyclically gated inhibitory inputs to Lkr neurons. Together, these findings reveal the dynamic nature of postprandial sleep. DOI: http://dx.doi.org/10.7554/eLife.19334.001 eLife Sciences Publications, Ltd 2016-11-22 /pmc/articles/PMC5119887/ /pubmed/27873574 http://dx.doi.org/10.7554/eLife.19334 Text en © 2016, Murphy et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Murphy, Keith R Deshpande, Sonali A Yurgel, Maria E Quinn, James P Weissbach, Jennifer L Keene, Alex C Dawson-Scully, Ken Huber, Robert Tomchik, Seth M Ja, William W Postprandial sleep mechanics in Drosophila |
title | Postprandial sleep mechanics in Drosophila |
title_full | Postprandial sleep mechanics in Drosophila |
title_fullStr | Postprandial sleep mechanics in Drosophila |
title_full_unstemmed | Postprandial sleep mechanics in Drosophila |
title_short | Postprandial sleep mechanics in Drosophila |
title_sort | postprandial sleep mechanics in drosophila |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119887/ https://www.ncbi.nlm.nih.gov/pubmed/27873574 http://dx.doi.org/10.7554/eLife.19334 |
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