Cargando…
Altered Metabolism During the Dark Period in Drosophila Short Sleep Mutants
Sleep is an almost universally required state in biology. Disrupted sleep has been associated with adverse health risks including metabolic perturbations. Sleep is in part regulated via circadian mechanisms, however, metabolic dysfunction at different times of day arising from sleep disruption is un...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634958/ https://www.ncbi.nlm.nih.gov/pubmed/37961245 http://dx.doi.org/10.1101/2023.10.30.564858 |
_version_ | 1785146266925137920 |
---|---|
author | Malik, Dania M. Sengupta, Arjun Sehgal, Amita Weljie, Aalim M. |
author_facet | Malik, Dania M. Sengupta, Arjun Sehgal, Amita Weljie, Aalim M. |
author_sort | Malik, Dania M. |
collection | PubMed |
description | Sleep is an almost universally required state in biology. Disrupted sleep has been associated with adverse health risks including metabolic perturbations. Sleep is in part regulated via circadian mechanisms, however, metabolic dysfunction at different times of day arising from sleep disruption is unclear. We used targeted liquid chromatography-mass spectrometry to probe metabolic alterations using high-resolution temporal sampling of two Drosophila short sleep mutants, fumin and sleepless, across a circadian day. Discriminant analyses revealed overall distinct metabolic profiles for mutants when compared to a wild type dataset. Altered levels of metabolites involved in nicotinate/nicotinamide, alanine, aspartate, and glutamate, glyoxylate and dicarboxylate metabolism, and the TCA cycle were observed in mutants suggesting increased energetic demands. Furthermore, rhythmicity analyses revealed fewer 24 hr rhythmic metabolites in both mutants. Interestingly, mutants displayed two major peaks in phases while wild type displayed phases that were less concerted. In contrast to 24 hr rhythmic metabolites, an increase in the number of 12 hr rhythmic metabolites was observed in fumin while sleepless displayed a decrease. These results support that decreased sleep alters the overall metabolic profile with short sleep mutants displaying altered metabolite levels associated with a number of pathways in addition to altered neurotransmitter levels. |
format | Online Article Text |
id | pubmed-10634958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-106349582023-11-13 Altered Metabolism During the Dark Period in Drosophila Short Sleep Mutants Malik, Dania M. Sengupta, Arjun Sehgal, Amita Weljie, Aalim M. bioRxiv Article Sleep is an almost universally required state in biology. Disrupted sleep has been associated with adverse health risks including metabolic perturbations. Sleep is in part regulated via circadian mechanisms, however, metabolic dysfunction at different times of day arising from sleep disruption is unclear. We used targeted liquid chromatography-mass spectrometry to probe metabolic alterations using high-resolution temporal sampling of two Drosophila short sleep mutants, fumin and sleepless, across a circadian day. Discriminant analyses revealed overall distinct metabolic profiles for mutants when compared to a wild type dataset. Altered levels of metabolites involved in nicotinate/nicotinamide, alanine, aspartate, and glutamate, glyoxylate and dicarboxylate metabolism, and the TCA cycle were observed in mutants suggesting increased energetic demands. Furthermore, rhythmicity analyses revealed fewer 24 hr rhythmic metabolites in both mutants. Interestingly, mutants displayed two major peaks in phases while wild type displayed phases that were less concerted. In contrast to 24 hr rhythmic metabolites, an increase in the number of 12 hr rhythmic metabolites was observed in fumin while sleepless displayed a decrease. These results support that decreased sleep alters the overall metabolic profile with short sleep mutants displaying altered metabolite levels associated with a number of pathways in addition to altered neurotransmitter levels. Cold Spring Harbor Laboratory 2023-11-02 /pmc/articles/PMC10634958/ /pubmed/37961245 http://dx.doi.org/10.1101/2023.10.30.564858 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Malik, Dania M. Sengupta, Arjun Sehgal, Amita Weljie, Aalim M. Altered Metabolism During the Dark Period in Drosophila Short Sleep Mutants |
title | Altered Metabolism During the Dark Period in Drosophila Short Sleep Mutants |
title_full | Altered Metabolism During the Dark Period in Drosophila Short Sleep Mutants |
title_fullStr | Altered Metabolism During the Dark Period in Drosophila Short Sleep Mutants |
title_full_unstemmed | Altered Metabolism During the Dark Period in Drosophila Short Sleep Mutants |
title_short | Altered Metabolism During the Dark Period in Drosophila Short Sleep Mutants |
title_sort | altered metabolism during the dark period in drosophila short sleep mutants |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634958/ https://www.ncbi.nlm.nih.gov/pubmed/37961245 http://dx.doi.org/10.1101/2023.10.30.564858 |
work_keys_str_mv | AT malikdaniam alteredmetabolismduringthedarkperiodindrosophilashortsleepmutants AT senguptaarjun alteredmetabolismduringthedarkperiodindrosophilashortsleepmutants AT sehgalamita alteredmetabolismduringthedarkperiodindrosophilashortsleepmutants AT weljieaalimm alteredmetabolismduringthedarkperiodindrosophilashortsleepmutants |